Title of Invention	N-SUBSTITUTED HYDROXYPYRIMIDINONE CARBOXAMIDE INHIBITORS OF HIV INTEGRASE
Abstract	N-substituted 5-hydroxypyrimidin-6-one-4-carboxamides of formula: are described as inhibitors of HIV integrase and inhibitors of HIV replication, wherein R<sup>1</sup>, R<sup>2</sup>, R<sup>3</sup> and R<sup>4</sup> are defined herein. These compounds are useful in the prevention and treatment of infection by HIV and in the prevention, delay in the onset, and treatment of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The j compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of preventing, treating or delaying the onset of AIDS and methods of preventing or treating infection by HIV are also described.

Title of Invention

N-SUBSTITUTED HYDROXYPYRIMIDINONE CARBOXAMIDE INHIBITORS OF HIV INTEGRASE

Abstract

N-substituted 5-hydroxypyrimidin-6-one-4-carboxamides of formula: are described as inhibitors of HIV integrase and inhibitors of HIV replication, wherein R1, R2, R3 and R4 are defined herein. These compounds are useful in the prevention and treatment of infection by HIV and in the prevention, delay in the onset, and treatment of AIDS. The compounds are employed against HIV infection and AIDS as compounds per se or in the form of pharmaceutically acceptable salts. The j compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of preventing, treating or delaying the onset of AIDS and methods of preventing or treating infection by HIV are also described.

Full Text	TITLE OF THE INVENTION N-SUBSTITUTED 11YDROXYPYR1MIDINONE CARBOXAMIDE INHIBITORS OF HIV INTEGRASE FIELD OF THE INVENTION The present invention is directed to N-substituted 5-hydroxy-6~oxo-l,6-dihydropyrimidinc-4-carboxamides and pharmaceutically acceptable salts thereof, their synthesis, and their use as inhibitors of the HIV intcgrase enzyme. The compounds and pharmaceutically acceptable salts thereof of the present invention are useful for preventing or treating infection by HIV and for treating or delaying the onset of AIDS. BACKGROUND OF THE INVENTION A retrovirus designated human immunodeficiency virus (HIV) is the etiological agent of the complex disease that includes progressive destruction of the immune system (acquired immune deficiency syndrome; AIDS) and degeneration of the central and peripheral nervous system. This virus was previously known as LAV. HTLV-II1, or ARV. A common feature of retrovirus replication is the insertion by virally-encoded integrase of proviral DNA into the host cell genome, a required step in HIV replication in human T-lymphoid and monocytoid cells. Integration is believed to be mediated by integrase in three steps: assembly of a stable nucleoprotein complex with viral DNA sequences; cleavage of two nucleotides from the 3' termini of the linear proviral DNA; covalent joining of the recessed 3* OH termini of the proviral DNA at a staggered cut made at the host target site. The fourth step in the process, repair synthesis of the resultant gap, may be accomplished by cellular enzymes. Nucleotide sequencing of HIV shows the presence of a pol gene in one open reading frame [Ratner, L. et al., Nature, 313, 277(1985)]. Amino acid sequence homology provides evidence that the pol sequence encodes reverse transcriptase, integrase and an HIV protease [Toh, H. et al., EMBO J. 4, 1267 (1985); Power, M.D. et al.. Science, 231, 1567 (1986); Pearl, L.H. et al.. Nature, 329. 351 (1987)]. All three enzymes have been shown to be essential for the replication of HIV. It is known that some antiviral compounds which act as inhibitors of HIV replication are effective agents in the treatment of AIDS and similar diseases, including reverse transcriptase inhibitors such as azidothymidine (AZT) and efavirenz and protease inhibitors such as indinavir and nelftnavir. The compounds of this invention are inhibitors of HIV integrase and inhibitors of HIV replication. The inhibition of integrase in vitro and HIV replication in cells is a direct result of inhibiting the strand transfer reaction catalyzed by the recombinant integrase in vitro in HIV infected cells. The particular advantage of the present invention is highly specific inhibition of HIV integrase and HIV replication. SUMMARY OF Till- INVENTION The present invention is directed to novel hydroxypyrimidinone carboxamides. These compounds are useful in the inhibition of HIV integrase, the prevention of infection by HIV. the treatment of infection by HIV and in the prevention, treatment, and delay in the onset of AIDS and/or ARC, either as compounds or their pharmaceutical^ acceptable salts or hydrates (when appropriate), or as pharmaceutical composition ingredients, whether or not in combination with other HIV/AIDS antivirals, anti-infectives, immunomodulators, antibiotics or vaccines. More particularly, the present invention includes a compound of Formula (1): wherein Rl is (1) -H. (2) -C1 _6 alkyl, which is optionally substituted with one or more subsliluents (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH, -CN, -0-C1-6 alkyl, -O-C1-6 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(-0)Ra, -N(RaRb), -C(=0)-C()-6 alkyl-N(RaRb), N(Ra)-C(0)-C()-6 alkyl-N(RbRc), -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), -N(Ra)-C(=0)Rb, N(R2)C(==0)C(=O)N(RaRb), (3) -Rk (4) -C1_6 alkyl-Rk, wherein: (i) the alkyl is optionally substituted with one or more substituents(e.g., optionally from 1 to 6, or 1 to 5, or I to 4, or 1 to 3. or I or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH, -CN, -O-C1-6 alkyl, -O-C1-6 haloalkyl, -N(RaRb), -N(Ra)C02Rb, -N(Ra)C(--=0)-Co-6 alkyl-N(RbRC), 0r -N(Ra)-C2-6 alkyl-OH with the proviso that the -OH is not attached to the carbon alpha to N(Ra); and (ii) the alkyl is optionally mono-substituted with -Rs, -C1_6 alkyi-Rs, -N(Ra)-C(=0)-C()-6 alkyl-Rs, -N(Ra)-Co-6 alkyl-Rs, -O-Co-6 alkyl-Rs, or -N(Ra)-C(=O)-C0-6 alkyl-RS; wherein Rs is (a) aryl which is optionally substituted with one or more substituents (e.g., optionally from 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH, -C1-6 alkyl, -C1-6 alkyl-ORa -C1-6 haloalkyl, -O-C1-6 alkyl, -O-C1-6 haloalkyl, melhylenedioxy attached to two adjacent carbon atoms, or aryl; (b) a 4- to 8- membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; wherein the saturated heterocyclic ring is optionally substituted with one or more substituents (e.g., optionally from I to 6, or 1 to x or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -C1-6 alkyl, -C1-6 alkyl-ORa, -C1-6 haloalkyl, -O-C1-6 alkyl, -0-C\|_6 haloalkyl, -C(=0)Ra, -CX)2Ra, -C(=0)-Co-6 alkyl-N(RaRb), -S02Ra, oxo. aryl. or - (c) a 5- to 7-membercd heteroaromatic ring containing from 1 to 4 hetcroatoms independently selected from N, O and S; wherein the heteroaromatic ring is optionally substituted with one or more substituents (e.g.. optionally 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -C 1 -6 alkyl, -C 1 -6 alkyl-ORa, -C i -6 haloalkyl, -O-C \| -6 alkyl, -O-C1-6 haloalkyl, oxo, or aryl; (5) -Co-6 alkyl-O-Co-6 alkyl-Rk (6) -Co-6 alkyl-S(O)irC0-6 alkyl-Rk (7) -0-C1-6alkyl-ORk, (8) -O-C 1-6 alkyl-O-C1-6 alkyl-Rk, (9) -0-C1-6alkyl-S(0)nRk, (10) -Co-6 alkyl-N(Ra).Rk, (11) -Co-6 alkyl-N(Ra)-C1-6 alkyl-Rk, (12) -Co-6 alkyl-N(Ra)-C 1-6 alkyl-ORk, (13) -Co-6 alkyl-C(-0-Rk (14) -Co-6 alkyl-C(=O)N(Ra)-C0-6 alkyl-Rk (15) -Co-6 alkyl-N(Ra)C(=0)-Co-6 alkyl-Rk, (16) -Co-6 alkyl-N(Ra)C(=0)-0-Co-6 aikyl-Rk, or (17) -Co-6 alkyl-N(Ra)C(=0)C(=0)Rk; R2 is -C1-6 alkyl which is optionally substituted with one or more substituents (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently (1) halogen, (2) -Oil, (3) -CN, (4) -O-C 1-6 alkyl, (5) -O-C 1-6 haloalkyl, (6) -C(=0)Ra, (7) -CO?.Ra (8) -SRa, (9) -S(==0)Ra, (10) -N(RaRb). (11) -C( O)N(RaRb), (12) -N(Ra)-C(-0)-C1-6 alkyl-N(RbRc), (13) -SG>2Ra, (14) -N(Ra)S02Rb, (15) -S02N(RaRb), (16) -N(Ra)-C(Rb)-(), (17) -C3-8 cycloalkyl, (18) aryl, wherein the aryl is optionally substituted with one or more substituents (e.g., optionally from 1 to 5. or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -C1-6 alkyl, -C1-6 haloalkyl, -0-C1_6 alkyl, -O-C1-6 haloalkyl, -Co-6 alkyl-N(RaRb), or -C1-6 alkyl substituted with a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; wherein the saturated heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -Ci-6 alkyl, oxo, or a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; or (19) a 5- to 8-membcred monocyclic helerocycle which is saturated or unsaturated and contains from 1 to 4 heteroatoms independently selected from N, O and S; wherein the helerocycle is optionally substituted with one or more substituents (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently -Ci-6 alkyl, -0-C1-6 alkyl, oxo, phenyl, or naphthyl; R3 is-H or-CI-6 alkyl; R4 is (1) H, (2) C1-6 alky! which is optionally substituted with one or more substituents (e.g., optionally from 1 to 6. or 1 to 5, or 1 to 4. or 1 to 3. or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH, 0-C1_6 alky I, -O-C1-6 haloalkyl, -NO2, -N(RaRb), -C(=0)Ra, -C()2Ra. -SRa, -S(=0)Ra, -S02Ra, or «N(Ra)C02Rb, (3) C1_6 alkyl which is optionally substituted with one or more substituents (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH. or O-C1-4 alkyl, and which is substituted with 1 or 2 substituents each of which is independently: (i) C3-8 cycloalkyl, (ii) aryl, (iii) a fused bicyclic carbocycle consisting of a benzene ring fused to a C5-7 cycloalkyl, (iv) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, (v) a 5- or 6-membered hcteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, or (vi) a 9- or 10-membered fused bicyclic heterocycle containing from 1 to 4 heteroatoms independently selected from N. O and S, wherein at least one of the rings is aromatic, (4) C2-5 alkynyi optionally substituted with aryl, (5) C3-8 cycloalkyl optionally substituted with aryl, (6) aryl, (7) a fused bicyclic carbocycle consisting of a benzene ring fused to a 05.7 cycloalkyl, (8) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, (9) a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, or (10) a 9- or 10-mcmbcred fused bicyclic heterocycle containing from 1 to 4 heteroatoms independently selected from N, O and S, wherein at least one of the rings is aromatic; wherein each aryl in (3)(ii) or the aryl (4), (5) or (6) or each fused carbocycle in (3)(iii) or the fused carbocycle in (7) is optionally substituted with one or more substiluents (e.g., optionally from 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 subslituents; or is optionally mono-subslituted) each of which is independently halogen, -OH, -C1-6 alkyl, -C1-6 alkyl-ORa, -Cj-6 haloalkyl, -0-C\|_6 alkyl, -O-C 1-6 haloalkyl, -CN, -N02, -N(RaRb), -C1_6 alkyi-N(RaRb). -C(=0)N(RaRb), -C(" 0)Ra. -C02Ra, -C1-6 aIky!-C02Ra, -OC02Ra, -SRa, -S(0)Ra, -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), -N(Ra)C(=0)Rb, -N(Ra)C02Rb, ~Cl-6 alkyl-N(Ra)C02Rb, aryl, -C1-6 alkyl-aryl, -O-aryl, or -Co-6 alkyl-het wherein het is a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, and het is optionally fused with a benzene ring, and is optionally substituted with one or more substiluents (e.g., optionally from I to 5, or 1 to 4, or 1 to 3, or 1 or 2 subslituents; or is optionally mono-substituted) each of which is independently -C)_6 alkyl, -C1-6 haloalkyl, -O-C1-6 alkyl, -O-C1-6 haloalkyl, oxo, or -CCbRa: each saturated heterocyclic ring in (3)(iv) or the saturated heterocyclic ring in (8) is optionally substituted with one or more subslituents (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substiluents; or is optionally mono-substituted) each of which is independently halogen, -C]_6 alkyl, -C1-6 haloalkyl, -0-C1_6 alkyl, -O-C \| -6 haloalkyl, oxo, aryl, or a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; and each heteroaromatic ring in (3)(v) or the heteroaromatic ring in (9) OY each fused bicyclic heterocycle in (3)(vi) or the fused bicyclic heterocycle in (10) is optionally substituted with one or more substiluents (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substiluents; or is optionally mono-substituted) each of which is independently halogen, -C\|-6 alkyl, -C]-6 haloalkyl, -O-C1-6 alkyl, -O-C1-6 haloalkyl, oxo, aryl, or-C1-6alkyl-aryl; or alternatively R3 and R4 together with the N to which both are attached form a C3-7 a/aeycloalkyl which is optionally substituted with one or more substituentsXe.g., optionally from 1 to 6, or I to 5, or 1 to 4, or 1 to 3, or I or 2 substituents; or is optionally mono-substituted) each of which is independently -Ci-6 alkyl or oxo; each Ra, Rb, RC? and Rd is independently -H or -C ] -6 alkyl; Rk is carbocycle or hcterocycle, wherein the carbocycle or heterocycle is optionally substituted with one or more substituents (e.g., optionally from I to 7, or 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or I or 2 substituents; or is optionally mono-substituted) each of which is independently (1) halogen, (2) -OIL (3) -CN, (4) -CI -6 alkyl, which is optionally substituted with one or more substituents (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH, -CN, -O-Ci-6 alkyl, -O-C1-6 haloalkyl, -C(0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb)!_C(-O)-(CH?)0-2N(RaRb), N(Ra)_c(=O)-(CH2)0-2N(RbRc), -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=0, (5) -O-C1 _6 alkyl, which is optionally substituted with one or more substituents (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or I or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH, -CN, -O-Cj-6 alkyl, -O-C16 haloalkyl, -C(K))Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb),_C(=O)-(CH2)0-2N(RaRb), N(Ra)-C(-O)-(CH2)0-2N(RbRC), -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb> =o, (6) -NO2, (7) oxo, (8) -C(K))Ra. (9) -C02Ka, (10) -SRa, (11) -S(0)Ra. (12) -N(RaRb), (13) -C(==())N(RaRb), (14) -C(-0)-C 1 -6 alkyl-N(RaRb), (15) -N(R>i)C( 0)Rb, (16) -S02Ra, (17) -S02N(RaRb), (18) -N(Ra)S02Rb, (19) -Rin, (20) -C\|_6 alkyl-Rni, wherein the alkyl is optionally substituted with one or more substituenls (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH, -CN, -C\|-6 haloalkyl, -O-Ci-6 alkyl. -O-Cj-6 haloalkyl, -C(=0)Ra, -C02Ra, -SRa -S(=0)Ra, -N(RaRb), -N(Ra)C02Rb, -S02R3, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=0, (21) -Co-6 alkyl-N(Ra)-Co-6 alkyl-Rm, (22) -Co-(, alkyl-O-Co-6 alkyl-Rm, (23) -Co-6 alkyl-S-Co-6 alkyl-Rm, (24) -Co-6 alkyl-C( (25) -C(- O)-O-C'0-6 alkyl-Rm, (26) -C("0)N(Ra)-Co-6 alkyl-Rm, (27) -N(Ra)C(0)-Rm, (28) -N(R»)C( 0)-C1_6 alkyl-Rm, wherein the alkyl is optionally substituted with one or more substituenls (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH, -CN, -C\|-6 haloalkyl, -O-Ci-6 alkyl, -O-C'i-6 haloalkyl, -C(=0)Ra. -CC)2Ra, -SRa, -S(=0)Ra, -N(RaRb), -N(Ra)C02Rb. -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(R«)-C(Rb)=0, (29) -N(Ra)-C(-O)-N(Rb)-C0-6 alkyl-Rm. (30) -N(Ra)-C(-0)-0-Co-6 alkyl-Rm, (31) -N(Ra)-C( -0)-N(Rb)-S02-Co-6 alkyl-R™, (32) -C(-0)-C(--0)-N(RaRb), (33) -C(-())-Ci_6 aIkyl-S02Ra, or (34) -C(-0)-C(-0)Rm; carbocycle in Rk is (i) a C3 to C8 monocyclic, saturated or unsaturated ring, (ii) a C7 to C]2 bicyclic ring system, or (iii) a C11to C16 tricyclic ring system, wherein each ring in (ii) or (iii) is independent of or fused to the other ring or rings and each ring is saturated or unsaturated; heterocycle in Rk is (i) a 4- to 8-membered, saturated or unsaturated monocyclic ring, (ii) a 7- to 12-membercd bicyclic ring system, or (iii) an 11 to 16-membered tricyclic ring system; wherein each ring in (ii) or (iii) is independent of or fused to the other ring or rings and each ring is saturated or unsaturated; the monocyclic ring, bicyclic ring system, or tricyclic ring system contains from 1 to 6 heteroatoms selected from N, O and S and a balance of carbon atoms; and wherein any one or more of the nitrogen and sulfur heteroatoms is optionally be oxidized, and any one or more of the nitrogen heteroatoms is optionally quatcrnized; each Rm is independently C3-.8 cycloalkyl; aryl; a 5- to 8-membered monocyclic heterocycle which is saturated or unsaturated and contains from 1 to 4 heteroatoms independently selected from N, O and S; or a 9- to 10-membcred bicyclic heterocycle which is saturated or unsaturated and contains from I to 4 heteroatoms independently selected from N, O and S; wherein any one or more of the nitrogen and sulfur heteroatoms in the heterocycle or bicyclic heterocycle is optionally oxidized and any one or more of the nitrogen heteroatoms is optionally quaternized; and wherein the cycloalkyl or the aryl defined in Rm is optionally substituted with one or more substituents (e.g., optionally from 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -C[_6 alkyl optionally substituted with -0-C]_4 alkyl, -C1-6 haloalkyl, -0-C\|-6 alkyl, -O-C1-6 haloalkyl. -N(RaRb), aryl, or -C1-6 alkyl-aryl; and the monocyclic or bicyclic heterocycle defined in Rm is optionally substituted with one or more substitucnts (e.g., optionally from I to 6, or 1 to 5, or 1 to 4, or I to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -C\.(> alkyl, -Ci-6 haloalkyl, -O-Cj-6 alkyl, -O-Ci-6 haloalkyl, oxo, aryl, -C\|_6 alkyl-aryl, -C(0)-aryl, -C02-aryl, -C02-C1_6 alkyl-aryl, a 5- or 6-membered saturated heterocyclic ring containing from I to 4 heteroatoms independently selected from N, O and S, or a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; and each n is independently an integer equal to zero, 1 or 2; or a pharmaceutical iy acceptable salt thereof. The present invention also includes pharmaceutical compositions containing a compound of the present invention and methods of preparing such pharmaceutical compositions. The present invention further includes methods of treating AIDS, methods of delaying the onset of AIDS, methods of preventing AIDS, methods of preventing infection by HIV, and methods of treating infection by HIV. Other embodiments, aspects and features of the present invention are either further described in or will be apparent from the ensuing description, examples and appended claims. DETAILED DESCRIPTION OF THE INVENTION The present invention includes the N-substituted hydroxypyrimidinone carboxamides of Formula (I) above. These compounds and pharmaceutically acceptable salts thereof are HIV integrase inhibitors. An embodiment of the present invention is a compound of Formula (I) exactly as defined above, except that in the definition of Rk, Rk js optionally substituted with one or more substitucnts each of which is independently one of the substituents (1) to (18), and is optionally mono-substituted with one of the substituents (19) to (34). Another embodiment of the present invention is a compound of Formula (I) as orieinallv defined above, exceot that the definition of R2 includes a proviso that none of the following optional substituents is attached to the carbon atom in the -C1-6 alkyl group that is attached to the ring nitrogen: halogen, -OHv-0-C1-6 alkyl, -O-C1-6 haloalkyl. -SRa, -S(=0)Ra or -N(Ra)-C(Rb) O. Stated another way, none of these substituents is attached to the carbon atom alpha to the ring nitrogen. Another embodiment of the present invention is a compound of Formula (I) as originally defined above except that in the definition of Rj, Rl is one of substitutcnts (1) to (16) and in the definition of Rk, Rk is optionally substituted with one or more substituents (e.g., optionally from 1 to 7, or 1 to 6, or 1 to 5, or 1 to 4, or I to 3, or 1 to 2 substituents, or is optionally monosubstituted) each of which is independently one of substitutcnts (1) to (31). Another embodiment of the present invention is a compound of Formula (I), wherein Rl is: (1) -H, (2) -C1_6 alkyl, which is optionally substituted with one or more substituents each of which is independently halogen, -OH, -CN, -O-C1-6 alkyl, -0-C[-6 haloalkyl, -C(-0)Ra, -C02Ra, -SRa, -S(==0)Ra, -N(RaRb), -C(=O)-(CH2)0-3-N(RaRb), N(Ra)-C( O)-(CH2)0-3-N(RbRC),-S02Ra,-N(Ra)S02Rb, -S02N(RaRb), -N(Ra)-C(0)Rb, FT or -N(R2)C(==0)C(=0)N(RaRb), (3) -Rk (4) -(CH2)l-3-Rk. wherein: (i) the -(Cll2)l-3- moiety is optionally substituted with one or more substituents each of which is independently halogen, -OH, -CN, -O-C1-6 alkyi, -0-C)-6 haloalkyl, -N(RaRb), -N(R'>)C02Rb, -N(Ra)C(=O)-(CH2)0-3-N(RbRC), or -N(Ra)-(('H2)2-3-OH with the proviso that the -OH is not attached to the carbon alpha to N(Ra); and (ii) the -(Cll2)l-3- moiety is optionally mono-substituted with -Rs, -C1-6 alkyl-R-s, -N(Ra)-C(=O)-(CH2)0-3-Rs, -N(Ra)-(CH2)0-3-Rs, -0-(C! l2)0-3-Rs, or -N(Ra)-C(-O)-(CH2)0-3-Rs; wherein RS is (a) aryl which is optionally substituted with one or more substituents each of which is independently halogen, -OH, -C \| _6 alkyl, -C1-6 alkyl-ORa, -C 1_6 haloalkyl, -C1-6 alkyl, -O-C1-6 haloalkyl, methylenedioxy attached to two adjacent carbon atoms, or aryl; (b) a 4- to 8- membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; wherein the saturated heterocyclic ring is optionally substituted with one or more substituents each of which is independently halogen, -C1-6 alkyl, -C1_6 alkyl-ORa, -C\|-6 haloalkyl, -O-C1-6 alkyl, -O-Ci-6 haloalkyl, -C(-=0)Ra -C02Ra- -C(=O)-(CH2)0-3-N(RaRb). -S02Ra, oxo, aryl, or -(Cll2)l-3-aryl;or (c) a 5- to 7-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; wherein the heteroaromatic ring is optionally substituted with one or more substituents each of which is independently halogen, -C\|-6 alkyl, -C1-6 alkyl-ORa, -Cj-6 haloalkyl, -O-C1-6 alkyl, -O-C1-6 haloalkyl, oxo, or aryl; (5) -(CH2)0-3-O-(CH2)0-3-Rk, (6) -(CH2)0-3-S(O)n-(CH2)0-3-Rk, (7) -(CH2)l-3-ORk, (8) -(CH2)l-3-0-(CH2)l-3-Rk, (9) -0-(Cll2)l-3-S(0)nRk (10) -(CH2)0-3-N(Ra)-Rk (11) -(CH2)0-3-N(Ra)-(CH2)l-3-Rk, (12) -(Cll2)0-3-N(Ra)-(CH2)l-3-ORk, (13) -(CH2)0-3-C(=-O)-Rk (14) -(CH2)0-3-C(=O)N(Ra)-(CH2)0-3-Rk, (15) -(CH2)0-3-N(Ra)C(=O)-(CH2)0-3-Rk. (16) -(Cll2)0-3-N(Ra)C(=O)-O-(CH2)0-3-Rk- (17) -C(CI-l3)2N(Ra)C(=0)Rb, (18) -C(Cll3)2N(Ra)C(=0)Rk, or (19) -C(CI-l3)2N(Ra)C(=0)C(=0)N(RbRc); and all other variables are as originally defined above; or a pharmaeeutically acceptable salt thereof. In an aspect of this embodiment, R' is one of groups (1) to (16). Another embodiment of the present invention is a compound of Formula (I), wherein Rl is: (1) -H, (2) -C1-4 alkyl, which is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -OH, -CN, -O-C1-4 alkyl, -O-C1-4 haloalkyl, -C(=0)Ra, -CC>2Ra, -SRa. -S(=0)Ra, -N(RaRb), -C(=O)-C0-4 alkyl-N(RaRb), N(Ra)-C(==0)-Co-4 alkyl-N(RbRC), -S02R3, -N(Ra)S02Rb, s -S02N(RaRb), -N(Ra)-C(=0)Rb, -N(R2)C(0)C( O)N(RaRb), (3) -Rk, (4) -C1-4 alkyl-Rk, wherein: (i) the alkyl is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -OH, -CN, -O-Ci-4 alkyl, -O-C1-4 haloalkyl, -N(RaRb), -N(Ra)C02Rb, -N(Ra)C(=0)-Co-4 alkyl-N(RbRC), or -N(Ra)-(CH2)2-4-OH; and (ii) the alkyl is optionally mono-substituted with -Rs, -N(Ra)-C(-0)-Co-4 alkyl-Rs, -N(Ra)-Co-4 alkyi-Rs, -O-Co-4 alkyl-Rs. or -N(Ra)-C(-O)«C0-4 alkyl-RS; wherein Rs is (a) aryl which is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -OH, -C\|-4 alkyl, -C1-4 alkyl-ORa, -C1.4 haloalkyl, -0-C1-4 alkyl, -O-C1-4 haloalkyl. methylenedioxy attached to two adjacent carbon atoms, or phenyl; (b) a 5- or 6-membercd heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; wherein the heteroaromatic ring is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C\|-4 alkyl, -C1-4 alkyl-ORp, -C1-4 haloalkyl, -O-C1-4 alkyl, -O-C1-4 haloalkyl, oxo, or phenyl; or (c) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 hetcroatoms independently selected from N, O and S; wherein the saturated heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C1-4 alkyl, -C1-4 alkyl-ORa, -C1-4 haloalkyl, -O-CM alkyl, -O-CM haloalkyl, -C(0)Ra, -C()2Ra, -C(=0)-Co-4 alkyl-N(RaRb), -S02Ra, oxo, or phenyl, (5) -(CH2)0-3-C(O)N(Ra)-(CH2)0-3-Rk- (6) -C(C1_4 alkyl)2N(Ra)C(=0)Rb, (7) -C(C 1-4 alkyI)2N(Ra)C(=0)Rk, or (8) -C(Cl-4alkyl)2N(Ra)C(=0)C(-0)N(RbRc); and all other variables arc as originally defined above; or a pharmaceuticallyacceptable salt thereof. In an aspect of this embodiment, Rl is one of groups (1) to (5). Another embodiment of the present invention is a compound of Formula (I), wherein Rl is: (1) -H, (2) -CI -4 alkyl, which is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -O-C1-4 alkyl, -O-C1-4 haloalkyl, -C(0)Ra, -C02Ra, -N(RaRb), 0r -C(=O)-(CH2)0-2-N(RaRb), (3) -Rk, (4) -(Cll2)l-4-Rk, wherein: (i) the -(CH2)l-4- moiety is optionally substituted with 1 or 2 substituents each of which is independently halogen, -OH, -O-C1-4 alkyl, -O-C1-4 haloalkyl, or -N(RaRb); and (ii) the -(CIl2)l-4- moiety is optionally mono-substituted with -Rs or -N(Ra)-(CH2)l-2-Rs; wherein Rs is (a) phenyl which is optionally substituted with from 1 to 3 substituents each of which is independently halQgen, -C1-4 alkyl, -C1.4 alkyl-ORa, -C1-4 haloalkyl, -O-C1-4 alky!, or -O-C1-4 haloalkyl; or (b) a 5- or 6-mcmbered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; wherein the heteroaromatic ring is optionally substituted with from 1 to 3 substituents each of which is independently halogen. -C\|_4 alkyl, -C14 alkyl-ORa, -C1-4 haloalkyl, -0-C1_4 alkyl, or -0-C1-4 haloalkyl; or (c) a 5- or 6-mcmbered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; wherein the saturated heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C1_4 alkyl, -C]_4 alkyI-ORa, -C\|-4 haloalkyl, -O-C1-4 alkyl, -O-CM haloalkyl, -C(=0)Ra or -C02Ra, (5) -C(=O)N(Ra)-(CH2)0-3-Rk(6) -C(CH3)2N(Ra)C(=0)Rb (7) -C(CH3)2N(Ra)C(=0)Rk (8) -C(CI-l3)2N(Ra)C(=0)C(K))N(RbRc); and all other variables arc as originally defined above; or a pharmaceutically acceptable salt thereof. In an aspect of this embodiment, Rl is one of groups (1) to (5). Another embodiment of the present invention is a compound of Formula (I), wherein Rk is C3-8 cycloalkyi; aryl selected from phenyl and naphthyl; a bicyclic carbocycle selected from indanyl and telrahydronaphthyl; a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N. O and S; or a bicyclic heterocyclc which is a benzene ring fused to a 5- or 6-membered saturated or unsaturated heterocyclic ring containing from I to 3 heteroatoms independently selected from N, O and S; wherein the cycloalkyl, aryl, bicyclic carbocycle, saturated heterocyclic ring, hcteroaromatic ring, or bicyclic heterocycle is optionally substituted with from 1 to 4 substituents each of which is independently (1) halogen, (2) -OH, (3) -CN, (4) -CM haloalkyl, (5) -C1-4 alkyl, which is optionally substituted with from 1 to 3 substituents each of which is independently -01 f, -CN, -O-C1-4 alkyl, -0-C\|-4 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra -N(RaRb), -C(=O)-(CH2)0-2N(RaRb), N(Ra)-C(=0)-(Cl l2)0-2N(RbRc),-S02Ra, -N(Ra)S02Rb, -S02N(RaRb), 0r -N(Ra)-C(Rb)=C), (6) -O-C1 -4 haloalkyl (7) -O-C 1-4 alkyl, which is optionally substituted with from 1 to 3 substituents each of which is independently -OH, -CN, -O-C1_6 alkyl, -0-C1-6 haloalkyl, -C(K))Ra, -C02R3, -SRa -S(=0)Ra, -N(RaRb), -C(=O)-(CH2)0-2N(RaRb), N(Ra)-C(=O)-(CH2)0-2N(RbRc),-S02R3, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=0, (8) -N02, (9) oxo, (10) -C(0)Ra, (11) -C02Ra, (12) -SRa, (13) -S(-0)Ra. (14) -N(RaRb), (15) -C(=0)N(RaRb), (16) -C(=0)-C1-6 alkyl-N(RaRb), (17) -N(Ra)C(=0)Rb, (18) -S02Ra, (18) -S02N(RaRb), (19) -N(Ra)S02Rb, (20) -Rm, (21) -C i .4 alkyl-Rm, (22) -(CH2)0-2-N(Ra)-(CH2)0-2-F^ (23) -(CH2)0-2-O-(CH2)0-2-Rm, (24) -(CMl2)()-2-S-(CH2)0-2-Rm, (25) -(CI l2)0-2-C(==O)-(CH2)0-2-Rm, (26) -C(-O)-O-(CH2)0-2-Rm, (27) -C(-0)N(Ra)-Rmj 0r (28) -C(-0)-C(=0)N(RaRb); and all other variables are as originally defined above; or a pharmaceutically acceptable salt thereof. In an aspect of this embodiment, the eycloalkyl, aryl, bicyclic carbocycle, saturated heterocyclic ring, heteroaromatic ring, or bicyclic heterocycle is optionally substituted with from I to 4 substituents each of which is independently selected from the groups (1) to (27). In an aspect of this embodiment, Rk (i.e., the eycloalkyl, aryl, bicyclic carbocycle, saturated heterocyclic ring, heteroaromatic ring, or bicyclic heterocycle) is optionally substituted with from 1 to 4 substituents each of which is independently one of the substituents (1) to (19), and is optionally mono-substituted with one of the substituents (20) to (28). In a feature of this aspect, Rk js optionally substituted with from 1 to 4 substituents each of which is independently one of the substituents (1) to (19). and is mono-substituted with one of the substituents (20) to (28). In another aspect of this embodiment, each Rm is independently C3-7 eycloalkyl; aryl selected from phenyl and naphthyl; a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; a 5- or 6-membcred heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, wherein any N is optionally oxidized to form an N-oxide; or a bicyclic heterocycle which is a benzene ring fused to a 5- or 6-membered, saturated or unsaturated heterocyclic ring containing from I to 3 -heteroatoms selected from N, O and S; wherein the cycloalkyl or the aryl defined in Rm is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -C\|_4 alkyl, -CM haloalkyl, -()-C\|-4 alkyl, -0-C\|-4 haloalkyl, -N(RaRb), phenyl, or -(CH2)l-2-p'ienyl; the saturated heterocyclic ring defined in Rm is optionally substituted with from 1 to 4 substituents each of which is independently -C]-4 alkyl optionally substituted with -0-C1_4 alkyl, -C]_4 haloalkyl, -O-Ci-4 alkyl, -0-C1_4 haloalkyl, oxo, phenyl, -(CI 12) 1 -2~phcnyU -C(=0)-phenyl, -C02-phenyI, -C09-(Cll2)l-2-phenyK a 5- or 6-membered saturated heterocyclic ring containing from I to 4 heteroatoms independently selected from N, O and S, or a 5- or 6-mcmbered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; and the heteroaromatic ring or the bicyclic heterocycle defined in Rm is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -C1-4 alkyl, -C1-4 haloalkyl, -O-C1-4 alkyl, -0-Ci_4 haloalkyl, oxo, phenyl, or -(CH2)]-2-phenyl. Another embodiment of the present invention is a compound of Formula (I), wherein Rk is phenyl; a 5- or 6-membered saturated heterocyclic ring containing 1 or 2 heteroatoms selected from 1 or 2 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; a 5- or 6-membered heteroaromatic ring containing 1 or 2 heteroatoms selected from 1 or 2 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; or a bicyclic heterocycle which is a benzene ring fused to a 5- or 6-membered saturated heterocyclic ring containing 1 or 2 nitrogen atoms; and all other variables are as originally defined; or a pharmaceutically acceptable salt thereof. In an aspect of this embodiment, (a) the phenyl, the saturated heterocyclic ring, heteroaromatic ring, or bicyclic heterocycle is optionally substituted with from I to 3 substituents each of which is independently (1) -- fiuoro. (2) chloro, (3) bromo, (4) -OH (5) -Cl-3, (6) -C1-4 alkyl, which is optionally substituted with 1 or 2 substituents each of which is independently -OH, -CN, -O-Ci-4 alkyl, -OCF3, -N(RaRb), -C(-0)N(RaRb), or N(Ra)-C(=O)-(CH2)0-2N(RbRC), (7) -OCF3, (8) -O-C 1.4 alkyl (9) -CCO)Ra, (10) -C02Ra, (11) -SRa, (12) -SRa, (13) -N(RaRb), (14) -C(-=0)N(RaRb), (15) -C(=0)-(CH2) 1 -2-N(RaRb), (16) -N(Ra)C(=0)Rb, or (17) -S02Ra; (b) the phenyl is optionally mono-substituted with (1) -(CH2)l-2-Rm,or (2) -(CH2)0-2-N(Ra).(CH2)0-2-Rm: and (c) the saturated heterocyclic ring, hetcroaromatic ring, or bicyclic hcterocycle is optionally mono- or di-substituted with (1) oxo (2) -(CH2)l-2-Rm, (3) -0-(CH2)l-2-Rm,or (4) -(CH2)()-\|-C(=O)-(CH2)0-2-Rm- In a feature of the preceding aspect, each Rni is independently cyclopropyl; phenyl; a 5- or 6-membered saturated heterocyclic ring selected from pyrrolidinyl, imidazolidinyl, pyrazolidinyl, piperidinyl, pipcrazinyl. and morpholinyl; or a 5- or 6-membered hetcroaromatic ring selected from thicnyl, pyridyl optionally in the form of an N-oxide, imidazolyl, pyrrolyl, pyrazolyl, thiazolyl, isothiazolyl, oxazolyl, isooxazolyl, oxadiazolyl, thiadiazolyl, pyrazinyl, pyrimidinyl, triazolyl, tetrazolyl, furanyl, and pyridazinyl; wherein the cyclopropyl is unsubstituted; the phenyl is optionally substituted with from i to 3 substituents each of which is independently halogen, -Ci_4 alkyl, -CF3, -0-C1-4 alkyl, -OCF3, or-N(RaRb); the saturated heterocyclic ring is optionally substituted with 1 or 2 subslituents each of which is independently -C1-4 alkyl, -CF3, -0-C]-4 alkyl, -OCF3, oxo, phenyl, -(CH2)l-2-phenyI, -C(= 0)-phcnyl, -C02-phenyl, or -C02-CH2-phenyl; and the heteroaromatic ring is optionally substituted with 1 or 2 substituents each of which is independently -C1.4 alkyl, -CF3, -0-C]-4 alkyl, -OCF3, oxo, phenyl, or -(CH2)l-2~phenyl. Another embodiment of the present invention is a compound of Formula (I), wherein R.2 is: (1) -C1-6 alkyl, (2) -C1 _6 alkyl substituted with -N(RaRb), (3) -C1 _(i alkyl substituted with phenyl, wherein the phenyl is: (a) optionally substituted with from 1 to 4 substituents each of which is independently halogen, -C1-4 alkyl, -C]_4 haloalkyl. -O-C1--4 alkyl, -0-C1_4 haloalkyl, or -C0-4 alkyl-N(RaRb); and (b) optionally mono-substituted with -C1-4 alkyl substituted with a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms selected from 1 or 2 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -C]-6 alkyl, oxo, or a 5- or 6-mcmbercd heteroaromatic ring containing from I to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atom, and 0 or 1 S atom; or (4) -C1 -6 alkyl optionally substituted with -OH and substituted with a 5- or 6-membered saturated monocyclic heterocycle which contains from 1 to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heterocycle is optionally substituted with from 1 to 4 substituents each of which is independently -Cl-6 alkyl, -O-C 1 -6 alkyl, oxo, or phenyl; or (5) -C 1-6 alkyl substituted with a 5- or 6-membered heteroaromatic ring which contains from 1 to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heteroaromatic ring is optionally substituted with from 1 to 4 substituents each of which is independently -Cl-6 alkyl, -0-C]_6 alkyl, oxo, or phenyl; and all other variables are as originally defined above; or a pharmaceutical ly acceptable salt thereof. Another embodiment of the present invention is a compound of Formula (I) exactly as defined in the immediately preceding embodiment, except that when R2 is -C1-6 alkyl substituted with -N(RaRb) it js with the proviso that -N(RaRb) js not attached to the carbon atom in the -C \| _6 alkyl group that is attached to the ring nitrogen (i.e., that the -N(RaRb) group is not attached to the carbon atom alpha to the ring nitrogen). Another embodiment of the present invention is a compound of Formula (I), wherein R2 is methyl; and all other variables are as originally defined above; or a pharmaceutical^ acceptable salt thereof. Another embodiment of the present invention is a compound of Formula (I), wherein lO is -H or -C1-4 alkyl; and all other variables are as originally defined above; or a pharmaceutical!) acceptable salt thereof. In an aspect of this embodiment, R3 is -11 or methyl. In another aspect of this embodiment, R3 is -11. Another embodiment of the present invention is a compound of Formula (I), wherein R4 js C1.4 alkyl substituted with an aryl, which is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -OH, -C1-4 alkyl, -C\|_4 alkyl-ORa, -CM haloalkyl, -O-C1-4 alkyl, -O-C1-4 haloalkyl, -CN, -NO2, -N(RaRb), -CM alkyl-N(RaRb). -C(-0)N(RaRb), -C(0)Ra, -C02Ra, -C1-4 alkyl-C02Ra, -OC02Ra, -SRa -S(-0)Ra, -S02Ra, -N(Ra)S02Rb, . -S()2N(RaRb), -N(Ra)C(0)Rb, -N(Ra)C02Rb, -C1-4 alkyl-N(Ra)C02Rb, methylencdioxy attached to two adjacent ring carbon atoms, phenyl, -C1_4 alkyl-phenyl, -O-phenyl, or -(CH2)0-2-het; wherein hct is a 5- or 6-membercd hetcroaromatic ring containing from I to 4 heteroatoms independently selected from N, O and S, and het is optionally fused with a benzene ring, and is optionally substituted with 1 or 2 substituents each of which is independently -Ci_4 alkyl, -C]-4 haloalkyl, -O-Ci-4 alkyl, -O-Cj-4 haloalkyl, or -C02Ra; and all other variables are as originally defined above; or a pharmaceutically acceptable salt thereof. Another embodiment of the present invention is a compound of Formula (I), wherein R4 is -CI l2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -C1-4 alkyl, -C1-4 fluoroalkyl, -O-Ci-4 alkyl, -O-C1-4 fluoroalkyl, -(CH2)l-2-N(RaRb), -S02Ra. -(CH2)0-2-CO2Ra, -(CH2)0-2-N(Ra)CO2Rb, -NO2, -SRa -N(RaRb) or phenyl; each Raand Rb is independently is H or-C1_4 alkyl; and all other variables are as originally defined above; or a pharmaceutical!)' acceptable salt thereof. In an aspect of the preceding embodiment, R4 is -CH2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents, each of which is independently -F, -Br, -CI, -011, -C1-4 alkyl, -C1-4 fluoroalkyl, -O-C1.4 alkyl, -SO2-C1_4 alkyl, -S-C]_4 alkyl, -N(CH3)2 or -O-Cl-4 fluoroalkyl. In another aspect of the preceding embodiment, R4 is/;-fluorobenzyI or 2,3-dimethoxybenzyI. In another aspect of the preceding embodiment, the phenyl is optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -C]_4 alkyl, -C]_4 fluoroalkyl, -O-Cl-4 alkyl, -0-C)„4 fluoroalkyl, -(CH2)\|-2-N(RaRb), -S02Ra, -(CH2)0-2-CO2Ra -(Cll2)0-2-N(Ra)CO2Rb, -NO2, or phenyl. In an aspect of the preceding embodiment, the phenyl is optionally substituted with from 1 to 3 substituents, each of which is independently -F. -Br, -CI, -OH. -C1-4 alkyl, -CM fluoroalkyl, -0-C1_4 alkyl, or -O-C1-4 fluoroalkyl. In another aspect of the preceding embodiment, R4 is/>fluorobenzyl or 2,3-dimethoxybcnzyl. A class of compounds of the present invention includes any compound of Formula (1), wherein Rl is-Rk; Rk is phenyl which is (a) optionally substituted with from 1 to 3 substituents each of which is independently: (1) halogen, (2) -Cl-6 alkyl, which is optionally substituted with 1 or 2 substituents each of which is independently -O-C1-6 alkyl, -O-C1-6 haloalkyl. -C(-0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb), -C(O)-(CH2)0-2N(RaRb), N(Ra)-C(=OHCH2)0-2N(RbRcX-SO2Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=0, (3) -C1_6 haloalkyl, (4) -O-C1_6 haloalkyl, (5) -C(=0)Ra, (6) -C02Ra, (7) -C(=0)N(RaRb), or (8) -C(0)-C]-6 alkyl-N(RaRb); and ;• (b) optionally mono-substituted with (1) -C1-4alkyI-Rm, or (2) -Co-4 alkyl-N(Ra)-Co-4 alkyl-R™; wherein Rm is aryl selected from phenyl and naphlhyl; a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; or a 5- or 6-membered heteroaromatic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; wherein the aryl defined in Rm is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C]-4 alkyl, -CF3, -O-C1-4 alkyl -OCF3, or -N(RaRb); the saturated heterocyclic ring defined in Rm is optionally substituted with from I to 3 substituents each of which is independently -C]-4 alkyl or oxo, and is additionally optionally mono-substituted with phenyl, -(CH2)l-2-phcnyl, -C( 0)-phenyl, -C02-phenyl, -C02-(CH2)l-2-phenyl, or a 5- or 6-mcmbcred heteroaromatic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; and the heteroaromatic ring defined in Rm is optionally substituted with 1 or 2 substituents each of which is independently -C1--4 alkyl or oxo; and all other variables arc as originally defined above; or a pharmaceutical ly acceptable salt thereof. A sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (1), wherein R2 is methyl; R3 is-H; R4 is: (1) -CI-l2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -C1-4 alkyl, -C1-4 fluoroalkyk -O-Ci-4 alky!, -0-Ci_4 fluoroalkyl -(CH2)l-2-N(RaRb), -S()2Ra, -(CH2)0~2-CO2Ra -(CI l2)0-2-N(Ra)CO2Rb, -N02, -SRa, - N(RaRb) or phenyl; or (2) a fused bicyclic carbocycle selected from 71 pl- each Ra and Rb is independently is H or -C1-4 alkyl; and all other variables are as defined in the class; or a pharmaceuticallyacceptable salt thereof. Another sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (1), wherein R4 is 4-fluorobenzyl or 2,3-dimethoxybenzyl; and all other variables arc as defined in the class; or a pharmaceutically acceptable salt thereof. Still another sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (1), wherein R2 is methyl; R3 is -II; R4 is 4-fluorobenzyl or 2,3-dimethoxybenzyl; each Ra and Rb is independently is H or -C1--4 alkyl; and all other variables are as defined in the class; or a pharmaceutically acceptable salt thereof. Another class of the present invention includes any compound of Formula (II): wherein Qis: (1) methyl which is optionally substituted with 1 or 2 of -O-C1-4 alkyl, (2) phenyl which is optionally substituted with from 1 to 3 substitucnts each of which is independently -F, -CI, Eir, -C\-4 alkyl, -CF3, -O-Cj-4 alkyl, -OCF3, methylenedioxy attached to two adjacent carbon atoms, or phenyl, or (3) a 5- or 6-mcmbercd saturated heterocyclic ring containing from 1 to 3 hetcroatoms independently selected from N, O and S; wherein the saturated heterocyclic ring is optionally substituted with 1 or 2 substituents each of which is independently -F, -CI, -Br, -C]_4 alkyl, oxo, phenyl, or -C(=0)-phenyl; T is: (1) -H, (2) -OH, (3) methyl or ethyl, optionally substituted with -OH or -O-C1-4 alkyl, (4) -O-C1-4 alkyl (5) -N(RaRb), (6) -N(Ra)-(CH2)2-OH, (7) -N(Ra)-C02Rb, (8) -N(Ra)-C(=0)-(CH2) 1 -2-N(RaRb), (9) -Rs, (10) -(CH2)l-2-Rs,or (11) -(Cll2)0-2-N(Ra)-(CH2)0-3-Rs; Rs is: (1) phenyl optionally substituted with from 1 to 4 substituents each of which is independently halogen, -C1-4 alkyl. -C1_4 alkyI-ORa, -C1_4 haloalkyl, -O-CM alkyl, -O-CM haloalkyl, or -N(RaRb); (2) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 hctcroatoms independently selected from N, O and S; which is optionally substituted with from 1 to 4 substituents each of which is independently-C1--4 alkyl, -C1_4 alkyl-ORa, -C1-4 haloalkyl, -O-C1-4 alkyl, -O-C1-4 haloalkyl, -C( 0)Ra, oxo, phenyl, or -CH2-phenyI; or (3) a 5- or 6-membered heteroaromatic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; which is optionally substituted with from I to 4 substituents each of which is independently -C1-4 alkyl, -C1-4 alkyl-ORa, -C1-4 haloalkyl, -O-CM alkyl, -O-C1-4 haloalkyl, or oxo; R2 is (1) -C1- -4 alkyl, (2) -C1 -4 alkyl substituted with -N(RaRb), or (3) -C1-4 alkyl substituted with a 5- or 6-membered saturated monocyclic heterocycle which contains from 1 to 3 heteroatoms selected from 1 to 3 N atoms. 0 or 1 O atoms, and 0 or 1 S atoms; wherein the saturated heterocycle is optionally substituted with from 1 to 4 substituents each of which is independently a -CM alkyl; R3 is-H or-C1-4 alkyl; R4 is -CH2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -C]-4 alkyl, -C1-2 fluoroalkyl, -O-C1-2 alkyl, -O-CM fluoroalkyl, ~(CH2)]-2-N(RaRb), -S02Ra, -(CIl2)0-2-CO2Ra, -(Cll2)0-2-N(Ra)CO2Rb, -N02, -SRa, -N(RaRb) or phenyl; each Ra and Rb is independently is H or -C]_4 alkyl: and s is an integer equal to zero, ], or 2; or a pharmaceutical!)' acceptable salt thereof. In an aspect of this class, R4 is -CFb-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substitucnts each of which is independently fluoro, bromo, chloro, -Oil, -C\|-4 alkyl, -Ci-4 fluoroalkyl, -O-Cj-4 alkyl, -O-Cj-4 fluoroalkyl, -(CH2)\|-2-N(RaRb), -S02Ra, -(CH2)0-2-CO2Ra, -(Cil2)0-2-N(Ra)C()2Rb, -NO2, or phenyl A sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (11) exactly as defined in the preceding class, except that when R2 is -C-i_4 alkyl substituted with -N(RaRb), it is with the proviso that -N(RaRb) is not attached to the carbon atom in the -C\-4 alkyl group that is attached to the ring nitrogen (i.e., that the -N(RaRb) group is not attached to the carbon atom alpha to the ring nitrogen). Another sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (11), wherein Q is phenyl; T is: (1) -H, (2) -N(RaRb), (3) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; which is optionally substituted with 1 or 2 substituents each of which is independently -C1-4 alkyl or -C(-~0)Ra, or (4) -N(Ra)-(CH2)l-2-heteroaromatic, wherein the heteroaromatic is a 5- or 6-mcmbered ring containing I or 2 N atoms; R2 is methyl; R3 is -H; and R.4 is -CH2-phenyl, wherein the phenyl is optionally substituted with 1 or 2 substituents each of which is independently-F, -CI, -Br, -Cj-4 alkyl, -CF3, -O-Cj-4 alkyl, -SO2CH3, -SCH3, -N(CH3)2 or-OCF3; each Ra and Rb is independently -H, methyl or ethyl; and s is an integer equal to zero or 1; or a pharmaceutical^ acceptable salt thereof. In an aspect of this subclass, R4 is -Cll2-phenyl, wherein the phenyl is optionally substituted with I or 2 substituents each of which is independently -F, -CI, -Br, -C1-4 alky], -CF3, -0-C\|-4 alkyl, or-OCF3. Another class of compounds of the present invention includes any compound of Formula (I), wherein Rl is-Rk; Rk is (i) a 5- or 6-membered saturated heterocyclic ring containing from 0 to 1 oxygen atoms and from 1 to 3 nitrogen atoms or (ii) a bicyclic heterocycle which is a benzene ring fused to a 5- or 6-membcred saturated heterocyclic ring containing from 0 to 1 oxygen atoms and from 1 to 3 nitrogen atoms; wherein the saturated heterocyclic ring or bicyclic heterocycle is optionally substituted with from 1 to 3 substituents each of which is independently (1) -Ci_4 alkyl, which is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -O-C1-4 alkyl, -O-C1-4 haloalkyl, -C(=0)Ra, -CC>2Ra, -SRa -S(=0)Ra, -N(RaRb), -C(=O)-(CH2)0-2N(RaRb), N(Ra)-C(=O)-(Cl)2)0-2N(RbRC),-S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra>C(Rb)=0, (2) -Oil, (3) -C(-0)Ra (4) -C02Ra, (5) -Ct O)N(RaRb), (6) -C(- ())-C \| _6 alkyl-N(RaRb), (7) -SRa. (8) -S( 0)Ra, (9) -SCnRa, (10) -N(RaRb), (11) -Km, (12) -C]_4 alkyl-Rm, wherein the alkyl is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -OH, -CN, -CM haloalkyl, -O-C-M alkyl, -O-C1-4 haloalkyl, -C(-0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb), -N(Ra)C02Rb, -SC>2Ra, -N(Ra)S02Rb, -SC>2N(RaRb), 0r -N(Ra)-C(Rb)=0, (13) -C()-4 alkyl-N(Ra)-Co-4 alkyl-Rm, (14) -C(M alkyl-O-Co-4 alkyl-Rm, (15) -Co-4 alkyI-S-CO-4 alkyl-Rm, (16) -Co_4 alkyl-C(=0)-Co-4 alkyl-Rm, (17) -C( -O)-()-C0-4 alkyl-Rm, or (18) -C( C))N(Ra)-Co-4 alkyl-Rm; wherein each Rm is independently -C3.6 cycloalkyi; aryl selected from phenyl and naphthyl; a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; or a 5- or 6-membered heteroaromatic ring conlaining from 1 to 3 heteroatoms independently selected from N, () and S, wherein any N is optionally oxidized to form an N-oxide; wherein the aryl is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -Ci-4 alkyl, -CF3, -O-Ci-4 alkyl, -OCF3, or -N(RaRb); the saturated heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -C\|_4 alkyl or oxo, and is additionally optionally mono-substituted with phenyl, -(CH2)l-2-phenyl, -C(=0)-phcnyl, -C()2-phenyl, or-C02-(CH2)l-2-phenyl; and the heteroaromatic ring is optionally substituted with 1 or 2 substituents each of which is independently halogen, -C1.4 alkyl, or oxo; and all other variables are as originally defined above; or a pharmaceutieally acceptable salt thereof. A sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (I), wherein R8 is: (1) -II, (2) -C]-4 alkyl, which is optionally substituted with 1 or 2 substituents each of which is independently -OH, -O-Ci-4 alkyl. -OCF3, -C(=0)Ra, -C()2Ra, -SRa, -N(RaRb), or -C( O)N(RaRb), (3) -C(=0)Ra, (4) -C02Ra, (5) -C(-0)N(RaRb), (6) -C(=0)-(CH2) 1 -2-N(RaRb), (7) -SO?Ra, (8) -(CII2)l-2-Rm, (9) -(CM2)0-2-C(=O)-(CH2)0-2-Rm, (10) -C(=O)-O-(CH2)0-2-Rm, or (11) -C(-O)N(Ra)-(CH2)0-2-Rm; R10 is -H, -OH, -C \| -4 alkyl, -O-C i .4 alkyl, -N(RaRb), or -0-(CH2) 1 -2-Rm ; R12 is (1) -II, (2) -C1_4 alkyl, which is optionally substituted with 1 or 2 substituentseach of which is independently -OH, -O-C 1.4 alkyl, -OCF3, -C(=0)Ra, -C02Ra, -SRa, -N(RaRb), or -C( O)N(RaRb), (3) -C( 0)Ra, (4) -C02Ra, (5) -C(K))-(CH2) 1 -2-N(RaRb), or (6) -S()2Ra; R2 is methyl; R3 is -H or methyl; R4 is -CH2-phenyl. wherein the phenyl is optionally substituted with from 1 to 3 substiluents each of which is independently fluoro, brorno, chloro, -OH, -C)-4 alkyl, -Ci_4 fluoroalkyl. -O-C 1.4 alkyl, -O-C 1.4 fluoroalkyl, -(CH2)l-2-N(RaRb), -S02Ra, -(CI l2)0-2-CO2Ra, -(CI h)0-2-N(Ra)CO2Rb, -NO2, -SRa, -N(RaRb) or phenyl; and each Ra and Rb is independently -H or -C]-4 alkyl; or a pharmaceutically acceptable salt thereof. In an aspect of this subclass, R4 is -Cll2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents-each of which is independently fluoro, bromo, chloro, -Ol-l, -C\|-4 alkyl, -Cj-4 fluoroalkyl, -O-Ci-4 alkyl. -O-Cj-4 fluoroalkyl, -(CH2) I -2-N(RaRb), -S02Ra, -(CH2)0-2-CO2Ra, -(CM2)0-2-N(Ra)C()2Rb, -NO?, or phenyl. Another elass of the present invention includes any compound of Formula (III): wherein R2 is: (1) -C1-6 alkyl, (2) -C \| -6 alkyl substituted with -N(RaRb), (3) -C 1 _6 alkyl substituted with phenyl which is: (a) optionally substituted with from 1 to 4 substituents each of which is independently halogen, -C1_4 alkyl, -C1-4 haloalkyl, -0-C]-4 alkyl, -O-C1-4 haloalkyl, or -Co-6 alkyl-N(RaRb); and (b) optionally mono-substituted with -C1-4 alkyl substituted with a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms selected from 1 or 2 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -C1-6 alkyl, oxo, or a 5- or 6-membered heteroaromatic ring containing from 1 to 3 heteroatoms selected from 1 to 3 N atoms. 0 or 1 O atom, and 0 or 1 S atom; (4) -C1-6 alkyl optionally substituted with -OH and substituted with a 5- or 6-membered saturated monocyclic hetcrocycle which contains from 1 to 3 heteroatoms selected from I to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heterocycle is optionally substituted with from 1 to 4 substituents each of which is independently -Ci-6 alkyl, -0-C\|_6 alkyl, oxo, or phenyl; or (5) -C \| _6 alkyl substituted with a 5- or 6-membered heteroaromatic ring which contains from 1 to 3 heteroatoms selected from I to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heteroaromatic ring is optionally substituted with from 1 to 4 substituents each of which is independently -C i _6 alkyl, -O-C \| _6 alkyl, oxo, or phenyl; and all other variables are as originally defined above; or a pharmaceutical ly acceptable salt thereof. A sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (111) exactly as defined in the preceding class, except that when R2 is -C \| _6 alkyl substituted with -N(RaRb), it is with the proviso that -N(RaRb) is not attached to the carbon atom in the -Cj_6 alkyi group that is attached to the ring nitrogen (i.e., that the -N(RaRb) group is not attached to the carbon atom alpha to the ring nitrogen). Another sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (111), wherein R2 is: (1) -C1-4 alkyl, (2) -(CH2)l-3-N(RaRb), (3) -(CH2)l-3-phenyl, wherein the phenyl is: (a) optionally substituted with from 1 to 3 substituents each of which is independently fluoro, chloro, bromo, -C1--4 alkyl, -CF3, -0-C1-4 alkyl, -O-CF3, or -(CH2)l-3-N(RaRb);and (b) optionally mono-substituted with -(CH2) 1 -3-saturated heterocyclic which is a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms atoms, wherein the heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -C\|_4 alkyl or pyridyl; (4) -(CH2)l-.Vsalurated heterocycle, wherein the -(CH2)l-3- moiely is optionally substituted with an -011 and the saturated heterocycle is a 5- or 6-membered saturated monocyclic heterocycle which contains from 1 to 3 heteroatoms selected from I to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heterocycle is optionally substituted with from 1 to 3 substituents each of which is independently a -C]-4 alkyl; or (5) -(CH2)l-3-pyridyl; R3 is -H or methyl; R4 is -CI l2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bronio, chloro, -OH, -C]_4 alkyl, -Ci-4 fluoroalkyl, -O-C1-4 alkyl, -O-C1-4 fluoroalkyl, -(CH2)l-2-N(RaRb), -S02Ra, -(CH2)0-2-CO2Ra, -(CH2)0-2-N(Ra)CO2Rb, -N02, -SRa -N(RaRb) 0r phenyl; and each Ra and Rb is independently is H or -C1-4 alkyl; or a pharmaceutical!)' acceptable salt thereof. In an aspect of this subclass, R4 is -CH2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -Oil, -C\|_4 alkyl, -C1-4 fluoroalkyl. -0-C1_4 alkyl, -O-Cj-4 nuoroalkyi, -(CH2)l-2-N(RaRb), -S02Ra, -(CH2)0-2-CO2Ra, -(CI l2)0-2-N(Ra)CO2Rb, -NO2, or phenyl. Another class of compounds of the present invention includes any compound of Formula (1), wherein RI is -C( Rk is (i) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected from N. O and S, or (ii) a 5- or 6-membered heteroaromatic ring containing from 1 to 3 heteroatoms independently selected from N.OandS; and all other variables are as originally defined above; or a pharmaceutically acceptable salt thereof. A sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (I), wherein Rl is -C(==0)NH-(CI-l2)l-2-Rk ; and Rk is (i) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected from N, O and S, or (ii) a 5- or 6-membered heteroaromatic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; R2 is methyl; R3 is -H or methyl; R4 is -CH2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -C1-4 alkyl, -C1-4 iluoroalkyl, -O-CM alkyl, -O-C1-4 fluoroalkyl, -(CH2)l-2-N(RaRb), -S02Ra, -(CI l2)0-2-CO2Ra, -(CIl2)0-2-N(Ra)CO2Rb, -N02- -SRa, -N(RaRb) 0r phenyl; and each Ra and Rb is independently -H or -C1-4 alkyl; or a pharmaceutical ly acceptable salt thereof. In an aspect of this subclass, R4 is -CI l2-phenyl. wherein the phenyl is optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -C\|_4 alkyl, -Ci-4 fluoroalkyk -O-Ci-4 alkyl, -O-Cj-4 fluoroalkyl, -(CH2)l-2-N(RaRb), -S02Ra, -(CH2)0-2-CO2Ra, -(CI l2)0-2-N(Ra)CO2Rb, -NO2, or phenyl. It is to be understood that additional embodiments of the present invention include, but arc not limited to, compounds of Formula I wherein each of two or three or more of R1, R2. R3, R4, Ra, Rb, Rc, Rd, Rk and Rm is independently defined in accordance with its definition in one of the embodiments or an aspect thereof as set forth above, or in accordance with its definition in one of the foregoing classes set forth above or a sub-class or feature thereof. Any and all possible combinations of these variables in Formula I are additional embodiments within the scope of the present invention. An aspect of the present invention is a compound selected from the group consisting of N-(2-ethoxybenzyl)--5-hydroxy-l-methyl-2-(4-methylphenyl)-6-oxo-l,6-dihydropyrimidinc-4-carboxamide; N-(2,3-dimethoxybenzyl)-5-hydroxy-1 -methyl-2-(4-methylphenyl)-6-oxo-1,6-dihydropyrimidine-4-carhoxamidc; N-(2J-dimethoxybenzyl)-2-{4-\|(dimethylamino)methyl]phenyl}-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-nuorobenzyl)-2-{4-\|(dimethylamino)methyl]phenyI}-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamidc; N-(2,3-dimethoxyben/yl)-5-hydroxy-l-methyl-6-oxo-2-[4-(pyrrolidin-l-ylmethyl)phenyl]-l,6-dihydropyrimidine-4-carboxamide; N-(4-lluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-[4-(pyrrolidin-l-ylmethyI)phenyl]-l,6-dihydropyrimidine-4-carboxamide; N-(4»fluorobenzyl)-5-hydroxy-l~methyl-6-oxo-2-[4-(piperidin-l-ylmethyl)phenyl]-l,6-dihydropyrimidinc-4-carboxamide; N-(23-dimethoxybenzyr)-5-hydroxy-l-methyl-2-\|4-(morplu)lin-4-ylmethyl)phenyl]-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-nuorobenzyl)-5-hydroxy-l-methyl-2-\|'4-(morphoIin-4-ylmethyI)pheny\|]-6-oxo-],6-dihydropyrimidinC'4-carboxamide; N-(4-nuorobenzyl)-5-hydroxy-l-methyl-2-{4'[(4-methvlpiperazin-l-yl)mcthyl [phenyl }-6-oxo-l,6-dihydropyrimidinc-4-carboxamide; 2-{4-[(diethyIamino)methyljphenyl}-N-(2,3-dimethc)\ybenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-{4-\|(diethylamino)melhyr]phcnyl}-N-(4-flLioroben/.yl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-earboxamide; 2-[(dimethylamino)(phenyl)methylJ-N-(4-nuorobcnzyl)-5-hydroxy-l-methyl-6-oxo-l^-dihydropyrimidine-4-carboxamide; N-(4--nuorobenzyl)-2-[(4-formylpiperazin-l-yl)(phenyl)methyl]-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-{phcnyl[(pyridin-3-ylmethyl)amino]methyl}-l,6-dihydropyrimidinc-4-carboxamide; 2-benzyl-1-[2-(dimethylamino)ethyl]-N-(4-fluorobenzyl)-5-hydroxy-6-oxo-1,6-dihydropyrimidine-4-carboxamide; l-[2-(dimethylamino)ethyl\|-N-(4-fluorobenzyI)-5-hydroxy-2-(2-methylphenyl)-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-nuorobenzyl)-5-hydroxy-l-methyl-2-(4-mcthylphcnyr)-6-oxo-K6-dihydropyrimidine-4-carboxamide; 2-bcnzyl-N-(23-dimethoxybenzyl)-l-[2-(dimcthylamino)cthyl]-5-hydroxy-6-oxo-l,6-dihydropyrimidinc-4-carboxamide; 2-{4-[(4-ethylpipcrazin-l-yl)methyl]phenyl}-N-(4-fluorobenzyl)-5-hydroxy-l -methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-lluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-{4-[(2-pyridin-3-ylpiperidin-l-yI)mcthyr\|phenyI}-I,6-dihydropyrimidine-4-carboxamide; N-(4-nuorobenzyI)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(2,3-dimcthoxybcnzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidinc-4-carboxamide; N-l4-nuoro-2-(trifluoromethyl)benzyl]-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamidc; N-(3-chIoro-4-mcthyIben/.yl)-5-hydroxy-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 5-hydroxy-N-[(lR,2S)-2-hydroxy-2,3-dihydro-lH-indcn-l-yl]-l-methyl-2-{4-\|(4-methylpiperazin-l-yl)methylJphenyl}-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-2-(4-{[(2R)-2-(methoxymelhyl)pyrrolidin-l-yl\|methyl}phenyI)-l-methyI-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-lluorobenzyi)-5-hydroxy-2-(4-{[(2S)-2-(methoxymethyi)pyrrolidin-l-yl]mcthyl} phenyl)-1 -methyl-6-oxo-l,6-dihydropvrimidine-4-carboxamide; N-(4-nuorobenzyl)-2-(4-{\|(4-nuorobenzyl)aminoJmethyl}phenyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyriinidine-4-carboxamide; 2-benzyl-N-(4-fluorobenzyI)-5-hydroxy-l-(2-morpholin-4-ylethyl)-6-oxo-l,6-dihydropyrimidine-4-carboxamide; l-f2-(dimethylamino)cthyr\|-N-(4-fluorobenzyl)-5-hydroxy-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyI)-5-hydroxy-6-oxo-l-(pyridin-3-ylmethyI)-l,6-dihydropyrimidine-4-carboxamide; 2-bcnzyl-N-(4-fluorobenzyl)-5-hydroxy-6-oxo-l-(2-pyrrolidin-I-ylethyl)-l,6-dihydropyrimidine-4-carboxamide; 2-bcnzyl-N-(4-fluorobcnzyl)-5-hydroxy-6-oxo-l-(2-pipcridin-l-ylethyl)-l,6-dihydropyrimidinc-4-carboxamide; 2-(l-bcnzylpiperidin-2-yl)-N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidinc-4-carboxamide; N-(4-nuorobcnzyl)-5-hydroxy-l-methyl-2-(l-methylpipcridin-2-yl)-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-( 1 -benzylpiperidin-3-yl)-N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide; l-{3-[(dimethyIamino)rncthyl\|bcnzyl}-N-(4-nuorobenzyl)-5-hydroxy-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(2,3-dimethoxybcnzyI)-l-[2-(dimethylamino)ethylj-5-hydroxy-6-oxo-l,6-dihydropyrimidine-4 -carboxamide; N-(2,3-dimethoxybenzyl)-5-hydroxy-6-oxo-l-(pyridin-3-ylmethyl)-l,6-dihydropyrimidine-4-carboxamide; N4-(4-fluorobenzyl)-5-hydroxy-l-methyl-N2-(2-morpholin-4-ylethyl)-6-oxO"l,6-dihydropyrimidine-2,4-dicarboxamide; N-(4-fluorobenzyl)-5-hydroxy-6-oxo-l-f3-(pyrrolidin-l-ylmcthyl)benzyl]-l,6-dihydropyrimidine-4-carboxamidc; N-(4-fluorobcnzyl)-5-hydroxy-1 -[3-(morphoiin-4-ylmelhyl)benzyl]-6-oxo-1.6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-l-{3-\|X4-methyIpipcra//in-l-yl)methyl]ben/yl} -6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-6-oxo-l-{3-[(4-pyridin-2-y!piperazin-l-yl)methyl]benzyl}-1.6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-l-I2-(morpholin-4-ylmctliyI)benzyl]-6-oxo-l,6-dihydropyrimidinc-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-6-oxo-l-{2-[(4-pyridin-2-ylpiperazin-l-yl)methyI\|benzyl}-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-pyrrolidin-2-yl-l,6-dihydropyrimidine-4-carboxamidc; N4-(4-fluorobenzyI)-5-hydroxy-1 -methyi-6-oxo-N2-(pyridin-2-yimethyl)-1,6-dihydropyrimidine-2,4-dicarboxamide; N-(4-fluorobenzyl)~5-hydroxy-1 -(2-hydroxy-3-morpholin-4-yIpropyl)~6-oxo-1,6-dihydropyrimidine-4-carboxamidc; N-(4-fluorobenzyl)-5-hydroxy-l-[4-(morpholin-4-ylmcthyl)bcnzyi]-6-oxo-l,6-dihydropyrimidine-4-carboxarnide; N-(4-fluorobenzyl)-5-hydroxy-1 -methyI-2-(2-morpholin-4-ylethyl)-6-oxo-1,6-dihydropyrimidine-4-earboxarnide; 2-(2,2-dimethoxyethyl)-N-(4-fluorobcnzyl)-5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide; 2-(2.3-dihydro-llI-indol-2-yl)-N-(4-fluorobenzyl)-5-hydroxy"l-methyI-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-[2-(4-benzoylpipcrazin-l-yl)ethyl]-N-(4-fluorobenzyl)-5-hydroxy-I-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxarnide; 2-\ l-(N,N-dimethyIglycyt)pipcridin-2-yl]-N-(4-fluorobenzyI)-5-hydroxy-l-mcthyI-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyi)-5-hydroxy-l-methyl-2-(]-methyl-2,3-dihydro-l H-indol-2-yi)-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-!-methyl-6-oxo-2-(l,2,3.4-tctrahydroquinoIin-2-yI)-1.6-dihydropyrimidine-4-carboxamide; N-(4-iluorobcnzyl)-5-hydroxy-i-methyl-2-(l-methyl-1,2,3,4-tetrahydroquinolin-2-yI)-6-oxo-l,6-dihydropyrimidinc-4-carboxamide; tcrt-butyl (2S,4R)-4-(bcnzyloxy)-2-(4-{[(4-fluorobcnzyl)amino]carbonyl}-5-hydroxy-l-mcthyl-6-oxo-l,6-dihydropyrimidin-2-yl)pyrrolidine-l-carboxylate; tcrt-butyl (2S,4R)-2-(4-{[(4-fluorobenzyl)aminojcarbonyl}-5-hydroxy-l-mcthyl-6-oxo»K6-dihydropyrimidin-2-yl)-4-hydroxypyrrolidine-l-carboxylate; 2-[(2S,4R)-4-(benzyIoxy)pyrrolidin-2-yl]-N-(4-fluorobcnzyr)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-lluorobenzyl)-5-hydroxy-2-[(2S,4R)-4-hydroxypyrrolidin-2-yl]-l-methyl-6-oxo-I,6-dihydropyrimidinc-4-carboxamide; N-(4-nuorobenzyl)-5-hydroxy-2-[(2S,4R)-4-hydroxy-l-methylpyrrolidiri'2-yl]-l-methvl-6-oxo-l,6-dihydropyrimidinc-4-carboxamidc; 2-( (2S,4R)-4-(benzyloxy)-1 -mcthylpyrrolidin-2-yl \|-N-(4-fluorobenzyl)-5-hydroxy-1 -mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamidc; 2-l(2S,4R)-l-benzoyl-4-(bcnzyloxy)pyrrolidin-2-yl]-N-(4-nuorobenzyI)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-[i-(N,N-dimethylglycyl)-2,3-dihydro-lH-indol-2-ylj-N-(4-fluorobenzyl)-5-hydroxy-I -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide; 2-( 1 -benzoyl-2,3-dihydro- ] I I-indol-2-yi)-N-(4-fluorobcnzyl)-5-hydroxy-1 -methyi-6-oxo-l,6-dihydropyrimidinc-4-carboxamide; N-(4-iluorobenzyl)~5-hydroxy-1 -methyl-6-oxo-2-\| 1 -(pyridin-2-ylcarbonyl)-2,3-dihydro-1 H-indol-2-yl\|- l,6-dihydropyrimidine-4-carboxamide; tcrt-butyl 3-(4-{[(4-Huorobcnzyl)amino\|carbonyl}-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidin-2-yl)-4-mcthylpiperazinc-I-carboxyIate; N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-2-(4-methylmorpholin-3-yl)-6-oxo-1.6-dihydropyrimidine-4-earboxamide; (+)-N-(441uorobenzyI)-5-hydroxy-1 -methyl-2-(4-methylmorphoIin-3-yl)-6-oxo-1,6-dihydropyrimidine-4-carboxamide (-)-N-(4-fiuorobenzyl)-5-hydroxy-1 -methyl-2-(4-methylmorpholin-3 -yl)-6-oxo-1,6-dihydropyrimidine-4-carboxamide 2-(l-ethyI-2,3-dihydro-]II-indol-2-yl)-N-(4-fluorobcnzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-(l-benzoylpiperidin-2-yl)-N-(4-fluorobenzyI)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-]-methyI-6-oxo-2-(l-(pyridin-2-ylcarbonyl)piperidin-2-yi\|-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyI)-5-hydroxy-1 -methyl-2-(2-methyl-1,2,3,4-tetrahydroisoquinolin-3-yl)-6-oxo-l,6-dihydropyrimidinc-4-carboxamidc; 2-( 1 -bcnzoy]pyrrolidin-2-yl)-N-(4-fluorobenzyl)-5-hydroxy- i -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-\| i-(pyridin-2-ylcarbonyl)pyrrolidin-2-yI\|-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-2-( 1 -methylpyrrolidin-2-yl)-6-ox 1.6-dihydropyrimidine-4-carboxamide; 2-\|(2S,4RH-(benzyloxy)-)-(pyridin-2-ylcarbony])p>Trolidin-2-yl]-N-(4-fluorobenzyl)-5-hydroxy-1 -mcthyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide; 2-\| l-(dimethylamino)-2-phcnylcthyl]-N-(4-nuorobcnzyl)-5-hydroxy-l-rnethyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-[(2S,4R)"l-benzoyl-4-hydroxypyrrolidin-2-yI\|-N'(4-fluorobenzyI)-5-hydroxy-l-mcthyl-6-oxo-l56-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyI)-5-hydroxy-2-(l-isobutyl-2J-dihydro-lH-indol-2-yl)-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-2-( 1-isopropyi-2,3-dihydro-1 H-indoi-2-yI)-1-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-\|l-(N,N-dimethylglycyl)pyrrolidin-2-yI]-N-(4-nuorobcnzyl)-5-hydroxy-l-methyl-6-oxo-L6-dihydropyrimidine-4-carboxamide; 2-{ l-[(6-bromopyridin-2-yl)carbonyljpyrrolidin-2-yl}-N-(4-fluorobenzyl)-5-hydroxy-I-mcthyI-6-oxo~l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)o-hydroxy-1 -methyl-2-( 1 -methylpiperazin-2-yl)-6-oxo-1,6-dihydropyrimidine-4-earboxamide; 2-(! -bcnzoyl-4-mcthylpipcrazin-2-yI)-N-(4-iluorobcnz\l)-5--hydroxy-1 -methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyI)-5-hydroxy-1 -methyI-6-oxo-2-\| 1 -(pyridin-2-ylcarbonyI)-1,2,3,4-tetrahydroquinoIin-2-yI]-I,6-dihydropyrimidine-4-carboxamide; 2-( i -acetylpyrroIidin-2-yI)-N-(4-fluorobenzyI)-5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide; 2-[ I -(cyclopropyicarbonyl)pyrrolidin-2-yl]-N-(4-nuorobenzyl)-5-hydroxy-1 -methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-l-methyl-2-\| l-(methylsulfonyI)pyrrolidin-2-yI\|-6-oxo-l,6-dihydropyrimidinc-4-carboxamide; N-(4-iluorobenzyl)-5-hydroxy-l-methyl-2-{l-[(4-mcthylmorpholin-3-yl)carbonylJpyrrolidin-2-yl}-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-( 1,4-dimethylpipcrazin-2-yl)-N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo-1.6-dihydropyrimidine-4-carboxamide; N-(4-nuorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-[I-(pyridin-3-ylcarbonyl)pyrrolidin-2-yi ]-1,6-dihydropyrimidine-4-carboxamide; 2-[(2S.4R)-]-acetyl-4-(benzyloxy)pyrrolidin-2-yl]-N-(4-fluorobenzyI)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyI)-5-hydroxy-2-( 1-isonicotinoylpyrrol idin-2-yl)-1-mcthyl-6-oxo-1,6-dihydropyrimidine-4-carboxamidc; 2-{ I-[(ethylamino)carbonyl\|pyrroIidin-2-yi}-N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide; N-(4-lluorobenzyl)-5-hydmxy-l-methyl-2-{ 1-[(1-methyl-1 H-imidazol-2-yl)carbonyl]pyrrolidin-2-yI}-6-oxo-1,6-dihydropyrim id ine-4-carboxamide; 2--[(2S,4R)-I-acetyl-4-hydroxypyrrolidin-2-yl]-N-(4-riuorobenzyl)-5-hydroxy-l- methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; . 2-\| l-(anilinocarbonyl)pyrrolidin-2-ylJ-N-(4-lluoroben/yl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carbo\amide; 2-(4-cthyl-l-methylpipera/in-2-yl)-N-(4-fluorobcnzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4~nuorobenzyl)-5-hydroxy-1 -methyl-2-{ 1 -\|( I -oxidopyridin-2-yl)carbonyl\|pyrrolidin-2-yi}-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyI)-5-hydroxy-1 -methy!-6-oxo-2-\| I -(pyrazin-2-ylcarbonyl)pyrrolidin-2-yl \|-! ,6-dihydropyrimidine-4-carboxamide; 2-[(4R)-3-acetyl-l,3-thiazolidin-4-yl]-N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-1.6-dihydropyrimidinc-4-carboxamide; N-(4-nuorobenzyl)-5-hydroxy-I-melhyl-2-\| l-methyl-4-(methylsulfonyl)pipcrazin-2-yI\|-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-nuorobenzyl)-5-hydroxy-l-methyI-2-(4-methyIthiomorpholin-3-yl)-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-[4-nuoro-2-(mcthylsulfbnyI)benzyl]-5-hydroxy-Uinethyl-6-oxo-2-[l-(pyrazin-2-ylcarbonyI)pyrrolidin-2-yI]-l,6-dihydropyrimidinc-4-carboxamide; 2-(i-acetylpyrrolidin-2-yi)-N-(4-fluoro-2-(mcthyIsuironyI)benzyl]-5-hydroxy-l-methyl-6-oxo-I,6-dihydropyrimidine-4-carboxamidc; 2-(3-acctyI-l,3-thiazolidin-2-yl)-N-(4-fluorobcnzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-( I-(acetylamino)-l-melhylethyl]-N-(4-fluorobcnzyI)-5-hydroxy-l-methyl-6-oxo-l,6-dihvdropyrimidine-4-carboxamide; 2-( I -acetylpyrrolidin-2-yl)-N-(2-ethoxybenzyl)-5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidinc-4-carboxamide; 2-(4-acetyl-l-methylpiperazin-2-yI)-N-(4-fluorobcnzyl)-5-hydroxy-l-methyl-6-oxo-1.6~dihydropyrimidinc-4-carboxamide; N-(4-fluorobenzyI)-5~hydroxy-1 -methyl-2-[ 1 -meihyl-4-(pyrazin-2-ylcarbonyl)piperazin-2-yl \|-6-oxo- 1,6-dihydropyrim id inc-4-carboxamide; 2-(l-acetylpyrrolidin-2-yI)-5-hydroxy-l-methyl-N-[2-(methylthio)benzyl]-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-nuorobenzyl)-5-hydroxy-2-{l-[(lH-imidaxol-5-ylcarbonyl)amino]-l-mcthylethyl}-l-mcthyi-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-\| l-benzoyl-4-(pyrazin-2-ylcarbonyl)piperazin-2-yl]-N-(4-fluorobenzyl)-5-hydroxy-i-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxcimide; 2-(4-benzoyl-l-mcthylpiperazin-2-yl)-N-(4-fIuorobenzyl)-5-hydroxy-I-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-[4-(benzyloxy)-l-(pyrazin-2-ylcarbonyl)pyrrolidin-2-yl]-N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidinc-4-carboxamide; 2-( I -acetyIpyrrolidin-2-yl)-N-(2,3-dimethoxybenzyl)-5 -hydroxy- l-methyl-6-oxo-1,6-dihydropyrimidinc-4-carboxamide; 2-( i -acetyIpyrroIidin-2-yl)-5-hydroxy-N-(2-methoxybenzyl)-l -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide; Nl-\|'l-(4-{[(4-fluorobcnzyI)amino]carbonyI}-5-hydroxy-l-melhyl-6-oxo-l,6-dihydropyrimidin-2-yl)-!~methyIethyl)-N2,N2-dimethylethancdiamidc; 2-(I-acetyIpyrroIidin-2-yl)-N-\|2-(dimethylamino)benzyI]-5-hydrox> l-methyl-6-oxo-l,6-dihydropyrimidinc-4-carboxamide; 2-\| (2S)-1 -acetylpyrrolidin-2-yl]-N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-earboxamide; N-(4~lluorobenzyl)-5-hydroxy-2-f4-hydroxy-l-(pyra/.in-2-y!carbonyl)pyrrolidin-2-yI]-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamidc; N-\| l-(4-{[(4-fluorobcnzyl)amino]carbonyl}-5-hydroxy-]-mcthyl-6-oxo-l,6-dihydropyrimidin-2-yl)-l-methylethyl]imidazo[2J-b]\| l,3]thiazo!e-6-carboxamide; 2-\|(2S,4S)-l-acctyI-4-nuoropyrroIidin-2-ylJ-N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidinc-4-carboxamide; N-(4-iluorobenzyl)-5-hydroxy-1-methyl-2-{l-methyl-4-[(l-methyl-1 H-imidazol-2-yI)carbonyljpiperazin-2-yl}-6-oxo-I,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-1 -methyI-2-( I -methyl-1 -{[(5-methyI-1,3,4-oxadiazol-2-yl)carbonyl]amino}ethyl)-6-oxo-l,6-dihydropyrimidine-4-carboxamide; Nl-J l-[4-({f4-fluoro-2-(methylsuIfonyl)benzyl]amino}carbonyl)-5-hydroxy-I- mcthyi-6-oxo-l,6-dihydropyrimidin-2-yl]-l-methylethyI}-N2,N2- dimethylethanediamide; 2-(4-acetyI-l,2-dimethylpiperazin-2-yl)-N-(4-fluorobcnzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-\| I-(pyrimidin-4-ylcarbonyl)pyrrolidin-2-yl]-l,6-dihydropyrimidine-4-earboxamide; N-(4-fluorobenzyl)~5-hydroxy-l-methyl-6-oxo-2-[ l-(pyrimidin-5-yIearbonyl)pyrrolidin-2-yl]-I,6-dihydropyrimidine-4-earboxamide; N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-2-{ 1 -methyl-1 -[(1 H-pyrazol-5-yIcarbonyl)amino\|ethyl}-6-oxo-I,6-dihydropyrimidine-4-carboxamide; 2-[(2R,4R)-l-acelyl-4-methoxypyrroIidin-2-yrj-N-(4-ilLiorobenzyl)o-hydroxy-l-methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide; 2-{ l-[(dimethylamino)(oxo)acetyl]pyrrolidin-2-yl}-N-(4-fluorobenzyl)-5-hydroxy-l-methyI-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-{l-\|"4-({[4-fluoro-2-(mcthylsulfonyI)benzyl]amino)carbonyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidin-2-yl]-l-methyiethyl}imidazo[2, l-b][l,3]thiazole-6-carboxamide; 2-\| _(2R,4R)-1 -bcnzoyI'4-iTiclhoxypyrrolidin-2-yrj-N-(4-l1uorobenzyl)-5-hydroxy-1 -meth\i-6-oxo-l,6-dihydropyrimidine-4-carboxamidc; N-(4-(luorobenzyl)-5-hydroxy-2-[4-(isopropylsulfonyl)-l-methylpiperazin-2-yl]-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-[l,2-dimcthyl-4-(mcthylsulfonyi)piperazin-2-yl]-N-(4-fluorobenzy!)-5-hydroxy-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-2-[(2S,4R)-4-methoxy-l-methyIpyrrolidin-2-yl]-l-methyl-6-oxo-l,6-dihydixipyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-l-methyl-2-{l-\|"(rnethylsulfonyl)acetyI]pyrroIidin-2-yl}-6-oxo-I,6-dihydropyrimidinc-4-carboxamide; 2-[(2S)-l-acetyl-4,4-difluoropyrroIidin-2-yl]-N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo- l,6-dihydropyrimidinc-4-carboxamide; 2-l(2R,4R)-l-acctyI-4-ethoxypyrrolidin-2-ylJ-N-(4-iliK)robcnzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-\|(2S)-4,4-difluoro-l-methylpyrrolidin-2-yij-N-(4-nuorobenzyl)-5-hydroxy-]-methyI-6-oxo-l,6-dihydropyrimidine-4-carboxamidc; N-(2.3-dimethoxybenzyl)-5-hydroxy-1 -methyl-6-oxo-2-l 1 -(pyridazin-3-ylcarbonyl)pyrrolidin-2-y!]-I,6-dihydropyrimidinc-4-carboxamide; N-(4-fluorobenzyI)-5-hydroxy-1 -methyl-2-( 1 -methyl-1 - {[morpholin-4-yl(oxo)acetyI]amino} cthyl)-6-oxo-1,6-dihydropyrim idine-4-carboxamide; 2-{(2R,4R)-l-f(diinethylamino)(oxo)acetyIj-4-mcthoxypyrrolidin-2-yl}-N-(4-fluorobenzyl)-5-hydroxy-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-((2S)-4,4-difluoro-l-(pyrazin-2-ylcarbonyI)pyrrolidin-2-ylJ-N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyI)-5-hydroxy-1 -methyl-2-{(2S,4S)-1 -methyI-4-[(mcthylsulfonyl)amino \|pyrrol id in-2-yl}-6-oxo-1,6-dihydropyrim idine-4-carboxamide; 2-{l-[(dimethylamino)sulfonyi\|pyrroIidin-2-yl}-N-(4-fluorobcnzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamicic; 2-{(2R,4R)-4-ethoxy-l-((methylamino)(oxo)acetyl]pyrrolidin-2-yl}-N-(4-fluorobenzyl)-5-hydroxy-l-mcthyI-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-\|(2S)-4,4-difluoro-l-(pyridazin-3-ylcarbonyI)pyrrolidin-2-yl]-N-(4~tluorobenzyl)-5-hydroxy-]-methyl-6-oxo-K6-dihydropyrimidinc-4-carboxamide; 2-[(2S)-4,4-difluoro-l-(pyridiiv2-ylcarbonyl)pyrrolidin-2-ylj-N-(4-fluorobenzyl)-5-hydroxy-]-methyl-6-oxo-i,6-dihydropyrimidine-4-carboxamide; 2-{(2S)-l-[(dimethylamino)(oxo)acctylj-4,4-dinuoropyrrolidin-2-yl}-N-(4-fluorobenzyl)-5-hydroxy-l -mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide: N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-2-{ 1 ~[morpholin-4-yl(oxo)acety!]pyrrolidin-2-yl)-6-oxo-l,6-dihydropyrimidine-4-carboxamidc; 2-{(2S)-l-[(dimethylamino)(oxo)acetyl]pyrrolidin-2-yI}-N-(4-fluorobenzyl)-5-hydroKy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamidc; 2-{(2S)-l-[(dimethyIamino)(oxo)acetyl]pyrrolidin-2-yl}-N-(4-fluoro-2-mcthoxybenzyl)-5-hydroxy-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; Nl-\| l-(4-{[(4-fluorobcnzyl)amino]carbonyl}-5-hydroxy-l-methyl-6-oxo-l16-dihydropyrimidin-2-yl)-l-mcthylethyl]-Nl,N2,N2-lrimclhylcthanediamide; 2-((2S)-l-acetylpyrroIidin-2-y!l-N-(4-fluoro-2-methoxybenzyl)-5-hydroxy-l-methyI-6~oxo-l,6-dihydropyrimidinc-4-carboxamide; N-(4-nuorobenzyl)-2-[(2S,4S)-4-nuoro-l-rnethylpyrrolidin-2-yI]-5-hydroxy-l-methyI-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-{(2S,4S)-]-[(dimcthylamino)(oxo)acetyl]-4-fluoropyrrolidin-2-yl}-N-(4-niiorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; Nl-\| i-(4-{[(3-chloro-4-iluorobenzyl)amino]carbonyl}-5-hydroxy-l-mcthyl-6-oxo-K6'dihydropyrimidin-2-yl)-l-mcthylethyl]-N2,N2-dimethylethanediamide; and pharmaceutically acceptable salts thereof. Another aspect of the present invention is a compound selected from the group consisting of: N-(4-nuorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-f l-(pyrazin-2-ylcarbonyI)pyrrolidin-2-yl \|-1,6-dihydropyrimidine-4-carboxamide; 2~\|(2S,4R)-l-benzoy]-4-hydroxypyrrolidin-2-yl]-N-(4-fluoiobenzyl)-5-hydroxy-l-methyl-6-oxo-K6-dihydropyrimidine-4-carboxamidc; N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-2-{ 1 -((1 -oxidopyridin-2-yI)carbonyl]pyrrolidin-2-yij~6-oxo-i,6-dihydropyrimidine-4-carboxamide;, 2-( I -acetylpyrrolidin-2-yI)-N-(4-f1uorobenzyl)-5-hydroxy-1 -methyl-6-oxo-1.6-dihydropyrimidine-4-carboxamide; 2-f(2S,4R)-4-(benzyloxy)-l-(pyridin-2-ylcarbonyI)pyrrolidin-2-yl]-N-(4-fliior()benzyl)-5-hydroxy-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-1 -methyI-2-(4-methylmorpholin-3-yl)-6-oxo-1,6-dihydropyrimidine-4-carboxamide; (0-N-(4-fluorobenzyl)-5-hydro\y-1 nriethyl-2-(4-methylmorpholin-3-yl)-6-oxo-1,6-dihydropyrimidine-4-carboxamide (-) -N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-2-(4-mcthylmorpholin-3-yl)-6-oxo-1,6-dihydropyrimidine-4-carboxamide N-(4-(luorobenzyl)-5-hydroxy-1 -methyl-6-oxo-2-[ 1 -(pyridin-2-ylcarbonyI)pyrroiidin-2-yl\|-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyI)~5-hydroxy-1 -methyl-6-oxo-2-[ 1 -(pyridin-2-ylcarbonyl)-1,2,3,4-tctrahydroquinolin-2-yl]-1,6-dihydropyrimidine-4-carboxamide; 2-[(2S.4R)-l-benzoyl-4-(bcnzyloxy)pyrroiidin-2-yl]-N-(4-lluorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamidc; 2-[(2S,4R)-I-acetyl-4-(bcnzyIoxy)pyrroIidin-2-yl]-N-(4-fluorobenzyI)-5-hydroxy-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamidc; N-(4-nuorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-\| I-(pyridin-3-ylcarbonyl)pyrrolidin-2-yl \|-1,6-dihydropyrimidinc-4-carboxamide; N-(4-nuorobenzyI)-5-hydi'oxy-2-(l-isonicotinoylpyrrolidin-2-yl)-l-methyl--6-oxo-K6-dihydropyrimidinc-4-carboxamide; 2-( 1,4-dimethylpiperazin-2-yI)-N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-qxo-1,6-dihydropyrimidinc-4-carboxamide; N-(4-nuorobenzyi)-5-hydroxy-1 -methyl-2-{ 1 -\| (I -methyl-1 H-imidazol-2-yl)carbonyI]pyrrolidin-2-yl}-6-oxo-1,6-dihydropyrim id ine-4-carboxamide; 2-(l-benzoylpyrrolidin-2-yl)-N-(4-i1uorobenzyI)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-l-methyi-2-( l-(methylsulfonyl)pyrrolidin-2-yI\|-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-\|(4R)-3-acetyl-l,3-thiazolidin-4-ylJ-N-(4-nuorobenzyl)-5-hydroxy-l-methyl-6-oxo-1,6-dihydropyrim idinc-4-carboxamide; 2-{ l-\|(ethylamino)carbonyl\|pyrrolidin-2-yl}-N-(4-nuorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; 2-(4-ethyl-l-methylpiperazin-2-yl)-N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-1.6-dihydropyrimidine-4-carboxamide; 2-\|(2S,4R)-4-(benzyloxy)-l-methylpyrrolidin-2-yl]-N-(4-fluorobenzyl)-5-hydroxy-l-melhyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo-2-[ 1 -(pyridin-2-ylcarbonyl)-2,3-dihydro-lH-indol-2-yl]-I,6-dihydropyrimidine-4-carboxamide; N-(4-fluorobenzyl)-5-hydroxy-1 -mcthyl-2-( 1 -methyl-1,2,3,4-tetrahydroquinolin-2-yl)-6-oxo-l,6-dihydropyrimidine-4-carboxamide; N-(4-nuorobenzyl)-5-hydroxy-l-methyl-2-(2-mcthyl-1,2,3,4-tetrahydroisoquinoIin-3-yl)-6-oxo-I,6-dihydropyrimidine-4-carboxamide; 2-j 1 -(dimethylamino)-2-phenylethyl]-N-(4-fluoroben/.yl)-5-hydroxy-1 -methy 1-6-oxo- l,6-dihydropyrimidine-4-carboxamidc; ;■. 2-\|(dimethylamino)(phenyl)methyl]-N-(4-fluoroben/yl)-5-hydroxy-l-methy 1-6-oxo-I,6~dihydropyrimidine-4-carboxamide; N-(2,3-dimethoxybenzyl)-5-hydroxy-l-methyl-2-(4-(morpholin-4-ylmethyl)phenyl]-6-oxo-1,6-dihydropyrimidine-4-carboxamide; and pharmaceuticaliy acceptable salts thereof. Other embodiments of the present invention include the following: (a) A pharmaceutical composition comprising a compound of Formula (1) and a pharmaceutically acceptable carrier. (b) A pharmaceutical composition which comprises the product prepared by combining (e.g., mixing) an effective amount of a compound of Formula (I) and a pharmaceutically acceptable carrier. (c) The pharmaceutical composition of (a) or (b), further comprising a therapeutically effective amount of an HIV infection/AIDS treatment agent selected from the group consisting of HIV/AIDS antiviral agents, immunomodulators, and anti-infective agents. (d) The pharmaceutical composition of (c), wherein the HIV infection/AIDS treatment agent is an antiviral selected from the group consisting of HIV protease inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, and nucleoside HIV reverse transcriptase inhibitors. (e) A combination useful for inhibiting HIV integrase, for treating or preventing infection by HIV, or for preventing, treating or delaying the onset of AIDS, which is a therapeutically effective amount of a compound of Formula (I) and a therapeutically effective amount of an HIV infection/AIDS treatment agent selected from the group consisting of HIV/AIDS antiviral agents, immunomodulators. and anti-infective agents. (i) The combination of (e), wherein the HIV infection/AIDS treatment agent is an antiviral selected from the group consisting of HIV protease inhibitors, non-nucleoside HIV reverse transcriptase inhibitors and nucleoside HIV reverse transcriptase inhibitors. (g) A method of inhibiting HIV integrase in a subject in need thereof which comprises administering to the subject a therapeutically effective amount of a compound of Formula (I). (h) A method of preventing or treating infection by HIV in a subject in need thereof which comprises administering to the subject a therapeutically effective amount of a compound of Formula (I). (i) The method of (h), wherein the compound of Formula (I) is administered in combination with a therapeutically effective amount of at least one antiviral selected from the group consisting of HIV protease inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, and nucleoside HIV reverse transcriptase inhibitors. (j) A method of preventing, treating or delaying the onset of AIDS in a subject in need thereof which comprises administering to the subject a therapeutically effective amount of a compound of Formula (I). (k) The method of (j), wherein the compound is administered in combination with a therapeutically effective amount of at least one antiviral selected from the group consisting of HIV protease inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, and nucleoside HIV reverse transcriptase inhibitors (I) A method of inhibiting HIV integrase in a subject in need thereof which comprises administering to the subject the pharmaceutical composition of (a), (b). (c) or (d) or the combination of (e) or (f). (m) A method of preventing or treating infection by HIV in a subject in need thereof which comprises administering to the subject the pharmaceutical composition of (a), (b), (c) or (d) or the combination of (e) or (f). (n) A method of preventing, treating or delaying the onset of AIDS in a subject in need thereof which comprises administering to the subject the pharmaceutical composition of (a), (b), (c) or (d) or the combination of (e) or (f). The present invention also includes a compound of the present invention (i) for use in, (ii) for use as a medicament for. or (iii) for use in the preparation of a medicament for: (a) inhibiting HIV protease, (b) preventing or treating infection by HIV, or (c) preventing, treating or delaying the onset of AIDS. In these uses, the compounds of the present invention can optionally be employed in combination with one or more HIV/AIDS treatment agents selected from HIV/AIDS antiviral agents, anti-infective agents, and immunomodulators. Additional embodiments of the invention include the pharmaceutical compositions, combinations and methods set forth in (a)-(n) above and the jjses set forth in the preceding paragraph, wherein the compound of the present invention employed therein is a compound of one of the embodiments, aspects, classes, subclasses, or features of the compounds described above. In all of these embodiments, the compound may optionally be used in the form of a pharmaceutical^ acceptable salt. As used herein, the term tkC) _6 alkyl" (or "C l -C6 alkyl") means linear or branched chain alkyl groups having from 1 to 6 carbon atoms and includes all of the hexyl alkyl and pentyl alkyl isomers as well as n-, iso-, sec- and t-butyl, n- and isopropyl, ethyl and methyl. "C]-4 alkyl" means n-, iso-, sec- and t-butyl, n- and isopropyl, ethyl and methyl. The term "Co" as employed in expressions such as UCQ-6 alkyl" means a direct covalent bond. For example, when Rl in Compound 1 is -CO-6 alkyl-O-Co-6 alkyl-Rk, then Rl is -O-Rk when both alkyl groups are Co alkyl. Similarly, when an integer defining the presence of a certain number of atoms in a group is equal to zero, it means that the atoms adjacent thereto are connected directly by a bond. For example, the compound of Formula (II) has T as a substituent at the 2- position of the pyrimidinone ring, wherein s is an integer equal to zero, 1 or 2. When s is zero, the substituent has the following structure: T The term M-Cj-6 alkyl-" refers to a Ci to C^ linear or branched alkyl group as just defined which is bivalent. It can alternatively be referred to as "Ci-6 alkylene" or "Ci-6 alkancdiyl". A class of alkylenes of particular interest with respect to the invention is -(CH2)l-6-- and sub-classes of particular interest include -(CH2)l-4-, -(CH2)l-3% -(CH2)l-2-, and -CH2-. The term "C?-5 alkynyl" (or "C2-C5 alkynyl") means linear or branched chain alkynyl groups having from 2 to 5 carbon atoms and includes all of the pentynyl isomers as well as 1-bulynyl, 2-butynyl, 3-butvnyl. 1-propynyl, 2-propynyl, and ethynyl (or acctylenyl). Similar terms such as "C'2-3 alkynyl" have an analogous meaning. The term "C3-8 cycloalkyl" (or "C3-C8 cycloalkyl") means a cyclic rinu of an alkane having three to eight total carbon atoms (i.e.. cvclooroDvL cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyt). The terms "C3-7 cycloalkyP", "C3-6 cycloalkyl", "C5-7 cycloalky!" and the like have analogous meanings. The term "C3-7 azacycloalkyr (or "C3-C7 azacycloalkyl") means a saturated cyclic ring consisting of one nitrogen and from three to seven carbon atoms (i.e., azetidinyl, pyrrolidinyl, piperidinyl, or azepanyi). The term "halogen" (or "halo'1) refers to fluorine, chlorine, bromine and iodine (alternatively referred to as fluoro, chloro, bromo, and iodo). The term "Cj-6 haloalkyl" (which may alternatively be referred to as "C]-Cg haloalkyl" or "halogenated C]-C6 alky I'") means a C] to Cfr linear or branched aikyl group as defined above with one or more halogen substituents. The term "C1-4 haloalkyl" has an analogous meaning. The term "C\|_6 fluoroalkyl'" has an analogous meaning except that the halogen substituents are restricted to fluoro. Suitable fluoroalkyls include the series (CH2)0-4CT3 (i.e., trifluoromethyl, 2,2,2- trilluoroethyl, 3,3,3-trifluoro-n-propyl, etc.). The term "carbocycle" (and variations thereof such as "carbocyclic" or "carbocyclyl") as used herein refers to (i) a C3 to Cg monocyclic, saturated or unsaturated ring, (ii) a C7 to C]2 bicyclic ring system, or (iii) aCn to C\^ tricyclic ring system, wherein each ring in (ii) or (iii) is independent of or fused to the other ring or rings and each ring is saturated or unsaturated. The carbocycle may be attached to the rest of the molecule at any carbon atom which results in a stable compound. The fused bicyclic carbocycles are a subset of the carbocycles; i.e., the term "fused bicyclic carbocycle" generally refers to a C7 to C]0 bicyclic ring system in which each ring is saturated or unsaturated and two adjacent carbon atoms are shared by each of the rings in the ring system. Fused tricyclic carbocycles have an anaiogous meaning. A subset of the fused bicyclic carbocycles are those bicyclic carbocycles in which one ring is a benzene ring and the other ring is saturated or unsaturated, with attachment via any carbon atom that results in a stable compound. Representative examples of this subset include the following: The term "aryl" refers to aromatic mono- and poly-carbocyclic ring systems, wherein the individual carbocyclic rings in the polyring systems are fused or attached to each other via a single bond. Suitable aryl groups include phenyl, naphthyl, and biphenylenyl. The term "heterocycle" (and variations thereof such as "heterocyclic" or "heterocyclyl") broadly refers to (i) a 4- to 8-membered, saturated or unsaturated monocyclic ring, (ii) a 7- to 12-membered bicyclic ring system, or (iii) an 1 1 to 16-mcmbcrcd tricyclic ring system; wherein each ring in (ii) or (iii) is independent of or fused to the other ring or rings and each ring is saturated or unsaturated, and the monocyclic ring, bicyclic ring system, ortricyclic ring system contains one or more hcteroatoms (e.g., from I to 6 heteroatoms, or from 1 to 4 heteroatoms) selected from N, O and S and a balance of carbon atoms (the monocylic ring typically contains at least one carbon atom and the ring systems typically contain at least two carbon atoms); and wherein any one or more of the nitrogen and sulfur heteroatoms is optionally be oxidized, and any one or more of the nitrogen heteroatoms is optionally quaternizcd. The heterocyclic ring may be attached at any heteroatom or carbon atom, provided that attachment results in the creation of a stable structure. When the heterocyclic ring has substituents, it is understood that the substituents may be attached to any atom in the ring, whether a heteroatom or a carbon atom, provided that a stable chemical structure results. Saturated heterocyclics form a subset of the heterocycles; i.e., the term "saturated heterocyclic" generally refers to a heterocycle as defined above in which the entire ring system (whether mono- or poly-cyclic) is saturated. The term "saturated heterocyclic ring" refers to a 4- to 8-membered saturated monocyclic ring which consists of carbon atoms and one or more heteroatoms selected from N, O and S. Representative examples include piperidinyl, piperazinyl, azepanyl, pyrrolidinyl, pyrazolidinyl, imidazolidinyl, oxazolidinyl, isoxazolidinyl, morpholinyl, thiomorpholinyl, thiazolidinyi, isothiazolidinyl, and tetrahydrofuryl (or tetrahydrofuranyi). Hcteroaromatics form another subset of the heterocycles; i.e.. the term "heteroaromatic" (alternatively "'heteroaryr) generally refers to a heterocycle as defined above in which the entire ring system (whether mono- or poly-cyclic) is an aromatic ring system. The term "heteroaromatic ring" refers a 5- or 6-membered monocyclic aromatic ring which consists of carbon atoms and one or more hcteroatoms selected from N, O and S. Representative examples of heteroaromatic rings include pyridyl, pyrrolyl, pyrazinyl, pyrimidinyL pyridazinyl, thienyl (or thiophenyl), thiazolyl, furanyl, imidazolyl, pyrazolyi, triazolyi, tetrazolyl, oxazolyl, isooxazolyl, oxadiazolyl, thiazolyl, isothiazoiyl, and Ihiadiazolyl. Representative examples of bicyclic heterocycles include benzotriazolyl, indolyl. isoindolyl, indazolyl, indolinyl, isoindolinyl, quinoxalinyl, quinazolinyl, cinnolinyl, chromanyl, isochromanyl, tetrahydroquinolinyl, quinolinyl, tctrahydroisoquinolinyl, isoquinolinyl, 2,3-dihydrobenzofuranyl, 2,3-dihydrobenzo- two adjacent carbon atoms. Representative examples of tricyclic heterocycles include phenothiazinyl, carbazolyl, beta-carbolinyl, tetrahydro-beta-carboiinyl, acridinyl, phenazinyl, and phenoxazinyl. Unless expressly stated to the contrary, an "'unsaturated" ring is a partially or fully unsaturated ring. For example, an "unsaturated monocyclic C(> carbocycle" refers to cyclohexene, cyclohexadiene, and benzene. Unless expressly stated to the contrary, all ranges cited herein are inclusive. For example, a heterocycle described as containing from "1 to 4 heteroatoms" means the heterocycle can contain 1, 2, 3 or 4 heteroatoms. When any variable (e.g., Ra, Rt\ Rc, Rk, etc.) occurs more than one time in any constituent or in Formula 1 or in any other formula depicting and describing compounds of the invention, its definition on each occurrence is independent of its definition at every other occurrence. Also, combinations of substituents and/or variables are permissible only if such combinations result in stable compounds. The term "substituted" (e.g., as in "aryl which is optionally substituted with ont or more substituents ...") includes mono- and poly-substitution by a named substituent to the extent such single and multiple substitution (including multiple substitution at the same site) is chemically allowed. The compounds of the present invention may have asymmetric centers and may occur, except when specifically noted, as mixtures of stereoisomers or as individual diastereomers, or enantiomers, with all isomeric forms being included in the present invention. The N-substituted hydroxypyrimidinone compounds of the present invention may also occur as lautomers thereof. It is understood that the present invention includes all tautomcrs of the hydroxypyrimidinone compounds of Formula 1, both singly and in mixtures. The compounds of the present invention are useful in the inhibition of HIV integrase, the prevention or treatment of infection by human immunodeficiency virus (HIV) and the prevention, treatment or the delay in the onset of consequent pathological conditions such as AIDS. Preventing AIDS, treating AIDS, delaying the onset of AIDS, or preventing or treating infection by HIV is defined as including, but not limited to, treatment of a wide range of states of HIV infection: AIDS, ARC (AIDS related complex), both symptomatic and asymptomatic, and actual or potential exposure to HIV. For example, the compounds of this invention are useful in treating infection by HIV after suspected past exposure to HIV by such means as blood transfusion, exchange of body fluids, bites, accidental needle stick, or exposure to patient blood during surgery. The compounds of this invention are useful in the preparation and execution of screening assays for antiviral compounds. For example, the compounds of this invention are useful for isolating enzyme mutants, which are excellent screening tools for more powerful antiviral compounds. Furthermore, the compounds of this invention arc useful in establishing or determining the binding site of other antivirals to HIV integrase, e.g., by competitive inhibition. Thus the compounds of this invention are commercial products to be sold for these purposes. Compounds representative of the present invention have been tested for inhibition in an assay for the strand transfer activity of integrase. The assay is conducted in accordance with Wolfe, A.L. et al., J, Virol. 1996, 70: 1424-1432, for recombinant integrase, except that: (i) the assay uses preassembled integrase strand transfer complexes; (ii) the strand transfer reaction is performed in the presence of inhibitor in 2.5 mM MgCl2 using 0.5 to 5 nM of a 3" ITFC labeled target DNA substrate as described in WO 02/30930 and (iii) strand transfer products are detected using an alkaline phosphatase conjugated anti-FITC antibody and a chemiluminescent alkaline phosphatase substrate. Representative compounds (e.g., the compounds set forth in Table 1 below) tested in the integrase assay demonstrated !C50's of about 5 micromolar or less. Further description on conducting the assay using preassembled complexes is found in Hazuda et al., J. Virol. 1997, 7J_: 7005-701 1; Hazuda et al., Drug Design and Discovery 1997, J_5: 17-24; and Hazuda et al., Science 2000, 287: 646-650. Certain compounds representative of the present invention have also been tested in an assay for inhibition of acute HIV infection of T-iymphoid cells, conducted in accordance with Vacca, J.P. et al., Proc. Natl. Acad. Sci. USA 1994, 9J_: 4096. These compounds demonstrated IC95's of about 20 micromolar or less. The compounds of the present invention may be administered in the form of pharmaceutical^ acceptable salts. The term "pharmaceutically acceptable salt" refers to a salt which possesses the effectiveness of the parent compound and which is not biologically or otherwise undesirable (e.g., is neither toxic nor otherwise deleterious to the recipient thereof). Suitable salts include acid addition salts which may, for example, be formed by mixing a solution of the compound of the present invention with a solution of a pharmaceutically acceptable acid such as hydrochloric acid, sulfuric acid, acetic acid, trifluoroacetic acid, or benzoic acid. When the compounds of the invention carry an acidic moiety, suitable pharmaceutically acceptable salts thereof can include alkali metal salts (e.g., sodium or potassium salts), alkaline earth metal salts (e.g., calcium or magnesium salts), and salts formed with suitable organic ligands such as quaternary ammonium salts. Also, in the case of an acid (-COOH) or alcohol group being present, pharmaceutically acceptable esters can be employed to modify the solubility or hydrolysis characteristics of the compound. For the purpose of preventing or treating HIV infection or preventing, treating or delaying the onset of AIDS, the compounds of the present invention may be administered orally, parenterally (including subcutaneous injections, intravenous, intramuscular, intrasternal injection or infusion techniques), by inhalation spray, or rectal ly, in the form of a unit dosage of a pharmaceutical composition containing a therapeutically effective amount of the compound and conventional non-toxic pharmaceutically-acceptable carriers, adjuvants and vehicle The term "administration" and variants thereof (e.g., "administering" a compound) in reference to a compound of the invention mean providing the. compound or a prodrug of the compound to the individual in need of treatment. When a compound of the invention or a prodrug thereof is provided in combination with one or more other active agents (e.g., antiviral agents useful for treating HIV infection or AIDS), "administration" and its variants are each understood to include concurrent and sequential provision of the compound or prodrug and other agents. As used herein, the term "composition" is intended to encompass a product comprising the specified ingredients in the specified amounts, as well as any product which results, directly or indirectly, from combining the specified ingredients in the specified amounts. By "pharmaceutical^ acceptable" is meant that the ingredients of the pharmaceutical composition must be compatible with each other and not deleterious to the recipient thereof. The term "subject" (alternatively referred to herein as "patient") as used herein refers to an animal, preferably a mammal, most preferably a human, who has been the object of treatment, observation or experiment. The term "therapeutically effective amount" as used herein means that amount of active compound or pharmaceutical agent that elicits the biological or medicinal response in a tissue, system, animal or human that is being sought by a researcher, veterinarian, medical doctor or other clinician, which includes alleviation of the symptoms of the disease being treated. When the active compound (i.e., active ingredient) is administered as the salt, references to the amount of active ingredient are to the free acid or free base form of the compound. The pharmaceutical compositions may be in the form of oral ly- administrable suspensions or tablets or capsules, nasal sprays, sterile injectible preparations, for example, as sterile injectible aqueous or oleagenous suspensions or suppositories. These compositions can be prepared by methods and contain excipients which are well known in the art. Suitable methods and ingredients are described in Remington's Pharmaceutical Sciences, 18th edition, edited by A. R. Gennaro, Mack Publishing Co., 1990, which is herein incorporated by reference in its entirety. The compounds of this invention can be administered orally in a dosage range of 0.001 to 1000 mg/kg of mammal (e.g.. human) body weight per day in a single dose or in divided doses. One preferred dosage range is 0.01 to 500 mg/kg body weight per day orally in a single dose or in divided doses. Another preferred doses. For oral administration, the compositions can be provided in the form of tablets or capsules containing 1.0 to 500 milligrams of the active ingredient, particularly 1,5, 10, 15,20.25,50, 75, 100, 150, 200. 250, 300, 400, and 500 milligrams of the active ingredient for the symptomatic adjustment of the dosage to the patient to be treated. 'The specific dose level and frequency of dosage for any particular patient may be varied and will depend upon a variety of factors including the activity of the specific compound employed, the metabolic stability and length of action of that compound, the age, body weight, general health, sex, diet, mode and time of administration, rate of excretion, drug combination, the severity of the particular condition, and the host undergoing therapy. As noted above, the present invention is also directed to use of the HIV integrase inhibitor compounds of the present invention with one or more agents useful in the treatment of HIV infection or AIDS. For example, the compounds of this invention may be effectively administered, whether at periods of pre-exposure and/or post-exposure, in combination with effective amounts of one or more of the HIV/AIDS antivirals, imunomodulators, antiinfectives, or vaccines useful for treating HIV infection or AIDS. Suitable antiviral agents include those listed in the following Table: PI — protease inhibitor nnRTI = non-nuclcosidc reverse transcriptase inhibitor nRTI = nucleoside reverse transcriptase inhibitor A compound of the present invention can also be administered in combination with another HIV integrase inhibitor such as a compound described in WO 99/62513, WO 99/62520, or WO 99/62897. A compound of the present invention can also be administered in combination with a CCR5 receptor antagonist, such as a compound described in WO 99/04794, WO 99/09984, WO 99/38514, WO 00/59497, WO 00/59498, WO 00/59502, WO 00/59503, WO 00/76511, WO 00/76512, WO00/76513, WO 00/765 14, WO 00/76792, or WO 00/76793. The compounds of this invention may be effectively administered, whether at periods of pre-exposure and/or post-exposure, in combination with effective amounts of one or more HIV/AIDS antivirals, immunomodulators, antiinicctives, or vaccines useful for treating HIV infection or AIDS disclosed in the Table in WO 01/38332, which is herein incorporated by reference in its entirety. It will be understood that the scope of combinations of the compounds of this invention with HIV/AIDS antivirals, immunomodulators, anti-infectives or vaccines is not limited to those listed above or listed in the above-referenced Table in WO 01/38332, but includes in principle any combination with any pharmaceutical composition useful for the treatment of AIDS. The HIV/AIDS antivirals and other agents will typically be employed in these combinations in their conventional dosage ranges and regimens as reported in the art, including the dosages described in the Physicians' Desk Reference, 54lh edition, Medical Economics Company, 2000. The dosage ranges for a compound of the invention in these combinations are the same as those set forth above. Abbreviations used in the instant specification, particularly the Schemes and Examples, include the following: AIDS " acquired immunodeficiency syndrome ARC AIDS related complex BOC or Boc := t-butyloxycarbonyl Bn ~-: benzyl Bz - benzoyl CBZ or Cbz = carbobenzoxy (alternatively, benzyloxycarbonyl) DMAD - dimethylacetylenedicarboxylate DMAP r dimethylaminopyridine DMF '-'-'- N,N-dimethylformamide Ht ^ ethyl LtOAc -■ ethyl acetate FIA-MS -" How injection analysis mass spectrometi^ HIV ■■"-"■ human immunodeficiency virus I -I PLC "" high performance liquid chromatography m-CPBA - meta-chloroperbenzoic acid Me - methyl NMP :": N-methyl pyrrolidinone NMR nuclear magnetic resonance Ph L-~ phenyl TFA ; trilluoroacetic acid THF ~:z tetrahydrofuran The compounds of the present invention can be readily prepared according to the following reaction schemes and examples, or modifications thereof, using readily available starting materials and reagents. In these reactions, it is also possible to make use of variants which are themselves known to those of ordinary skill in this art, but arc not mentioned in greater detail. Furthermore, other methods for preparing compounds of the invention will be readily apparent to the person of ordinary skill in the art in light of the following reaction schemes and examples. Unless otherwise indicated, all variables are as defined above. The compounds of the present invention can be prepared by coupling suitable substituted alkyl l-alkyI-l,6-dihydro-5-hydroxy-6-oxopyrimidine-4-carboxylates (or carboxylic acids or halides) with the appropriate amines, as represented by Scheme I. In the scheme, P is H or a protective group, typically an ester (e.g., benzoate or pivalate) that is normally removed under the conditions employed to convert the the methyl ester to the amide. The ester protective group is typically used to purify the 2-substituted-5,6 dihydroxypyrimidine-4-carboxylates after their synthesis when the unprotected product cannot be crystallized from the reaction crude and/or for synthetic reasons. Methods for coupling carboxylic acid derivatives with amines to form carboxamides are well known in the art. Suitable methods are described, for example, in Jerry March, Advanced Organic Chemistry, 3rd edition. John Wiley & Sons, 1985, pp. 370-376. Amines of formula 1-1 can be prepared using the methods described in Richard Larock, Comprehensive Organic Transformations. VCH Publishers Inc, 1989, pp 385-438, or routine variations thereof. Methyl l-alkyl-l,6-dihydro-5-hydroxy-6-oxopyrimidine-4-carboxylates of formula 1-2 can be prepared as shown in Scheme 2, wherein amidoxime 2-1 can be reacted with DMAD in an appropriate solvent and at a suitable temperature to give the intermediate dihydroxypyrimidine 2-2, followed by protection of the 5-hydroxy group in 2-2 with a suitable protecting agent such as benzoate or pivalate to give 2-3, and then alkylation of nitrogcn-1 to afford 1-2. This procedure is described in the literature [Culbertson et al., J Ileterocycl Chew, 1979, J_6 (7): 1423-24]. Dihydroxypyrimidine 2-2 can be isolated or directly protected to give 2-3. The alkyl group can be introduced on Ni by reaction of 2-3 with an alkylating agent in the presence of an inorganic base (e.g., cesium carbonate). If a mixture of N- and O-alkylated derivatives results, the desired N-alkylated product 1-2 can be separated by flash chromatography. Scheme 2 is exemplified in Example 1. Scheme 2 (- ~i Methyl l-alkyl-l,6-dihydro-5-hydroxy-6-oxopyrimidine-4-carboxyIates of formula 1-2 can be prepared as shown in Scheme 3, wherein an N-alkylamidoxime 3-1 can be reacted with dimethylacetylenedicarboxylate to give the unprotected 1-2 (P- 11). The unprotected compound can be isolated as such or it can be converted to 1-2 by reaction with a suitable protecting group. Scheme 3 is exemplified in Example 2. Scheme 3 Amidoximes 2-1 and 3-1 are prepared from the corresponding nitriles by chemistry described herein (see Example 1, Step 1 and Example 2, Step 2). Nitriles can be prepared from carboxylic acids by various procedures known in the an. including, for example, conversion to carboxamides by the procedure of of Pozdnev {Tetrahedron Lett. 1989, 30: 5193) (see also, Example 6, Step 2), and dehydration of the amide by the procedure of Waldmann {Tetrahedron 1994, 50: 11865) (see also, Example 6, Step 3). Compounds of the present invention of general formula 3-3 or 3-6 can be prepared in accordance with Scheme 3, Parts 1 and 2, wherein haloderivative 3-1 or 3-4 can be synthesized by the bromination or chlorination of a suitable substrate affording a -CH2Br, -CI bCI, -CHBr-, or -CMC!- group, followed by displacement of the halogen with a nucleophile ("Nu") such as an amine, thiol, or alcoholatc to obtain the nucleophile-substituted methyl ester intermediate 3-2 or 3-5, which need not be isolated. Elaboration of the methyl ester functionality into the carboxamide will afford the final product 5-3 or 3-6. Scheme 3 is exemplified in Example 5. Scheme 3 - Part I Scheme 4 depicts the preparation of compounds of the invention that contain an alkylated aliphatic amine in the substituent at the 2 position. Nitrogen alkylation is achieved via a reductive amination or alkylation. The nitrogen alkylation can be performed before formation of the amide {via 4-3) or after formation of the amide {via 4-2) depending on the substrate, with suitable deprotection as necessary. Scheme 4 is exemplified in Examples 6 to 8 below. Compounds of the present invention with general formula 5-3 containing an acylated nitrogen or sulfonylated nitrogen in the substituent at the 2-position, can be prepared following Scheme 5. Acylation or sulfonylation of the nitrogen in the 2-substituent of the pyrimidine core provides compound 5-2, which can bo elaborated into the final amide 5-3 by reaction of a suitable amine in a polar solvent. Scheme 5 is exemplified in Examples 9 to 12 below. The preparation of compounds that feature a carboxamide at the 2 position of the pyrimidine core can be achieved as shown in Scheme 6, wherein a starting material bearing a 2-ethyl- and a 4-methylcarboxyIate functionality (6-1) is employed. This strategy will allow the regioselective elaboration of the 4-methyl ester into the carboxamide by reaction with a suitable amine. The other ester bond in the 2 position can then be further elaborated. Scheme 6 is exemplified in Example 13 below. Compounds of the present invention of formula 7-2 can be prepared by reaction of aldehydes or ketones 7-1 with suitable amines under reductive alkylation conditions, as shown in Scheme 7. Scheme 7 is cxcmplifed in Kxample 14 below. In the processes for preparing compounds of the present invention set forth in the foregoing schemes and exemplified in the examples below, functional groups in various moieties and substituents may be sensitive or reactive under the reaction conditions employed and/or in the presence of the reagents employed. Such sensitivity/reactivity can interfere with the progress of the desired reaction to reduce the yield of the desired product, or possibly even preclude its formation. Accordingly, it may be necessary or desirable to protect sensitive or reactive groups on any of the molecules concerned. Protection can be achieved by means of conventional protecting groups, such as those described in Protective Groups in Organic Chemistry, ed. J.F.W. McOmie, Plenum Press, 1973 and in T.W. Greene & P.G.M. Wuts, Protective Groups in Organic Synthesis, John Wiley & Sons, 1991. The protecting groups can be removed at a convenient subsequent stage using methods known in the art. For example, in preparing the compounds of the invention it is sometimes necessary to protect one or more amino groups (e.g., amino groups present in substituents at the 2-position of the pyrimidinone ring) with, for example, a 13oc or Cbz group or to protect hydroxy (e.g., the 5-hydroxy group on the with, for example, a benzoyl or benzyl group. The Boc group pan be removed by acid treatment (e.g., TFA) either before or after formation of the final amide at C-6 of the pyrimidinone nucleus. The Cbz and benzyl groups are typically removed by catalytic hydrogenation or under strong acid conditions, either prior to or following formation of the final amide. The benzoyl group can be removed concurrently with the formation of the final amide. Examples 6 and 12 below illustrate the use of a Boc protective group and of Boc, benzoyl and benzyl protective groups in the preparation of compounds of the invention. The preparation of compounds that feature a bis oxalamide at the 2 position of the pyrimidine core can be achieved as shown in Scheme 8. wherein a starling material bearing a basic nitrogen at the 2- position of the pyrimidinc carboxyamide (8-1) is employed. This strategy will allow to obtain the final compound (8-3) following two possible procedures: by simple coupling of monoamide oxalic acid to the amine (8-1) or by the acylation of the basic nitrogen of (8-1) with dimethyl oxalate to give the ester intermediate (8-2) that is converted to the final compound by heating in presence of amine in appropriate solvent. Scheme 8 is exemplified in Examples 17, 18, and 20 below. The following examples serve only to illustrate the invention and its practice. The examples are not to be construed as limitations on the scope or spirit of the invention. EXAMPLE I Methyl 5-(benzoyloxy)-2-[l-(/ Step 1: Tert-butyI-2-famino(hydroxyimino)methyl]pyrrolidine-l-carboxylate A solution of hydroxylamine hydrochloride (1.0 eq.) in MeOH was added at 0 °C to a solution of KOH (1.0 eq.) in MeOH. The resulting reaction mixture was filtered and added to a solution of/t7r/-butyl-2-cyanopyrrolidine-l-carboxylate (1.0 cq.) in methanol and stirred at 40 °C for 2 h.The solvent was removed //; vacuo and the residue treated with water; the solid was filtered and washed with a mixture of EhO: Petroleum Ether 1:1 to afford the title compound as a white solid as a mixture ofrotamers byNMR. 'H-NMR (DMSO-6, 400 MHz) 5 8.92 (s, 1 H),5.35(s,l H), 5.15 (s, I H), 4.25 (bs, 0.5 II), 4.10 (s, 0.5 II), 3.40-3.30 (m, 1 H), 2.10-1-70 (m, 4 H), 1.40 (s, 4.5 H),1.35 (s, 4.5 H), one signal is obscured by water. Stop J!: Methyl 5-(benzoyloxy)-2-[l-(^r/-butoxycarbonyl)pyrrolidin-2-yl\|-6- hydroxypyrimidine-4-carboxylate A solution of the product of Step 1 (1.0 eq.) and dimethyl acetylenedicarboxylate (1.05 eq.) in CHCbwas refluxed for 3 h. The reaction mixture was concentrated and the crude product was used directly in the next step without further purification. The crude product was dissolved in xylene and refluxed for 24 h. The solvent was removed in vacuo and the crude was dissolved in pyridine. Benzoic anhydride was added (1.5 eq.). The reaction mixture was stirred at room temperature until the starting material was consumed as determined by MS analysis. The reaction mixture was concentrated, and the resulting oil was diluted with ethyl acetate and washed with IN HO solution, saturated NaHCOi solution, saturated Nad solution. The crude oil obtained after organic solvent evaporation was purified by flash chromatography to obtain the title compound as a yellow solid. 'H-NMR(CDC-13, 400 MHZ) S 12.08 (bs, 1 H), 8.18 (d, J- 7.6 Hz, 2 H), 7.64 (t, J = 7.4 Hz, 1 H), 7.50 (t, J- 7.6 Hz, 2 H), 4.80-4.60 (m, I H), 3.82 (s, 3 H), 3.60-3.50 (m, I i I), 3.40-3.20 (m, 1 H), 2.50-2.10 (m, 2 H), 2.00-1.70 (m, 2 H), 1.50 (s, 9 H). MS/w/z444(M+H)+. StcpJV Methyl 5-(benzoyloxy)-2-\| l-(/er/-butoxycarbonyl)pyrrolidin-2-yl]-l- mcthyI-6-oxo-I,6-dihydropyrimidine-4-carboxylate To a stirred solution of the product of Step 2 (1.0 eq.) in THI\ Cs2C03 was added (1.2 eq.) followed by the addition of CH3I (2.0 eq.). The reaction was stirred at 40°C until the starting material was consumed as determined by MS analysis. The reaction was concentrated and the residue taken up with EtQAc, washed with I N HO, saturated solution of NaHCCb and brine. The organic phase was dried over anhydrous Na;>S04, filtered and concentrated. Reaction crude showed 3.4:1 ratio N (desired product) versus O methylation. The title product was purified by flash column chromatography (EtOAc: Petroleum Ether =: 1:1) and obtained as a 1:1 mixture of rotamers by NMR. lH-NMR(CDCI3!400MHz)5 8.12(d,y=7Hz, 2 II), 7.58 (t,J= 7 Hz, 1 11), 7.46 (t, 7= 7 Hz, 2 H), 4.97-4.95 (m, 0.5 H), 4.87-4.83 (m, 0.5 H), 3.74 (s, 1.5 H), 3.72 (s, 1.5 H), 3.63 (s, 1.5 H), 3.59 (s. 1.5 H), 3.56-3.42 (m, 1 H), 2.40-2.25 (m, 5 H), 1.41 (s, 4.5 H). 1.25 (s, 4.5 H). MS w/z458(M-i-H)'. Also obtained was the O-methylated compound of formula: as a mixture of rotamers by NMR. 'H-NMR (CDC13,400 MHz) 6 8.21 (d, J= 7.6 Hz, 211), 7.72 (t, J= 7.6 Hz, 111), 7.56 (t, J= 7.6 Hz, 2H), 5.10-5.05 (m, 0.3H), 5.00-4.95 (m, 0.7H), 4.01 (s, 3H), 3.87 (s, 3H), 3.80-3.60 (m, 2H), 2.50-2.40 (m, 1H), 2.15-2.00 (m, 2H), 2.00-1.85 (m, III), 1.61 (s, 2.7H), 1.40 (s, 6.3H). MSm/z458(M+H)EXAMPLE 2 Eicnzyl 2-[5-(benzoyloxy)-4-(methoxycarbonyl)-1 -methyl-6-oxo-1,6-dihydropyrimidin-2-yl\|indoline-l-carboxylate StepJj Benzyl 2-\|[hydroxy(methyl)aminoj(imino)methyl]indoline-l- carboxylale l-Benzyloxycarbonyl-2-cyanoindoiine was added to a solution of tricthylamine (2 eq.) and MeNHOH.HCl (2 cq.) in HtOH. After stirring overnight the reaction mixture was evaporated, dissolved in KtOAc, washed with water, dried over Na2S04and evaporated to afford the title compound. 'll NMR(DMSO-d6, 340K, 300 MHz) 8 7.68 (d,./ - 8.0 Hz, 1 H), 7.41-7.30 (m, 5 11), 7.19 (t, J =7.5 Hz, 2 11), 6.99 (t, J =7.6 Hz, 1 H). 5.53 (dd, J= 5.5, 10.9 Hz, I H), 5.22 (s, 2 H), 3.62 (dd, J- 11.0, 16.6 Hz, I H), 3.33 (s, 3 H), 3.01 (dd,J-5.5 Hz, 16.6 Hz, 1 H). MSIH/Z326(M+H)'Step 2: Benzyl 2-[5-(benzoyIoxy)-4-(methoxycarbonyl)-l-methyl-6-oxo-l,6- dihydmpyrimidi-2-yl]indoIine-l-carboxylate The product of Step 1 was dissolved in CHCI3 and dimethylacetylenediearboxylate was added dropwisc (1.2 eq.) at room temperature. After 4 h the mixture was evaporated, and the residue was dissolved in xylene and stirred at 160 °C for 2 days. The solvent was then evaporated, and the residue was dissolved in pyridine, after which (PhCO)20 (2 eq.) was added and the reaction mixture was stirred for 2 days. After evaporation, the resulting crude oil was diluted with EtOAc, washed with HC1 IN, dried over Na^SCXi and evaporated. The product was purified by flash chromatography on silica gel (F.tOAc/ petroleum ether, 1:4) to afford the title product. 1H NMR (DMSO-d6, 340 K, 400 MHz) 5 8.08 (d,./ ' 7.3 Hz, 2 H), 7.77 (L J - 7.4 Hz, 2 H), 7.62 (t, J -■ 7.6 Hz, 2 H), 7.31 -7.20 (m. 7 H). 7.00 (t, J = 7.3 Hz, 1H), 5.83 (dd. 7-4.6 Hz, 11.0 Hz, I H), 5.23-5.13 (m. 2 li). 3.76 (dd, ./= 11.1.16.6 Hz. 1 H), 3.65 (s, 3 H), 3.56 (s, 3 II), 3.27 (dd,./-4.4 Hz. 16.6 Hz, 1 II). \A£ ,.,A SA(\ f\A+\ n EXAMPLE 3 A^-(4-riuorobenzyl)-5-hydiu\y-l-methyl-2-(4-methylphcnyl)-6-oxo-l,6-dihydropyrimidine-4-carboxarnide To a stirred solution of methyl 5-[(2,2-dimelhylpropanoyI)oxy\|-l-methyl-2-(4-methylphenyl)-6-oxo-l,6-dihydropyrimidine-4-carboxylate (prepared from 4-methylbenzonitrile by procedures similar to those set forth in Examples 2 or 3) in DMF 3 equivalents of 4-fluorobenzyIamine were added and mixture was stirred at 90 °C for 2 h. The title product precipitated from the cooled reaction mixture after the addition of 2 N MCI, and was collected by filtration and washed with diethyl ether. !HNMR(DMSO-d6,400MHz)5 12.45 (s, 1 H), 9.3 I (bt, .7=6.0 Hz, 1 H), 7.62 (m, 2 H), 7.40-7.32 (m, 4 II), 7.14 (t,./- 8.8 Hz, 2 H). 4.45 (d, J= 6.0 Hz, 2 H), 3.35 (s, 3 H), 2.48 (s, 3 H). MS/w/z368(M+H)EXAMPLE 4 A^-(4-fluorobenzyl)"5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide Step 1: 4,5-Dihydroxy-6-(methoxycarbonyI)pyrimidine-2-carboxylic acid 2-l:thc)\ycarbonyI-4,5-Dihydroxy-6-(melhoxycarbonyI)pyrimidine [obtained from ethyl amino(hydroxyimino)ethanoate (Branco, P.S. et al, Tetrahedron 1992, 40: 6335) by procedures similar to those set forth in Example 1] was suspended in dioxane/TTIF 2:1 and IN NaOH was added. After 20 min the mixture was acidified with IN f ICI solution, concentrated and filtered to give the title product. 'lI-NMRCDMSO-d, 400 MHz) 5 13.10 (bs, 1 H), 11.11 (bs, 1 H), 3.82 (s, 3 H). MS m/z 2\3 (M-ll). Step 2: Methyl 5,6-dihydroxypyrimidine-4-carboxyiate A solution of the product of Step I in HC1 IN solution was stirred for 6 hours at 90°C. Reaction mixture was filtered and the solid washed with HCI IN. Evaporation of the filtrate afforded the title product as a solid. !H NMR (DMSO-d6, 300 K, 400 MHz) 5 7.75 (s, I H), 3.82 (s, 3 H). ,3C NMR (DMSO-d6, 300 K, 400MHz)5 165.66, 158.20, 147.14, 139.00, 127.85,52.16. Step 3: Methyl 5-\|(2,2-dimethylpropanoyl)oxy]-6-hydroxypyrimidine-4- carboxylate Pivaloyi chloride I.I eq. was added to a solution of the product of Step 2 in pyridine, and the mixture was heated to 40°C for 10 minutes. HPLC showed the complete conversion of starting material. The reaction mixture was concentrated, the resulting oil was diluted with ethyl acetate and washed with 1 N MCI solution. The title product was obtained as a brown solid after evaporation of the organic phase and trituration with diethyl ether. 'll NMR (DMSO-dr,, 400 MHz) 5 13.35 (s,l H), 8.18 (s, 1 II), 3.85 (s, 3 H),1.28 (s, 9 H). Slep._4: Methyl 5-\|(2,2-dimethylpropanoyl)oxy]-l-methyI-6-oxo-I,6- dihyclropyrimidine-4-carboxylatc Dimethyl sulfate (1.5 eq.) was added to a solution of the product of Step 3 (1 eq.) in THF containing cesium carbonate (1.5 eq.). The reaction was carried out at 50°C for thirty minutes. The solvent was evaporated and the resulting oil was dissolved in ethyl acetate, washed with IN HC1 solution. The crude title compound was recovered as yellow solid and used in the next step without purification. 'II NMR (DMSO-d6, 400 MHz) 5 8.43 (s,l H), 3.81 (s, 3 H), 3.45 (s, 3 H)J .30 (s, 9 H). Steji_5: A^-(4-fluorobenzyI)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine- 4-carboxamide 4-Fluorobenzylamine (3 eq.) was added to a solution of the crude product of Step 4 in DMF and the reaction mixture was heated to 90°C for one hour. The title compound was obtained by RP-HPLC (Cis, eluting with water and acetonitrile containing 0.1 % rfFA). ]H NMR(DMSO-d6,400MHz)5 12.5 (s,I H), 9.54 (t../- 6.2 Hz, 1 II), 8.05 (s, 1 H), 7.36 (dd, ./= 6.2, 8.4 Hz, 2 H), 7.14 (t, J= 8.4 Hz, 2 H), 4,45 (d, J = 6.2 Hz, 2 11), 3.44 (sj H). MS/H/Z276(M-H)EXAMPLE 5 N-(4-I'1uorobenzyl)-5-hydroxy-l-melhyI-2-[4-(morpholin-4-ylmethyl)phenyI]-6-oxo-l,6-dihydropyrimidine-4-carboxamide Step 1: Methyl 2-\|4-(bromornethyI)phenylJ-5-l(2,2-dimethylpropanoyl)oxy]-l- methyl-6-oxo-I,6-dihydropyrimidine~4-carboxylate To a vigorously boiling solution of methyl 5-[(2,2-dimclhylpropanoyl)oxy]-I-methyl-2-(4-methyIphenyI)-6-oxo-l,6-dihydropyrimidine-4-carboxylate in carbon tetrachloride N-bromosuccinimide (1 eq.) and benzoyl peroxide (0.05 eq.) were added as dry powders. After 4 hr the mixture was allowed to reach room temperature and the precipitated succinimide was filtered off. The filtrate was evaporated under vacuum and the solid residue was used as such. 'H NMR (DMSO-dr,, 400 Ml Ix) S 7.68-7.57 (ITU 4 H), 4.77 (s, 2 H), 3.80 (s, 3 H), 3.27 (s, 3 H), 1.30 (s, 9 11). Steg_2: N-(4-I;luorobcn/yl)-5-hydroxy-l-methyl-2-[4-(morphoIin-4- ylmethyI)phenyi\|-6-oxo-l,6-dihydropyrimidine-4-carboxamide A THF solution of methyl 2-[4-(bromomcthyl)phenylJ-5-[(2,2-dimcthylpropanoyl)oxy]-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxylate was reacted with 4 eq. of morpholine for 0.5 h at room temperature. After evaporation of volatiles, the oily residue was taken into DMF and treated with 3 eq. of 4-fluorobenzylamine at 90°C for 2 h. Title product was isolated as its trifluoroacetate salt by RP-HPLC (CI 8,water/acctonitrile with 1 % of TFA as eluant). 1H-NMR(DMSO-d6.400MH/)8 12.45 (s, 1 H), 10 (bs, 1 H), 9.3 1 (bt, 1 H), 7.74 (m, 2 11), 7.62 (m, 2 11), 7.35 (m, 2 II), 7.14 (t, J-8.8 Hz, 2 H), 4.54-4.38 (m, 4 H), 4.1-3.9 (m, 2 H), 3.9-3.7 (m, 2 H), 3.68-3.51 (m, 2 H), 3.31 (s, 3 H), 3.2-3.1 (m, 2 H). MS: m/z 453 (M+H)HXAMPLE6 N-(4-nuorobenzyI)-5-hydroxy-l-methyl-2-(4-methyImorpholin-3-yl)-6-oxo-l,6-dihydropyrimidine-4-carboxamide Step 1: 4-(/^r/"Butoxycarbonyl)morpholine-3-carboxylic acid ( To a vigorously stirred solution of 3-morpholinecarboxylic acid and triethylamine (1.11 cq.) in MeOU (1.4 M) at 50 °C was added di-t-butyl dicarbonate (2 cq.). Stirring was continued at 50 °C for 5 min and at room temperature overnight. -- The reaction mixture was then concentrated to obtain an oily residue and suspended between EtOAc (500 ml) and saturated NaUC03 (500 ml). The organic layer was extracted with saturated NaHCCh (2x250 ml) and 112() (250 ml). Combined aqueous layers were brought to pi I =: 2.0 with 3 M HC1 and immediately extracted with EtOAc (2x500 ml). The combined organic layers were washed with dilute HCI, dried, filtered and evaporated to give the title compound as a pale yellow oil, a 1:1 mixture of rotamers by NMR. 5 'II NMR (400 MHz, DMSO-d6) 12.93 (bs, 1 H), 4.32 (s, 0.5 H), 4.29 (s, 0.5 H), 4.2-4.1 (m, 1 H), 3.83-3.74 (m, I II), 3.58-3.52 (m, 2 H), 3.36-3.31 (m, 1 H), 3.16(t, JH 1.4 Hz, 0.5 H). 3.00 (t, J-1 1.4 Hz, 0.5 H). 1.40 (s, 4.5 H), 1.36 (s, 4.5 H). MS//7/z232(M+H)Step 2: /er/-Butyl 3-(aminocarbonyl)morpholinc-4-carboxyIate To a stirred solution of the compound prepared in Step 1 (1 eq.), pyridine (0.6 eq.) and di-/-butyl dicarbonate (1.3 eq.) in dioxane (0.6 M), NH4HCO3 (1.26 eq.) was added and the mixture was stirred at room temperature for 20 hours. Mixture was concentrated, taken up in BtOAc and washed with water and brine. Organics were dried over Na2S04 and evaporated giving the title product as an oil which crystallized at room temperature. 1H-NMR(DMSO-d6.300MHz)5 7.35(bs, 1 H), 7.06 (bs, 1 H), 4.15 (bs, 2 H), 3.76 (bs, I H), 3.57-3.51 (m, 2 H), 3.28 (m, 1 II), 3.18 (m, 1 H), 1.36 (s, 9 H). MSA/;/Z231 (M+H)'. Step.3: ^r/-Liutyl 3-cyanomorpholine-4-carboxylate A solution of the product of Step 2 (I eq.) and triethylamine (2.1 eq.) in CH2CI2 (0.1 M) was cooled to 0 °C and trifluoroacetic anhydride (1.1 eq.) added dropwise under nitrogen. Stirring was continued 3.5 hours more at room temperature and volatilcs removed in vacuo. Residues taken in ElOAc were washed with water, brine and dried over Na2S04. Evaporation gave the title compound as a brown solid. '11 NMR (DMSO-d6, 400 MHz) 5 5.04 (d, J = 2.7 Hz, 1 H), 3.96 (d, 7=12.2 Hz, 1 H), 3.86 (dd,7- 11.5, 2.6 Hz, 1 H), 3.69 (d, 7=12.4 Hz, 1 H), 3.56 (dd,7 = 12.2, 3.2 Hz, 1 H),3.40(td,7 = 11.9,2.89 Hz, 1 H), 2.97 (m, 1 II), 1.43(s,9H). MS/w/z213(M+H)Step 4: /er/-Butyl 3-[(Z)-amino(hydroxyimino)methyl]morphoIine-4- carboxylate A solution of of the product of Step 3 (1 eq.), hydroxylamine hydrochloride (1.4 cq.) and triethylamine (1.7 eq.) in HtOH (0.5 M) was re fluxed under nitrogen for 5 hours. Mixture was concentrated and residues taken up in EtOAc and washed with water and brine. Combined organics were dried over Na2S04 and evaporated giving the title compound as a yellow solid. !I I NMR (DMSO-d6, 400 MHz) 8 9.16 (bs, 1 H), 5.32 (bs, 2 H), 4.30 (bs, 1 H), 4.08 (d, 7- 11.6 Hz, 1 H), 3.75 (d, 7= 6.8 Hz, 1 H), 3.50-3.33 (m, 4 H), 1.38 (s, 9 H). MS: m/z246(M+H)Ste\|2..5: DimcthyI-2-({2-amino-2-[4-(/er/-butoxycarbonyl)morphoIin-3- yl]ethenyl}oxy)but-2-enedioate A solution of the product of Step 4 (1 eq.) and dimethyiacetylencdicarboxylate (1.2 eq.) in CHCI3 was refluxed for 1 hour under nitrogen and solution concentrated. Residue was purified by flash chromatography on silica gel, cluents petroleum ether/EtOAc 7:3 -> 1:1, to give the desired product as a mixture of two isomers H/Z (76:14). !l 1 NMR (DMSO-dft, 400 MHz, 300K) 5 6.60 and 6.20 (2 bs, 2 H), 5.58 and 5.41 (2s, 1 II), 4.36 (bs, 1 II), 4.04 (bs, 1 H), 3.8 (bs, 1 H), 3.76 and 3.72 (2 s, 3 H), 3.63 and 3.58 (2 s, 3 H), 3.53 (td,./- 13.6, 3.7 Hz, 1 H), 3.44 (t, J- 10.4 Hz, 1 H), 3.31 (m, 2 11), (s, 9 11). MS/w/z388(M+H)St^E_6- /er/-Butyl-3-[4,5-dihydroxy-6-(methoxycarbonyl)pyrimidin-2- yl]morpholine-4-carboxylate The adducts of Step 5 were refluxed in xylenes for 24 hours. Then the reaction was cooled down and concentrated in vacuo. Ethyl ether was added until precipitation of a solid that was filtered, washed with ethyl ether and dried to give the title pyrimidinc as an orange solid. 'HNMR(DMSO-d6, 400 MHz, 340 K) 8 4.62 (s, HI). 4.15 (d, J-12 Hz, 111). 3.84 (bs. Ill), 3.82 (s, 3H), 3.70 (dd. J= 12.3, 4 Hz, I H). 3.61 (dd, Jr= 12.2,3.8 Hz, ] H), 3.56(1, J- 13 Hz, III), 3.43 (tdj= 11.5, 3.4 Hz, HI). 1.35 (s,9H). MS m/z 356 (M i-\l)Step 7: /^r/-Butyl-3-f5-(benzoyloxy)-4-hydroxy-6- (methoxycarbonyl)pyrimidin-2-yl]morpholine-4-carboxylatc The pyrimidine from Step 6 in dry pyridine (0.2 M), was treated with ben/.oic anhydride (2 eq.) overnight at room temperature. The mixture was evaporated, taken in EtOAc and washed with HCI 1N, NaHCC>3 and brine. Organics were dried over Na^S04, and filtered, evaporated and purified by flash chromatography on silica gel, cluents EtOAc/Petroleum Ether: 7/3. "H NMR (DMSO-dr,, 300 MHz, 340K) 5 13.3 (bs, 1 H), 8.07 (d, J = 7.5 Hz, 2 H), 7.76 (t, J =7.5 Hz, 1 II), 7.61 (t, J= 7.5 Hz, 2 H), 4.73 (s, 1 H), 4.22 (d,y = 12.4 Hz, 1 11), 3.86 (d, J- II.OHz, 1H), 3.78 (dd, J- 12.4,3.9 Hz, 1 H), 3.73 (s, 3 H), 3.58 (t, y- 13.9 Hz, 2 H), 3.47 (td, J = 10.7, 3.6, 1 H), 1.36 (s. 9 H). MS w/z 600 (M-i-H). The pyrimidine product of Step 7 in dry THF (0.6 M) was treated with cesium carbonate (1.5 eq.) and dimethyl sulfate (1.5 eq.) at 50 °C for 1 hour. Solvent was removed in vacuo and residue taken in EtOAc, washed with HCI IN and brine. Organics were dried over Na2SO^, filtered and evaporated to obtain a crude which was purified by flash chromatography on silica gel, (elucnts BtOAc/PetroIeum Ether: 3/7) to separate the two compounds 8A and 8B (ratio 8A/8B 1/0.85). An alternative route was also employed as follows: The pyrimidine product of Step 7 was added to a suspension of LiH (1.1 eq) in dioxane at room temperature. The mixture was aged 45 min at 38 °C and was then cooled to room temperature. Dimethylsulfate (1.3 eq) was added and the mixture was warmed to 38 °C (4h) and 56 °C (4h). The reaction mixture was cooled to 16 °C and glacial acetic acid (0.1 eq) was added, followed by water and EtOAc. The aqueous layer was separated and extracted with EtOAc. The combined organic layer was dried (Na2S04) and concentrated to an oil, which was chromatographed through silica gel, eluting with 50-55% EtOAc/hexanes to separated compound 8A from 8B. The fractions were evaporated to a foamy solid. This solid was dissolved in ether and re-evaporated to foamy solid that could be scraped out easily. This solid was dried in a vacuum oven overnight at 40 °C to afford 8B as a pale yellow solid. The ratio of 8A/8B is variable with this route, from 1:4 to 1:12. /cv/-Butyl-3-[5-(benzoyloxy)-4-methoxy-6-(methoxycarbonyl)pyrimidin-2-yl] rnorpholine-4-carboxylate (8A). 'll NMR (300 MHz, DMSO-d6+TFA, 330K) 5 8.10 (d, J=7.9 Hz, 2 H), 7.77 (t, J=7.3 Hz. 1 H),7.61 (t, J-7.4Hz,2H),4.94(bs, 1H), 4.50 (d, J-l 1.6 Hz, 1H), 4.0 (s, 3H), 3.85-3.81 (m, 2 II), 3.76 (s, 3 H), 3.66 (d, J-10.4 Hz, 1H), 3.49-3.45 (m, 2 11), 1.35 (bs, 9 H). MS w//z474(M + H)". /er/-Fiutyl-3-[5-(benzoyloxy)-4-(methoxycarbonyl)-!-methyl-6-oxo-l,6-dihydropyrimidin-2-yl]morpholine-4-carboxyiate (8B). 'H NMR (DMSO-d6, 400 MHz, 330K,) 5 8.09 (d, ./■-= 7.3 Hz, 2 H), 7.77 (t, J = 7.5 Hz. 1 H),7.62(t,y-7.8Hz,2H),5.08(d,y-3.4Hz, 1 H).4.21 (±J= 12.3 Hz, 1 H), 3.95-3.85 (m, 3 11), 3.76 (s, 3 H), 3.58 (s, 3 H), 3.55-3.50 (m, 2 H), 1.34 (s, 9 H). MS////z474(M-f H)Step 9: tert-Butyl-3'(4-{[(4-fluorobenzyl)amino\|carbonyl}-5-hydroxy-l- mcthyI-6-OKO-l,6-dihydropyrimidin-2-yl\|-morpholine-4-carboxylate The methyl ester 8B in dry MeOH was treated with 4-fluorobcnzylaminc (2.5 eq.) at reflux for 2 hours. Solvent was removed in vacuo and residue triturated with Et.->() to obtain the title product. 'llNMR(300MH/., DMSO-d6, 320K)8 11.95(bs, I 11), 8.32 (t, J= 6.0 Hz, 1 H), 7.39-7.35 (m, 2 H), 7.19-7.13 (m, 2 H), 4.96 (dd,./-4.25, 2.42 Hz, 1 H), 4.62 (dd, J= 14.9, 6.95 Hz, 111), 4.49 (dd, J= 14.9, 5.83 Hz, III), 4.16 (dd, J= 12.2, 2.0 Hz, 1H), 3.87-3.79 (m, 211), 3.70-3.64 (m, HI), 3.55-3.45 (m, 5H), 1.23 (s, 9H). MSm/z463 (M+M)+. Step 10: N-(4-nuorobenzyl)-5-hydroxy-1 -methyl-2-morpholin-3-yl-6-o.\o-1,6- dihyclropyrimidine-4-carboxamide The compound from Step 9 was treated with a mixture of dichloromethane/TFA (2/1) for 1 hour at room temperature. Organics were removed in vacuo to give the title compound as a solid. '11 NMR(300 MHz, DMSO-dr„ 300 K) 5 9.45 (bs, 1 H), 7.39-7.36 (m, 2 H), 7.19-7.15 (m, 2 H), 4.93 (d,.7-9.2 Hz, 1 H), 4.64 (dd../- 15.4, 6.7 Hz, 1 H), 4.55 (dd, 7-15.4, 6.2 Hz, 1 II), 4.35 (d,./= 12.8 Hz, 1 II), 4.08 (d,7- 12.6 Hz. I H), 3.77 (t, J = 12.4 Hz, 1 H), 3.55 (s, 3 H), 3.55-3.46 (m, 2 H), 3.40-3.34 (m, 1 H). MS /»/z363(M + H)+. Step 11: N-(4-nuorobcnzyl)-5-hydroxy-l-mcthyl-2-(4-methyImorpholin-3-yl)-6- oxo-l,6-dihydropyrimidine-4-carboxamide The compound from Step 10 was dissolved in MeOH and treated with triethylamine (1 eq.), sodium acetate (1.6 eq.), formaldehyde 37% w/w aq. soin. (3 eq.), and sodium cyanoborohydride (1.43 eq.). The mixture was left stirring at room temperature for 1 hour. The reaction mixture was concentrated and the title compound was obtained by RP-IIPLC purification (C\|«, eluting with water and acetonitrile containing 0.1 % TFA), as its trifluoroacetate salt. 'H NMR (400 MHz, l)MSO-d6■♦TFA) 5 12.33 (bs, 1 II), 10.05 (bs, 1 H), 9.48 (t, J = 6.4Ilz, 1 H), 7.35-7.33 (m. 2 II), 7.15-7.12 (m, 2 11), 4.98 (d, ./ = 8.8 Hz, 1 H), 4.57 (d,./-6.4Hz, 2H). 4.36(d,./- 12.7 Hz, 1 H), 4.13 (d.7- 12.4 Hz, 1 H), 3.77 (t, 7 = 12.5 Hz, 1 H), 3.69 (d,./ 12.8 Hz, 1 H), 3.54 (s, 3 H), 3.48-3.41 (m, 2 H), 2.83 (s, 3 H). MS wi/z 377 (M-H I) N-(4-lluorobenzyl)-5-hydroxy-l-methyl-2-(4-methylmorpholin-3-yl)-6-oxo-l,6-dihydropyrimidine-4-earboxamide has been resolved into its enantiomers by semi preparative chiral UPLC using the following conditions: Solvents: a mixture of 1:1 0.2%TFA in Hexanes : EtOH Column: chiralpak AS column, 250 x 46 mm at 1 .Oml/min, collected by absorbtion at 260 nM The first eluate is the (f) enatiomer (MeOH, c - 0.24, 25C): fa]D=(+) 55.42. The second eluate is the (-) enantiomer (MeOH, c^0.215, 25C) [a]D- (-) 51.63. EXAMPLE 7 2-(4-ethyI-l-methyIpiperazin-2-yl)-//-(4-fluorobenzyl)-5-hydroxy-l-methyI-6-oxo-I,6-dihydropyrimidine-4-carboxarnide Step 1: Methyl l-methyl-2-(4-/eA7-butoxycarbonylpiperazin-2-y!))-5- benzoyloxy-6-oxo-l,6-dihydropyrimidine-4-carboxylate Methyl l-methyl-2-(4-/er/-butoxycarbonyl-l-ben/yloxycarbonyIpipcrazin-2-yi))-5-bcnzoyloxy-6-oxo-l,6-dihydropyrimidine-4-carboxylate (prepared from 1-[(ben/.yioxy)carbonyI\|-4-(/er/-butoxycarbonyl)pipera/,ine-2-carboxylic acid (Bigge et al, Tetrahedron Lett. 1989, 3_0: 5193) by procedures similar to those set forth in Examples 2 or 3 in combination with a deprotection step) was dissolved in MeOH and hydrogenated at atm pressure on 10% Pd/C for 1 hour. The crude title product was obtained after filtration and evaporation. Step 2: N-(4-fIuorobcn/.yl) l-methyl-2-(4-/er/-butoxycarbony!piperazin-2-yl))- 5-hydroxy-6-oxo-l,6-dihydropyrimidine-4-carboxamide The crude product from Step 1 was dissolved in MeOH and 4-fluorobenzylamine (3.5 eq.) added. After being relluxed overnight, the precipitate was filtered and washed with Ct20 to afford the title product. Step 3: N-(4~fluorobenzyl) l-methyl-2-(4-/^/7-butoxycarbonyl-l- methylpiperazin-2-yi))-5-hydroxy-6-oxo-l,6-dih)drop>rimidine-4-carboxamide The solid product from Step 2 was dissolved in MeOH and NaCNBH3 (1.4 eq.), AcONa (1.6 eq.), IICH0 37%(1 eq.) were added. The reaction mixture was stirred at room temperature for 2 days, and then evaporated to afford the crude title product. 'II NMR (DMSOd6 f TI;A, 340K, 400MHz) 5 7.40-7.35 (m, 2H), 7.18-7.10 (m, 2H), 4.83 (d, J- 7.3 Hz, IH). 4.59 (d, J - 6.3 Hz, 2H), 4.41 (d, J - 14.9 Hz, IH), 4.20-4.10 (m, 1H), 3.75-3.60 (m, IH), 3.54 (s, 3H), 3.38-3.25 (m, 2H), 3.15-3.05 (m, 1H), 2.85 (s. 311), 1.45 (s, 911). MS (Elf) m/z - 476 (M+H)S.^ep_4: Ar-(4-fluorobenzyI)-5-hydroxy-l-methyl-2-(l-methylpiperazin-2-yI)-6- oxo-I,6-dihydropyrimidine-4-carboxamide The crude product from Step 3 was stirred in CH2CI2/TFA (1:1) for 2 hours to remove the Boc protective group from the piperazinyl nitrogen. 'H NMR (DMSOd6, 340K, 400MHz) 5 12.25 (bs, 111), 9.03 (bs, IH), 7.42-7.35 (m, 211), 7.20-7.10 (m, 211), 4.62-4.45 (m, 2H), 4.14-4.09 (m, IH), 3.62 (s. 3H), 3.62-3.52 (m, IH), 3.48-3.32 (m, IH), 3.25-3.15 (m, IH), 3.15-3.05 (m, 2H), 2.44-2.32 (m, IH), 2.34 (s, 3H). MS(El+)n//z = 376(M+H)'Step 5 : 2-(4-ethyl-1-methylpiperazin-2-yl)-A'-(4-fluorobenzyI)-5-hydroxy-1 - methyl-6-oxo-l,6-dihydropyrimidinc-4-carbo.\amide Triethylamine (2 eq.). NaCNBH3 (1.4 eq.), AcONa (1.6 eq.) and CH3CHO (1 eq.) were added to a methanolic solution of the crude product obtained in step 4. The reaction was stirred at room temperature for 1 hour. The title product was obtained as its trifluroacelate salt by preparative RP-HPLC purification (CI8, gradient of CH3CN/H2O + O.OI %TFA). 'H NMR (DMSO-d6 i TFA, 300 MM/.) 8 9.40 (l J- 5.9 Hz, 1 H), 7.34 (t, J= 8.02 Hz. 2 H), 7.14 (t,./ - 8.7 11/, 2 II), 5.00 (d,./-9.9 Hz, 1 H), 4.54 (d, 7= 6.1 Hz, 2 H), 4.04-3.82 (m, 3 H), 3.55-3.43 (m, 4 H), 3.30-3.22 (m, 4 H), 2.87 (s, 3 H), 1.21 (t, y = 7.14 Hz, 3 H). MS m/z 404 (MM\)EXAMPLE 7B Step 1: A^-(4-fluorobenzyI)-5-hydroxy-2-[4-(isopropylsulfonyl)-l- methylpiperazin-2-yl]-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide 4-fluorobenzyl 2-(1.2-dimethylpiperazin-2-yl) -5-hydroxy- 1-methyl -6-oxo- 1,6-dihydropyrimidine-4-carboxylate , obtained during the preparation of the compound in example 7 step 4, was dissolved in THF/NaOH 2N (1:1) followed by the addition of iPrSC^CI (4 eq). After being stirred at room temperature overnight, further addition of iPrSChCl (2.4 eq) and NaOH 2N (2.4 eq) were made to complete the reaction. After 3 hours NaOH 2N (10 eq) was added and the reaction mixture was stirred for 10 minutes at room temperature. The title product was isolated by preparative HPLC (Column C18, gradient of CH3CN/H20 + 0.01 %TFA). 'H NMR (DMSOdftT TFA, 300K, 300MHz) 5 9.48 (bt, J =-■ 6.5 Hz,lH), 7.39-7.35 (m, 211). 7.7.22-7.12 (m„ 211), 4.96 (d, J = 8.4 Hz, 1H), 4.57 (d, J = 6.3 Hz, 211), 4.23 (d, J = 14.4 Hz, HI), 3.96 (d, J - 10.8 Hz, 1H), 3.76 (d, J - 10.2 Hz, 1H), 3.53 (s, 3H), 3.50-3.35 (m, 3H), 3.23-3.15 (m, HI), 2.87 (s, 311), 1.25 (d, J - 6.9 Hz, 6H). MS: m/z 482 (M+H)EXAMPLE 8 A/-(4-nuorobenzyI)"5-hydroxy-l-methyl-2-(l-mcthyIpipericiiii-2-yl)-6-oxo-l,6--dihydropyrimidine-4-carboxamidc Methyl 5-(bcnzoyloxy)-1 -methyl-6-oxo-2-piperidin-2-yl-1,6-dihydropyrimidinc-4-carboxylate (prepared from l-(benzyloxycarbonyl)piperidine-2-carboxylic acid by procedures similar to those set forth in Examples 1 or 2 in combination with a deprotcction step) was suspended in THF and treated with 3 eq. of triethylamine and 3 eq. of methyl iodide at 40 °C. After stirring for 5 h, THF was evaporated and residue poured into EtOAc and washed with brine. Organic phase was dried (Na^SC^), filtered and concentrated under reduced pressure. The oily residue was taken into EtOAc and treated with 3 eq. of 4-fluorobenzylamine at 90 °C for 0.5 h. The title product was isolated as its trifluoroacctic salt by preparative RP-HPLC (CI 8, 5 ^iM, acetonitrile/water containing 0.1% TFA as eluant). ,HNMR(DMSO-dft,400MHz)8 12.28 (bs, 1 H), 9.50(bt, I H), 9.31 (bs, 1 H), 7.37 (dd, J = 5.6 Hz, 8.4 Hz, 2 H), 7.18 (t, J = 8.8 Hz, 2H), 4.8-4.6 (m, 1 II), 4.57 (d, J = 6.4 Hz, 2 H), 3.70-3.60 (m, I 11), 3.50 (s, 3 H), 3.4-3.3 (m, 1 H), 2.78 (bs, 3 H), 2.4-2.3 (m, 1 H), 1.92-1.46 (m, 511). MS/w/z375(M+H)"EXAMPLE 9 2-( I -AcetyIpyrrolidin-2-yl)-A/-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide Methyl-5-(bcnzoyloxy)-2-[l-(/cr/-butoxycarbonyl)pyrroIidin-2-yl]-6-hydroxypyrimidine -4-carboxyIate was treated with TFAiCH^Cb (3:7) at 0 °C. The solution was warmed to room temperature and the progress of the reaction was monitored by MS analysis. After lh the reaction was complete and the solvent was removed under reduced pressure using a rotatory evaporator. The title product was precipitated with Et20 and collected by filtration. !H-NMR(CDCI3,400MHz)8 8.17(d,J=7.4Hz, 2 H), 7.67 (t, J = 7.6 Hz, 1 H), 7.52 (t, J= 7.6 Hz, 2 H), 5.45 (dd, J= 7.6, 6.7 Hz, 1 II), 3.82 (s, 3 H), 3.66 (s, 3 H), 3.61 (t, .7= 7.0 Hz, 2 11), 2.78-2.69 (m, 1 H), 2.40-2.00 (m, 3 H). MS/w/358(M+H)+. Sicj"?_2- 2-(l-Acetylpyrrolidin-2-yl)-A^-(4-[luorobcnzyl)-5-hydroxy-l-methyI-6- oxo-l,6-dihydropyrimidine-4-carboxamide To a stirred solution of the product of Step I (1.0 eq.) in CIICI3, trielhylamine (3.0 eq.) was added followed by the addition of acetyl chloride (1.5 eq.). The reaction was stirred at room temperature until the starting material was consumed as determined by MS analysis. The reaction mixture was concentrated and the crude product was used directly in the subsequent step without further purification. A solution of the crude product from above (1.0 eq.) in NMP was treated with 4-fluorobenzylamine (2.0 eq.). The solution was stirred at reflux until the reactants were consumed as determined by MS analysis. The title compound was obtained by RP-HPLC purification (Cis, eluting with water and acetonitrile containing 0.1 % trifluoroacetic acid) as a 4:1 mixture of rotamers by NMR. 'll-NMR (DMSO-d6, 400 MHz) 5 12.11 (bs, 1 H), 8.49 (t, .7=6.2 Hz, 0.8 H), 8.30 (t, y=--6.2 Hz? 0.2 H), 7.4-7.3 (m, 2 II), 7.15 (t, J-8.8 Hz, 2 M), 5.22 (dd, J=$A 3.2 Hz, 0.2 H). 5.02 (dd, .7-8.0, 3.2 I Iz, 0.8 H), 4.60-4.47 (m, 2 H), 3.95-3.85 (m, 0.8 H), 3.80-3.70 (m, 0.2 H), 3.59-3.57 (m, 0.8 H), 3.55 (s, 2.4 H), 3.52 (s, 0.6 H), 3.43-3.37 (m, 0.2 H), 2.40-1.7 (m, 4 H), 2.5 (s, 2.4 H), 1.75 (s, 0.8 H). MSw/z389(M+H)+. EXAMPLE 10 2-(l-benzoyI-2,3-dihvdro-l//-indol-2-yl)-A/r-(4-lluorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide Step I: Methyl 2-(2,3-dihydro-1//-indol-2-yl)-1 -methyl-5-benzoy!oxy-6-oxo- l,6-dihydropyrimidine-4-carboxyIate ^^ BenzvI 2-[ 5-(bcnzoyioxy)-4-(methoxyearbonyl)-1 -methyl-6-oxo-1 ?6-dihydropyHmidi-2-yI\|indoIinc-l-carboxyIate was dissolved in EtOAc and hydrogenated at atmospheric pressure on 10% Pd/C overnight. The crude title product was obtained after filtration and evaporation Step 2: Methyl 2-(l-benzoyl-2,3-dihydro-l//-indol-2-yl)-5-benzoyloxy-l- methyI-6-oxo-l,6-dihydropyrimidine-4-carboxylate THF was added to the crude product of Step 1, followed by pyridine (2 cq.) and PhCOCI (I eq.). After being stirred at room temperature overnight, the reaction mixture was evaporated to give the crude title product. Stee_3: 2-(l-benzoyI-2,3-dihydro-l//-indol-2-yl)-yV-(4-tluorobenzyl)-5- hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide The crude product of Step 2 was dissolved in MeOH and 4- fluorobenzylaminc (3.5 eq.) added. The solution was stirred at 60 °C over night. The title product was obtained by preparative RP-HPLC (CI8, gradient of CH3CN/H2O + 0.01 %TFA). !HNMR(DMSO-d6 i TFA, 340 K, 400 MHz) 5 7.75-7.80 (m, 1 H), 7.45-6.97 (m, 13 H). 5.77(dd,y= 10, 3.6Ilz, 1 H), 4.35-4.50 (m, 2 11), 3.72 (dd, J = 16, 10 Hz, 1 H), 3.35 (s, 3 H),3.16(dd,J- 16, 3.6 Hz, 1 H). MS m/z 499 (M+H)EXAMPLE 1 1 Ar-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-[ l-(pyridin-2-ylcarbonyl)-l,2,3,4-tetrahydroquinolin-2-yl]-l,6-dihydropyrimidine-4-carboxamide Benzyl 2-\|5-(bcnzoyloxy)-4-(methoxycarbonyI)-1 -methyl-6-oxo-1,6-dihydropyrimidi-2-yI\|-l,2,3,4-tetrahydroquinoline-l-carboxylate (prepared from tclrahydroquinoline-2-carboxylic acid (RobI et al, Tetrahedron Letters 1995, 36: 1593) by protection of the nitrogen and following procedures similar to those set forth in Examples 1 or 2 in combination with a deprotection step) was dissolved in EtOAc and hydrogenated at atmospheric pressure on 10% Pd/C at room temperature overnight. The title product was obtained as the residue after filtration and evaporation of the organic solvent. Sjep_2: Methyl 5-benzoyloxy-!-methyl-6-oxo-2-\| l-(pyridin-2-ylcarbonyl)- l,2,3,4-tetrahydroquinolin-2-yl]-l,6-dihydropyrimidine-4-carboxylate The residue of Step 1 was dissolved in dichloromethane. Pyridine, picolinoyl chloride hydrochloride and a catalytic amount of DMAP were added. A further addition of the reactants was made alter two hours. After evaporation of the solvent, the residue was diluted with EtOAc, the organic phase washed with water, dried (Na2S04) and evaporated to afford the title product. Step 3: A^-(4-fluorobenzyl)-5-hydroxy-I-methyl-6-oxo-2-[l-(pyridin-2- ylcarbonyl)-l,2,3,4-tetrahydroquinolin-2-yl]-l,6-dihydropyrimidine-4-carboxamide The residue of Step 2 was dissolved in DMF and 4-fluorobenzylamine (3 eq.) was added. The reaction mixture was stirred at 90°C for 1 h. The title compound was purified by preparative HPLC and isolated as its trifluoroacetic salt (CI 8, gradient of CH3CN/H20 f 0.01% TFA). lH-NMR(DMSO-d6+TFA,400MHz,340K)5 8.35(d,y=4.2Hz, 1 H),7.81 (t,V = 7.4 Hz, I H), 7.54 (bt. 1 II), 7.49 (d, J= 7.7 Hz, 1 H), 7.37 (dd, J = 5.2 Hz, 7.0 Hz, 1 H), 7.25-7.22 (m, 2 II), 7.17-7.09 (in, 3 H), 6.90 (t, J = 7.3 Hz, 1 H), 6.62 (t,./- 7.3 Hz. I H), 6.43 (bs, 1 H), 5.74 (t, 7-7.6 Hz, 1 H), 4.42 (dd, ^=6.4 Hz, 14.8 Hz,lH), 4.32(dd, .7=6.4 Hz, 14.8 Hz, 1 H), 3.65 (s, 3 H), 2.80-2.70 (m, 3 H), 1.85-1.75 (m, 1 H). MS/w/z514(M+H)f. EXAMPLE 12 2-\ (2SAR)-\ -benzoyl-4-hydroxypyrrolidin-2-yI]-iV-(4-nuorobenzyI)-5-hydrpxy-l-methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide Methyl 2-f(25,4/?)-1 -tert-butyloxycarbonyl-4-(benzyIoxy)pyrrolidin-2-yl\|-5-(benzoyloxy)-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxylate [obtained from N-Boc-O-benzyl-L-hydroxyproline using chemistry similar to those set forth in Examples 1 or 2; the stereochemistry of products of Steps 1 to 3 is based on that of starting material] was dissolved in dichloromethane (0.03 M), followed by addition of an excess of TFA. The mixture was stirred at room temperature for 1 hour. The solvent was evaporated in vacuo. To the residue dissolved in pyridine, benzoic anhydride (2 eq.) was added. The mixture was stirred at room temperature for 5 hours. Pyridine was evaporated in vacuo and the residue dissolved in EtOAc was washed with HC1 (1M), saturated aqueous NaHC03 and brine, dried on Na2S(>4, filtered and evaporated in vacuo to give the title product as a yellow solid. 'U NMR (DMSO-d6, 400 MHz, 330 K) 5 8.07 (d, J- 7.6 Hz, 2 H), 7.77 (t, .7-7.3 Hz, H), 7.62 (t, 7=7.74 I Iz, 2 11), 7.52-7.49 (m, 5 H), 7.33-7.30 (m, 5 H), 5.47 (bt, 1 H), 4.53 (d,J= 12.1 Hz, i H), 4.44 (d. J-12.0 Hz. 1 H),4.36(bs. I H), 3.87-3.84 (m, 1 H), 3.76(s, 3 H), 3.73 (s, 3 H), 3.57 (d, 7=11.2 Hz, 1 11)2.70 (t, 7=12.2 Hz, I H), 2.31-2.28 (m, 1 H). SICJL.2: 2-\|(2.V,47e)-Nbenzoyl-4-(benzyloxy)pyrrolidin-2-yl]-A^-(4- nuorobenzyl)-5-hydroxy-l-methyi-6-oxo-l,6-dihydropyrimidine-4-carboxamide The compound of Step 1 was dissolved in methanol and 4-fluorobenzylamine (5 eq.) was added. The mixture was refluxed overnight. After cooling, the reaction mixture was filtered and washed with ethyl ether to obtain the title product as a white solid. 'HNMR (DMSO-d6,400MHz, 300 K) 5 12.15 (s, 1 11), 9.00 (br t, lH),7.48(d, .7-7.6 Hz, 2 H) 7.41-7.20 (m, 10 H), 7.12 (t,./= 8.8 Hz, 2H), 5.27 (t, J= 8Hz, 1 H), 4.63 (dd, J= 14.9, 7.3 Hz, 1 H), 4.56-4.38 (m, 2 H), 4.26 (bs, 1 H) 4.25 (d, 7=11.4 Hz, 2 H) 3.68 (s, 3 H), 3.52 (d, 7= 11.2 Hz, 1 H), 2.66-2.63 (m, 1 H), 2,26-2.20 (m, 1 H). MS/w/z557(M+H)Step 3: 2-1X25,4/?)-] -bcnzoyl-4-hydroxypyrrolidin-2-yl]-A^-(4-fiuorobenzyl)-5- hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide The title compound of Step 2 was dissolved in AcOH and 10% Pd/C (10% weight) was added. The mixture was stirred under Hsat atmosphere overnight. Pd/C was filtered, AcOl I evaporated in vacuo, and the resulting title compound was washed with methanol. 'H NMR(DMSO-d(i, 400 MHz) S 12.1 (s, 1 H), 9 (bt, 1 H), 7.51-7.47 (m, 3 11), 7.41- 7.33 (m, 4 H) 7.11 (t, 7= 8.8 Hz, 2 H), 5.27 (t, 7= 8 Hz, I H), 5.08 (d, 7=3.2 Hz, 1 H), 4.63 (dd, 7=14.8 Hz, 7.3 Hz, I H), 4.43-4.39 (m, 2 II), 4.20 (d, J- 7.4 Hz, 1 H), 3.67 (s. 3 H), 2.41-2.36 (m, I II). 2.2-2.1 (m, I H). MS w/z467(M-H-I)EXAMPLE 13 yW-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo-yV^-(pyridin-2-ylmcthyI)-1.6-dihydropyrimidine-2,4-dicarboxamide 2-Ethyl 4-methyl 5-[(2,2-dimethylpropanoyl)oxy]-1 -methyl-6-oxo-1,6-dihydropyrimidine-2,4-dicarboxylate (made by protection and alkylation of the starting material of Example 4, Step I using procedures similar to those set forth in Examples I or 2) was dissolved in DME, 4-fluorobenzyIamine (3.1 eq.) was added and the mixture was stirred at 90 °C overnight. After concentration of the solvent, the residue was taken into EtOAc, washed with 1 N HO, dried over Na2SC>4 and evaporated to obtain crude A^-(4-fluorobenzyl)-2-ethoxycarbonyM-methyl-5-hydroxy-6-oxo-l,6-dihydropyrimidine-4-carboxamide. To this crude product was added 2-picolylamine (8 eq.), and the reaction was stirred at 90 °C overnight. The title product was obtained as its trifluoroacetic salt by preparative RP-HPLC purification (CI8 gradient of CH3CN/H20 f- 0.01% TFA). !H NMR (DMSO-d6, 300K, 400 MHz) 5 12.70 (bs, 1 H), 9.75-9.65 (m, 2 H), 8.56 (d, 7==4.4Hz, 1 H), 7.90-7.80 (m, 1 H), 7.44 (d, J= 8.0 Hz, 1 H), 7.40-7.35 (m, 3 H), 7.17 (t, J -■= 9.2, 2 H), 4.60 (d, J - 6.0 Hz, 2 H), 4.54 (d, J - 6.0 Hz, 2 H), 3.67 (s, 3H). MS/v//z4I2(M-HI)EXAMPLE 14 2-[2-(4-benzoylpiperazin-l-yl)elhyI]-A^-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-L6-dihydropyrimidine-4-carboxamide Methyl 2-(2,2-dimethoxyethyl)-5-benzoyIoxy-l-methyl-6-oxo-I,6-dihydropyrimidine-4-earboxylate (1.0 eq.) (prepared from 3,3-dimethoxypropionitrile by procedure similar to those set forth in Examples 1 or 2) in dry MeOH was treated with 4-fluorobenzyl amine (2.5 eq.) at reflux for 2 hours. Solvent was removed in vacuo and residue triturated with Et20 to obtain the title product. !H NMR (DMSO-d6, 300K, 400 MHz) 5: 9.80 (br s, III), 7.41-7.38 (m, 2H), 7.15 (t, J = 8.7 Hz, 2H), 5.04 (br s, IH), 4.47 (d, J = 6.2 Hz, 2H), 3.46 (s, 3H), 3.28 (s, 6H), 3.01 (d,J = 5.5Hz,2H). MS: w/z366(M-H)-f Stcp 2: N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-(2-oxoethyl)-l,6- dihydropyrimidine-4-carboxamide The product of Step 1 was treated with a mixture HC1 IN/IT IF for 1 hour at 40 °C. Organics were removed in vacuo and residue extracted in DCM, dried over Na2SC)4 and concentrated to give the title compound as a foam which was immediately reacted in the following reductive amination. MS: m/z 320 (M HI-H)--h Step 3: 2-[2-(4-ben/oylpiperazin-l-yl)ethyIj-Ar-(4-fluorobenzyl)-5-hydroxy-l- methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide The product of Step 2 was dissolved in MeOI-f and treated with sodium acetate (1.6 eq.), 1-benzoylpiperazine (2 eq.), and sodium cyanoborohydride (1.43 cq.). The mixture was left stirring at room temperature for 1 hour. The reaction mixture was concentrated and the title compound was obtained by RP-HPLC purification ( Cis, eluting with water and acetonitrile containing 0.1 % TFA). IHNMR(CDCl3+TFA,273K,600MHz)8: 10.431 (br s, I H), 8.38 (t, J - 5.7 Hz, 1H), 7.61 (t, J = 6.4 Hz, 1H), 7.52 (t, J = 7.7 Hz, 2H), 7.41 (d, J = 7.4 Hz, 2H), 7.28 (2H, overlapped by CMCI3), 7.07 (t, J - 8.5 Hz, 2H), 4.97 (d, J - 14 Hz, 1H), 4.63 (d, J - 5.7 Hz, 2H), 4.10 (d, J = 14 Hz, 1H), 3.93 (d, J - 1 1.9 Hz, 1H), 3.82-3.74 (m, 4H), 3.61 (s,3H), 3.47(t, J= 12.6 Hz, 1H), 3.41 (br s, 211), 3.29-3-26 (m, 1H), 3.15-3.14 (m, HI). MS: /w/z494(M + H)+. EXAMPLE 15 A/-(4-t1uorobenzyl)-5-hydroxy-l-(2-hydroxy-3-morpholin-4-ylpropyl)-6-oxo-l,6-dihydropyrimidine-4-earboxamide Methyl 5-j(2,2-dimethylpropanoyl)oxy]-6-hydroxy-1,6-dihydropyrimidinc-4-carboxylate (see Example 4, Step 3) was dissolved in THF, then allyl bromide (2 eq.) and CS2CO3 (2 eq.) were added. The reaction mixture was rcfluxed for 2h, then evaporated. The residue was diluted with EtOAc, washed with IN MCI, dried (Na2S04) and the solvent evaporated. The product was purified by flash chromatography on silica gel eluting with a gradient of petroleum ether/EtOAc. !H-NMR (DMSO-d6, 400 MM/, 300K) 8 8.47 (s, Ml), 5.99-5.92 (m, 1H), 5.25-5.14 (m, 2M), 4.58 (d, J = 5.5 Hz, 211), 3.82 (s, 3H), 1.28 (s, 9H). Sl£R_2: yV-(4-tluorobenzyl)-5-hydroxy-l-(2-hydroxy-3-morpholin-4-ylpropyl)- 6-oxo-l,6-dihydropyrimidine-4-carboxamide 2a. The compound of Step 1 was dissolved in dichloroethane and m-CPBA was added (5 eq.). The reaction mixture was refluxed until the starting material was completely consumed, then evaporated. MS m/z 311 (M+H). 2b. Crude material from step 2a was dissolved in MeOM and morpholine (6 eq.) was added. The reaction mixture was refluxed for 3h, then evaporated. MS (Elf) m/z 398 (M+H)+. 2c. Crude material from step 2b was dissolved in DMF and 4-fluorobenzylamine (3 eq.) was added. The reaction mixture was stirred at 90 °C for 3h. The title compound was obtained as its trifluoroacetate salt by RP-HPLC purification (gradient of CMjCN/H20 + 0.01% TEA). 'll-NMR (DMSO-d6 +TFA, 400 MHz, 340K) o 9.27 (bt, III), 7.94 (s, 1H), 7.40-7.36 (m, 211), 7.15-7.11 (m, 211), 4.48 (d, J= 6.4 Hz, 2H), 4.30-4.36, (m, 1H), 4.09 (dd, J= 13.6, 4.0 Hz, 1H), 3.91-3.86 (m. 5H), 3.34-3.30 (m, 5H), 3.18 (dd, J= 13.6 ,4.0 Hz, 111). MSw/z407(M+H)EXAMPLE 16 2-\|(2S,4S)-l-acetyI-4-nuoropyrrolidin-2-yl]-N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo- 1.6-dihvdropvrimidine-4-carboxamide l-benzyl-2-methyl(2S,4R) 4-hydroxypyrrolidine-l,2 dicarboxylate in dichloromethane was added dropwise to a solution, precooled to -78 °C, oi"N,N- diethylaminosulfur trifluoride (1.0 eq.) in dichloromethane. The reaction was stirred while the temperature was allowed to increase to 25 °C. The solvent was concentrated under vacuum and the crude was purified by flash chromatography (eluent: petroleum ether: EtOAc = 1:1) to give the title compound. 'H NMR (CDC13, 300 MHz, 300 K) 8 7.42-7.30 (m, 5H), 5.35-5.10 (m, 3H), 4.65 (d, J-9.6 Hz, 0.5H), 4.57 (d, J- 9.4Hz, 0.5H), 3.99-3.62 (m, 211), 3.79 (s, 1.5H), 3.68 (s, 1.5H). 2.62-2.29 (m,2H). MS:m/z282(MMl)'. Step 2: (4S)-l-[(Benzyloxy)carbonyl]-4-fluoro-L-proline .. /■ l-Bcnzyl-2-methyl-(2S,4S)-4-fluoropynx)lidine-l,2-dicarboxylate dissolved in methanol was treated with NaOH IN (2 eq.) and the reaction mixture was stirred at 50 °C for 3 hours. Alter concentration of the solvent, HC1 IN was added until pH=l and the aqueous layer was extracted three times with dichloromethane. The organic phase was washed with brine, dried over Na2SO;j and filtered to give, after concentration, title compound. 'llNMR (CDCI3, 400 MHz, 300 K) 5 7.45-7.30 (m, 5H), 5.33-5.18 (m, 3H), 4.70-4.60 (bm, IH), 4.00-3.65 (m, 211), 2.85-2.25 (m, 2H). MS:m/z268(M+H)+. Step 3: Benzyl-(2S,4S)-2-aminocarbonyl-4-(luoropyrrolidine-l-carboxylate A stirred solution of (4S)-l-[(Bcnzyloxy)carbonylJ-4-fiuoro-L-proline in dioxane was treated with pyridine (0.7 eq.) and B0C2O (1.3 eq.), then ammonium bicarbonate (1.26 eq.) was added and the mixture was stirred at room temperature for 15 hours. Dioxane was concentrated and the residue was taken up in ethyl acetate, washed with 1 N MCI and brine, dried over Na2SC>4 to give, after filtration and concentration, title compound. {l 1 NMR (DMSO-d6, 400 MHz, 340 K) § 7.40-7.28 (m, 511), 5.25 (dt. JM_r-- 53.6 Hz, J = 4.5 Hz, 1H), 5.13-5.06 (m, 211), 4.28 (d, J= 9.6Hz, 1H), 3.80-3.63 (m. 2H), 2.45- 2.21 (m, 2H). MS:m/z267(M-H-l). Step 4: Benzyl-(2S,4S)-2-cyano-4-fluoropyrrolidine-!-carboxylate Bcnzyl-(2S,4S)-2-aminocarbonyl-4-nuoropyrroIidine-]-carboxylate in dichloromethane was treated al 0 °C with Et3N (2.1 eq.) and trifluoroacetic anhydride was added dropwise. The reaetion mixture was stirred at 0 °C for 0.5 hour and 10 minutes at room temperature. Then, it was diluted with dichloromethane, washed with HCI IN and brine, dried over Na2SO.\| and filtered to give, after concentration, title compound. 'li NMR (DMSO-dr„ 400 MHz, 340 K) 5 7.42-7.30 (m, 5H), 5.40 (dbt, JH_\|.-= 52.3 Hz, HI). 5.20 (d, JH2.7 Hz, HI), 5.16 (d, J- 12.7 Hz, III), 4.94 (d, J= 8.4Hz. 1 H), 3.68- 3.56 (m, 211), 2.63-2.41(m, 211). MS: m/z 249 (M+H)'Step_rV Benzyl-(2S,4S)-2-[amino(hydroxyimino)methyl]-4-fluoropyrrolidine- I-carboxylate BenzyI-(2S,4S)-2-cyano-4-fluoropyrroiidine~l-carboxylate dissolved in absolute ethanol was treated with triethyl amine (1.5eq.) and hydroxylamine hydrochloride (1.3 cq.). The reaction mixture was stirred at 50 °C for 3 hours and then the solvent was removed under reduced pressure. The residue was partitioned between water and dichloromethane and the aqueous layer was extracted with dichloromethane three times. The organic phase was dried over Na2SO.j and filtered. The solid obtained by concentration was then recrystallized from MeOH to give title compound. 'H NIMR (DMSO-dft. 400 MH/, 300 K) 5 9.10 (bs, III), 7.40-7.25 (m, 5H), 5.35-5.15 (m, 3H), 5.07 (m, 211), 4.43 (d. J = 9.1 Hz, 1H), 3.72-3.56 (m. 2H), 2.45-2.20(m, 2H). MS: m/z282(M+lir. Stcp..6j. Dimcthyl-2-{[(amino-{(2S,4S)-l-[(benzyloxy)carbonyl]-4- fluoropyrrolidin-2-yl} methyl idenc)amino]oxy}but-2-enedioatc /"/" ft A _ BcnzyI-(2S,4S)-2-[amino(hydroxyimino)methyl]-4-nuoropyrrolidine-I-carboxylate in chloroform was treated with dimethylacetylene dicarboxylate for 3 hours at 60 °C. The chloroform was then concentrated to give the title compound as a 8:2 mixture of isomers. 'II NMR (DMSO-d(1. 400 MHz, 300 K) 5 7.45-7.25 (m, 5H), 6.51 (bs, 1.6 H), 6.14 (bs, 0.4 H), 5.64 (s, 0.8H), 5.61 (s, 0.2 H), 5.30 (dt, J».F= 53.9 Hz, J= 4.6 Hz, 1H), 5.15-5.04 (m, 2H), 4.51 (t, J-8.8 Hz, 0.8H), 4.44 (bt, 0.4H), 3.85-3.48 (m, 8H), 2.67- 2.23 (m, 2H). MS:m/z424(M+H)T. Step 7: Methyl-2-{(2S,4S)-l-[(benzyloxy)carbonyl]-4-fluoropyrroIidin-2-yl}- 5,6-dihydroxypyrimidine-4-carboxylate Dimethyl-2-{[(amino-{(2S,4S)-l-[(benzyloxy)carbon>T\|-4- fluoropyrrolidin-2-yl}methylidene)amino]oxy}but-2-enedioate was refluxcd for 6 hours in ortho-xylene. The reaction mixture was then cooled down to room temperature and petroleum ether was added. A light brown solid precipitated to give after filtration title compound, that was not purified furthermore, but used as such in the following reaction. SlepJL Methyl-5-(benzoyloxy)-2-{(2S,4S)-l-((benzyloxy)carbonyl\|-4- fluoropyrrolidin-2-yl}-6-hydroxypyrimidine-4-carboxylate Methyl-2-{(2S,4S)-l-[(ben/yloxy)carbonylJ-4-nuoropyrrolidin-2-yl}-5,6-dihydroxypyrimidine-4-carboxylate in pyridine was treated with benzoic anhydride (1.3 eq.) and the reaction mixture was stirred at room temperature overnight. Pyridine was concentrated and the residue was taken up in ethyl acetate and washed with HC1 IN and brine. The organic phase was dried over Na2S04 and filtered to give after concentration a crude that was purified by Hash chromatography , (eluent: petroleum ether: ethyl acetate- 1:1) to give title compound. 'II NMR (DMSO-d6, 400 MHz, 300 K) 5 13.50 (bs, 1H), 8.09 (d, J=7.7Hz, 2H), 7.80 (t, J- 7.35 Hz, 1H), 7.64 (t, J=7.8 Hz, 211), 7.45-7.15 (m, 5H), 5.36 (dbt, JH-r=54 Hz, 111), 5.14 (m, 2H),5.02-4.93 (m, 1H), 3.95-3.60 (m, 211), 3.76 (s, 3H), 2.80-2.36 (m, 211). MS:m/z496(M+H)+. Step 9 : Methyl-5-(benzoyloxy)-2-{(2S,4S)-l-[(benzyloxy)carbonylJ-4- fluoropyrrolidin-2-yI}-l-methyl-6-oxo-1.6-dihydropyrimidine-4-carboxylate . Melhyl-5-(benzoyI()xy)-2-{(2S,4S)-l-[(bcnzyloxy)carbonyl\|-4-fluoropyrroiidin-2-yl}-6-hydroxypyriinidinc-4-carboxylate, dissolved in dry dioxane, was added to a suspension of lithium hydride (1.2 eq.) in dry dioxane. The reaction mixture was stirred at 38 °C for 45 minutes and then cooled down to room temperature. Dimethyl sulfate (1.3 eq.) was added and the mixture was heated to 58 °C and stirred at this temperature for 3 hours. The reaction mixture was then cooled down and glacial acetic acid (0.2 eq.) was added, followed by water and ethyl acetate. The aqueous layer was separated and extracted with ethyl acetate; the organic phase was dried over Na2S04 and filtered to give, after concentration, a crude that was purified by flash chromatography (clucnt petroleum ether: ethyl acetate from 4:6 to 2:8) to give the title compound as a 4.6:5.4 mixture of rotamers by NMR. 'I-I NMR (DMSO-d6, 400 MHz, 300 K) 5 8.08 (d, J-7.5 Hz, 2H), 7.79 (t. J- 7.3 Hz, 111). 7.63 (t, J=7.5 Hz, 2H)S 7.37-7.11 (m, 5H), 5.48-5.38 (m, 2H), 5.20 (d, J= 12.8 Hz. 0.46H), 5.12 (d, J-11.8 Hz, 0.54H), 5.10 (d, J=I2.5 Hz, 0.54H), 4.92 (d. J=12.8 Hz, 0.46H), 4.00-3.75 (m. 2H), 3.72 (s, 3H), 3.59 (s, 1.6H), 3.52 (s, 1.4H), 2.90-2.65 (m, 211). MS:m/z5I0(IVMlf. Step 1.0: Mcthyl-2-j(2S,4S)-1 -acetyi-4-fluoropyrrolidin-2-yl]-5-(benzoyloxy)-6- hydroxypyrimidine-4-carboxylate. Methyl-5-(benzoylo\y)-2-{(2S,4S)-l-[(benzyIoxy)carbonyI\|-4-fluoropyrrolidin-2-yl}-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxylate. dissolved in ethyl acetate was treated with Pd/C 10% (10%w/w) and acetic anhydride (1 eq.) and submitted under H2 atmosphere at room temperature. The reaction mixture was stirred at room temperature for 18 hours and then the suspension was filtered over celite to give the title compound as a 7:3 mixture of rotamers by NMR. ]H NMR (DMSO-d6, 400 MHz, 300 K) 5 8.07 (m, 2H), 7.78 (m, 1H), 7.62 (m, 2H), 5.75-5.26 (m, 2H), 4.13-3.60 (m, 2H), 3.72 (s, 3H), 3.59 (s, 3H), 2.79-2.36 (m, 2H), 2.03 (s, 2.1 H), 1.87 (s, 0.9U). MS:m/z418(MHI)Stcp_.LL: 2-((2S>4S)-l-acetyl-4-fluoropyrrolidin-2-yl]-N-(4-fluorobenzy))-5- hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide. Methyl-2-[(2S,4S)-l-acetyl-4-fluoropyrroIidin-2-yl]-5-(benzoyIoxy)-6-hydroxypyrimidine-4-carboxylate was dissolved in MeOH (0.12 N) and treated with 4-F-benzylamine (3 eq.) in a sealed tube. The reaction mixture was stirred at 65 °C for 18 hours, then it was cooled down. The solvent was evaporated and the residue was washed with ethyl ether several times to obtain a solid that was recrystallized from ethanol and washed again with ethyl ether to give the title compound as a 7.3:2.7 mixture of rotamers by NMR. 'il NMR (DMSO-d6, 500 MHz, 300 K) 5 12.01 (bs, I H). 8.52 (t, J = 6.3 Hz, 0.7H), 8.34 (t, J = 6.3 Hz, 0.311), 7.34-7.29 (m, 2H), 7.18-7.12 (m, 2H), 5.39 (dbt, JH-F=54.3 Hz. 0.7H), 5.29 (dt, J[M- 54.2 Hz, J-4.4 Hz, 0.3 II), 5.38 (d, J=8.9 Hz, 0.3H), 5.18 (dd, J-9.2 and 1.6 Hz, 0.7H), 4.55-4.47 (m, 2H), 4.20-3.78 (m, 2H), 3.51 (s, 2.1H), 3.50(s, 0.9H), 2.75-2.54 (m, 1H), 2.47-2.27 (m, 1H), 2.00 (s, 2.1 H), 1.81 (s. 0.9H). MS: m/z 407 (M+M)+. EXAMPLE 17 2-{(2.S',4/^)-l-[(diiTiethylamino)(oxo)acetyl]-4-methoxypyrrolidin-2-yl}-AA-(4-fliiorobenzyi)-5-hydroxy-l-mcthyl-6-oxo-I,6-dihydropyrimidine-4-carboxamide Step I: (4/?)-1 -\|(Benzyloxy)carbonyl]-4-mcthoxy-L-proline ^■^ la/lb Synthesized following the procedure reported on Journal of Medicinal Chemistry 1988,31,875-885. Step 2: Benzyl-(2.V,4y?)-2-cyano-4-methoxypyrroIidine-l-carboxylate To compound (4y?)-l-[(I3enzyioxy)carbonylJ-4-mcthoxy-L-prolinc dissolved in dioxane, Hoc anhydride (1.3 eq), NH4HCO3 (1.26 eq.) and pyridine were added. The mixture was stirred overnight at room temperature. Dioxane was removed in vacuo and the residue, dissolved in ethyl acetate, was washed with HC1 IN, saturated aqueous NaHC03 and brine, dried over Na2S04, filtered and concentrated,in vacuo to get the primary amide. The crude product was dissolved in dichioromethane and tricthylamine (2.1 eq,) was added. The mixture was cooled down to 0° C and trifiuoroacetic anhydride (1.1 cq.) was added. After I hour the dichioromethane solution was diluted and washed with HC1 IN, saturated aqueous NaHCC>3 and brine, dried over Na2SO.j, filtered and evaporated in vacuo. The compound was purified by flash chromatography on silica gel (eluent ethyl acetate: petroleum ether = 20%:80%) as a 4:6 mixture of rotamers by NMR. 'II NMR (DMSO-d6. 400 MHz, 300 K) 5 7.45-7.3 (nru 5H), 5.20 (d, J-12 Hz, 0.4H), 5.14 (s, 1.211), 5.12 (d, J- 12 Hz, 0.4H), 4.75 (t, J- 7 Hz, 0.4H), 4.64 (t, J 7.8 Hz, 0.611), 4.02 (bs, 111), 3.6-3.45 (m, 2H), 3.21 (s, 311), 2.45-2.40 (partially under DMSO)(m, 1H), 2.40-2.25 (m, 1H). St^P. 3: Benzyl-(2.,4/0-2-famino(hydroxyimino)methylJ-4methoxypyrrolidine -1-carboxylate To benzyl-(25,,4/?)-2-cyano-4-methoxypyrrolidine- 1-carboxylate, dissolved in ethanol (0.4 M), hydroxylamine hydrochloride (1.3 eq.) and tricthylamine (1.5 eq.) were added. The mixture was stirred at 40°C for 4 hours then at room temperature overnight. The mixture was concentrated in vacuo and the residue dissolved in ethyl acetate washed with brine, dried over Na2S04, filtered and concentrated to give title compound. !I1 NMR (DMSO-d(1, 400 MHz, 300 K) 5 9.05 (bs, 1H), 7.45-7.25 (m, 5H). 5.4 (bs, 211). 5.10 (d, J- 13 Hz, HI), 5.03 (d, J=13 Hz, 1H), 4.26 (t, J= 7.4 Hz, 111), 3.97 (bs, HI). 3.63-3.45 (m, 211), 3.22 (s, 3H) 2.3-2.03 (m, 211). Step 4: Uimcthyl-2-{\|(amino-{(2 mcthoxypyrrolidin-2-yI} methyl idene)amino]oxy}but-2-enedjoate 7o benzyl-(2iS',47^)-2-[amino(hydroxyimino)methyl]-4methoxypyrroIidine -I-carboxylate, dissolved in chloroform, dimethyl acetylendicarboxylate (1.1 eq.) was added. The mixture was refluxed for 1 hour and left stirring at 40° C overnight. The chloroform was removed in vacuo and the crude product purified by flash chromatography on silica gel (eluent ethyl acetate: petroleum ether = 40: 60). Two isomers were present in ratio 7:3. 1II NMR (DMSO-d6, 400 Mil/, 300 K) 8 7.40-7.23 (m, 5H), 6.7-6.55 (2bs, 1.4 H), 6.35-6.2 (bs, 0.6H). 5.61 (s, 0.7H), 5.59 (s, 0.3M), 5.10 (d, J=13 Hz, 0.7H), 5.08 (s, 0.611), 5.02 (d, JH3 Hz, 0.7H), 4.30-4.20 (m, HI), 3.97 (bs, 1H), 3.78 (s, 2.IH), 3.73 (s, 0.9H), 3.62 (s, 0.9H), 3.59 (s, 2.1H), 3.65-3.50 (m, 2H), 3.22 (s, 3H), 2.37-2.23 (m, 1H), 2.10-1.95 (m, 1H). Step 5: Methyl 5-(bcn/oyloxy)-2-{(25',4/0-l-[(benzyloxy)carbonyl]-4- methoxypyrrolidin-2-yl}-6-hydroxypyrimidine-4-carboxylate Dimethyl-2- {[(amino- {(2SAK)- l-[(ben/yloxy)carbonylJ-4-methoxypyrrolidin-2-yl}mcthylLdene)amino]oxy}but-2-enedioate were dissolved in xylene and the solution stirred at 150°C for 3 hours and at room temperature overnight. Xylene was concentrated in vacuo. To the crude compound, dissolved in pyridine, benzoic anhydride (1.3 eq.) was added and the reaction mixture was stirred at room temperature overnight. The solution was concentrated in vacuo and the crude dissolved in ethyl acetate washed with 1 N HO, saturated aqueous NaHCOi and brine, dried on Na^SO^ filtered and evaporated in vacuo. The crude product was purified by flash chromatography on silica gel (eluent ethyl acetate: petroleum ether = 10:90) and showed a 1:1 mixture of rotamers by NMR. jH NMR (DMSO-d6, 400 MHz, 300 K) S 13.5 (s, 1H), 8.09 (t, J- 7.0 Hz, 2H), 7.82-7.75 (m, 1H), 7.66-7.61 (m, 211), 7.40-7.25 (m, 4 H), 7.12-7.06 (m, lH),5.10(s, 1H), 5.09 (d, J- 12.5 Hz, 0.5H), 4.88 (d, J= 12.5 Hz, 0.5H), 4.66 (dd, J 16.2 and 8.0 Hz, 111), 4.10-4.00 (m, 1H), 3.74 (s, 3H), 3.75-3.60 (m, 211), 3.25 (s, 3H), 2.45-2.40 (partially under DMSO) (m, IH), 2.13-2.03 (m, 111). Stcp._6: Methyl-5-(benzoyloxy)-2-{(25,4y^)-l-[(benzyloxy)carbonyl]-4- methoxypyrrolidin-2-yl} -1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxylate To methyl 5-(ben7.oyloxy)-2-{(25;47?)-l-[(benzylox\)carbonyl]-4-methoxypyrrolidin-2~yI}~6-hydroxypyrimidinc-4-carboxylate, dissolved in dioxane, LiH (1.4 eq.) was added and the reaction mixture stirred at 38° C for 40 minutes. The temperature was raised to 60°C and dimethyl sulphate (1.3 eq.) was added dropwise. After two hours the reaction mixture was cooled down to 0°C and HC1 I N was added to quench the reaction. The reaction mixture was extracted with ethyl acetate and the organic phase washed with HC1 IN, saturated aqueous NaHCCb and brine, dried on Na2SO.i, filtered and concentrated in vacuo. The desired product was isolated by flash chromatography on silica gel (eluent ethyl acetate: petroleum ether = 30:70) as a 1:1 mixture of rotamers by NMR: '11 NMR (DMSO-d 7.66-7.61 (m, 2H), 7.38-7.22 (m, 4H), 7.08-7.02 (m, 1H), 5.18-5.12 (m, 111), 5.13 (d, J= 13.1 Hz, 0.5H), 5.07 (d, J= 13.1 Hz, 0.5H), 5.06 (d, J= 12.4 Hz, 0.5H), 4.84 (d, J= 12.4 Hz, 0.5H), 4.08-4.17 (m. 1H), 3.73 (s, 3H), 3.75-3.55 (m, 2H), 3.65 (s, 1.5H), 3.44 (s, 1.5H), 3.26 (s, 311), 2.62-2.52 (partially under DMSO) (m, 1H), 2.30-2.15 (m, 1H). MS: tn/z 522 (M+H)" Step 7: Benzyl-(2tS',4/?)-2-(4-{[(4-fluorobenzyl)aminojcarbonyl}-5-hydroxy-l- methyl-6-oxo-l,6-dihydropyrimidin-2-yl)-4-methoxypyrrolidine-l-carboxylate To methyl-5-(benzoy!oxy)-2-{(2.S\4/?)-l-[(benzyloxy)carbonyl]-4-methoxypyrrolidin-2-yl}-l-methyl-6-oxo-1.6-dihydropyrimidine-4-carboxylate,dissolved in methanol, 4-F-benzylamine (3 eq.) was added. The reaction mixture was stirred at reflux overnight. Methanol was removed in vacuo and the residue triturated with ethyl ether to give the title product as a 4:6 mixture of rotamers by NMR: 'll NMR (DMSO-dr, + TFA, 400 MHz, 300 K) 5 14.0 (bs, 1H), 8.92 (t, J = 6.4 Hz, 0.4H), 8.73 (t, J = 5.9 Hz, 0.6H), 7.35-7.25 (m, 4H), 7.20-7.05 (m, 4H), 6.93 (d, J= 7.5 Hz, 1H), 5.09-4.95 (m, HI), 5.09 (d, J= 12.3 Hz, 0.6H), 4.75 (d, J= 12.3 Hz. 0.6H), 5.05 (d, J= 13 Hz, 0.4H), 4.98 (d, J= 13 Hz, 0.4H), 4.52-4.43 (m, 211), 4.12-4.06 (bm, 0.411), 4.06-4.02 (bm, 0.611), 3.87 (dd, J= 11.5 and 4.5Hz, 0.4H), 3.84 (dd, J - 12 and 2.7Hz, 0.6H), 3.65-3.55 (m, ll-I),3.59(s, 1.2H), 3.41 (s. 1.8H), 3.25 (s, 311). 2.45-2.40 (partially under DMSO) (m, 1H), 2.30-2.15 (m, 1H). MS: m/z511 (MHI)' StepJJ: A^-(4-nuorobenzyl)-5-hydroxy-2-\|(2.S;4/0-4-methoxypyrroWdin-2-yl]- l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide Bcn/yl-(2.S\4/?)-2-(4-{[(4-i1uon)bcnzyl)amino]carbonyl}-5-hydroxy-l-rnethyI-6-oxo-1.6-dihydropyrimidin-2-yl)-4-methoxypyrrolidine-l-carboxylate was dissolved in methanol and Pd/C I0%wt (14%w/\v) was added. The mixture was stirred under H2 atmosphere at room temperature. After 2 hours the reaction mixture was filtered and methanol was removed in vacuo to give title compound. H NMR (DMSO-d6-fTFA, 400 MHz, 300 K) 5 12.58 (bs, 1H), 10.16 (bs, 1H), 9.74 (t, J= 6.3 Hz, 1H), 8.90 (bs, 111), 7.36 (dd, J - 8.5 and 5.7 Hz, 2H), 7,19 (t, J= 8.8 Hz, 2H), 5.01 (bs, IH), 4.50-4.60 (m, 2H), 4.19 (bs, IH), 3.55-3.45 (m, 1H), 3.47 (s, 3H), 3.45-3.35 (m, IH), 3.32 (s, 3H), 2.74 (dd, J= 13.9 and 7.5 Hz, IH), 2.17-2.10 (m, IH). MS:m/z377(M+H)'f Step 9: 2-{(2(V,4/^)-l-[(dimethylamino)(oxo)acctyl]-4-methoxypyrrolidin-2- yI}-A'-(4-fluorobcnzyl)-5-hydroxy-l-melhyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide To JV-(4-fluorobenzyl)-5-hydroxy-2-[(25,4/?)-4-methoxypyrrolidin-2-yI]-l-methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide, triethylamine (1 eq.) was added. The reaction mixture was cooled down to 0°C and methyl chlorooxoacetate (3 eq.) was added. After 1 hour the reaction mixture was concentrated and a big excess of dimelhylamine 2M in II IF (30 eq.) was added The reaction mixture was concentrated and the desired compound was isolated by HPLC purification (Waters, Symmetry CJS, 5um, 19x50mm eluting with water and acetonitrile containing 0.1% trifluoroacetic acid) as a 2:8 mixture of rotamcrs by NMR: 'H NMR (DMSO-d6, 400 MHz, 340 K) 5 11.9 (bs, HI). 8.99 (bs, 0.8H), 8.85 (bs, 0.2H), 7.40-7.30 (m, 2H), 7.14 (t, J= 8.8 Hz, 2H), 5.21 (t, J= 7.5 Hz, iH), 4.54 (dd, J= 14.9 and 6.7 Hz, 111), 4.45 (dd, J = 14.9 and 6.4 Hz, HI), 4.10 (bs, IH), 3.91 (dd, J = 11.6 and 4.6 Hz, 0.2H), 3.79 (dd, J= 11.2 and 4.4 Hz, 0.8H), 3.60-3.50 (m, 1 H), 3.58 (s, 2.4H), 3.48 (s, 0.6H), 3.29 (s, 0.6H), 3.27 (s, 2.4H), 2.87 (s, 2.4H), 2.81 (s, 2.4H), 2.64 (s, 0.6H), 2.57 (s, 0.6H), 2.70-2.50 (m, IH), 2.30-2.20 (m, 0.8H), 2.20-2.10 (m, 0.211). MS:m/z476(M+H)+ EXAMPLE 18 N]-\ l-(4-{[(4-fluorobenzyl)amino]carbonyl}-5-hydroxy-l-methyl-6-oxo-l,6-dihyclropyrimidin-2-yl)-l-]nethyicthylJ-A^ ,;V"-dimcthylethancdiamide (11). Organic Synthesis Coll. Vol.II pg 29 Acetone cyanohydrin was diluted with MeOU (approx. 3 mmol/mL). The solution was cooled and saturated with ammonia gas, and the reaction mixture was allowed to stand for one day. The excess of ammonia and methyl alcohol were evaporated by rotary evaporation. Residue consisted in the title product. Step 2: Benzyl 1 -cyano-1 -methylethylcarbamate To a suspension of 2-amino-2-methyIpropanenitrile in water an equimolar amount of Na2C03 and a slight excess (1.1 eq) of benzylchloroformate were added, with an external cooling. Reaction mixture was stirred o/n at room temperature, extracted in EtOAc and the organic phase was washed with Nal ICOjss, dried (Na2S04), filtered and concentrated. Product was obtained as a white solid. 'll-NMR (CDCI3) S 7.48-7.33 (bs, 5 H), 5.15 (s, 2 11), 4.98 (bs, 1 H). 1.68 (s, 6 H); 13C-NMR(CDC13)S 153.33, 13.81, 127.81, 127.63, 127.55, 120.64,66.56,46.19, 26.67; MS(M+1)/I//J219. Step 3: Benzyl 2-amino-2-(hydroxyimino)-l.l-dimcthylethylcarbamate. Hydroxylamine hydrochloride in methanol was added to an equimolar stirred solution of potassium hydroxide in methanol. The mixture was stirred for 15 min and the precipitated potassium chloride was removed by filtration. The filtrate was added to an equimolar amount of the nitrile and the solution stirred overnight at 40 °C, then cooled to room temperature and concentrated. The resulting residue was triturated with water and the white solid, after drying under vacuum, consists mainly in the title product. 'II-NMR(DMSO) 59.12 (bs, 1 H), 7.48 (bs, 5 H), 7.08 (bs. I H), 5.33 (bs, 2 H), 4.98 (s, 2 11), 1.39 (s, 6 1 f): MS (Mi I) m/z 252. Step 4: Methyl 2-( l-{[(benzyIoxy)carbonyl]amino}-l-methylethyI)-5,6- dihydroxypyrimidine-4-carboxylate. Benzyl 2-amino-2-(hydraxyimino)-l,l-dimethylethylcarbamate was suspended in chloroform and treated with 1.2 eq of dimethylacetylcnedicarboxylate and reaction was refluxed overnight. Alter cooling at room temperature, volatiles were evaporated and the residue was taken into xylene and heated at 145 °C for 48 h. The reaction mixture was stirred at room temperature overnight to allow the precipitation of the product (5) as a light brown solid. This solid was collected by filtration and washed with diethyl ether. 'H-NIMRCDMSCOS 12.54 (S, I H), 10.21 (s, 1 H), 7.44 (bs, 1 H), 7.30 (bs, 5 H), 4.95 (s, 2 H), 3.80 (s, 3 H), 1.47 (s, 6 H); MS (M+l) m/z 362. -Si£lL5: Methyl 5-(benzoyloxy)-2-(l-{[(bcnzyloxy)carbonyI]amino}-l- methylethyl)-6-hydroxypyrimidine-4-carboxylate. To a stirred solution of methyl 2-(l-{[(benzyloxy)carbonyl]amino}-l-methylethyI)-5,6-dihydroxypyrimidine-4-carboxyIate in pyridine. 1.1 eq of benzoic anhydride were added and stirring prolonged at room temperature over night. Pyridine was evaporated and residue was taken in eihyl acetate and washed with 1 N HC1 and brine. Organic layer was separated, dried (Na2S04), filtered and concentrated by rotary evaporation and residue was purified by Hash column chromatography (Si02, petroleum ether/ethyl acetate 60/40 v/v as eluant). Collection and evaporation of appropriate fractions afforded title product. lH-NMR(CDCI3)5 12.2 (bs, 1 II), 8.15 (d, J= 7.4 Hz, 2 H), 7.65 (t, J = 7.4 Hz, 1 H), 7.50 (t, 7 = 7.5 Hz, 2 H), 7.32 (bs, 5 H), 5.54 (bs, 1 11), 5.05 (s, 2 H), 3.82 (s. 3 H), 1.67 (s, 6 H); MS (M+l) m/z 466. Step 6: Methyl 5-(benzoyloxy)-2-(l-{[(benzyloxy)carbonyl]amino}-l- mcthylethyl)-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxylate To a stirred solution of Lif I (1.1 eq) in dioxane, methyl 5-(benzoyIoxy)-2-(l-{[(benzyloxy)carbonyl]amino}-l-methylethyl)-6-hydroxypyrimidine-4-carboxylate was added and the mixture was stirred at 38 °C for 45 min. After cooling down to room temperature, dimethylsulfate (1.3 eq) was added and reaction mixture was heated at 60 °C for 2 h. Mixture was then cooled to room temperature, dioxane evaporated and residue was purified by flash chromatography, eluting with 65/55 v/v petroleum ether/ethyl acetate. Collection and evaporation of appropriate fractions afforded the title product. lH-NMR(CDCl3)5 8.19(d,7=7.3 Hz, 2 H), 7.65 (t, .7- 7.3 Hz, 1 H), 7.51 (t, .7=7.6 Hz, 2 H), 7.33 (bs, 5 II), 5.63 (bs, 1 H), 5.03 (s, 2 H). 3.80 (s, 3 H), 3.63 (bs, 3 H), 1.72 (s, 6 H); MS (M+l) m/z 480. Step._8: Benzyl l-(4-{[(4-fluorobenzyl)aminoJearbonyl}-5-hydroxy-l-methyl- 6-oxo-l,6-dihydropyrimidin-2-yI)-l-methylethyIcarbamate. To a mcthanolic solution of methyl 5-(benzoyloxy)-2-(l-{[(bcnzyloxy)carbonyl]amino}-l-methyIethyl)-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxylate,/)-fluoro benzylamine (3 cq) was added and mixture was refluxed over nighl. After evaporation of methanol, residue was taken in BtOAc, washed with IN I1C1 and brine, dried (Na2S04), filtered and evaporated to obtain the title product. 'll-NMR(CDCl3)8 I1.9(bs, 1 H), 7.79 (bt, 1 H), 7.35-7.29 (m, 7 II), 7.07 (t, y = 8.6 Hz, 2 H), 5.27 (bs, 1 H), 5.02 (bs, 2 H), 4.58 (d, J- 6.2 Hz, 2 H), 3.67 (s. 3 H), 1.70 (s,6H);MS(M+l)m/z469. S]ej2_9: 2-( 1 -amino-1 -mcthyIethyl)-//-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6- oxo-l,6-dihydropyrimidine-4-carboxamide. A mcthanolic solution of Benzyl l-(4-{[(4-fluorobenzyl)amino]carbonyl}-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidin-2-yl)-Nmethylethylcarbamate was stirred over night under a hydrogen atmosphere in the presence of catalytic 10% Pd/C. Catalyst was then filtered oft"through celite, and the filtrate was concentrated. Product was obtained after trituration with ethyl ether. 'H-NMR(DMSO)8 12.31 (bs, 1 H), 9.68 (bt, J-6.6 Hz, 1 H), 8.60 (bs, 2 H), 7.43 (dd, J = 8.4 Hz, J = 5.7 Hz, 2 H), 7.20 (t, y = 8.8 Hz, 2 H), 4.54 (d, J 6.6 1 iz, 2 H), 3.56 (s, 3 H), 1.73 (s, 6 II); MS (M+l) m/z 335. Step 10: Methyl {[l-(4-{[.(4-fluorobcnxyl)amino]carbonyI}-5-hydroxy-I- methyl-6-oxo-l,6-dihydropyrimidin-2-yl)-l-methylethyI]amino}(oxo)acetate. To a stirred mixture of 2-(l-amino-l-methyIethyl)-A^-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide (4) and triethyl amine (3 eq) in chloroform, methyl chlorooxoacetate (1.5 eq) was added with an external cooling. Finished the addition, the ice bath was removed and the mixture was stirred at room temperature for 3h. Reaction mixture was then partitioned between chloroform and IN IICI. Organic layer was separated, washed with brine, dried (Na2SC>4), filtered and concentrated to obtain title product. 'H-NMR (DMSO) 5 12.2 (bs, 1 H), 9.47 (s, 1 II), 9.04 (t, 7= 6.3 Hz, 1 H), 7.38 (dd, J-8.4 Hz, 7=5.7 Hz, 2 11), 7.16 (t, 7=8.8 Hz, 2 H), 4.50 (d, 7= 6.3 Hz, 2 H), 3.78 (s, 3 H), 3.45 (s, 3 11), 1.67 (s, 6 H); MS (M+l) m/z 421. Step 11: N] -[ 1 -(4- {[ (4-fluorobenzyl)amino]carbonyl} -5-hydroxy-1 -methyl-6- oxo~l,6-dihydropyrimidin-2-yl)-I-methylethyI]-A/' ,N -dimethylethanediamide (11). Methyl {[ 1 -(4-{[(4-fluorobenzyl)amino]carbonyl} -5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidin-2-yl)-l-methylethyl]amino}(oxo)acetate was refluxed in an excess of 2 M solution of dimethylamine in THF for 2 h. Reaction mixture was cooled to room temperature, evaporated and residue was purified by RP HPLC (CI8, water/acetonitrile containing 0.1% of trifluoroacetic acid as eluant). Collection and lyophilization of appropriate fractions afforded the title product. ,H-NMR(DMSO)8 12.19 (s, 1 H), 9.32 (s, 1 H), 9.06 (t, 7= 6.4 Hz, 1 H), 7.40 (dd, 7 -8.5 Hz, 7= 5.7 Hz, 2 H), 7.18 (t, 7= 8.8 Hz, 2 11), 4.51 (d, 7 = 6.4 Hz, 2 H), 3.55 (s, 3 11), 2.93 (s, 3 H), 2.87 (s, 3 H), 1.68 (s, 6 H); 13C-NMR (DMSO) 5 168.23, 163.76, 163.09, 161.20 (d, 7= 96.4 Hz), 158.46, 151.90, 145.49, 134.77, 129.40 (d, 7 - 3.2 Hz). 124.29, 115.05 (d, 7= 8.5 Hz), 56.50, 41.51, 35.46, 33.42, 32.68, 26.85; MS (Mr 1) m/z 434; MS (M+l) m/z 434. EXAMPLE 19 Step 1: Af-(4-fluorobenzyl)-5-hydroxy-1 -mcthyl-2-( I -methyl-1 -{[(5-methyl- 1,3,4-oxadiazol-2-yl)carbonyl]amino) ethyl)-6-oxo-1,6-dihydropyrimidine-4-carboxamide A solution of S-methyl-l^^-oxadiazoIe^-carboxylic acid was treated with 1.9 equivalents of oxalyl chloride and a few drops of anhydrous A'.Af-dimethylformamide. After 1 h, mixture was concentrated, residue was triturated with /-z-hexane and directly added to an equimolar solution of 2-(l -amino-1 -methylethyI)-jV-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-K6-dihydropyrimidinc-4-carboxamide (described in step 9, example 18) in acctonitrile. Tricthyl amine (3 eq) was added to the mixture and the reaction was stirred overnight at room temperature. Title product was isolated by prep RP HPLC (CI8, acetonitrile/water containing 0.1% of trifluoroacetic acid as eluant). 1H-NMR(DMSO)8 12.2 (bs, I H), 9.84 (s, 1 H), 9.05 (t, J - 6.5 Hz , 1 H),7.38(dd,J = 8.4 Hz, 7- 5.6 Hz, 2 11), 7.17 (t, J= 8.8 Hz, 2 H), 4.50 (d, J= 6.5 Hz, 2 11), 2.56 (s, 3 H), 1.74 (s, 6 H), one methyl signal obscured by water, MS(M+1)/M/Z445. EXAMPLE 20 2-{(2,ST)-l-\|(dimethylamino)(oxo)acelyr]-4,4-difluoropyrrolidin-2-yl}-iV-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide A solution of dimethyl sulfoxide (2.1 eq) in dry dichloromethane was added dropwise to a stirred solution of oxalyl chloride (1.01 eq) in dry dichloromethane (1.25 N) at-78 °C under N2 atmosphere. After 15 min, a solution of the commercially available 1-benzyl-2-methyl-(2LS\4#)-4-hydroxypyrrolidine-1,2-dicarboxylate in dry dichloromethane was added slowly, and stirring was continued for 30 min at -78 °C. Alter addition of triethylaminc (5 eq), the mixture was gradually warmed up to room temperature. The mixture was quenched with water and aqueous layer was separated and extracted with dichloromethane. The extract was washed with brine and dried over Na2SC>4. Concentration of the solvent in vacuo gave a residue, which was purified by flash cromatography (ethyl acetate:petroleum ether = 3:7) to give title product as a yellow oil. "H NMR (DMSO-de+TFA, 400 MHz, 330 K) 5 7.40-7.32 (m, 5H), 5.20-5.09 (m, 2H), 4.79 (d, J = 9.7 Hz, 1H), 3.95 (d, J = 17.9 Hz, HI), 3.78 (d, J - 17.9 Hz, 1H), 3.64 (s, 311), 3.13 (dd, J- 18.7 and 10.6, 1H), 2.62 (dd, J = 18.7 and 2.7 Hz, 1H). MS: m/z278(M+H)+ Step 2: 1-Benzyl 2-methyl (2,Sr)-4,4-difluoropyrrolidine-l,2-dicarboxylate A solution of l-benzyl-2-mcthyl-(25)-4-oxopyrrolidine-l,2-dicarboxylate in dichloromethane was slowly added to a solution of diethylaminosulfur fluoride in dichloromethane precooled to - 78 °C. The reaction mixture was warmed to room temperature and mixed with cold water. The organic layer was separated, washed with water, dried over Na2S04 and evaporated to give title compound as a yellow oil. 'II NMR (DMSO-d6, 400 MHz, 330K) 8 7.40-7.32 (m, 5H), 5.16-5.12 (m, 211), 4.63 (br s, 1H), 3.96-3.80 (m, 2H), 3.65 (s, 3H), 3.15-2.86 (m, 1H), 2.56-2.45 (partially under DMSO) (m, 111). I9F NMR 'll-l9F dec (DMSO-d6, 400 MHz, 330 K) 8 - 98.13 (d, J = 223.7 Hz) + -98.72 (d, J = 223.6 Hz) (rotamera), -101.38 (d, J == 190.7 Hz)+ -102.00 (d, J = 191.3 Hz) (rotamer b) (2F). MS m/z 300 (M + 11)+. Step 3: l-[(Benzyloxy)carbonyl]-4,4-difluoro-L-proline A solution of 1-benzyl 2-methyl (2S)-4,4-difluoropyrrolidine-l,2-dicarboxylate in methanol was refluxed with 2N NaOH (2 eq) for 2 hours. Methanol was removed and pH adjusted to 1 with 3 N HC1 obtaining a suspension which was extracted several times with ethyl acetate. Combined organics were dried overNa2S04 and evaporated to give title product as a dark brown oil. II NMR(DMSO-dr,,400MHz,330K)5 12.96 (brs, 111), 7.36-7.31 (m, 511), 5.11 (s, 2H).4.50(bs, 1H), 3.91-3.80 (m, 2H), 3.01-2.82 (m. 111), 2.56-2.41 (partially under DMSO)(m, 1H). MS: m/z284(M-H)Step 4; BenzyI-(2S)-2-aminocarbonyi-4,4-difiuoropyrrolidine-l-carboxylate To a stirred solution of l-[(bcn/yloxy)carbonyl]-4,4-dinuoro-L-proline, pyridine (0.6 eq.) and di-t-butyl dicarbonate (1.3 eq) in dioxane, ammonium bicarbonate (1.26 eq) was added and the mixture was stirred at room temperature for 20 hours. Dioxane was concentrated and the residue dissolved in ethyl acetate and washed with HC1 1 N, saturated aqueous NaHCC^ and brine, dried over Na2S04, filtered and evaporated in vacuo to obtain a yellow oil. Two sets of signals, two con formers (ratio 1:1) were present. 'II NMR (DMSO-d6,400 MHz, 300 K) 5 7.56 (d, J - 15.4 Hz, 1H), 7.39-7.34 (m, 5H), 7.17 (d, J - 19.3 Hz, 1H), 5.10-5.08 (m, 211), 4.42 (dd, J = 9.3 and 4.7, 0.5 H), 4.34 (dd, J - 9.2 and 4.6 Hz, 0.5 H), 3.92-3.73 (m, 211), 2.90-2.72 (m, 1H), 2.43-2.30 (m, 111). MS:m/z285(M+H)Step 5: Benzyl-(2.V)-2-cyano-4,4-difluoropyrrolidine-l-carboxylate A solution of benzyl-(2S)-2-aminocarbonyl-4,4-difiuoropyrrolidine-l-carboxylate and triethylamine (2.1 eq.) in dichloromethane was cooled to 0°C and trifluoroacetic anhydride (1.1 eq.) was added dropwise under nitrogen. Stirring was continued for 1 hour allowing the mixture to reach room temperature. Volatiles removed in vacuo and residue taken up in ethyl acetate, washed with HC1 IN, brine and dried over Na2S04. Evaporation gave title compound as brown oil. 'H NMR (DMSO-d Stej3_6: Benz.yl-(25)-2-famino(hydroxyimino)methyl]-4,4-difluoropyrrolidine- 1-carboxylate A solution of benzyI-(2.S)-2-cyano~4,4-difluoropyrrolidine-l -carboxylate, hydroxylamine hydrochloride (1.4 eq.) and triethylamine (1.7 eq.) in ethanol was refluxcd under nitrogen for 5 hours. Mixture was concentrated and residues taken up in ethyl acetate and washed with water and brine. Combined organics were dried over Na2SC>4 and evaporated to give title compound as a foam. !H NMR (DMSO-dG, 300 MHz, 330 K) 8 9.12 (bs, HI), 7.38-7.34 (m, 5H), 5.36 (bs, 2H), 5.13 (dj - 14.4 Hz, 1H) + 5.09 (d, J - 14.4 Hz, I H), 4.56 (dd, J = 8.6 and 4.9 Hz, 1H), 4.07-3.76 (m, 211), 2.80-2.71 (m 1H), 2.60-2.51 (partially under DMSO) (m, 1H). MS:m/z300(M+H)+. Step_7: Dimethyl-2-{f(amino-{(2lSr)-l-[(benzyloxy)carbonyl]-4,4- difluoropyrrolidin-2-yl}methylidene)amino]oxy}but-2-enedioate F A solution of benzyi-(25)-2-[amino(hydroxyimino)methyl]-4,4-difluoropyrrolidine-l-carboxylate and dimethylacetylcndicarboxylate (1.2 eq.) in chloroform was refluxed for 1 hour under nitrogen and the solution was concentrated. Residue was purified by flash chromatography on silica gel, (eluent: petroleum ethercthyl acetate = 7.5:2.5), to give the desired product as a 3:1 mixture of two isomers by 'H NMR. 'H NMR (DMSO-d6, 300 MHz, 330 K) 5 7.45 -7.25 (m, 5H), 6.63 (bs, 1.5H), 6.30 (bs, 0.5H), 5.62 (s, 0.7511), 5.60 (s, 0.25H), 5.13 (s, 211), 4.58 (dd, J = 9.1 and 4.9 Hz) + 4.57 (dd, partially overlapped) (1H), 3.96-3.86 (m, 2H), 3.79 (s, 2.2H), 3.74 (s, 0.8H), 3.66 (s, 0.8H), 3.61(s, 2.2H), 2.93-2.81(m, 1H), 2.56-2.43 (partially under DMSO)(m, 1H). MS:m/z442(M+H)+. Step_8: Methyl-2-{(2S)-l-[(benzyloxy)carbonyiJ-4,4-difluoropyrrolidin-2-yl}- 5,6-dihydroxypyrimidine-4-carboxylale A solution ofdimethyl-2-{[(amino-{(2tS>l-[(benzyIoxy)carbonyl]-4,4-dinuoropyrroIidin-2-yI}methylidene)amino]oxy}bul-2-enedioate in o-xylene was re fluxed for 6 hours. Then the reaction was cooled down and concentrated at rotavapor. Ethyl ether was added until precipitation of a solid that was filtered, washed with other ethyl ether and dried to give the title pyrimidine as a brown solid. Two sets of signals, two rotamers (ratio 1:1) were present. '11 NMR (DMSO-d6, 400 MHz, 300 K) S 12.97 (s, 1H). 10.38 (s, 1H), 7.40-7.29 (m, 311), 7.22-7.15 (m, 1H); 7.10-7.05 (m, 1H), 5.12 (d, J - 12.6 Hz, 0.5H) 5.10 (s, 1H), 4.89 (d, J = 12.6 Hz, 0.5H), 4.86-4.72 (m, 1H), 4.10 3.86 (m, 2H), 3.81 (s, 3H), 2.90-2.85 (m, 1H), 2.64-2.53 (partially under DMSO) (m, 111). MS:m/z410(M+H)+. Step 9: Methyl 5-(benzoyloxy)-2-{(2i>!-[(benzyloxy)carbonyl]-4,4- diiluoropyrrolidin-2-yl}-6-hydroxypyrimidine-4-carboxylate Mcthyl-2-{(25)-l-[(benzyloxy)carbonyI]-4,4-dilluorop\rrolidin-2-yl}-5,6-. dihydroxypyrimidine-4-carboxylate in dry pyridine was treated with benzoic anhydride (2 eq.) overnight at room temperature. The mixture was evaporated, taken up in ethyl acetate and washed with HC1 IN and brine. Organics were dried over Na2S04, filtered and evaporated to obtain an oil which was purified by flash chromatography on silica gel (eluent: ethyl acetate:petroleum ether = 7:3). !H NMR (DMSO-d6, 300 MHz, 330 K) 8 13.51 (bs, 1H), 8.10 (d, J - 7.6 Hz, 2H), 7.79 (t, J - 7.1 Hz, 1H), 7.64 (t, J = 7.6 Hz, 2H), 7.33-7.17 (m, 5H), 5.13 (s, 2H), 4.99 (t, J - 7.3 Hz, 1H), 4.09-3.97 (rn, 2H), 3.77 (s, 3H), 3.02-2.99 (m, 2H). MS:m/z514(M+H)+. Step 10: MethyI-5^(benzoyloxy)-2-{(2iS)-l-i(benzyloxy)carbonyl]-4,4- difluoropyrrolidin-2-yl}-l-methyi-6-oxo-l,6-dihydropyrimidine-4-carboxylate I Methyl 5-(benzoyloxy)-2-{(2iS>l-[(benzyloxy)carbonylJ-4,4-difluoropyrrolidin-2-yl}-6-hydroxypyrimidine-4-carboxylate dissolved in dry 1,4-dioxane was added to a suspension of Lill (1.4 eq.) in dioxane. The mixture was stirred at 38° C for 45 minutes and then cooled down to room temperature. Dimethyl sulphate (1.3 eq.) was added and the mixture was warmed to 58 °C for 1 hour. The reaction mixture was cooled down to 16 °C and glacial acetic acid (0.1 eq) was added, followed by water and ethyl acetate. The combined organic layers were dried (Na2SC>4), filtered and concentrated to an oil which was cromatographed through silica gel (eluent: ethyl acetate:petroleum ether^3:7) to give the desired compound as a 1:1 mixture of two rotamers bv ]H NMR 'H NMR (DMSO-de, 300 MHz, 300 K) 5 8.11-8.08 (m. 2H), 7.80 (t, J= 7.7 Hz, 1H), 7.67 - 7.65 (m, 2H), 7.36-7.10 (m, 5H), 5.50 (dd, J = 9.2 and 4.7 Hz, 1H), 5.22 (d, J = 12.9 Hz, 0.5H), 5.14 4.95 (m, 1H), 4.93 (d, J = 12.3 Hz, 0.5H), 4.16-3.79 (m, 2H), 3.74 (s, 3H), 3.61 (s,1.5H), 3.45 (s,1.5H), 3.25-3.11 (m, 1H), 2.89-2.74 (m. 1H). MS: m/z 528 (NM-H)+. Step ..J.I: Benzyl-(2.S)-4,4-difluoro-2-(4-{[(4-fluorobenzyl)amino]carbonyl}-5- hydroxy-1 -methyl-6-oxo-l ,6-dihydropyrimidin-2-yl)pyrrolidine-1 -carboxylate Methyl-5-(benzoyIoxy)-2-{(2^-l-[(benzyloxy)carbonyI\|-4,4-difluoropyrrolidin-2-yl}-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxylatc in dry MeOH was treated with 4-fiuorobenzyl amine (2.5 eq.) at reflux for 2 hours. Solvent was removed in vacuo and the residue was taken up in ethyl acetate, washed with HC1 IN, brine, dried over Na^SOa- The filtrate was concentrated in vacuo and triturated with ethyl ether to obtain the title compound as a 1.5:1 mixture of two rotamers by NMR. 'll NMR (DMSO-de-iTFA, 300 MHz, 300 K) 5 8.92 (bt, 0.4H), 8.69 (bt, 0.6H), 7.36-7.31 (m, 411), 7.20 -7.09 (m, 4H), 6.97 (dJ - 7.2 Hz, 1II), 5.34-5.25 (m, 1H), 5.14 (d, J = 12.4 Hz, 0.411 ), 5.07-4.99 (m, 1.2H), 4.81 (d, J - 12.2 Hz, 0.4H), 4.51-4.48 (m, 211), 4.38-4.21 (m, 1H), 4.07-3.96 (m, 1H), 3.59 (s, 1.2H),3.48 (s, 1.8H), 3.05-2.95 (m, 1H), 2.78-2.68(m, 1H). MS:m/z517(M+H)Step 12: (2.S,)-4,4-difluoro-2-(4-{[(4-fiuorobcnzyl)amino]carbonyl}-5-hydroxy- 1 -methyl-6-oxo-1,6-dihydropyrimidin-2-yl)pyrrolidinium trifluoroacetate A solution of benzyl-(2.V)-4,4-difiuoro-2-(4-{f(4-fluorobenzyl)amino]carbonyl}-5-hydroxy-l-methyi-6-oxo-l,6-dihydropyrimidin-2-yl)pyrrolidine-l-carboxylate in MeOH was treated with Pd/C 10%wt (10% w/w) for 3 hours at room temperature under H2 atmosphere. The mixture was filtrated over a celite pad, concentrated in vacuo and treated with trifiuoroacetic acid (10 eq.). The acid in excess was removed in vacuo to obtain title product as a pale yellow solid after trituration with ethyl ether. 'H NMR (DMS0-d6+TFA, 300 MHz, 340K) S 9.60 (bt, 1H), 7.39 (t, J = 8 Hz, 2H), 7.17 (t, J - 8,8 Hz, 211), 5.35 (t, J = 8.4 Hz, HI), 4.62 (dd, J - 15.3 and 6.6;-Hz, 1H), 4.55 (dd, J - 15.2 and 6.3 Hz, 1H), 4.05--3.87 (m, 2H), 3.48 (s, 3H), 3.30-3.14 (m, 1H), 2.96-2.78 (m, 1H). MS: m/z 383 (M+H)+. Step 13: 2-{(26>l-\|(dimethylamino)(oxo)acctyll-4,4-difluoropyrrolidin-2-yl}- A^-(4-nuorobenzyl)-5~hydroxy-l-methy!-6-oxo-l,6-dihydropyrimidine-4-carboxamide A solution of (2iS,)-4,4-diiluoro-2-(4-{[(4-nuorobenzyl)aminoJcarbonyl}-5-hydroxy-l-methyI-6-oxo-l,6-dihydropyrimidin-2-yl)pyrrolidinium trifluoroacetate in chloroform and triethylamine (1.01 eq.) was treated with methyl chlorooxacetate (2 eq.) at 0 °C. The mixture was allowed to reach room temperature for 2 hours. Dimethylamine (30 eq.) was added at room temperature and the mixture left stirring over night. The mixture was concentrated in vacuo and purified by preparative HPLC (Column: Cis, eiuent: acetonitrile and water containing 0.1 % trifluoroacetic acid). To obtain the title product two rotamers (ratio 4:1) were found in 11 NMR. Hi NMR (DMSO-d6+TFA, 300 MHz, 300 K) 5 9.23 (t, J = 6.5 Hz, 0.8H), 9.10 (bt, 0.2H), 7.34 - 7.31 (m, 2H), 7.11 (t, J - 8.8 Hz, 2H), 5.48 (dd, J = 8.9 and 5.7 Hz, 1H), 4.53 (dd, J = 15.0 and 6.7 Hz, 1H), 4.42 (dd, J = 15.0 and 6.2 Hz, 1H), 4.24-4.16 (m, 111), 4.05-4.02 (t, J = 11.8 Hz, 1H), 3.52 (s, 2.4H), 3.45 (s, 0.6H), 3.15-3.04 (m, 1.6H), 2.84 (s, 2.411), 2.80 (s. 2.4H), 2.79 - 2.65 (m, 0.4H), 2.63 (s, 0.6H), 2.57 (s, 0.6H). MS:m/z482(M+H)+. EXAMPLE 21 * 2-\|l,2-dimethyl-4-(methylsulfonyl)piperazin-2-yI]-A/-(4-fluorobenzyl)-5-hydroxy-l- methyI-6-oxo-l,6-dihydropyrimidine-4-carboxamide To a cooled (-75 °C) solution of LDA 2M in heptane/THF (1.5 eq) in THF, a solution of 1 -[(benzyloxy)carbonyl\|-4-(/er/-butoxycarbonyl)piperazine-2-carboxylic acid (Bigge et al, Tetrahedron Lett. 1989, 30: 5193) in THF was added dropwise at -75°C. After being stirred for 1 hour at -75 °C, Mel (1.5 eq) was added. After 2 hours at -75 °C the reaction mixture was left warming to r.t., evaporated, diluted with AcOEt, washed with NaHC03, water, brine and dried over Na2S04. The crude was purified by flash chromatography on silica gel (petroleum ether/AcOEt, 85:15) to obtain the title compound . 1II NMR (DMSOd6, 340K, 300MHz) 5 7.45-7.30 (m, 5H), 5.19 (AA' system, J = 13 Hz, 2H), 4.05 (d, J = 14 Hz, 1H), 3.87-3.78 (m, HI), 3.66 (d, J = 14 Hz, 1H), 3.62-3.35 (m, 3H), 1.66 (s, 3H), 1.45 (s, 9H). MS: m/z 360 (M+H)+. Step_2: 1-benzyl 4-/e/7-hutyl 2-[(Z)-amino({[(lA>3-methoxy-l- (methoxycarbonyl)-3-oxoprop-l-enyr]oxy}imino)methyl]-2-methyl piperazine-l,4-dicarboxylate. A solution of 1-benzyl 4-/eri~buty\ 2-cyano-2-methylpiperazine-l,4-dicarboxylate in EtOIl was added to a solution of Et3N (3.2 eq) and NU20I1 HCI (3 eq) in EtOH. The mixture was stirred 2 hr at 40 °C. After evaporation of the solvent, the residue was diluted with AcOEl, washed with water, dried over Na2S04, filtered and concentrated. The residue was further dissolved in chloroform and dimethylacetylenedicarboxylate (1.5 cq) added to the stirred solution. Reaction was refluxed over night. The mixture was evaporated and the residue was purified by flash chromatography on silica gel (petroleum ether/AcOEt, 65:35) affording the title compound as mixuture of isomers in 3.5:1 ratio. !H NMR (DMSOd6, 340K? 300MHz). Two sets of signals were observed due to the presence of the geometric isomers: 5 7.48-7.25 (m, 5H), 6.31( bs, 1.56 H), 6.01 (bs, 0.44 H), 5.63 ( s,0.78 H), 5.55 (s, 0.22 H), 5.12-5.02 (m, 2H), 3.85-3.60 (m, 9H), 3.60-3.45 (m,2H), 3.45-3.31 (m, 1H), 1.51 (s, 2.4H), 1.45 (s, 0.66 H), 1.41 (s, 9H). MS:m/z535(M+H)+. ^tcp_3: 1 -benzyl 4-(ert-buty\ 2-[5-(benzoyloxy)-4-hydroxy-6- (methoxycarbonyl) pyrimidin-2-yl]-2-methylpiperazine-l,4-dicarboxylate 1-benzyl 4-/m-butyl 2-[(Z)-amino({[(l£)-3-methoxy-l-(methoxycarbonyl)-3-oxoprop-l-enyl]oxy}imino)methyl]-2-methylpipcrazine-L4-dicarboxylate was dissolved in xylene and stirred at 155 °C for 8h. After evaporation of the solvent, the residue was dissolved in pyridine and benzoic anhydride (1.5 eq) was added. The reaction mixture was stirred at room temperature over night, then pyridine was evaporated. The residue was diluted with AcOEt, the organic phase washed with HC1 IN, dried (Na2S04) and evaporated. The title product was obtained by flash chromatography (cluent: petroleum ether/AcOEt 70/30). !H-NMR (DMSOd6, 340K, 400MHz) 8 12.96 (bs, 1H), 8.07 (d, J=12 Hz, 2 H), 7.76 (t, .7-7.6 Hz, HI), 7.62 (t, ,7-7.6 Hz, 2H), 7.37-7.22 (m, 5H), 5.03 (s, 2H), 3.96 (dt ,7,-13.6 Hz, J2==5.8!lz, 111), 3.80-3.52 (m, 7H), 3.47-3.40 (m, 1H), 1.65 (s, 3H), 1.35 (s, 911). MS:m/z607(MHI)Step 4: 1-benzyl 4-/er/-butyl 2-[5-(benzoyloxy)-4-(methoxycarbonyl)-l- methyl-6-oxo-l,6-dihydropyrimidin-2-yl]-2-methylpiperazine»l,4-dicarboxylate. 1-Benzyl 4-/er/-butyI 2-\|"5-(benzoyloxy)-4-hydroxy-6-(methoxycarbonyl) pyrimidin-2-yl]-2-methylpiperazine-l,4-dicarboxyIate was added to a suspension of LiH (1.1 eq) in dioxane (7 ml/mmol) at room temperature. The mixture was stirred at 40 °C for 45 min. then dimethylsulfalc (1.3 eq) was added and the temperature was raised to 60 °C. After 1 h glacial acetic acid (0.1 eq) was added to the reaction mixture, followed by water (7 ml/mmol) and EtOAc (7 ml/mmol). The aqueous layer was separated and extracted with EtOAc. The combined organic layers were dried (Na2SC>4) and concentrated. The crude was purified by flash chromatography on silica gel (AcOEt/petroleum ether, 1:4) to separate the title compound A from B (ratio A/B 1.3/1). A: 'll NMR (CD3CN, 320K, 300MHz) 5 8.18 (d, ,/=7.2 Hz, 2H), 7.80 (t, .7=7.5 Hz, 1H), 7.63 (t, .7=7.8 Hz, 2H), 7.45-7.22 (m, 5H), 5.08 (AA' system, J = 12 Hz, 2H), 4.18-3.88 (m, 3M), 3.81 (s, 3H), 3.68-3.46 (m, 5H, at 3.58 (s)), 3.40-3.22 (m, 1H), 1.75 (s,3H), 1.49 (s,9H). MS:m/z621 (M+H)+. Stejl-5: Methyl 5-(benzoyloxy)-2-\|4-(/er/-buloxycarbonyl)-2-methylpiperazin- 2-yl ]-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxylate 1 -Benzyl 4~/er/-butyl 2-[5-(benzoyloxy)-4-(mcthoxycarbonyl)-l-methyl-6-oxo-l,6-dihydropyrimidin-2-yt]--2-methylpiperazine-l,4-dicarboxylatc was dissolved in AcOEt (20 rnl/mmol) and hydrogenated at atm pressure on 10% (w/w) Pd/C over night. After filtration of the catalyst, solvent was evaporated to give crude product. 'H NMR (DMSOd6 4 TFA, 340K, 400MHz) 8 8.08 (d, J - 7.1 Hz, 2H), 7.787 (t, J = 7.4 Hz, 1H), 7.63 (t, J -7.8 Hz, 2H), 4.30 (d, J - 15.2 Hz, III), 3.90-3.50 (m, 10H), 3.35-3.25 (m, 1H), l.81(s,3H), 1.37 (s, 911). MS (EI+) m/z 487 (M+H)+. Step_6: 2-\|l,2-dimethyl-4-(methylsulfonyl)pipeaizin-2-yl]-/V-(4-fluorobenzyl)- 5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide . Crude methyl 5-(benzoyloxy)-2-[4-(/er/-butoxycar.bonyi)-2-methylpiperazin-2-yl]-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxylate was dissolved in MeOH,/> fluorobenzylamine (3.0 eq) was added and the mixture was refluxed over night. Evaporation of the solvent afforded crude product. MS:m/z476(M+H). Crude obtained in the previous step was dissolved in MeOH (20 ml/mmol) and NaCNBH3 (2.8 eq), AcONa (3.2 eq) and HCHO 37 % in H20 (4eq) were added. The reaction mixture was stirred at room temperature over night, evaporated and the crude solid (4-fluorobenzyI 2-[4-(/er/-butoxycarbonyl)-l,2-dimethylpiperazin-2-yl\|-5- hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxylate) obtained washed with Et20. MS(BI+)w/z490(jM+-H)f. Deprotection of Boc group was carried out in DCM/TFA (1:1, 10 ml/mmol) for 1 hour. MS (1:1+) m/z 390 (M+H)+. The crude product was dissolved in DCM , Et3N (3.3 eq) and MeS02Ci (2.6 eq) were added and the reaction was stirred at room temperature over night. The reaction mixture was evaporated and the crude residue purified by preparative HPLC (CI8, gradient of CH3CN/H20 + 0.01% TFA) to obtain the title product. 'II NMR (CD3CN + TFA, 320K, 400MHz) 8 8.51 (bs, IH), 7.46-7.36 (m, 2H), 7.15-7.10 (m, 2H), 4.64 (d, J - 6.4 Hz, 2H), 4.04 (dd, J, - 14.4 Hz, J2 - 2.2 Hz, IH), 3.88-3.80 (m, IH), 3.68 (dt, J, - 13.6 Hz, J2 - 3.3 Hz, 111), 3.61 (s, 3H), 3.60-3.50 (m, IH) 3.42-3.3 l(m, 2H), 2.94 (s, 3H), 2.81 (s, 3H), 1.92 (s, 311). MS:m/z468(M+H)+. Tables 1 and 2 below list compounds of the present invention which have been prepared. The tables provide the structure and name of each compound, the mass of its molecular ion plus 1 (M+) or molecular ion minus 1 (M~) as determined via F1A-MS. and the synthetic scheme employed to prepare the compound. When the compound was prepared as a salt, the identity of the salt is included with the compound name. The synthetic scheme identified as "1" in Table 1 is identical to Scheme 1 above, except for an additional deprotection step to remove Boc, Cbz, or benzyl present in the 2-substituent in the pyrimidinone ring. While the foregoing specification teaches the principles of the present invention, with examples provided for the purpose of illustration, the practice of the invention encompasses all of the usual variations, adaptations and/or modifications that come within the scope of the following claims. I/WE CLAIM: 1. A compound of Formula (I): wherein Rl is (1) -H, (2) -C1-6 alkyl, which is optionally substituted with one or more substituents each of which is independently halogen, -OH, -CN, -O-C1-6 alkyl, -O-C1-6 haloalkyl, -C(0)Ra, -CC>2Ra, -SRa, -Sl=0)Ra, -N(RaRb), -C(=0)-Co-6 alkyl-N(RaRb), N(Ra)-C(O)-C0-6 alkyl-N(RbRc), -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), (i) the alkyl is optionally substituted with one or more substituents each of which is independently halogen, -OH, -CN, -0-C]_6 alkyl, -0-C1-6 haloalkyl, -N(RaRb), -N(Ra)C02Rb, -N(Ra)C(=0)-Co-6 alkyl-N(RbRc), or -N(Ra)-C2-6 alkyl-OH with the proviso that the -OH is not attached to the carbon alpha to N(Ra); and (ii) the alkyl is optionally mono-substituted with -Rs, -C1-6 alkyl-Rs, -N(Ra)-C(=O)-C0-6 alkyl-Rs, -N(Ra)-Co-6 alkyURs, -O-CO-6 alkyl-Rs, or -N(Ra)-C(-O)--C0-6 alkyl-RS; wherein Rs is (a) aryl which is optionally substituted with one or more substituents each of which is independently halogen, -OH, -C1-6 alkyl, -Cj-6 alkyl-ORa, -C1-6 haloalkyl,-0-C1-6 alky I, -O-C1-6 haloalkyl, methylcnedioxy attached to two adjacent carbon atoms, or aryl; (b) a 4- to 8- membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; wherein the saturated heterocyclic ring is optionally substituted with one or more substituents each of which is independently halogen, -C1 _6 alkyl, -C1 -6 alkyl-ORa, -C1-6 haloalkyl, -0-C]-6 alkyl, -0-C\|_6 haloalkyl, -C(=0)Ra -C02Ra, -C(=0)-Co-6 alkyl-N(RaRb), -S02Ra, oxo, aryl, or -C1-6 alkyl-aryl; or (c) a 5- to 7-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; wherein the heteroaromatic ring is optionally substituted with one or more substituents each of which is independently halogen, -C1-6 alkyl, -C1-6 alkyl-ORa, -C 1-6 haloalkyl, -0-C[_6 alkyl, -O-Ci-6 haloalkyl, oxo, or aryl; (5) -Co-6 alkyl-O-Co-6 alkyl-Rk, (6) -Co-6 alkyl-S(0)n-Co-6 alkyl-Rk (7) -O-C1-6 alkyORk, (8) -O-C1-6 alkyl-O-C i -6 alkyl-Rk, (9) -0-C\|-6alkyl-S(0)nRk (10) -Co-6 alkyi-N(Ra)-Rk, (11) -Co-6 alkyl-N(Ra)-C1-6 alkyl-Rk, (12) -Co-6 a!kyl-N(Ra)-C1-6 alkyl-ORk, (13) -Co-6 alkyl-C(-0)-Rk, (14) -Co-6 alkyl-C(-0)N(Ra)-Co-6 alkyl-Rk, (15) -Co-6 alkyl-N(Ra)C(=0)-Co-6 alkyl-Rk, (16) -Co-6 alkyI-N(Ra)C(=0)-0-Co-6 alkyl-Rk, or (17) -Co-6 aIkyl-N(Ra)C(=0)C(=O)Rk; R- is -C1-6 al'kyl which is optionally substituted with one or more substituents each of which is independently (1) halogen, (2) -OH, (3) -CN, (4) -0-C1-6 alkyl, (5) -0-C1-6aloalkyl, (6) -C(K))Ra, (7) -C02Ra (8) -SRa (9) -S(=0)Ra (10) -N(RaRb), (11) -C(=0)N(RaRb), (12) -N(Ra)-C(=0)-C 1 -6 alkyl-N(RbRC), (13) -S02Ra (14) -N(Ra)S02Rb, (15) -S02N(RaRb), (16) -N(Ra)-C(Rb)K), (17) -C3-8cycloalkyl, (18) aryl, wherein the aryl is optionally substituted with one or more substituents each of which is independently halogen, -C1-6 alkyl, , -C;1 -6 haloalkyL -O-C1-6 alkyl, -O-C1-6 haloalkyl, -Co-6 alkyl-N(RaRb), or -C1_6 alkyl substituted with a 5- or 6- membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; wherein the saturated heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -C1-6 alkyl, oxo, or a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; or (19) a 5- to 8-membered monocyclic heterocycle which is saturated or unsaturated and contains from 1 to 4 heteroatoms independently selected from N, O and S; wherein the heterocycle is optionally substituted with one or more substituents each of which is independently -Cl-6 alkyl, -0-C\|-6 alkyl, oxo, phenyl, or naphthyl; with the proviso that none of the following substituents is attached to the carbon atom in the -C1-6 alkyl group that is attached to the ring nitrogen: halogen, -OH, -O-C1-6 alky!, -0-C1-6 haloalkyl, -SRa, -S(-0)Ra, or -N(Ra)-C(Rb)-0; R3 is -II or-C1-6 alkyl; R4 is((2) C\|_6 alkyl which is optionally substituted with one or more substituents each of which is independently halogen, -OH, O-C1-6 alkyl, -O-C1-6 haloalkyl, -NO2, -N(RaRb), -C(0)Ra, -C02Ra, -SRa, -S(---C)Ra, -S02Ra, or -N(Ra)C02Rb, (3) C\-(y alkyl which is optionally substituted with one or more substituents each of which is independently halogen, -OH, or 0-C]_4 alkyl, and which is substituted with 1 or 2 substituents each of which is independently: (i) C3-8 cycloalkyl, (ii) aryl, (iii) a fused bicyclic carbocycle consisting of a benzene ring fused to a C5-7 cycloalkyl, (iv) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, (v) a 5- or 6-membered heteroaromatic ring containing from I to 4 heteroatoms independently selected from N, O and S, or (vi) a 9- or 10-membered fused bicyclic heterocycle containing from 1 to 4 heteroatoms independently selected from N, O and S, wherein at least one of the rings is aromatic, (4) C2-5 alkynyl optionally substituted with aryl, (5) C3-8 cycloalkyl optionally substituted with aryl, (6) aryl. (7) a fused bicyclic carbocycle consisting of a benzene ring fused to a C5-7 cycloalkyl, (8) a 5- or 6-mcmbered saturated heterocyclic ring containing frorp 1 to 4 heteroatoms independently selected from N, O and S, (9) a 5- or 6-mcmbered heteroaromatic ring containing from I to 4 heteroatoms independently selected from N, O and S, or (10) a 9- or 10-membcred fused bicyclic heterocycle containing from 1 to 4 heteroatoms independently selected from N, O and S, wherein at least one of the rings is aromatic; wherein each aryl in (3)(ii) or the aryl in (4), (5) or (6) or each fused carbocycle in (3)(iii) or the fused carbocycle in (7) is optionally substituted with one or more substituents each of which is independently halogen, -OH, -C]-6 alky!, -C]-6 alkyl-ORa, ~C\|_6 haloalkyl, -O-C1-6 alky I, -0-C]-6 haloaikyl, -CN, -NO2, -N(RaRb), -C1-6 alkyl-N(RaRb), -C(0)N(RaRb), -C(=0)Ra, -CC>2Ra, -Ci-6 alkyl-C02Ra, -OC02Ra, -SRa, -S(0)Ra -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), -N(Ra)C(=0)Rb, -N(Ra)C02Rb, -C1-6 alkyl-N(Ra)CC)2Rb, aryl, -Ci-6 alkyl-aryl, -O-aryl, or -Co-6 alkyl-het wherein hct is a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, and het is optionally fused with a benzene ring, and is optionally substituted with one or more substituents each of which is independently -C1-6 alkyl, -C1-6 haloalkyl, -0-C]-6 alkyl, -O-Cl-6 haloalkyl, oxo, or -C02Ra; each saturated heterocyclic ring in (3)(iv) or the saturated heterocyclic ring in (8) is optionally substituted with one or more substituents each of which is independently halogen, -C1-6 alkyl, -C1-6 haloalkyl, -O-C1-6 alkyl, -O-C1--6 haloalkyl, oxo, aryl, or a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; and each heteroaromatic ring in (3)(v) or the heteroaromatic ring in (9) or each fused bicyclic heterocycle in (3)(vi) or the fused bicyclic heterocycle in (10) is optionally substituted with one or more substituents each of which is independently halogen, -C1_6 alky-Ci-6 haloalkyl, -0-C1_6 alkyl, -O-C1-6 haloalkyl, oxo, aryl, or-C]-6l, alkyl-aryl; or alternatively R3 and R4 together with the N to which both are attached form a C3-7 i azacycloalkyl which is optionally substituted with one or more substituents each of which is independently -C1-6 alkyl or oxo; each Ra, Rb, Rc, and Rd is independently -H or -C1-6 alkyl; Rk is carbocycle or heterocycle, wherein the carbocycle or heterocyele is optionally substituted with one or more substituents each of which is independently (1) halogen, (2) -OH, (3) -CN, (4) -C1-6 alkyl, which is optionally substituted with one or more substituents each of which is independently halogen, -OH, -CN, -O-C1-6 alkyl, -O-C1-6 haloalkyl. -C(=0)Ra, -C02Ra. -SRa, -S(=0)Ra, -N(RaRb), -C(=O)-(CH2)0-2N(RaRb), N(Ra)-C(=O)-(CH2)0-2N(RbRc), -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(RbH), (5) -O-C1-6 alkyl, which is optionally substituted with one or more substituents each of which is independently halogen, -OH, -CN, -O-C1-6 alkyl, -O-C1-6 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra -N(RaRb), -C(=O)-(CH2)0-2N(RaRb), N(Ra)-C(-O)-(CH2)0-2N(RbRC), -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), 0r -N(Ra)-C(Rb)=0, (6) -NO2, (7) oxo, (8) -C(=0)Ra (9) -C02Ra, (10) -SRa (11) -S(=0)Ra, (12) -N(RaRb), (13) -C(=0)N(RaRb), (14) -C(==0)-C 1 -6 alkyl-N(RaRb), (15) -N(Rii)C(K))Rb (16) -S02Ra (17) -S02N(RaRb), (18) -N(Ra)S02Rb, (19) -Rm. (20) -C i -6 alkyl-Rm, wherein the alkyl is optionally substituted with one or more substituents each of which is independently halogen, -OH, -CN, -C1-6 haloalkyl, -O-C1-6 alkyl, -O-C1-6 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb). -N(Ra)CC)2Rb, -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=o, (21) -Co-6 alkyl-N(Ra)-Co-6 alkyl-Rm, (22) -Co-6 alkyl-O-Co-6 alkyl-Rm, (23) -Co-6 alkyl-S-Co-6 alkyl-Rm, (24) -Co-6 alkyi-C(K))-Co-6 alkyl-Rm, (25) -C(=0)-0-Co-6 alkyl-Rm, (26) -C(-0)N(Ra)-Co-6 alkyl-Rm, (27) -N(Ra)C(=())-Rm, (28) -N(Ra)C(= 0)-C 1 -6 alkyl-Rm, wherein the alkyl is optionally substituted with one or more substituents each of which is independently halogen, -OH, -CN, -Cl-6 haloalkyl, -O-C1-6 alkyl, -O-C1-6 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra -N(RaRb), -N(Ra)C02Rb, -S02Ra -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=0, (29) -N(Ra)-C(=0)-N(Rb)-Co-6 alkyl-Rm, (30) -N(Ra)-C(~-0)-0-Co-6 alkyl-Rm, (31) -N(Ra)-C(-0)-N(Rb)-S02-Co-6 alkyl-Rm, (32) -C(K))-C(-0)-N(RaRb), (33) -C(=0)-C 1 -6 alkyl-S02Ra, or (34) -C(=0)-C(=0)Rm; carbocycle in Rk is (i) a C3 to Cs monocyclic, saturated or unsaturated ring, (ii) a C7 to C\|2 bicyclic ring system, or (iii) a C11 to C16 tricyclic ring system, wherein each ring in (ii) or (iii) is independent of or fused to the other ring or.-rings and each ring is saturated or unsaturated; heterocycle in Rk is (i) a 4- to 8-membered, saturated or unsaturated monocyclic ring, (ii) a 7- to 12-membered bicyclic ring system, or (iii) an 11 to 16-membered tricyclic ring system; wherein each ring in (ii) or (iii) is independent of or fused to the other ring or rings and each ring is saturated or unsaturated; the monocyclic ring, bicyclic ring system, or tricyclic ring system contains from 1 to 6 heteroatoms selected from N, O and S and a balance of carbon atoms; and wherein any one or more of the nitrogen and sulfur heteroatoms is optionally be oxidized, and any one or more of the nitrogen heteroatoms is optionally quaternized; each Rm is independently C3-8 cycloalkyl; aryl; a 5- to 8-membered monocyclic heterocycle which is saturated or unsaturated and contains from 1 to 4 heteroatoms independently selected from N, O and S; or a 9- to 10-membered bicyclic heterocycle which is saturated or unsaturated and contains from 1 to 4 heteroatoms independently selected from N, O and S; wherein any one or more of the nitrogen and sulfur heteroatoms in the heterocycle or bicyclic heterocycle is optionally oxidized and any one or more of the nitrogen heteroatoms is optionally quaternized; and wherein the cycloalkyl or the aryl defined in Rm optionally substituted with one or more substituents each of which is independently halogen, -C1-6 alkyl optionally substituted with -0-C1-4 alkyl, -C1-6 haloalkyl, -OC1-6 alkyl, -O-C1-6 haloalkyl, -N(RaRb), aryl, or -C1-6 alkyl-aryl; and the monocyclic or bicyclic heterocycle defined in Rm is optionally substituted with one or more substituents each of which is independently halogen, -C1-6 alkyl, -C1-6 haloalkyl, -O-C1-6 alkyl, -O-C1-6 haloalkyl, oxo, aryl, -C1-6 alkyl-aryl, -C(=0)-aryl, -C02-aryl, -CO2-CI-6 alkyl-aryl, a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, or a 5- or .6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; and each n is independently an integer equal to zero, 1 or 2; or a pharmaceutical!)' acceptable salt thereof. 2. The compound according to claim 1, wherein R1 is: (1) -H, (2) -Cl-4 alkyl, which is optionally substituted with from I to 4 substituents each of which is independently halogen, -OH, -CN, -O-Ci-4 alkyl, -O-Cj-4 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb), -C(-0)-C()-4 alkyl-N(RaRb), N(Ra)-C( -S02N(RaRb), _N(Ra)-C(-0)Rb, -N(Ra)C(=0)Rk, or -N(Ra)C(=O)C(=0)N(RbRc) (3) -Rk (4) -Ci_4 alkyl-Rk, wherein: (i) the alkyl is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -OH, -CN, -0-C]_4 alkyl, -O-C1-4 haloalkyl, -N(RaRb), -N(Ra)C02Rb, -N(Ra)C(-0)-Co-4 alkyl-N(RbRc), or -N(Ra)-(CH2)2-4-OH; and (ii) the alkyl is optionally mono-substituted with -Rs, -N(Ra)-C(=0)-Co-4 alkyl-Rs, -N(Ra)-Co-4 alkyl-Rs, -0-C()-4 alkyl-Rs, or -N(Ra)-C(0)-C()-4 alkyl-RS; wherein Rs is (a) aryl which is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -OH, -C1-4 alkyl, -Cl-4 alkyl-ORa, -C\|_4 haloalkyl, -O-C1-4 alkyl, -O-C1-4 haloalkyl, methylcnedioxy attached to two adjacent carbon atoms, or phenyl; (b) a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; wherein the heteroaromatic ring is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C1_4 alkyl, -C1--4 alkyl-ORa, -C1_4 haloalkyl, -O-C1-4 alkyl, -0-C1-4 haloalkyl, oxo, or phenyl; or (c) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 hetcroatoms independently selected from N, O and S; wherein the saturated heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C1-4 alkyl, -C1-4 alkyl-ORa, -C1_4 haioalkyl, -O-C]-4 alkyl, -0-C\|_4 haloalkyl, -C(-0)Ra, -C02Ra, -C(=0)-C()-4 alkyl-N(RaRb), -S02Ra, oxo, or phenyl, or (5) -(CH2)0-3-C(-O)N(Ra)-(CH2)0-3-Rk; or a pharmaceutically acceptable salt thereof. 3. The compound according to claim 2, wherein R' is: (1) -H, (2) -C1-4 alkyl, which is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -O-Cj-4 alkyl, -O-C1-4 haloalkyl, -C(=0)Ra -CO2Ra, -N(RaRb), or (3) -Rk, (4) -(CH?)l-4-Rk, wherein: (i) the -(CH2)l-4- moiety is optionally substituted with 1 or 2 substituents each of which is independently halogen, -OH, -O-C1-4 alkyl, -0-C1_4 haloalkyl, or -N(RaRb); and (ii) the -(CH2)l-4- moiety is optionally mono-substituted with -Rs or -N(Ra)-(CH2)l-2-Rs; wherein Rs is (a) phenyl which is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C i -4 alkyl, -C l .4 alkyl-ORa, -C1-.4 haloalkyl, -O-C1.4 alkyl, or -O-C 1 -4 haloalkyl; or (b) a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; wherein the heteroaromatic ring is optionally. substituted with from 1 to 3 substituents each of which is independently halogen, -C1.4 alkyl, -C \| -4 alkyl-ORa, -C1-4 haloalkyl, -0-C1_4 alkyl, or -O-C1-4 haloalkyl; or (c) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; wherein the saturated heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C1-4 alkyl, -C1_4 alkyl-ORa, -C0_4 haloalkyl, -O-C1-4 alkyl, -O-C1.4 haloalkyl, -C(K))Ra or -C02Ra, (5) -C(-O)N(Ra)-(CH2)0-3-Rk, (6) -C(ClI3)2N(Ra)C(=0)Rb? (7) -C(CM3)2N(Ra)C(-0)Rk, or (8) -C(CII3)2N(Ka)C(=0)C(-0)N(RbRc); or a pharmaceutical^ acceptable salt thereof. 4. The compound according to claim 1, wherein Rk is C3-8 cycloalkyl; aryl selected from phenyl and naphthyl; a bicyclic carbocycle selected from indanyl and tetrahydronaphthyl; a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; or a bicyclic heterocyele which is a benzene ring fused to a 5- or 6-membered saturated or unsaturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; wherein the cycloalkyl, aryl, bicyclic carbocycle, saturated heterocyclic ring, heteroaromatic ring, or bicyclic heterocyele is optionally substituted with from 1 to 4 substituents each of which is independently (1) halogen, (2) -OH, (3) -CN, (4) -C1-4 haloalkyl, (5) -C1_4 alkyl, which is optionally substituted with from 1 to 3 substituents each of which is independently -OH, -CN(, -O-Cj-4 alkyi, -O-C1.4 haloalkyl, -C(=0)Ra, -C02Ra,-SRa, -S(=0)Ra, -N(RaRb), -C(=O)-(CH2)0-2N(RaRb), N(Ra)-C(=O)-(CH2)0-2N(RbRC),-SO2Ra, -N(Ra)S02Rb, -S02N(RaRb), 0r -N(Ra)-C(Rb)=0, (6) -O-C1_4 haloalkyl (7) -O-C 1-4 alkyl, which is optionally substituted with from 1 to 3 substituents each of which is independently -OH, -CN, -O-Cl-6 alkyl, -O-C1 -6 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb), -C(=O)-(CH2)0-2N(RaRb), N(Ra)-C(=O)-(CH2)0-2N(RbRC),-SO2Ra -N(Ra)S02Rb, -S02N(RaRb), or-N(Ra)-C(Rb)=0, (8) -N02, (9) oxo, (10) -C(0)Ra, (11) -C02Ra, (12) -SRa, (13) -S(=0)Ra, (14) -N(RaRb), (15) -C(=0)N(RaRb), (16) -C(=0)-C 1 -6 alkyl-N(RaRb), (17) -N(R3)C(=0)Rb, (18) -S02Ra, (18) -S02N(RaRb), (19) -N(Ra)S02Rb, (20) -Rm, (21) -Ci_4alkyl-Rm, (22) -(CH2)0-2-N(Ra)-(CH2)0-2-Rm. (23) -(CH2)0-2-O-(CH2)0-2-Rm, (24) -(CH2)0-2-S-(CH2)0-2-Rm, (25) -(CH2)0-2-C(=O)-(CH2)0-2-Rm. (26) -C(-O)-O-(CH2)0-2-Rm, (27) -C(-0)N(Ra)-Rm, Gr (28) -C(0)-C(=0)N(RaRb); or a pharmaceuticaliy acceptable salt thereof. 5. The compound according to claim 4, wherein each Rm is independently C3-7 cycloalkyl; aryl selected from phenyl and naphthyl; a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, wherein any N is optionally oxidized to form an N-oxide; or a bicyclic heterocycle which is a benzene ring fused to a 5- or 6-membered, saturated or unsaturated heterocyclic ring containing from 1 to 3 heteroatoms selected from N, O and S; wherein the cycloalkyl or the aryl defined in Rm is optionally substituted with from 1 to 4 substiluents each of which is independently halogen, -C\|-4 alkyl, -C1-4 haloalkyl, -O-CM alkyl, -OC1_4 haloalkyl, -N(RaRb), phenyl, or -(CH2)l-2-phenyl; the saturated heterocyclic ring defined in Rm is optionally substituted with from I to 4 substituents each of which is independently -C1_4 alkyl optionally substituted with -O-C1-4 alkyl, -C1.4 haloalkyl, -0-C1_4 alkyl, -O-C1-4 haloalkyl, oxo, phenyl, -(CH2)l-2-phenyl, -C(=0)-phenyl, -C02-phenyI, -C02-(CH2)l-2-phenyl, a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, or a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; and the heteroaromatic ring or the bicyclic heterocycle defined in Rm is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -C 1.4 alkyl, -C1-4 haloalkyl, -O-Ci-4 alkyl, -O-Ci-4 haloalkyl, oxo, phenyl, or -(CH2)l-2-phenyl; or a pharmaceutical]}' acceptable salt thereof. 6. The compound according to claim 4, wherein Rk is phenyl; a 5- or 6-membered saturated heterocyclic ring containing 1 or 2 heteroatoms selected from I or 2 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; a 5- or 6-membered heteroaromatic ring containing 1 or 2 hcteroatoms selected from 1 or 2 N atoms, 0 or 1 O atoms, and 0 or I S atoms; or a bicyclic heterocycle which is a benzene ring fused to a 5- or 6-membered saturated heterocyclic ring containing 1 or 2 nitrogen atoms; wherein: (a) the phenyl, the saturated heterocyclic ring, heteroaromatic ring, or bicyclic heterocycle is optionally substituted with from 1 to 3 substituents each of which is independently (1) fluoro, (2) chloro, (3) bromo, (4) -OH (5) -CF3, (6) -C1-4 alkyl, which is optionally substituted with 1 or 2 substituents each of which is independently -OH, -CN, -0-C]_4 alkyl, -OCF3, -N(RaRb), -C(=0)N(RaRb), or N(Ra)-C(-O)-(CH2)0-2N(RbRC), (7) -OCF3, (8) -O-C1-4 alkyl (9) -C(0)Ra, (10) -C02Ra, (11) -SRa, (12) -SRa, (13) -N(RaRb), (14) -C(0)N(RaRb), (15) -C(=0)-(CH2) 1 -2-N(RaRb), (16) -N(Ra)C(=0)Rb, or (17) -S02Ra; (b) the phenyl is optionally mono-substituted with (1) -(CH2)l-2-Rm,or (2) -(CIl2)0-2-N(Ra)-(CH2)0-2-Rm;and (c) the saturated heterocyclic ring, heteroaromatic ring, or bicyclic heterocycle is optionally mono- or di-substituted with (1) oxo (2) -(CH2)l-2-Rm, (3) -0-(CH2)l-2-Rm, or (4) -(CH2)0-\|-C(-OHCH2)0-2-Rm; or a pharmaceutically acceptable salt thereof. 7. The compound according to claim 6, wherein each Rm is independently cyclopropyl; phenyl; a 5- or 6-membered saturated heterocyclic ring selected from pyrrolidinyl, imidazolidinyl, pyrazolidinyl, piperidinyl, piperazinyl, and morphoiinyl; or a 5- or 6-membered heteroaromatic ring selected from thienyl, pyridyl optionally in the form of an N-oxide, imidazolyl, pyrrolyl, pyrazolyl, thiazolyl, isothiazolyl, oxazolyl, isooxazolyl, oxadiazolyl, thiadiazolyl, pyrazinyl, pyrimidinyl, triazolyl, tetrazolyl, furanyl, and pyridazinyl; wherein the cyclopropyl is unsubstituted; the phenyl is optionally substituted with from I to 3 substituents each of which is independently halogen, -Ci_4 alkyl, -CF3, -O-Ci-4 alkyl, -OCF3, or -N(RaRb); the saturated heterocyclic ring is optionally substituted with 1 or 2 substituents each of which is independently -C]-4 alkyl, -CF3, -0-C]_4 alkyl, -OCF3, oxo, phenyl, -(^H2)\|-2-phenyl, -C0 -C02-CH2-phenyl;and the heteroaromatic ring is optionally substituted with 1 or 2 substituents each of which is independently -Ci-4 alkyl, -CF3, -O-C1-.4 alkyl, -OCF3, oxo, phenyl, or -(CIl2)]-2-phenyl; or a pharmaceutically acceptable salt thereof. 8. The compound according to claim 1, wherein R2 is: (1) -C1-6 alkyl, (2) -C1-6 alkyl substituted with -N(RaRb), with the proviso that -N(RaRb) is not attached to the carbon atom in the -C1 -6 alkyl group that is attached to the ring nitrogen, (3) -C]-6 alkyl substituted with phenyl, wherein the phenyl is: (a) optionally substituted with from 1 to 4 substitupnts each of which is independently halogen, -Cl-4 aikyl, -Ci-4 haloalkyl, -0-C\|-4 alkyl, -O-C1-4 haloalkyl, or -C0-4 alkyl-N(RaRb); and (b) optionally mono-substituted with -C1-4 alkyl substituted with a 5- or 6-rnembered saturated heterocyclic ring containing from 1 to 3 heteroatoms selected from 1 or 2 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -C\|_6 alkyl, oxo, or a 5- or 6-membered heteroaromatic ring containing from 1 to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atom, and 0 or 1 S atom; or (4) -C1-6 alkyl optionally substituted with -OH and substituted with a 5- or 6-membered saturated monocyclic heterocycle which contains from I to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heterocycle is optionally substituted with from 1 to 4 substituents each of which is independently -C1-6 alkyl, -O-C1-6 alkyl, oxo, or phenyl; or (5) -C1_6 alkyl substituted with a 5- or 6-membered heteroaromatic ring which contains from 1 to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heteroaromatic ring is optionally substituted with from I to 4 substituents each of which is independently-C1-6 alkyl, -O-C1-6 alkyl, oxo, or phenyl; or a pharmaceutically acceptable salt thereof. 9. The compound according to claim 8, wherein R2 is methyl; or a . pharmaceutically acceptable salt thereof, 10. The compound according to claim 1, wherein R3 is -H or -C]_4 alkyl; or a pharmaceutically acceptable salt thereof. 11. The compound according to claim 10, wherein R3 is -H or methyl; or a pharmaceuticaily acceptable salt thereof. 12. The compound according to claim 11, wherein R3 is -H; or a pharmaceuticaily acceptable salt thereof. 13. The compound according to claim 1, wherein R.4 is Cj-4 alkyl substituted with an aryl, which is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -OH, -C1-4 alkyl, -C]-4 alkyl-ORa, -C]-4 haloalkyl, -0-C1_4 alkyl, -O-Cj-4 haloalkyl. -CN, -NO2, -N(RaRb), -CM alkyl-N(RaRb), -C(-0)N(RaRb), -C(=0)Ra -C02Ra, -CM alkyl-C02Ra, -OC02Ra, -SRa, -S(==0)Ra, -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), -N(Ra)C(=0)Rb, -N(Ra)C02Rb, -CM alkyI-N(Ra)C02Rb, methylenedioxy attached to two adjacent ring carbon atoms, phenyl, -CM alkyl-phenyl, -O-phenyl, or -(CH2)0-2-het; wherein het is a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, and het is optionally fused with a benzene ring, and is optionally substituted with 1 or 2 substituents each of which is independently -C1-4 alkyl, -C1_4 haloalkyl, -O-C1-4 alkyl, -0-C1_4 haloalkyl, or-C02Ra; or a pharmaceuticaily acceptable salt thereof. 14. The compound according to claim 13, wherein R4 is -CH2-phenyI, wherein the phenyl is optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -Ci_4 alkyl, -Ci_4 fluoroalkyl, -O-Ci-4 alkyl, -O-Cj-4 fluoroalkyl, -(CH2)1-2-N(RaRb), -S02Ra, -(CH2)0-2-CO2Ra, -(CH2)0-2-N(Ra)CO2Rb, -NO2, -SRa, -N(RaRb) or phenyl; and each Ra and Rb is independently is H or -C1-_4 alkyl; or a pharmaceuticaily acceptable salt thereof. 15. The compound according to claim 14, wherein R4 is -CI l2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents, each of which is independently -F, -Br, -CI, -OH, -C1-4 alkyl, -C1-4 fluoroalkyl, -0-C\|_4 alkyl, -SO2-C1-4 alkyl, -S-C1-4 alkyl, -N(CH3)2, OZ-O-CM fluoroalkyl; or a pharmaceutically acceptable salt thereof. 16. The compound according to claim 15, wherein R4 is />fluorobenzyl or 2,3-dimethoxybenzyI; or a pharmaceutically acceptable salt thereof. 17. The compound according to claim 1, wherein: Rl is-Rk; Rk is phenyl which is (a) optionally substituted with from I to 3 substituents each of which is independently: (1) halogen, (2) -C]-6 alkyl, which is optionally substituted with 1 or 2 substituents each of which is independently -O-C] -6 alkyl, -O-C1-6 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb), -C(=O)-(CH2)0-2N(RaRb), N(Ra)-C(=O)-(CH2)0-2N(RbRc),-S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=o, (3) -C1-6 haloalkyl, (4) -O-C1-6 haloalkyl, (5) -C(=0)Ra, (6) -C02Ra, (7) -C(=0)N(RaRb), or (8) -C(=0)-Ci-6 alkyl-N(RaRb); and (b) optionally mono-substituted with (1) -C1_4alkyl-Rm, or (2) -Co-4 alkyl-N(Ra)-CQ-4 alkyl-R™; wherein Rm is aryl selected from phenyl and naphthyl; a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected*from N, O and S; or a 5- or 6-membercd heteroaromatic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; wherein the aryl defined in R™ is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C]-4 alkyl, -CF3, -O-C1-4 alkyl. -OCF3, or -N(RaRb); the saturated heterocyclic ring defined in Rm is optionally substituted with from I to 3 substituents each of which is independently -C]-4 alkyl or oxo, and is additionally optionally mono-substituted with phenyl, -(CH2)l-2-phenyl, -C(0)-phenyl, -CC>2-phenyl, -C02-(CH2)l-2-phenyl, or a 5- or 6-membered heteroaromatic ring containing from I to 3 heteroatoms independently selected from N, O and S; and the heteroaromatic ring defined in Rm is optionally substituted with 1 or 2 substituents each of which is independently -C]-4 alkyl or oxo; or a pharmaceutically acceptable salt thereof. 18. The compound according to claim 17, wherein R2 is methyl; R3 is -H; R4 is: (1) -CH2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -Cj-4 alkyl, -Ci_4 fluoroalkyl, -O-Ci-4 alkyl, -O-C1-4 fluoroalkyl, -(CH2)l-2-N(RaRb), -SC)2Ra, -(CH2)0-2-CO2Ra, -(CH2)0-2-N(Ra)CO2Rb, -N02, -SRa, -N(RaRb) or phenyl; or (2) a fused bicyclic carbocycle selected from each Ra and Rb is independently is H or -Ci-4 alkyl; or a pharmaceuticalty acceptable salt thereof. 19. The compound according to claim 18, wherein R4 is 4-fluorobenzyl or 2,3-dimethoxybenzyl; or a pharmaceutically acceptable salt thereof. 20. A compound of Formula (II): wherein Qis: (1) methyl which is optionally substituted with 1 or 2 of-O-Ci-4 alkyl, (2) phenyl which is optionally substituted with from 1 to 3 substituents each of which is independently -F, -CI, Br, -Cl-4 alkyl. -CF3, -O-Cj-4 alkyl, -OCF3, methylenedioxy attached to two adjacent carbon atoms, or phenyl, or (3) a 5- or 6-mcmbcrcd saturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; wherein the saturated heterocyclic ring is optionally substituted with 1 or 2 substituents each of which is independently -F, -CI, -Br, -C1.4 alkyl, oxo, phenyl, or -C(-0)-phenyI; ; T is: (1) -H, (2) -OH, (3) methyl or ethyl, optionally substituted with -OH or -O-Ci-4 alkyl, (4) -O-C1-4 alkyl (5) -N(RaRb), (6) -N(Ra)-(CH2)2-OH, (7) -N(Ra)-C02Rb, (8) -N(Ra)-C(=0)-(CH2)l-2-N(RaRb), (9) -Rs, (10) -(CH2)l-2-Rs,or (11) -(CH2)0-2-N(Ra)-(CH2)0-3-Rs; Rs is: (1) phenyl optionally substituted with from 1 to 4 substituents each of which is independently halogen, -Cl-4 alkyl, -C1.4 alkyl-ORa, -Ci_4 haloalkyl, -O-C)-4 alkyl, -O-C1-4 haloalkyl, or -N(RaRb); (2) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; which is optionally substituted with from 1 to 4 substituents each of which is independently -C1.4 alkyl, -Cl-4 alkyl-ORa, -Cl-4 haloalkyl, -O-C'1-4 alkyl, -O-C 1-4 haloalkyl, -C(=0)Ra, oxo, phenyl, or -CH2-phenyl; or (3) a 5- or 6-membered heteroaromatic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; which is optionally substituted with from 1 to 4 substituents each of which is independently -C1-4 alkyl, -C1-4 alkyl-ORa, _C1_4 haloalkyl, -O-C].4 alkyl, -O-C-4 haloalkyl, or1 oxo; R2 is (1) -C\|-4 alkyl, (2) -C l -4 alkyl substituted with -N(RaRb), with the proviso that -N(RaRb) r is not attached to the carbon atom in the -C1-4 alkyl group that is attached to the ring nitrogen, or (3) -C1-4 alkyl substituted with a 5- or 6-membered saturated monocyclic heterocyclic which contains from 1 to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the saturated heterocycle is optionally substituted with from 1 to 4 substituents each of which is independently a -C1-4 alkyl; R3 is-H or-C1-4 alkyl; R4 is -CH2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -CM alkyl, -C1-4-fluoroalkyl, -O-C1-4 alkyl, -O-CM fluoroalkyl, -(CH2)l-2-N(RaRb), -S02Ra, -(CH2)0-2-CO2Ra, -(CH2)0-2-N(Ra)CO2Rb, -N02, -SRa, -N(RaRb) 0r phenyl; each Ra and Rb is independently -H or -C1-4 alkyl; and s is an integer equal to zero, 1, or 2; or a pharmaceutically acceptable salt thereof. 21. The compound according to claim 20, wherein Q is phenyl; Tis: (1) -H, (2) -N(RaRb), (3) a 5- or 6-mcmbered saturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; which is optionally substituted with 1 or 2 substituents each of which is independently -C1-4 alkyl or -C(=0)RA. or (4) -N(Ra)-(CH2)l-2-heteroaromatic, wherein the heteroaromatic is a 5- or 6-membcred ring containing 1 or 2 N atoms; R2 is methyl; R3 is-H; and R4 is -CH2-phenyI, wherein the phenyl is optionally substituted with 1 or 2 substituents each of which is independently -F, -CI, -Br, -Cj-4 alkyl, -CF3, -O-C1-4 alkyl, -SO2CH3, -SCH3, -N(CI!3)2 or-OCF3; each Ra and Rb is independently -H, methyl or ethyl; and s is an integer equal to zero or 1; or a pharmaceutically acceptable salt thereof. 22. The compound according to claim 1, wherein Rl is-Rk; Rk is (i) a 5- or 6-membered saturated heterocyclic ring containing from 0 to I oxygen atoms and from I to 3 nitrogen atoms or (ii) a bicyclic heterocycle which is a benzene ring fused to a 5- or 6-membered saturated heterocyclic ring containing from 0 to 1 oxygen atoms and from 1 to 3 nitrogen atoms; wherein the saturated heterocyclic ring or bicyclic heterocycle is optionally substituted with from 1 to 3 substituents each of which is independently (1) -C1_4 alkyl, which is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -O-C1-4 alkyl, -O-C1-4 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb), -C(=O)-(CH2)0-2N(RaRb), N(Ra)-C(=O)-(CH2)0-2N(RbRC),.S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or-N(Ra)-C(Rb)=Of (2) -OH, (3) -C(=0)Ra, (4) -C02Ra, (5) -C(K))N(RaRb), (6) -C(=0)-C 1 -6 alkyl-N(RaRb), (7) -SRa, (8) -S(-C))Ra (9) -S02Ra, (10) -N(RaRb), (11) -Rm, (12) -C1-4 alkyl-Rm, wherein the alkyl is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -OH, -CN, -C]-4 haloalkyl, -O-C1.4 alkyl, -O-C1-4 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb), -N(Ra)CC>2Rb, -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=0, (13) -Co-4 alkyl-N(Ra)-Co-4 alkyl-Rm, (14) -Co-4 alkyl-O-Co-4 alkyl-Rm, (15) -Co-4 alkyl-S-CO-4 alkyl-Rm, (16) -Co-4 alkyl-C(=0)-Co-4 alkyl-Rm, (17) -C(=0)-0-Co-4 alkyl-Rm, 0r (18) -C(=0)N(Ra)-Co-4 alkyl-Rm; wherein each Rm is independently -C3-6 cycloalkyl; aryl selected from phenyl and naphthyl; a 5- or 6-mcmbered saturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; or a 5- or 6-membered heteroaromatic ring containing from 1 to 3 heteroatoms independently selected from N, O and S, wherein any N is optionally oxidized to form an N-oxide; wherein the aryl is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C]-4 alkyl, -CF3, -O-Ci-4 alkyl, -OCF3, or -N(RaRb); the saturated heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -C1.4 alkyl or oxo, and is additionally optionally mono-substituted with phenyl, -(CH2)l-2-phenyl, -C(=0)-phenyl, -C02-phenyl, or -C02-(CH2)l-2-phenyl; and the heteroaromatic ring is optionally substituted with 1 or 2 substituents each of which is independently halogen, -C1-4 alkyl, or oxo; or a pharmaceutically acceptable salt thereof. 23. The compound according to claim 22, wherein R8is: (1) -H, (2) -C \| -4 alkyl, which is optionally substituted with 1 or 2 substituents each of which is independently -OH, -O-C i .4 alkyl, -OCF3, -C(=0)Ra -C()2Ra, -SRa -N(RaRb), or -C(-0)N(RaRb), (3) -C(=0)Ra. (4) -CC)2Ra. (5) -C(-0)N(RaRb), (6) -C(=0)-(CH2) 1.2-N(RaRb>; (7) -S()2Ra, (8) -(CU2)l-2-Rm, (9) -(CH2)0-2-C(=O)-(CH2)0-2-Rm- (10) -C(=O)-O-(CH2)0-2-Rm, or (11) -C(=O)N(Ra)-(CH2)0-2-Rnn; RlO is-H, -OH, -C i .4 alkyl, -O-Ci-4 alky!, -N(RaRb), or -0-(CH2)l-2-Rm ; Rl2 is (1) -H, (2) -C \| _4 alkyl, which is optionally substituted with 1 or 2 subslituents each of which is independently-OH, -O-C1.4 alkyl, -OCF3, -C(=0)Ra -Co2Ra, -SRa, -N(RaRb), 0r -C(=0)N(R3Rb), (3) -C(=0)Ra, (4) -C02R3, (5) -C(=O)-(CH2)l-2-N(RaRb),0r (6) -S02Ra; R2 is methyl; R3 is -H or methyl; R4 is -CH2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 subslituents each of which is independently fluoro, bromo, chloro, -OH, -C1-4 alkyl, -C1-4 fluoroalkyl, -O-C1.4 alkyl, -O-C1-4 fluoroalkyl, -(CH2)l-2-N(RaRb), -S02Ra -(CH2)0-2-CO2Ra, -(Cll2)0-2-N(Ra)CO2Rb, -NO2, -SRa, -N(RaRb) or phenyl; and each Ra and Rb is independently -H or -C1.4 alkyl; or a pharmaceutically acceptable salt thereof. 24. The compound according to claim 1, which is a compound of Formula (III): wherein R2 is: (1) -C 1 -6 alkyl, (2) -C1-6 alky! substituted with -N(RaRb), with the proviso that -N(RaRb) is not attached to the carbon atom in the -C1-6alkyl group that is attached to the ring nitrogen, (3) -C1-6 alkyl substituted with phenyl which is: (a) optionally substituted with from 1 to 4 substituents each of which is independently halogen, -Cl-4 alkyl, -C1_4 haloalkyl, -0-C\|-4 alkyl, -O-C1-4 haloalkyl, or -Co-6 alkyl-N(RaRb); and (b) optionally mono-substituted with -C]-4 alkyl substituted with a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 hetcroatoms selected from 1 or 2 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -C]-6 alkyl, oxo, or a 5- or 6-mcmbered heteroaromatic ring containing from 1 to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atom, and 0 or 1 S atom; (4) -C]-6 alkyl optionally substituted with -OH and substituted with a 5- or 6-membered saturated monocyclic heterocycle which contains from 1 to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heterocycle is optionally substituted with from 1 to 4 substituents each of which is independently-C1-6 alkyl, -O-C1-6 alkyl, oxo, or phenyl; or (5) -C1-6 alkyl substituted with a 5- or 6-membered heteroaromatic ring which contains from 1 to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heteroaromatic ring is optionally substituted with from 1 to 4 substituents each of whjch is independently -C1_6 alkyl, -0-C\|-6 alkyl, oxo, or phenyl; or a pharmaceutically acceptable salt thereof. 25. The compound according to claim 24, wherein R2 is: (1) -C1-4 alkyl, (2) -(CH2)2-3-N(RaRb), (3) -(Cll2)\|-3-phenyl, wherein the phenyl is: (a) optionally substituted with from 1 to 3 substituents each of which is independently fluoro, chloro, bromo, -C1-4 alkyl, -CF3, -O-C1-4 alkyl, -O-CF3, or -(CM2)l-3-N(RaRb);and (b) optionally mono-substituted with -(CI l2)l-3-saturated heterocycle which is a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms selected from 1 or 2 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms, wherein the heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -C1 -4 alkyl or pyridyl; (4) -(CH2) 1-3-sauced heterocycle, wherein the -(CH2)l-3- moiety is optionally substituted with an -OH and the saturated heterocycle is a 5- or 6-membered saturated monocyclic heterocycle which contains from 1 to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heterocycle is optionally substituted with from 1 to 3 substituents each of which is independently a -Cl_4 alkyl; or (5) -(Cll2)l-3-pyridyI; R3 is -H or methyl; 31. A pharmaceutical composition, which comprises an effective amount of the compound according to claim 28, or a pharmaceutical^ accqptable salt thereof, and a pharmaceutically acceptable carrier. 31. A pharmaceutical composition comprising a therapeutically effective amount of a compound.according to claim 1, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. 32. A pharmaceutical composition, which comprises the product prepared by combining an effective amount of a compound according to claim 1, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

Full Text

TITLE OF THE INVENTION
N-SUBSTITUTED 11YDROXYPYR1MIDINONE CARBOXAMIDE INHIBITORS
OF HIV INTEGRASE
FIELD OF THE INVENTION
The present invention is directed to N-substituted 5-hydroxy-6~oxo-l,6-dihydropyrimidinc-4-carboxamides and pharmaceutically acceptable salts thereof, their synthesis, and their use as inhibitors of the HIV intcgrase enzyme. The compounds and pharmaceutically acceptable salts thereof of the present invention are useful for preventing or treating infection by HIV and for treating or delaying the onset of AIDS.
BACKGROUND OF THE INVENTION
A retrovirus designated human immunodeficiency virus (HIV) is the etiological agent of the complex disease that includes progressive destruction of the immune system (acquired immune deficiency syndrome; AIDS) and degeneration of the central and peripheral nervous system. This virus was previously known as LAV. HTLV-II1, or ARV. A common feature of retrovirus replication is the insertion by virally-encoded integrase of proviral DNA into the host cell genome, a required step in HIV replication in human T-lymphoid and monocytoid cells. Integration is believed to be mediated by integrase in three steps: assembly of a stable nucleoprotein complex with viral DNA sequences; cleavage of two nucleotides from the 3' termini of the linear proviral DNA; covalent joining of the recessed 3* OH termini of the proviral DNA at a staggered cut made at the host target site. The fourth step in the process, repair synthesis of the resultant gap, may be accomplished by cellular enzymes.
Nucleotide sequencing of HIV shows the presence of a pol gene in one open reading frame [Ratner, L. et al., Nature, 313, 277(1985)]. Amino acid sequence homology provides evidence that the pol sequence encodes reverse transcriptase, integrase and an HIV protease [Toh, H. et al., EMBO J. 4, 1267 (1985); Power, M.D. et al.. Science, 231, 1567 (1986); Pearl, L.H. et al.. Nature, 329. 351 (1987)]. All three enzymes have been shown to be essential for the replication of HIV.
It is known that some antiviral compounds which act as inhibitors of HIV replication are effective agents in the treatment of AIDS and similar

diseases, including reverse transcriptase inhibitors such as azidothymidine (AZT) and efavirenz and protease inhibitors such as indinavir and nelftnavir. The compounds of this invention are inhibitors of HIV integrase and inhibitors of HIV replication. The inhibition of integrase in vitro and HIV replication in cells is a direct result of inhibiting the strand transfer reaction catalyzed by the recombinant integrase in vitro in HIV infected cells. The particular advantage of the present invention is highly specific inhibition of HIV integrase and HIV replication.
SUMMARY OF Till- INVENTION
The present invention is directed to novel hydroxypyrimidinone carboxamides. These compounds are useful in the inhibition of HIV integrase, the prevention of infection by HIV. the treatment of infection by HIV and in the prevention, treatment, and delay in the onset of AIDS and/or ARC, either as compounds or their pharmaceutical^ acceptable salts or hydrates (when appropriate), or as pharmaceutical composition ingredients, whether or not in combination with other HIV/AIDS antivirals, anti-infectives, immunomodulators, antibiotics or vaccines. More particularly, the present invention includes a compound of Formula
(1):
wherein
Rl is
(1) -H.
(2) -C1 _6 alkyl, which is optionally substituted with one or more
subsliluents (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH, -CN, -0-C1-6 alkyl, -O-C1-6 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(-0)Ra, -N(RaRb), -C(=0)-C()-6 alkyl-N(RaRb), N(Ra)-C(0)-C()-6 alkyl-N(RbRc), -S02Ra,

-N(Ra)S02Rb, -S02N(RaRb), -N(Ra)-C(=0)Rb, N(R2)C(==0)C(=O)N(RaRb),
(3) -Rk
(4) -C1_6 alkyl-Rk, wherein:
(i) the alkyl is optionally substituted with one or more
substituents(e.g., optionally from 1 to 6, or 1 to 5, or I to 4, or 1 to 3. or I or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH, -CN, -O-C1-6 alkyl, -O-C1-6 haloalkyl, -N(RaRb), -N(Ra)C02Rb, -N(Ra)C(--=0)-Co-6 alkyl-N(RbRC), 0r -N(Ra)-C2-6 alkyl-OH with the proviso that the -OH is not attached to the carbon
alpha to N(Ra); and (ii) the alkyl is optionally mono-substituted with -Rs, -C1_6
alkyi-Rs, -N(Ra)-C(=0)-C()-6 alkyl-Rs, -N(Ra)-Co-6 alkyl-Rs, -O-Co-6 alkyl-Rs, or -N(Ra)-C(=O)-C0-6 alkyl-RS; wherein Rs is
(a) aryl which is optionally substituted with one or
more substituents (e.g., optionally from 1 to 5, or 1 to 4, or 1 to
3, or 1 or 2 substituents; or is optionally mono-substituted) each
of which is independently halogen, -OH, -C1-6 alkyl, -C1-6
alkyl-ORa -C1-6 haloalkyl, -O-C1-6 alkyl, -O-C1-6 haloalkyl,
melhylenedioxy attached to two adjacent carbon atoms, or aryl;
(b) a 4- to 8- membered saturated heterocyclic ring
containing from 1 to 4 heteroatoms independently selected from
N, O and S; wherein the saturated heterocyclic ring is
optionally substituted with one or more substituents (e.g.,
optionally from I to 6, or 1 to x or 1 to 4, or 1 to 3, or 1 or 2
substituents; or is optionally mono-substituted) each of which is independently halogen, -C1-6 alkyl, -C1-6 alkyl-ORa, -C1-6 haloalkyl, -O-C1-6 alkyl, -0-C|_6 haloalkyl, -C(=0)Ra, -CX)2Ra, -C(=0)-Co-6 alkyl-N(RaRb), -S02Ra, oxo. aryl. or -

(c) a 5- to 7-membercd heteroaromatic ring
containing from 1 to 4 hetcroatoms independently selected from
N, O and S; wherein the heteroaromatic ring is optionally
substituted with one or more substituents (e.g.. optionally 1 to
5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally
mono-substituted) each of which is independently halogen, -C 1 -6 alkyl, -C 1 -6 alkyl-ORa, -C i -6 haloalkyl, -O-C | -6 alkyl,
-O-C1-6 haloalkyl, oxo, or aryl;
(5) -Co-6 alkyl-O-Co-6 alkyl-Rk
(6) -Co-6 alkyl-S(O)irC0-6 alkyl-Rk
(7) -0-C1-6alkyl-ORk,
(8) -O-C 1-6 alkyl-O-C1-6 alkyl-Rk,
(9) -0-C1-6alkyl-S(0)nRk,
(10) -Co-6 alkyl-N(Ra).Rk,
(11) -Co-6 alkyl-N(Ra)-C1-6 alkyl-Rk,
(12) -Co-6 alkyl-N(Ra)-C 1-6 alkyl-ORk,
(13) -Co-6 alkyl-C(-0-Rk
(14) -Co-6 alkyl-C(=O)N(Ra)-C0-6 alkyl-Rk
(15) -Co-6 alkyl-N(Ra)C(=0)-Co-6 alkyl-Rk,
(16) -Co-6 alkyl-N(Ra)C(=0)-0-Co-6 aikyl-Rk, or
(17) -Co-6 alkyl-N(Ra)C(=0)C(=0)Rk;
R2 is -C1-6 alkyl which is optionally substituted with one or more substituents (e.g.,
optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently
(1) halogen,
(2) -Oil,
(3) -CN,
(4) -O-C 1-6 alkyl,
(5) -O-C 1-6 haloalkyl,
(6) -C(=0)Ra,
(7) -CO?.Ra
(8) -SRa,
(9) -S(==0)Ra,
(10) -N(RaRb).

(11) -C( O)N(RaRb),
(12) -N(Ra)-C(-0)-C1-6 alkyl-N(RbRc),
(13) -SG>2Ra,
(14) -N(Ra)S02Rb,
(15) -S02N(RaRb),
(16) -N(Ra)-C(Rb)-(),
(17) -C3-8 cycloalkyl,
(18) aryl, wherein the aryl is optionally substituted with one or more
substituents (e.g., optionally from 1 to 5. or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -C1-6 alkyl, -C1-6 haloalkyl, -0-C1_6 alkyl, -O-C1-6 haloalkyl, -Co-6 alkyl-N(RaRb), or -C1-6 alkyl substituted with a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S;
wherein the saturated heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -Ci-6
alkyl, oxo, or a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; or
(19) a 5- to 8-membcred monocyclic helerocycle which is saturated
or unsaturated and contains from 1 to 4 heteroatoms independently
selected from N, O and S; wherein the helerocycle is optionally
substituted with one or more substituents (e.g., optionally from 1 to
6, or 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently -Ci-6
alkyl, -0-C1-6 alkyl, oxo, phenyl, or naphthyl; R3 is-H or-CI-6 alkyl;
R4 is
(1) H,
(2) C1-6 alky! which is optionally substituted with one or more
substituents (e.g., optionally from 1 to 6. or 1 to 5, or 1 to 4. or 1 to 3.

or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH, 0-C1_6 alky I, -O-C1-6 haloalkyl, -NO2, -N(RaRb), -C(=0)Ra, -C()2Ra. -SRa, -S(=0)Ra, -S02Ra, or
«N(Ra)C02Rb,
(3) C1_6 alkyl which is optionally substituted with one or more
substituents (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3,
or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH. or O-C1-4 alkyl, and which is
substituted with 1 or 2 substituents each of which is independently: (i) C3-8 cycloalkyl,
(ii) aryl,
(iii) a fused bicyclic carbocycle consisting of a benzene ring fused to a C5-7 cycloalkyl,
(iv) a 5- or 6-membered saturated heterocyclic ring
containing from 1 to 4 heteroatoms independently selected from N, O and S,
(v) a 5- or 6-membered hcteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, or
(vi) a 9- or 10-membered fused bicyclic heterocycle
containing from 1 to 4 heteroatoms independently selected from N. O and S, wherein at least one of the
rings is aromatic,
(4) C2-5 alkynyi optionally substituted with aryl,
(5) C3-8 cycloalkyl optionally substituted with aryl,
(6) aryl,
(7) a fused bicyclic carbocycle consisting of a benzene ring fused to a 05.7
cycloalkyl,
(8) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S,
(9) a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, or
(10) a 9- or 10-mcmbcred fused bicyclic heterocycle containing from 1 to 4 heteroatoms independently selected from N, O and S, wherein at least one of the rings is aromatic;

wherein
each aryl in (3)(ii) or the aryl (4), (5) or (6) or each fused
carbocycle in (3)(iii) or the fused carbocycle in (7) is optionally
substituted with one or more substiluents (e.g., optionally from 1 to 5,
or 1 to 4, or 1 to 3, or 1 or 2 subslituents; or is optionally mono-subslituted) each of which is independently halogen, -OH, -C1-6 alkyl,
-C1-6 alkyl-ORa, -Cj-6 haloalkyl, -0-C|_6 alkyl, -O-C 1-6 haloalkyl, -CN, -N02, -N(RaRb), -C1_6 alkyi-N(RaRb). -C(=0)N(RaRb), -C(" 0)Ra. -C02Ra, -C1-6 aIky!-C02Ra, -OC02Ra, -SRa, -S(0)Ra, -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), -N(Ra)C(=0)Rb, -N(Ra)C02Rb, ~Cl-6 alkyl-N(Ra)C02Rb, aryl, -C1-6 alkyl-aryl, -O-aryl, or -Co-6 alkyl-het wherein het is a 5- or 6-membered
heteroaromatic ring containing from 1 to 4 heteroatoms independently
selected from N, O and S, and het is optionally fused with a benzene
ring, and is optionally substituted with one or more substiluents (e.g.,
optionally from I to 5, or 1 to 4, or 1 to 3, or 1 or 2 subslituents; or is optionally mono-substituted) each of which is independently -C)_6
alkyl, -C1-6 haloalkyl, -O-C1-6 alkyl, -O-C1-6 haloalkyl, oxo, or
-CCbRa:
each saturated heterocyclic ring in (3)(iv) or the saturated
heterocyclic ring in (8) is optionally substituted with one or more
subslituents (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3,
or 1 or 2 substiluents; or is optionally mono-substituted) each of which is independently halogen, -C]_6 alkyl, -C1-6 haloalkyl, -0-C1_6 alkyl, -O-C | -6 haloalkyl, oxo, aryl, or a 5- or 6-membered heteroaromatic
ring containing from 1 to 4 heteroatoms independently selected from N, O and S; and
each heteroaromatic ring in (3)(v) or the heteroaromatic ring in (9) OY each fused bicyclic heterocycle in (3)(vi) or the fused bicyclic heterocycle in (10) is optionally substituted with one or more substiluents (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substiluents; or is optionally mono-substituted) each of which is independently halogen, -C|-6 alkyl, -C]-6 haloalkyl, -O-C1-6 alkyl, -O-C1-6 haloalkyl, oxo, aryl, or-C1-6alkyl-aryl;

or alternatively R3 and R4 together with the N to which both are attached form a C3-7
a/aeycloalkyl which is optionally substituted with one or more substituentsXe.g.,
optionally from 1 to 6, or I to 5, or 1 to 4, or 1 to 3, or I or 2 substituents; or is optionally mono-substituted) each of which is independently -Ci-6 alkyl or oxo;
each Ra, Rb, RC? and Rd is independently -H or -C ] -6 alkyl;
Rk is carbocycle or hcterocycle, wherein the carbocycle or heterocycle is optionally substituted with one or more substituents (e.g., optionally from I to 7, or 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or I or 2 substituents; or is optionally mono-substituted) each of which is independently
(1) halogen,
(2) -OIL
(3) -CN,
(4) -CI -6 alkyl, which is optionally substituted with one or more
substituents (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or
1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH, -CN, -O-Ci-6 alkyl, -O-C1-6 haloalkyl, -C(0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb)!_C(-O)-(CH?)0-2N(RaRb), N(Ra)_c(=O)-(CH2)0-2N(RbRc), -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=0,
(5) -O-C1 _6 alkyl, which is optionally substituted with one or more
substituents (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or
1 to 3, or I or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH, -CN, -O-Cj-6
alkyl, -O-C16 haloalkyl, -C(K))Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb),_C(=O)-(CH2)0-2N(RaRb), N(Ra)-C(-O)-(CH2)0-2N(RbRC), -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb> =o,

(6) -NO2,
(7) oxo,
(8) -C(K))Ra.
(9) -C02Ka,

(10) -SRa,
(11) -S(0)Ra.
(12) -N(RaRb),
(13) -C(==())N(RaRb),
(14) -C(-0)-C 1 -6 alkyl-N(RaRb),
(15) -N(R>i)C( 0)Rb,
(16) -S02Ra,
(17) -S02N(RaRb),
(18) -N(Ra)S02Rb,
(19) -Rin,
(20) -C|_6 alkyl-Rni, wherein the alkyl is optionally substituted with
one or more substituenls (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH, -CN, -C|-6 haloalkyl, -O-Ci-6 alkyl. -O-Cj-6 haloalkyl, -C(=0)Ra, -C02Ra, -SRa -S(=0)Ra, -N(RaRb), -N(Ra)C02Rb, -S02R3, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=0,
(21) -Co-6 alkyl-N(Ra)-Co-6 alkyl-Rm,
(22) -Co-(, alkyl-O-Co-6 alkyl-Rm,
(23) -Co-6 alkyl-S-Co-6 alkyl-Rm,
(24) -Co-6 alkyl-C( (25) -C(- O)-O-C'0-6 alkyl-Rm,
(26) -C("0)N(Ra)-Co-6 alkyl-Rm,
(27) -N(Ra)C(0)-Rm,
(28) -N(R»)C( 0)-C1_6 alkyl-Rm, wherein the alkyl is optionally
substituted with one or more substituenls (e.g., optionally from 1 to 6, or 1 to 5, or 1 to 4, or 1 to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -OH, -CN, -C|-6 haloalkyl, -O-Ci-6 alkyl, -O-C'i-6 haloalkyl, -C(=0)Ra. -CC)2Ra, -SRa, -S(=0)Ra, -N(RaRb), -N(Ra)C02Rb. -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(R«)-C(Rb)=0,
(29) -N(Ra)-C(-O)-N(Rb)-C0-6 alkyl-Rm.
(30) -N(Ra)-C(-0)-0-Co-6 alkyl-Rm,

(31) -N(Ra)-C( -0)-N(Rb)-S02-Co-6 alkyl-R™,
(32) -C(-0)-C(--0)-N(RaRb),
(33) -C(-())-Ci_6 aIkyl-S02Ra, or
(34) -C(-0)-C(-0)Rm;
carbocycle in Rk is (i) a C3 to C8 monocyclic, saturated or unsaturated ring, (ii) a C7 to C]2 bicyclic ring system, or (iii) a C11to C16 tricyclic ring system, wherein each
ring in (ii) or (iii) is independent of or fused to the other ring or rings and each ring is saturated or unsaturated;
heterocycle in Rk is (i) a 4- to 8-membered, saturated or unsaturated monocyclic ring, (ii) a 7- to 12-membercd bicyclic ring system, or (iii) an 11 to 16-membered tricyclic ring system; wherein each ring in (ii) or (iii) is independent of or fused to the other ring or rings and each ring is saturated or unsaturated; the monocyclic ring, bicyclic ring system, or tricyclic ring system contains from 1 to 6 heteroatoms selected from N, O and S and a balance of carbon atoms; and wherein any one or more of the nitrogen and sulfur heteroatoms is optionally be oxidized, and any one or more of the nitrogen heteroatoms is optionally quatcrnized;
each Rm is independently C3-.8 cycloalkyl; aryl; a 5- to 8-membered monocyclic
heterocycle which is saturated or unsaturated and contains from 1 to 4 heteroatoms
independently selected from N, O and S; or a 9- to 10-membcred bicyclic heterocycle
which is saturated or unsaturated and contains from I to 4 heteroatoms independently
selected from N, O and S; wherein any one or more of the nitrogen and sulfur
heteroatoms in the heterocycle or bicyclic heterocycle is optionally oxidized and any
one or more of the nitrogen heteroatoms is optionally quaternized; and wherein
the cycloalkyl or the aryl defined in Rm is optionally substituted with
one or more substituents (e.g., optionally from 1 to 5, or 1 to 4, or 1 to 3, or 1
or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -C[_6 alkyl optionally substituted with -0-C]_4 alkyl,
-C1-6 haloalkyl, -0-C|-6 alkyl, -O-C1-6 haloalkyl. -N(RaRb), aryl, or -C1-6 alkyl-aryl; and

the monocyclic or bicyclic heterocycle defined in Rm is optionally substituted with one or more substitucnts (e.g., optionally from I to 6, or 1 to 5, or 1 to 4, or I to 3, or 1 or 2 substituents; or is optionally mono-substituted) each of which is independently halogen, -C\.(> alkyl, -Ci-6 haloalkyl, -O-Cj-6 alkyl, -O-Ci-6 haloalkyl, oxo, aryl, -C|_6 alkyl-aryl, -C(0)-aryl, -C02-aryl, -C02-C1_6 alkyl-aryl, a 5- or 6-membered saturated heterocyclic ring
containing from I to 4 heteroatoms independently selected from N, O and S, or a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; and
each n is independently an integer equal to zero, 1 or 2;
or a pharmaceutical iy acceptable salt thereof.
The present invention also includes pharmaceutical compositions containing a compound of the present invention and methods of preparing such pharmaceutical compositions. The present invention further includes methods of treating AIDS, methods of delaying the onset of AIDS, methods of preventing AIDS, methods of preventing infection by HIV, and methods of treating infection by HIV.
Other embodiments, aspects and features of the present invention are either further described in or will be apparent from the ensuing description, examples and appended claims.
DETAILED DESCRIPTION OF THE INVENTION
The present invention includes the N-substituted hydroxypyrimidinone carboxamides of Formula (I) above. These compounds and pharmaceutically acceptable salts thereof are HIV integrase inhibitors.
An embodiment of the present invention is a compound of Formula (I) exactly as defined above, except that in the definition of Rk, Rk js optionally substituted with one or more substitucnts each of which is independently one of the substituents (1) to (18), and is optionally mono-substituted with one of the substituents (19) to (34).
Another embodiment of the present invention is a compound of Formula (I) as orieinallv defined above, exceot that the definition of R2 includes a

proviso that none of the following optional substituents is attached to the carbon atom in the -C1-6 alkyl group that is attached to the ring nitrogen: halogen, -OHv-0-C1-6 alkyl, -O-C1-6 haloalkyl. -SRa, -S(=0)Ra or -N(Ra)-C(Rb) O. Stated another way,
none of these substituents is attached to the carbon atom alpha to the ring nitrogen.
Another embodiment of the present invention is a compound of Formula (I) as originally defined above except that in the definition of Rj, Rl is one of substitutcnts (1) to (16) and in the definition of Rk, Rk is optionally substituted with one or more substituents (e.g., optionally from 1 to 7, or 1 to 6, or 1 to 5, or 1 to 4, or I to 3, or 1 to 2 substituents, or is optionally monosubstituted) each of which is independently one of substitutcnts (1) to (31).
Another embodiment of the present invention is a compound of Formula (I), wherein Rl is:
(1) -H,
(2) -C1_6 alkyl, which is optionally substituted with one or more
substituents each of which is independently halogen, -OH, -CN, -O-C1-6 alkyl, -0-C[-6 haloalkyl, -C(-0)Ra, -C02Ra, -SRa, -S(==0)Ra, -N(RaRb), -C(=O)-(CH2)0-3-N(RaRb), N(Ra)-C( O)-(CH2)0-3-N(RbRC),-S02Ra,-N(Ra)S02Rb,
-S02N(RaRb), -N(Ra)-C(0)Rb, FT
or -N(R2)C(==0)C(=0)N(RaRb),
(3) -Rk
(4) -(CH2)l-3-Rk. wherein:
(i) the -(Cll2)l-3- moiety is optionally substituted with one or
more substituents each of which is independently halogen, -OH, -CN, -O-C1-6 alkyi, -0-C)-6 haloalkyl, -N(RaRb),
-N(R'>)C02Rb, -N(Ra)C(=O)-(CH2)0-3-N(RbRC), or
-N(Ra)-(('H2)2-3-OH with the proviso that the -OH is not
attached to the carbon alpha to N(Ra); and (ii) the -(Cll2)l-3- moiety is optionally mono-substituted with -Rs,
-C1-6 alkyl-R-s, -N(Ra)-C(=O)-(CH2)0-3-Rs, -N(Ra)-(CH2)0-3-Rs, -0-(C! l2)0-3-Rs, or -N(Ra)-C(-O)-(CH2)0-3-Rs; wherein RS is

(a) aryl which is optionally substituted with one or
more substituents each of which is independently halogen, -OH,
-C | _6 alkyl, -C1-6 alkyl-ORa, -C 1_6 haloalkyl, -C1-6 alkyl,
-O-C1-6 haloalkyl, methylenedioxy attached to two adjacent
carbon atoms, or aryl;
(b) a 4- to 8- membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; wherein the saturated heterocyclic ring is optionally substituted with one or more substituents each of which is independently halogen, -C1-6 alkyl, -C1_6 alkyl-ORa, -C|-6 haloalkyl, -O-C1-6 alkyl, -O-Ci-6 haloalkyl, -C(-=0)Ra -C02Ra- -C(=O)-(CH2)0-3-N(RaRb). -S02Ra, oxo, aryl, or -(Cll2)l-3-aryl;or
(c) a 5- to 7-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; wherein the heteroaromatic ring is optionally substituted with one or more substituents each of which is independently halogen, -C|-6 alkyl, -C1-6 alkyl-ORa, -Cj-6 haloalkyl, -O-C1-6 alkyl, -O-C1-6 haloalkyl, oxo, or aryl;

(5) -(CH2)0-3-O-(CH2)0-3-Rk,
(6) -(CH2)0-3-S(O)n-(CH2)0-3-Rk,
(7) -(CH2)l-3-ORk,
(8) -(CH2)l-3-0-(CH2)l-3-Rk,
(9) -0-(Cll2)l-3-S(0)nRk
(10) -(CH2)0-3-N(Ra)-Rk
(11) -(CH2)0-3-N(Ra)-(CH2)l-3-Rk,
(12) -(Cll2)0-3-N(Ra)-(CH2)l-3-ORk,
(13) -(CH2)0-3-C(=-O)-Rk
(14) -(CH2)0-3-C(=O)N(Ra)-(CH2)0-3-Rk,
(15) -(CH2)0-3-N(Ra)C(=O)-(CH2)0-3-Rk.
(16) -(Cll2)0-3-N(Ra)C(=O)-O-(CH2)0-3-Rk-
(17) -C(CI-l3)2N(Ra)C(=0)Rb,
(18) -C(Cll3)2N(Ra)C(=0)Rk, or
(19) -C(CI-l3)2N(Ra)C(=0)C(=0)N(RbRc);

and all other variables are as originally defined above;
or a pharmaeeutically acceptable salt thereof.
In an aspect of this embodiment, R' is one of groups (1) to (16).
Another embodiment of the present invention is a compound of Formula (I), wherein Rl is:
(1) -H,
(2) -C1-4 alkyl, which is optionally substituted with from 1 to 4
substituents each of which is independently halogen, -OH, -CN, -O-C1-4 alkyl, -O-C1-4 haloalkyl, -C(=0)Ra, -CC>2Ra, -SRa. -S(=0)Ra, -N(RaRb), -C(=O)-C0-4 alkyl-N(RaRb), N(Ra)-C(==0)-Co-4 alkyl-N(RbRC), -S02R3, -N(Ra)S02Rb,
s
-S02N(RaRb), -N(Ra)-C(=0)Rb,
-N(R2)C(0)C( O)N(RaRb),
(3) -Rk,
(4) -C1-4 alkyl-Rk, wherein:
(i) the alkyl is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -OH, -CN, -O-Ci-4 alkyl, -O-C1-4 haloalkyl, -N(RaRb), -N(Ra)C02Rb, -N(Ra)C(=0)-Co-4 alkyl-N(RbRC), or -N(Ra)-(CH2)2-4-OH; and
(ii) the alkyl is optionally mono-substituted with -Rs,
-N(Ra)-C(-0)-Co-4 alkyl-Rs, -N(Ra)-Co-4 alkyi-Rs, -O-Co-4 alkyl-Rs. or -N(Ra)-C(-O)«C0-4 alkyl-RS; wherein Rs is
(a) aryl which is optionally substituted with from 1
to 3 substituents each of which is independently halogen, -OH, -C|-4 alkyl, -C1-4 alkyl-ORa, -C1.4 haloalkyl, -0-C1-4 alkyl,
-O-C1-4 haloalkyl. methylenedioxy attached to two adjacent
carbon atoms, or phenyl;
(b) a 5- or 6-membercd heteroaromatic ring
containing from 1 to 4 heteroatoms independently selected from
N, O and S; wherein the heteroaromatic ring is optionally

substituted with from 1 to 3 substituents each of which is independently halogen, -C|-4 alkyl, -C1-4 alkyl-ORp, -C1-4
haloalkyl, -O-C1-4 alkyl, -O-C1-4 haloalkyl, oxo, or phenyl; or
(c) a 5- or 6-membered saturated heterocyclic ring
containing from 1 to 4 hetcroatoms independently selected from
N, O and S; wherein the saturated heterocyclic ring is
optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C1-4 alkyl, -C1-4 alkyl-ORa,
-C1-4 haloalkyl, -O-CM alkyl, -O-CM haloalkyl, -C(0)Ra,
-C()2Ra, -C(=0)-Co-4 alkyl-N(RaRb), -S02Ra, oxo, or phenyl,
(5) -(CH2)0-3-C(O)N(Ra)-(CH2)0-3-Rk-
(6) -C(C1_4 alkyl)2N(Ra)C(=0)Rb,
(7) -C(C 1-4 alkyI)2N(Ra)C(=0)Rk, or
(8) -C(Cl-4alkyl)2N(Ra)C(=0)C(-0)N(RbRc);
and all other variables arc as originally defined above;
or a pharmaceuticallyacceptable salt thereof.
In an aspect of this embodiment, Rl is one of groups (1) to (5).
Another embodiment of the present invention is a compound of Formula (I), wherein Rl is:
(1) -H,
(2) -CI -4 alkyl, which is optionally substituted with from 1 to 3
substituents each of which is independently halogen, -O-C1-4 alkyl, -O-C1-4 haloalkyl, -C(0)Ra, -C02Ra, -N(RaRb), 0r -C(=O)-(CH2)0-2-N(RaRb),
(3) -Rk,
(4) -(Cll2)l-4-Rk, wherein:
(i) the -(CH2)l-4- moiety is optionally substituted with 1 or 2
substituents each of which is independently halogen, -OH, -O-C1-4 alkyl, -O-C1-4 haloalkyl, or -N(RaRb); and (ii) the -(CIl2)l-4- moiety is optionally mono-substituted with -Rs or -N(Ra)-(CH2)l-2-Rs; wherein Rs is

(a) phenyl which is optionally substituted with from 1 to 3 substituents each of which is independently halQgen, -C1-4 alkyl, -C1.4 alkyl-ORa, -C1-4 haloalkyl, -O-C1-4 alky!, or -O-C1-4 haloalkyl; or
(b) a 5- or 6-mcmbered heteroaromatic ring
containing from 1 to 4 heteroatoms independently selected from
N, O and S; wherein the heteroaromatic ring is optionally
substituted with from 1 to 3 substituents each of which is independently halogen. -C|_4 alkyl, -C14 alkyl-ORa, -C1-4
haloalkyl, -0-C1_4 alkyl, or -0-C1-4 haloalkyl; or
(c) a 5- or 6-mcmbered saturated heterocyclic ring
containing from 1 to 4 heteroatoms independently selected from
N, O and S; wherein the saturated heterocyclic ring is
optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C1_4 alkyl, -C]_4 alkyI-ORa,
-C|-4 haloalkyl, -O-C1-4 alkyl, -O-CM haloalkyl, -C(=0)Ra
or -C02Ra,
(5) -C(=O)N(Ra)-(CH2)0-3-Rk(6) -C(CH3)2N(Ra)C(=0)Rb
(7) -C(CH3)2N(Ra)C(=0)Rk
(8) -C(CI-l3)2N(Ra)C(=0)C(K))N(RbRc);
and all other variables arc as originally defined above;
or a pharmaceutically acceptable salt thereof.
In an aspect of this embodiment, Rl is one of groups (1) to (5).
Another embodiment of the present invention is a compound of Formula (I), wherein
Rk is C3-8 cycloalkyi; aryl selected from phenyl and naphthyl; a bicyclic carbocycle
selected from indanyl and telrahydronaphthyl; a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N. O and S; or a bicyclic heterocyclc which is a benzene

ring fused to a 5- or 6-membered saturated or unsaturated heterocyclic ring containing from I to 3 heteroatoms independently selected from N, O and S;
wherein the cycloalkyl, aryl, bicyclic carbocycle, saturated heterocyclic ring, hcteroaromatic ring, or bicyclic heterocycle is optionally substituted with from 1 to 4 substituents each of which is independently
(1) halogen,
(2) -OH,
(3) -CN,
(4) -CM haloalkyl,
(5) -C1-4 alkyl, which is optionally substituted with from 1 to 3
substituents each of which is independently -01 f, -CN, -O-C1-4 alkyl, -0-C|-4 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra -N(RaRb), -C(=O)-(CH2)0-2N(RaRb),
N(Ra)-C(=0)-(Cl l2)0-2N(RbRc),-S02Ra, -N(Ra)S02Rb, -S02N(RaRb), 0r -N(Ra)-C(Rb)=C),
(6) -O-C1 -4 haloalkyl
(7) -O-C 1-4 alkyl, which is optionally substituted with from 1 to 3
substituents each of which is independently -OH, -CN, -O-C1_6 alkyl, -0-C1-6 haloalkyl, -C(K))Ra, -C02R3, -SRa -S(=0)Ra, -N(RaRb), -C(=O)-(CH2)0-2N(RaRb),
N(Ra)-C(=O)-(CH2)0-2N(RbRc),-S02R3, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=0,
(8) -N02,
(9) oxo,
(10) -C(0)Ra,
(11) -C02Ra,
(12) -SRa,
(13) -S(-0)Ra.
(14) -N(RaRb),
(15) -C(=0)N(RaRb),
(16) -C(=0)-C1-6 alkyl-N(RaRb),
(17) -N(Ra)C(=0)Rb,
(18) -S02Ra,

(18) -S02N(RaRb),
(19) -N(Ra)S02Rb,

(20) -Rm,
(21) -C i .4 alkyl-Rm,
(22) -(CH2)0-2-N(Ra)-(CH2)0-2-F^
(23) -(CH2)0-2-O-(CH2)0-2-Rm,
(24) -(CMl2)()-2-S-(CH2)0-2-Rm,
(25) -(CI l2)0-2-C(==O)-(CH2)0-2-Rm,
(26) -C(-O)-O-(CH2)0-2-Rm,
(27) -C(-0)N(Ra)-Rmj 0r
(28) -C(-0)-C(=0)N(RaRb);
and all other variables are as originally defined above;
or a pharmaceutically acceptable salt thereof.
In an aspect of this embodiment, the eycloalkyl, aryl, bicyclic carbocycle, saturated heterocyclic ring, heteroaromatic ring, or bicyclic heterocycle is optionally substituted with from I to 4 substituents each of which is independently selected from the groups (1) to (27).
In an aspect of this embodiment, Rk (i.e., the eycloalkyl, aryl, bicyclic carbocycle, saturated heterocyclic ring, heteroaromatic ring, or bicyclic heterocycle) is optionally substituted with from 1 to 4 substituents each of which is independently one of the substituents (1) to (19), and is optionally mono-substituted with one of the substituents (20) to (28). In a feature of this aspect, Rk js optionally substituted with from 1 to 4 substituents each of which is independently one of the substituents (1) to (19). and is mono-substituted with one of the substituents (20) to (28).
In another aspect of this embodiment, each Rm is independently C3-7
eycloalkyl; aryl selected from phenyl and naphthyl; a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; a 5- or 6-membcred heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, wherein any N is optionally oxidized to form an N-oxide; or a bicyclic heterocycle which is a benzene ring fused to a 5- or 6-membered, saturated or unsaturated heterocyclic ring containing from I to 3 -heteroatoms selected from N, O and S; wherein

the cycloalkyl or the aryl defined in Rm is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -C|_4 alkyl,
-CM haloalkyl, -()-C|-4 alkyl, -0-C|-4 haloalkyl, -N(RaRb), phenyl, or
-(CH2)l-2-p'ienyl;
the saturated heterocyclic ring defined in Rm is optionally substituted with from 1 to 4 substituents each of which is independently -C]-4 alkyl
optionally substituted with -0-C1_4 alkyl, -C]_4 haloalkyl, -O-Ci-4 alkyl, -0-C1_4 haloalkyl, oxo, phenyl, -(CI 12) 1 -2~phcnyU -C(=0)-phenyl, -C02-phenyI, -C09-(Cll2)l-2-phenyK a 5- or 6-membered saturated heterocyclic ring containing from I to 4 heteroatoms independently selected from N, O and S, or a 5- or 6-mcmbered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; and
the heteroaromatic ring or the bicyclic heterocycle defined in Rm is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -C1-4 alkyl, -C1-4 haloalkyl, -O-C1-4 alkyl, -0-Ci_4 haloalkyl, oxo, phenyl, or -(CH2)]-2-phenyl.
Another embodiment of the present invention is a compound of Formula (I), wherein Rk is phenyl; a 5- or 6-membered saturated heterocyclic ring containing 1 or 2 heteroatoms selected from 1 or 2 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; a 5- or 6-membered heteroaromatic ring containing 1 or 2 heteroatoms selected from 1 or 2 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; or a bicyclic heterocycle which is a benzene ring fused to a 5- or 6-membered saturated heterocyclic ring containing 1 or 2 nitrogen atoms;
and all other variables are as originally defined;
or a pharmaceutically acceptable salt thereof.
In an aspect of this embodiment, (a) the phenyl, the saturated heterocyclic ring, heteroaromatic ring, or bicyclic heterocycle is optionally substituted with from I to 3 substituents each of which is independently
(1) -- fiuoro.

(2) chloro,
(3) bromo,
(4) -OH
(5) -Cl-3,
(6) -C1-4 alkyl, which is optionally substituted with 1 or 2 substituents each of which is independently -OH, -CN, -O-Ci-4 alkyl, -OCF3, -N(RaRb), -C(-0)N(RaRb), or N(Ra)-C(=O)-(CH2)0-2N(RbRC),
(7) -OCF3,
(8) -O-C 1.4 alkyl
(9) -CCO)Ra,
(10) -C02Ra,
(11) -SRa,
(12) -SRa,
(13) -N(RaRb),
(14) -C(-=0)N(RaRb),
(15) -C(=0)-(CH2) 1 -2-N(RaRb),
(16) -N(Ra)C(=0)Rb, or
(17) -S02Ra;
(b) the phenyl is optionally mono-substituted with
(1) -(CH2)l-2-Rm,or
(2) -(CH2)0-2-N(Ra).(CH2)0-2-Rm: and
(c) the saturated heterocyclic ring, hetcroaromatic ring, or bicyclic
hcterocycle is optionally mono- or di-substituted with
(1) oxo
(2) -(CH2)l-2-Rm,
(3) -0-(CH2)l-2-Rm,or
(4) -(CH2)()-|-C(=O)-(CH2)0-2-Rm-
In a feature of the preceding aspect, each Rni is independently cyclopropyl; phenyl; a 5- or 6-membered saturated heterocyclic ring selected from pyrrolidinyl, imidazolidinyl, pyrazolidinyl, piperidinyl, pipcrazinyl. and morpholinyl; or a 5- or 6-membered hetcroaromatic ring selected from thicnyl, pyridyl optionally in the form of an N-oxide, imidazolyl, pyrrolyl, pyrazolyl, thiazolyl, isothiazolyl,

oxazolyl, isooxazolyl, oxadiazolyl, thiadiazolyl, pyrazinyl, pyrimidinyl, triazolyl, tetrazolyl, furanyl, and pyridazinyl; wherein
the cyclopropyl is unsubstituted;
the phenyl is optionally substituted with from i to 3 substituents each of which is independently halogen, -Ci_4 alkyl, -CF3, -0-C1-4 alkyl, -OCF3, or-N(RaRb);
the saturated heterocyclic ring is optionally substituted with 1 or 2 subslituents each of which is independently -C1-4 alkyl, -CF3, -0-C]-4 alkyl,
-OCF3, oxo, phenyl, -(CH2)l-2-phenyI, -C(= 0)-phcnyl, -C02-phenyl, or
-C02-CH2-phenyl; and
the heteroaromatic ring is optionally substituted with 1 or 2 substituents each of which is independently -C1.4 alkyl, -CF3, -0-C]-4 alkyl,
-OCF3, oxo, phenyl, or -(CH2)l-2~phenyl.
Another embodiment of the present invention is a compound of Formula (I), wherein R.2 is:
(1) -C1-6 alkyl,
(2) -C1 _6 alkyl substituted with -N(RaRb),
(3) -C1 _(i alkyl substituted with phenyl, wherein the phenyl is:
(a) optionally substituted with from 1 to 4 substituents each
of which is independently halogen, -C1-4 alkyl, -C]_4
haloalkyl. -O-C1--4 alkyl, -0-C1_4 haloalkyl, or
-C0-4 alkyl-N(RaRb); and
(b) optionally mono-substituted with -C1-4 alkyl
substituted with a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms selected from 1 or 2 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms;
wherein the heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -C]-6 alkyl, oxo, or a 5- or 6-mcmbercd heteroaromatic ring
containing from I to 3 heteroatoms selected from 1 to 3 N
atoms, 0 or 1 O atom, and 0 or 1 S atom; or
(4) -C1 -6 alkyl optionally substituted with -OH and substituted with a 5-
or 6-membered saturated monocyclic heterocycle which contains from 1 to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atoms, and 0

or 1 S atoms; wherein the heterocycle is optionally substituted with from 1 to 4 substituents each of which is independently -Cl-6 alkyl,
-O-C 1 -6 alkyl, oxo, or phenyl; or
(5) -C 1-6 alkyl substituted with a 5- or 6-membered heteroaromatic ring
which contains from 1 to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heteroaromatic ring is optionally substituted with from 1 to 4 substituents each of which is independently -Cl-6 alkyl, -0-C]_6 alkyl, oxo, or phenyl;
and all other variables are as originally defined above; or a pharmaceutical ly acceptable salt thereof.
Another embodiment of the present invention is a compound of
Formula (I) exactly as defined in the immediately preceding embodiment, except that when R2 is -C1-6 alkyl substituted with -N(RaRb) it js with the proviso that -N(RaRb) js not attached to the carbon atom in the -C | _6 alkyl group that is attached to the ring nitrogen (i.e., that the -N(RaRb) group is not attached to the carbon atom alpha to the ring nitrogen).
Another embodiment of the present invention is a compound of Formula (I), wherein R2 is methyl;
and all other variables are as originally defined above;
or a pharmaceutical^ acceptable salt thereof.
Another embodiment of the present invention is a compound of Formula (I), wherein lO is -H or -C1-4 alkyl;
and all other variables are as originally defined above; or a pharmaceutical!) acceptable salt thereof.

In an aspect of this embodiment, R3 is -11 or methyl. In another aspect of this embodiment, R3 is -11.
Another embodiment of the present invention is a compound of Formula (I), wherein R4 js C1.4 alkyl substituted with an aryl, which is optionally
substituted with from 1 to 4 substituents each of which is independently halogen, -OH, -C1-4 alkyl, -C|_4 alkyl-ORa, -CM haloalkyl, -O-C1-4 alkyl, -O-C1-4 haloalkyl, -CN, -NO2, -N(RaRb), -CM alkyl-N(RaRb). -C(-0)N(RaRb), -C(0)Ra, -C02Ra, -C1-4 alkyl-C02Ra, -OC02Ra, -SRa -S(-0)Ra, -S02Ra, -N(Ra)S02Rb, . -S()2N(RaRb), -N(Ra)C(0)Rb, -N(Ra)C02Rb, -C1-4 alkyl-N(Ra)C02Rb, methylencdioxy attached to two adjacent ring carbon atoms, phenyl, -C1_4 alkyl-phenyl, -O-phenyl, or -(CH2)0-2-het;
wherein hct is a 5- or 6-membercd hetcroaromatic ring containing from I to 4 heteroatoms independently selected from N, O and S, and het is optionally
fused with a benzene ring, and is optionally substituted with 1 or 2 substituents each of which is independently -Ci_4 alkyl, -C]-4 haloalkyl, -O-Ci-4 alkyl, -O-Cj-4
haloalkyl, or -C02Ra;
and all other variables are as originally defined above;
or a pharmaceutically acceptable salt thereof.
Another embodiment of the present invention is a compound of Formula (I), wherein R4 is -CI l2-phenyl, wherein the phenyl is optionally substituted
with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -C1-4 alkyl, -C1-4 fluoroalkyl, -O-Ci-4 alkyl, -O-C1-4 fluoroalkyl, -(CH2)l-2-N(RaRb), -S02Ra. -(CH2)0-2-CO2Ra, -(CH2)0-2-N(Ra)CO2Rb, -NO2, -SRa -N(RaRb) or phenyl;
each Raand Rb is independently is H or-C1_4 alkyl;
and all other variables are as originally defined above; or a pharmaceutical!)' acceptable salt thereof.

In an aspect of the preceding embodiment, R4 is -CH2-phenyl, wherein
the phenyl is optionally substituted with from 1 to 3 substituents, each of which is independently -F, -Br, -CI, -011, -C1-4 alkyl, -C1-4 fluoroalkyl, -O-C1.4 alkyl, -SO2-C1_4 alkyl, -S-C]_4 alkyl, -N(CH3)2 or -O-Cl-4 fluoroalkyl. In another aspect of the preceding embodiment, R4 is/;-fluorobenzyI or 2,3-dimethoxybenzyI.
In another aspect of the preceding embodiment, the phenyl is optionally
substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -C]_4 alkyl, -C]_4 fluoroalkyl, -O-Cl-4 alkyl, -0-C)„4 fluoroalkyl, -(CH2)|-2-N(RaRb), -S02Ra, -(CH2)0-2-CO2Ra
-(Cll2)0-2-N(Ra)CO2Rb, -NO2, or phenyl.
In an aspect of the preceding embodiment, the phenyl is optionally
substituted with from 1 to 3 substituents, each of which is independently -F. -Br, -CI, -OH. -C1-4 alkyl, -CM fluoroalkyl, -0-C1_4 alkyl, or -O-C1-4 fluoroalkyl. In
another aspect of the preceding embodiment, R4 is/>fluorobenzyl or 2,3-dimethoxybcnzyl.
A class of compounds of the present invention includes any compound of Formula (1), wherein
Rl is-Rk;
Rk is phenyl which is
(a) optionally substituted with from 1 to 3 substituents each of which is independently:
(1) halogen,
(2) -Cl-6 alkyl, which is optionally substituted with 1 or 2 substituents each of which is independently -O-C1-6 alkyl, -O-C1-6 haloalkyl. -C(-0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb), -C(O)-(CH2)0-2N(RaRb),
N(Ra)-C(=OHCH2)0-2N(RbRcX-SO2Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=0,
(3) -C1_6 haloalkyl,
(4) -O-C1_6 haloalkyl,
(5) -C(=0)Ra,
(6) -C02Ra,

(7) -C(=0)N(RaRb), or
(8) -C(0)-C]-6 alkyl-N(RaRb); and ;•
(b) optionally mono-substituted with
(1) -C1-4alkyI-Rm, or
(2) -Co-4 alkyl-N(Ra)-Co-4 alkyl-R™;
wherein Rm is aryl selected from phenyl and naphlhyl; a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; or a 5- or 6-membered heteroaromatic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; wherein
the aryl defined in Rm is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C]-4 alkyl, -CF3, -O-C1-4 alkyl -OCF3, or -N(RaRb);
the saturated heterocyclic ring defined in Rm is optionally substituted with from I to 3 substituents each of which is independently -C]-4 alkyl or
oxo, and is additionally optionally mono-substituted with phenyl, -(CH2)l-2-phcnyl, -C( 0)-phenyl, -C02-phenyl, -C02-(CH2)l-2-phenyl, or a
5- or 6-mcmbcred heteroaromatic ring containing from 1 to 3 heteroatoms
independently selected from N, O and S; and
the heteroaromatic ring defined in Rm is optionally substituted with 1 or 2 substituents each of which is independently -C1--4 alkyl or oxo;
and all other variables arc as originally defined above;
or a pharmaceutical ly acceptable salt thereof.
A sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (1), wherein
R2 is methyl;
R3 is-H;
R4 is:

(1) -CI-l2-phenyl, wherein the phenyl is optionally substituted with
from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -C1-4 alkyl, -C1-4 fluoroalkyk -O-Ci-4 alky!, -0-Ci_4 fluoroalkyl -(CH2)l-2-N(RaRb), -S()2Ra, -(CH2)0~2-CO2Ra -(CI l2)0-2-N(Ra)CO2Rb, -N02, -SRa, -
N(RaRb) or phenyl; or
(2) a fused bicyclic carbocycle selected from
71 pl-
each Ra and Rb is independently is H or -C1-4 alkyl;
and all other variables are as defined in the class;
or a pharmaceuticallyacceptable salt thereof.
Another sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (1), wherein R4 is 4-fluorobenzyl or 2,3-dimethoxybenzyl;
and all other variables arc as defined in the class;
or a pharmaceutically acceptable salt thereof.
Still another sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (1), wherein R2 is methyl; R3 is -II; R4 is 4-fluorobenzyl or 2,3-dimethoxybenzyl; each Ra and Rb is independently is H or -C1--4 alkyl; and all other variables are as defined in the class; or a
pharmaceutically acceptable salt thereof.

Another class of the present invention includes any compound of Formula (II):

wherein
Qis:
(1) methyl which is optionally substituted with 1 or 2 of -O-C1-4 alkyl,
(2) phenyl which is optionally substituted with from 1 to 3 substitucnts each of which is independently -F, -CI, Eir, -C\-4 alkyl, -CF3, -O-Cj-4
alkyl, -OCF3, methylenedioxy attached to two adjacent carbon atoms,
or phenyl, or
(3) a 5- or 6-mcmbercd saturated heterocyclic ring containing from 1 to 3
hetcroatoms independently selected from N, O and S; wherein the
saturated heterocyclic ring is optionally substituted with 1 or 2 substituents each of which is independently -F, -CI, -Br, -C]_4 alkyl,
oxo, phenyl, or -C(=0)-phenyl;
T is:
(1) -H,
(2) -OH,
(3) methyl or ethyl, optionally substituted with -OH or -O-C1-4 alkyl,
(4) -O-C1-4 alkyl
(5) -N(RaRb),
(6) -N(Ra)-(CH2)2-OH,
(7) -N(Ra)-C02Rb,
(8) -N(Ra)-C(=0)-(CH2) 1 -2-N(RaRb),
(9) -Rs,
(10) -(CH2)l-2-Rs,or
(11) -(Cll2)0-2-N(Ra)-(CH2)0-3-Rs;

Rs is:
(1) phenyl optionally substituted with from 1 to 4 substituents each of which is independently halogen, -C1-4 alkyl. -C1_4 alkyI-ORa, -C1_4 haloalkyl, -O-CM alkyl, -O-CM haloalkyl, or -N(RaRb);
(2) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 hctcroatoms independently selected from N, O and S; which is
optionally substituted with from 1 to 4 substituents each of which is independently-C1--4 alkyl, -C1_4 alkyl-ORa, -C1-4 haloalkyl, -O-C1-4 alkyl, -O-C1-4 haloalkyl, -C( 0)Ra, oxo, phenyl, or -CH2-phenyI; or
(3) a 5- or 6-membered heteroaromatic ring containing from 1 to 3
heteroatoms independently selected from N, O and S; which is optionally substituted with from I to 4 substituents each of which is independently -C1-4
alkyl, -C1-4 alkyl-ORa, -C1-4 haloalkyl, -O-CM alkyl, -O-C1-4 haloalkyl, or oxo;
R2 is
(1) -C1- -4 alkyl,
(2) -C1 -4 alkyl substituted with -N(RaRb), or
(3) -C1-4 alkyl substituted with a 5- or 6-membered saturated monocyclic
heterocycle which contains from 1 to 3 heteroatoms selected from 1 to
3 N atoms. 0 or 1 O atoms, and 0 or 1 S atoms; wherein the saturated
heterocycle is optionally substituted with from 1 to 4 substituents each of which is independently a -CM alkyl;
R3 is-H or-C1-4 alkyl;
R4 is -CH2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -C]-4 alkyl, -C1-2 fluoroalkyl, -O-C1-2 alkyl, -O-CM fluoroalkyl, ~(CH2)]-2-N(RaRb), -S02Ra, -(CIl2)0-2-CO2Ra, -(Cll2)0-2-N(Ra)CO2Rb, -N02, -SRa, -N(RaRb) or phenyl;
each Ra and Rb is independently is H or -C]_4 alkyl: and s is an integer equal to zero, ], or 2;

or a pharmaceutical!)' acceptable salt thereof.
In an aspect of this class, R4 is -CFb-phenyl, wherein the phenyl is
optionally substituted with from 1 to 3 substitucnts each of which is independently fluoro, bromo, chloro, -Oil, -C|-4 alkyl, -Ci-4 fluoroalkyl, -O-Cj-4 alkyl, -O-Cj-4
fluoroalkyl, -(CH2)|-2-N(RaRb), -S02Ra, -(CH2)0-2-CO2Ra, -(Cil2)0-2-N(Ra)C()2Rb, -NO2, or phenyl
A sub-class of the preceding class of compounds of the present
invention includes any compounds of Formula (11) exactly as defined in the preceding class, except that when R2 is -C-i_4 alkyl substituted with -N(RaRb), it is with the
proviso that -N(RaRb) is not attached to the carbon atom in the -C\-4 alkyl group that
is attached to the ring nitrogen (i.e., that the -N(RaRb) group is not attached to the carbon atom alpha to the ring nitrogen).
Another sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (11), wherein
Q is phenyl;
T is:
(1) -H,
(2) -N(RaRb),
(3) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3
heteroatoms independently selected from N, O and S; which is
optionally substituted with 1 or 2 substituents each of which is independently -C1-4 alkyl or -C(-~0)Ra, or
(4) -N(Ra)-(CH2)l-2-heteroaromatic, wherein the heteroaromatic is a 5- or
6-mcmbered ring containing I or 2 N atoms;
R2 is methyl;
R3 is -H; and

R.4 is -CH2-phenyl, wherein the phenyl is optionally substituted with 1 or 2 substituents each of which is independently-F, -CI, -Br, -Cj-4 alkyl, -CF3, -O-Cj-4 alkyl, -SO2CH3, -SCH3, -N(CH3)2 or-OCF3;
each Ra and Rb is independently -H, methyl or ethyl; and
s is an integer equal to zero or 1;
or a pharmaceutical^ acceptable salt thereof.
In an aspect of this subclass, R4 is -Cll2-phenyl, wherein the phenyl is
optionally substituted with I or 2 substituents each of which is independently -F, -CI, -Br, -C1-4 alky], -CF3, -0-C|-4 alkyl, or-OCF3.
Another class of compounds of the present invention includes any compound of Formula (I), wherein
Rl is-Rk;
Rk is (i) a 5- or 6-membered saturated heterocyclic ring containing from 0 to 1 oxygen atoms and from 1 to 3 nitrogen atoms or (ii) a bicyclic heterocycle which is a benzene ring fused to a 5- or 6-membcred saturated heterocyclic ring containing from 0 to 1 oxygen atoms and from 1 to 3 nitrogen atoms;
wherein the saturated heterocyclic ring or bicyclic heterocycle is
optionally substituted with from 1 to 3 substituents each of which is independently
(1) -Ci_4 alkyl, which is optionally substituted with from 1 to 4
substituents each of which is independently halogen, -O-C1-4 alkyl, -O-C1-4 haloalkyl, -C(=0)Ra, -CC>2Ra, -SRa -S(=0)Ra, -N(RaRb), -C(=O)-(CH2)0-2N(RaRb),
N(Ra)-C(=O)-(Cl)2)0-2N(RbRC),-S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra>C(Rb)=0,
(2) -Oil,
(3) -C(-0)Ra
(4) -C02Ra,
(5) -Ct O)N(RaRb),

(6) -C(- ())-C | _6 alkyl-N(RaRb),
(7) -SRa.
(8) -S( 0)Ra,
(9) -SCnRa,
(10) -N(RaRb),
(11) -Km,
(12) -C]_4 alkyl-Rm, wherein the alkyl is optionally substituted with
from 1 to 4 substituents each of which is independently halogen, -OH, -CN, -CM haloalkyl, -O-C-M alkyl, -O-C1-4 haloalkyl, -C(-0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb), -N(Ra)C02Rb, -SC>2Ra, -N(Ra)S02Rb, -SC>2N(RaRb), 0r -N(Ra)-C(Rb)=0,
(13) -C()-4 alkyl-N(Ra)-Co-4 alkyl-Rm,
(14) -C(M alkyl-O-Co-4 alkyl-Rm,
(15) -Co-4 alkyI-S-CO-4 alkyl-Rm,
(16) -Co_4 alkyl-C(=0)-Co-4 alkyl-Rm,
(17) -C( -O)-()-C0-4 alkyl-Rm, or
(18) -C( C))N(Ra)-Co-4 alkyl-Rm;
wherein each Rm is independently -C3.6 cycloalkyi; aryl selected from phenyl and
naphthyl; a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3
heteroatoms independently selected from N, O and S; or a 5- or 6-membered
heteroaromatic ring conlaining from 1 to 3 heteroatoms independently selected from
N, () and S, wherein any N is optionally oxidized to form an N-oxide; wherein
the aryl is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -Ci-4 alkyl, -CF3, -O-Ci-4 alkyl, -OCF3, or
-N(RaRb);
the saturated heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -C|_4 alkyl or oxo, and is
additionally optionally mono-substituted with phenyl, -(CH2)l-2-phenyl,
-C(=0)-phcnyl, -C()2-phenyl, or-C02-(CH2)l-2-phenyl; and
the heteroaromatic ring is optionally substituted with 1 or 2 substituents each of which is independently halogen, -C1.4 alkyl, or oxo;

and all other variables are as originally defined above;
or a pharmaceutieally acceptable salt thereof.
A sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (I), wherein

R8 is:
(1) -II,
(2) -C]-4 alkyl, which is optionally substituted with 1 or 2
substituents each of which is independently -OH, -O-Ci-4 alkyl. -OCF3, -C(=0)Ra, -C()2Ra, -SRa, -N(RaRb), or -C( O)N(RaRb),
(3) -C(=0)Ra,
(4) -C02Ra,
(5) -C(-0)N(RaRb),

(6) -C(=0)-(CH2) 1 -2-N(RaRb),
(7) -SO?Ra,
(8) -(CII2)l-2-Rm,
(9) -(CM2)0-2-C(=O)-(CH2)0-2-Rm,
(10) -C(=O)-O-(CH2)0-2-Rm, or
(11) -C(-O)N(Ra)-(CH2)0-2-Rm;
R10 is -H, -OH, -C | -4 alkyl, -O-C i .4 alkyl, -N(RaRb), or -0-(CH2) 1 -2-Rm ;
R12 is
(1) -II,
(2) -C1_4 alkyl, which is optionally substituted with 1 or 2
substituentseach of which is independently -OH, -O-C 1.4 alkyl, -OCF3, -C(=0)Ra, -C02Ra, -SRa, -N(RaRb), or -C( O)N(RaRb),
(3) -C( 0)Ra,
(4) -C02Ra,
(5) -C(K))-(CH2) 1 -2-N(RaRb), or
(6) -S()2Ra;
R2 is methyl;
R3 is -H or methyl;
R4 is -CH2-phenyl. wherein the phenyl is optionally substituted with from 1 to 3 substiluents each of which is independently fluoro, brorno, chloro, -OH, -C)-4 alkyl, -Ci_4 fluoroalkyl. -O-C 1.4 alkyl, -O-C 1.4 fluoroalkyl, -(CH2)l-2-N(RaRb), -S02Ra, -(CI l2)0-2-CO2Ra, -(CI h)0-2-N(Ra)CO2Rb, -NO2, -SRa, -N(RaRb) or phenyl; and
each Ra and Rb is independently -H or -C]-4 alkyl;
or a pharmaceutically acceptable salt thereof.
In an aspect of this subclass, R4 is -Cll2-phenyl, wherein the phenyl is
optionally substituted with from 1 to 3 substituents-each of which is independently

fluoro, bromo, chloro, -Ol-l, -C|-4 alkyl, -Cj-4 fluoroalkyl, -O-Ci-4 alkyl. -O-Cj-4 fluoroalkyl, -(CH2) I -2-N(RaRb), -S02Ra, -(CH2)0-2-CO2Ra, -(CM2)0-2-N(Ra)C()2Rb, -NO?, or phenyl.
Another elass of the present invention includes any compound of Formula (III):
wherein R2 is:
(1) -C1-6 alkyl,
(2) -C | -6 alkyl substituted with -N(RaRb),
(3) -C 1 _6 alkyl substituted with phenyl which is:
(a) optionally substituted with from 1 to 4
substituents each of which is independently halogen, -C1_4
alkyl, -C1-4 haloalkyl, -0-C]-4 alkyl, -O-C1-4 haloalkyl, or
-Co-6 alkyl-N(RaRb); and
(b) optionally mono-substituted with -C1-4 alkyl
substituted with a 5- or 6-membered saturated heterocyclic ring
containing from 1 to 3 heteroatoms selected from 1 or 2 N
atoms, 0 or 1 O atoms, and 0 or 1 S atoms;
wherein the heterocyclic ring is optionally substituted
with from 1 to 3 substituents each of which is independently -C1-6 alkyl, oxo, or a 5- or 6-membered heteroaromatic ring
containing from 1 to 3 heteroatoms selected from 1 to 3 N
atoms. 0 or 1 O atom, and 0 or 1 S atom;
(4) -C1-6 alkyl optionally substituted with -OH and substituted with a 5-
or 6-membered saturated monocyclic hetcrocycle which contains from 1 to 3 heteroatoms selected from I to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heterocycle is optionally substituted with

from 1 to 4 substituents each of which is independently -Ci-6 alkyl, -0-C|_6 alkyl, oxo, or phenyl; or (5) -C | _6 alkyl substituted with a 5- or 6-membered heteroaromatic ring
which contains from 1 to 3 heteroatoms selected from I to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heteroaromatic ring is
optionally substituted with from 1 to 4 substituents each of which is independently -C i _6 alkyl, -O-C | _6 alkyl, oxo, or phenyl;
and all other variables are as originally defined above; or a pharmaceutical ly acceptable salt thereof.
A sub-class of the preceding class of compounds of the present
invention includes any compounds of Formula (111) exactly as defined in the preceding class, except that when R2 is -C | _6 alkyl substituted with -N(RaRb), it is with the
proviso that -N(RaRb) is not attached to the carbon atom in the -Cj_6 alkyi group that
is attached to the ring nitrogen (i.e., that the -N(RaRb) group is not attached to the carbon atom alpha to the ring nitrogen).
Another sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (111), wherein
R2 is:
(1) -C1-4 alkyl,
(2) -(CH2)l-3-N(RaRb),
(3) -(CH2)l-3-phenyl, wherein the phenyl is:
(a) optionally substituted with from 1 to 3
substituents each of which is independently fluoro, chloro, bromo, -C1--4 alkyl, -CF3, -0-C1-4 alkyl, -O-CF3, or
-(CH2)l-3-N(RaRb);and
(b) optionally mono-substituted with
-(CH2) 1 -3-saturated heterocyclic which is a 5- or 6-membered
saturated heterocyclic ring containing from 1 to 3 heteroatoms

atoms, wherein the heterocyclic ring is optionally substituted
with from 1 to 3 substituents each of which is independently -C|_4 alkyl or pyridyl;
(4) -(CH2)l-.Vsalurated heterocycle, wherein the -(CH2)l-3- moiely is
optionally substituted with an -011 and the saturated heterocycle is a 5-
or 6-membered saturated monocyclic heterocycle which contains from
1 to 3 heteroatoms selected from I to 3 N atoms, 0 or 1 O atoms, and 0
or 1 S atoms; wherein the heterocycle is optionally substituted with from 1 to 3 substituents each of which is independently a -C]-4 alkyl;
or
(5) -(CH2)l-3-pyridyl;
R3 is -H or methyl;
R4 is -CI l2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bronio, chloro, -OH, -C]_4 alkyl, -Ci-4 fluoroalkyl, -O-C1-4 alkyl, -O-C1-4 fluoroalkyl, -(CH2)l-2-N(RaRb), -S02Ra, -(CH2)0-2-CO2Ra, -(CH2)0-2-N(Ra)CO2Rb, -N02, -SRa -N(RaRb) 0r phenyl; and
each Ra and Rb is independently is H or -C1-4 alkyl;
or a pharmaceutical!)' acceptable salt thereof.
In an aspect of this subclass, R4 is -CH2-phenyl, wherein the phenyl is
optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -Oil, -C|_4 alkyl, -C1-4 fluoroalkyl. -0-C1_4 alkyl, -O-Cj-4
nuoroalkyi, -(CH2)l-2-N(RaRb), -S02Ra, -(CH2)0-2-CO2Ra,
-(CI l2)0-2-N(Ra)CO2Rb, -NO2, or phenyl.
Another class of compounds of the present invention includes any compound of Formula (1), wherein
RI is -C( Rk is (i) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected from N. O and S, or (ii) a 5- or 6-membered

heteroaromatic ring containing from 1 to 3 heteroatoms independently selected from N.OandS;
and all other variables are as originally defined above;
or a pharmaceutically acceptable salt thereof.
A sub-class of the preceding class of compounds of the present invention includes any compounds of Formula (I), wherein
Rl is -C(==0)NH-(CI-l2)l-2-Rk ; and
Rk is (i) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected from N, O and S, or (ii) a 5- or 6-membered heteroaromatic ring containing from 1 to 3 heteroatoms independently selected from N, O and S;
R2 is methyl;
R3 is -H or methyl;
R4 is -CH2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -C1-4 alkyl, -C1-4 iluoroalkyl, -O-CM alkyl, -O-C1-4 fluoroalkyl, -(CH2)l-2-N(RaRb), -S02Ra, -(CI l2)0-2-CO2Ra, -(CIl2)0-2-N(Ra)CO2Rb, -N02- -SRa, -N(RaRb) 0r phenyl; and
each Ra and Rb is independently -H or -C1-4 alkyl;
or a pharmaceutical ly acceptable salt thereof.
In an aspect of this subclass, R4 is -CI l2-phenyl. wherein the phenyl is
optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -C|_4 alkyl, -Ci-4 fluoroalkyk -O-Ci-4 alkyl, -O-Cj-4
fluoroalkyl, -(CH2)l-2-N(RaRb), -S02Ra, -(CH2)0-2-CO2Ra, -(CI l2)0-2-N(Ra)CO2Rb, -NO2, or phenyl.

It is to be understood that additional embodiments of the present invention include, but arc not limited to, compounds of Formula I wherein each of two or three or more of R1, R2. R3, R4, Ra, Rb, Rc, Rd, Rk and Rm is independently defined in accordance with its definition in one of the embodiments or an aspect thereof as set forth above, or in accordance with its definition in one of the foregoing classes set forth above or a sub-class or feature thereof. Any and all possible combinations of these variables in Formula I are additional embodiments within the scope of the present invention.
An aspect of the present invention is a compound selected from the group consisting of
N-(2-ethoxybenzyl)--5-hydroxy-l-methyl-2-(4-methylphenyl)-6-oxo-l,6-dihydropyrimidinc-4-carboxamide;
N-(2,3-dimethoxybenzyl)-5-hydroxy-1 -methyl-2-(4-methylphenyl)-6-oxo-1,6-dihydropyrimidine-4-carhoxamidc;
N-(2J-dimethoxybenzyl)-2-{4-|(dimethylamino)methyl]phenyl}-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-nuorobenzyl)-2-{4-|(dimethylamino)methyl]phenyI}-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamidc;
N-(2,3-dimethoxyben/yl)-5-hydroxy-l-methyl-6-oxo-2-[4-(pyrrolidin-l-ylmethyl)phenyl]-l,6-dihydropyrimidine-4-carboxamide;
N-(4-lluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-[4-(pyrrolidin-l-ylmethyI)phenyl]-l,6-dihydropyrimidine-4-carboxamide;
N-(4»fluorobenzyl)-5-hydroxy-l~methyl-6-oxo-2-[4-(piperidin-l-ylmethyl)phenyl]-l,6-dihydropyrimidinc-4-carboxamide;
N-(23-dimethoxybenzyr)-5-hydroxy-l-methyl-2-|4-(morplu)lin-4-ylmethyl)phenyl]-oxo-l,6-dihydropyrimidine-4-carboxamide;

N-(4-nuorobenzyl)-5-hydroxy-l-methyl-2-|'4-(morphoIin-4-ylmethyI)pheny|]-6-oxo-],6-dihydropyrimidinC'4-carboxamide;
N-(4-nuorobenzyl)-5-hydroxy-l-methyl-2-{4'[(4-methvlpiperazin-l-yl)mcthyl [phenyl }-6-oxo-l,6-dihydropyrimidinc-4-carboxamide;
2-{4-[(diethyIamino)methyljphenyl}-N-(2,3-dimethc)\ybenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
2-{4-|(diethylamino)melhyr]phcnyl}-N-(4-flLioroben/.yl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-earboxamide;
2-[(dimethylamino)(phenyl)methylJ-N-(4-nuorobcnzyl)-5-hydroxy-l-methyl-6-oxo-l^-dihydropyrimidine-4-carboxamide;
N-(4--nuorobenzyl)-2-[(4-formylpiperazin-l-yl)(phenyl)methyl]-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-{phcnyl[(pyridin-3-ylmethyl)amino]methyl}-l,6-dihydropyrimidinc-4-carboxamide;
2-benzyl-1-[2-(dimethylamino)ethyl]-N-(4-fluorobenzyl)-5-hydroxy-6-oxo-1,6-dihydropyrimidine-4-carboxamide;
l-[2-(dimethylamino)ethyl|-N-(4-fluorobenzyI)-5-hydroxy-2-(2-methylphenyl)-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-nuorobenzyl)-5-hydroxy-l-methyl-2-(4-mcthylphcnyr)-6-oxo-K6-dihydropyrimidine-4-carboxamide;
2-bcnzyl-N-(23-dimethoxybenzyl)-l-[2-(dimcthylamino)cthyl]-5-hydroxy-6-oxo-l,6-dihydropyrimidinc-4-carboxamide;

2-{4-[(4-ethylpipcrazin-l-yl)methyl]phenyl}-N-(4-fluorobenzyl)-5-hydroxy-l -methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-lluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-{4-[(2-pyridin-3-ylpiperidin-l-yI)mcthyr|phenyI}-I,6-dihydropyrimidine-4-carboxamide;
N-(4-nuorobenzyI)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(2,3-dimcthoxybcnzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidinc-4-carboxamide;
N-l4-nuoro-2-(trifluoromethyl)benzyl]-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamidc;
N-(3-chIoro-4-mcthyIben/.yl)-5-hydroxy-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
5-hydroxy-N-[(lR,2S)-2-hydroxy-2,3-dihydro-lH-indcn-l-yl]-l-methyl-2-{4-|(4-methylpiperazin-l-yl)methylJphenyl}-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-2-(4-{[(2R)-2-(methoxymelhyl)pyrrolidin-l-yl|methyl}phenyI)-l-methyI-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-lluorobenzyi)-5-hydroxy-2-(4-{[(2S)-2-(methoxymethyi)pyrrolidin-l-yl]mcthyl} phenyl)-1 -methyl-6-oxo-l,6-dihydropvrimidine-4-carboxamide;
N-(4-nuorobenzyl)-2-(4-{|(4-nuorobenzyl)aminoJmethyl}phenyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyriinidine-4-carboxamide;
2-benzyl-N-(4-fluorobenzyI)-5-hydroxy-l-(2-morpholin-4-ylethyl)-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
l-f2-(dimethylamino)cthyr|-N-(4-fluorobenzyl)-5-hydroxy-6-oxo-l,6-dihydropyrimidine-4-carboxamide;

N-(4-fluorobenzyI)-5-hydroxy-6-oxo-l-(pyridin-3-ylmethyI)-l,6-dihydropyrimidine-4-carboxamide;
2-bcnzyl-N-(4-fluorobenzyl)-5-hydroxy-6-oxo-l-(2-pyrrolidin-I-ylethyl)-l,6-dihydropyrimidine-4-carboxamide;
2-bcnzyl-N-(4-fluorobcnzyl)-5-hydroxy-6-oxo-l-(2-pipcridin-l-ylethyl)-l,6-dihydropyrimidinc-4-carboxamide;
2-(l-bcnzylpiperidin-2-yl)-N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidinc-4-carboxamide;
N-(4-nuorobcnzyl)-5-hydroxy-l-methyl-2-(l-methylpipcridin-2-yl)-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
2-( 1 -benzylpiperidin-3-yl)-N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide;
l-{3-[(dimethyIamino)rncthyl|bcnzyl}-N-(4-nuorobenzyl)-5-hydroxy-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(2,3-dimethoxybcnzyI)-l-[2-(dimethylamino)ethylj-5-hydroxy-6-oxo-l,6-dihydropyrimidine-4 -carboxamide;
N-(2,3-dimethoxybenzyl)-5-hydroxy-6-oxo-l-(pyridin-3-ylmethyl)-l,6-dihydropyrimidine-4-carboxamide;
N4-(4-fluorobenzyl)-5-hydroxy-l-methyl-N2-(2-morpholin-4-ylethyl)-6-oxO"l,6-dihydropyrimidine-2,4-dicarboxamide;
N-(4-fluorobenzyl)-5-hydroxy-6-oxo-l-f3-(pyrrolidin-l-ylmcthyl)benzyl]-l,6-dihydropyrimidine-4-carboxamidc;
N-(4-fluorobcnzyl)-5-hydroxy-1 -[3-(morphoiin-4-ylmelhyl)benzyl]-6-oxo-1.6-dihydropyrimidine-4-carboxamide;

N-(4-fluorobenzyl)-5-hydroxy-l-{3-|X4-methyIpipcra//in-l-yl)methyl]ben/yl} -6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-6-oxo-l-{3-[(4-pyridin-2-y!piperazin-l-yl)methyl]benzyl}-1.6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-l-I2-(morpholin-4-ylmctliyI)benzyl]-6-oxo-l,6-dihydropyrimidinc-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-6-oxo-l-{2-[(4-pyridin-2-ylpiperazin-l-yl)methyI|benzyl}-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-pyrrolidin-2-yl-l,6-dihydropyrimidine-4-carboxamidc;
N4-(4-fluorobenzyI)-5-hydroxy-1 -methyi-6-oxo-N2-(pyridin-2-yimethyl)-1,6-dihydropyrimidine-2,4-dicarboxamide;
N-(4-fluorobenzyl)~5-hydroxy-1 -(2-hydroxy-3-morpholin-4-yIpropyl)~6-oxo-1,6-dihydropyrimidine-4-carboxamidc;
N-(4-fluorobenzyl)-5-hydroxy-l-[4-(morpholin-4-ylmcthyl)bcnzyi]-6-oxo-l,6-dihydropyrimidine-4-carboxarnide;
N-(4-fluorobenzyl)-5-hydroxy-1 -methyI-2-(2-morpholin-4-ylethyl)-6-oxo-1,6-dihydropyrimidine-4-earboxarnide;
2-(2,2-dimethoxyethyl)-N-(4-fluorobcnzyl)-5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide;
2-(2.3-dihydro-llI-indol-2-yl)-N-(4-fluorobenzyl)-5-hydroxy"l-methyI-6-oxo-l,6-dihydropyrimidine-4-carboxamide;

2-[2-(4-benzoylpipcrazin-l-yl)ethyl]-N-(4-fluorobenzyl)-5-hydroxy-I-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxarnide;
2-\ l-(N,N-dimethyIglycyt)pipcridin-2-yl]-N-(4-fluorobenzyI)-5-hydroxy-l-mcthyI-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyi)-5-hydroxy-l-methyl-2-(]-methyl-2,3-dihydro-l H-indol-2-yi)-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-!-methyl-6-oxo-2-(l,2,3.4-tctrahydroquinoIin-2-yI)-1.6-dihydropyrimidine-4-carboxamide;
N-(4-iluorobcnzyl)-5-hydroxy-i-methyl-2-(l-methyl-1,2,3,4-tetrahydroquinolin-2-yI)-6-oxo-l,6-dihydropyrimidinc-4-carboxamide;
tcrt-butyl (2S,4R)-4-(bcnzyloxy)-2-(4-{[(4-fluorobcnzyl)amino]carbonyl}-5-hydroxy-l-mcthyl-6-oxo-l,6-dihydropyrimidin-2-yl)pyrrolidine-l-carboxylate;
tcrt-butyl (2S,4R)-2-(4-{[(4-fluorobenzyl)aminojcarbonyl}-5-hydroxy-l-mcthyl-6-oxo»K6-dihydropyrimidin-2-yl)-4-hydroxypyrrolidine-l-carboxylate;
2-[(2S,4R)-4-(benzyIoxy)pyrrolidin-2-yl]-N-(4-fluorobcnzyr)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-lluorobenzyl)-5-hydroxy-2-[(2S,4R)-4-hydroxypyrrolidin-2-yl]-l-methyl-6-oxo-I,6-dihydropyrimidinc-4-carboxamide;
N-(4-nuorobenzyl)-5-hydroxy-2-[(2S,4R)-4-hydroxy-l-methylpyrrolidiri'2-yl]-l-methvl-6-oxo-l,6-dihydropyrimidinc-4-carboxamidc;
2-( (2S,4R)-4-(benzyloxy)-1 -mcthylpyrrolidin-2-yl |-N-(4-fluorobenzyl)-5-hydroxy-1 -mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamidc;
2-l(2S,4R)-l-benzoyl-4-(bcnzyloxy)pyrrolidin-2-yl]-N-(4-nuorobenzyI)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;

2-[i-(N,N-dimethylglycyl)-2,3-dihydro-lH-indol-2-ylj-N-(4-fluorobenzyl)-5-hydroxy-I -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide;
2-( 1 -benzoyl-2,3-dihydro- ] I I-indol-2-yi)-N-(4-fluorobcnzyl)-5-hydroxy-1 -methyi-6-oxo-l,6-dihydropyrimidinc-4-carboxamide;
N-(4-iluorobenzyl)~5-hydroxy-1 -methyl-6-oxo-2-| 1 -(pyridin-2-ylcarbonyl)-2,3-dihydro-1 H-indol-2-yl|- l,6-dihydropyrimidine-4-carboxamide;
tcrt-butyl 3-(4-{[(4-Huorobcnzyl)amino|carbonyl}-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidin-2-yl)-4-mcthylpiperazinc-I-carboxyIate;
N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-2-(4-methylmorpholin-3-yl)-6-oxo-1.6-dihydropyrimidine-4-earboxamide;
(+)-N-(441uorobenzyI)-5-hydroxy-1 -methyl-2-(4-methylmorphoIin-3-yl)-6-oxo-1,6-dihydropyrimidine-4-carboxamide
(-)-N-(4-fiuorobenzyl)-5-hydroxy-1 -methyl-2-(4-methylmorpholin-3 -yl)-6-oxo-1,6-dihydropyrimidine-4-carboxamide
2-(l-ethyI-2,3-dihydro-]II-indol-2-yl)-N-(4-fluorobcnzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
2-(l-benzoylpiperidin-2-yl)-N-(4-fluorobenzyI)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-]-methyI-6-oxo-2-(l-(pyridin-2-ylcarbonyl)piperidin-2-yi|-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyI)-5-hydroxy-1 -methyl-2-(2-methyl-1,2,3,4-tetrahydroisoquinolin-3-yl)-6-oxo-l,6-dihydropyrimidinc-4-carboxamidc;

2-( 1 -bcnzoy]pyrrolidin-2-yl)-N-(4-fluorobenzyl)-5-hydroxy- i -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-| i-(pyridin-2-ylcarbonyl)pyrrolidin-2-yI|-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-2-( 1 -methylpyrrolidin-2-yl)-6-ox 1.6-dihydropyrimidine-4-carboxamide;
2-|(2S,4RH-(benzyloxy)-)-(pyridin-2-ylcarbony])p>Trolidin-2-yl]-N-(4-fluorobenzyl)-5-hydroxy-1 -mcthyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide;
2-| l-(dimethylamino)-2-phcnylcthyl]-N-(4-nuorobcnzyl)-5-hydroxy-l-rnethyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
2-[(2S,4R)"l-benzoyl-4-hydroxypyrrolidin-2-yI|-N'(4-fluorobenzyI)-5-hydroxy-l-mcthyl-6-oxo-l56-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyI)-5-hydroxy-2-(l-isobutyl-2J-dihydro-lH-indol-2-yl)-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-2-( 1-isopropyi-2,3-dihydro-1 H-indoi-2-yI)-1-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
2-|l-(N,N-dimethylglycyl)pyrrolidin-2-yI]-N-(4-nuorobcnzyl)-5-hydroxy-l-methyl-6-oxo-L6-dihydropyrimidine-4-carboxamide;
2-{ l-[(6-bromopyridin-2-yl)carbonyljpyrrolidin-2-yl}-N-(4-fluorobenzyl)-5-hydroxy-I-mcthyI-6-oxo~l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)o-hydroxy-1 -methyl-2-( 1 -methylpiperazin-2-yl)-6-oxo-1,6-dihydropyrimidine-4-earboxamide;
2-(! -bcnzoyl-4-mcthylpipcrazin-2-yI)-N-(4-iluorobcnz\l)-5--hydroxy-1 -methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;

N-(4-fluorobenzyI)-5-hydroxy-1 -methyI-6-oxo-2-| 1 -(pyridin-2-ylcarbonyI)-1,2,3,4-tetrahydroquinoIin-2-yI]-I,6-dihydropyrimidine-4-carboxamide;
2-( i -acetylpyrroIidin-2-yI)-N-(4-fluorobenzyI)-5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide;
2-[ I -(cyclopropyicarbonyl)pyrrolidin-2-yl]-N-(4-nuorobenzyl)-5-hydroxy-1 -methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-l-methyl-2-| l-(methylsulfonyI)pyrrolidin-2-yI|-6-oxo-l,6-dihydropyrimidinc-4-carboxamide;
N-(4-iluorobenzyl)-5-hydroxy-l-methyl-2-{l-[(4-mcthylmorpholin-3-yl)carbonylJpyrrolidin-2-yl}-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
2-( 1,4-dimethylpipcrazin-2-yl)-N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo-1.6-dihydropyrimidine-4-carboxamide;
N-(4-nuorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-[I-(pyridin-3-ylcarbonyl)pyrrolidin-2-yi ]-1,6-dihydropyrimidine-4-carboxamide;
2-[(2S.4R)-]-acetyl-4-(benzyloxy)pyrrolidin-2-yl]-N-(4-fluorobenzyI)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyI)-5-hydroxy-2-( 1-isonicotinoylpyrrol idin-2-yl)-1-mcthyl-6-oxo-1,6-dihydropyrimidine-4-carboxamidc;
2-{ I-[(ethylamino)carbonyl|pyrroIidin-2-yi}-N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide;
N-(4-lluorobenzyl)-5-hydmxy-l-methyl-2-{ 1-[(1-methyl-1 H-imidazol-2-yl)carbonyl]pyrrolidin-2-yI}-6-oxo-1,6-dihydropyrim id ine-4-carboxamide;

2--[(2S,4R)-I-acetyl-4-hydroxypyrrolidin-2-yl]-N-(4-riuorobenzyl)-5-hydroxy-l-
methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide; .
2-| l-(anilinocarbonyl)pyrrolidin-2-ylJ-N-(4-lluoroben/yl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carbo\amide;
2-(4-cthyl-l-methylpipera/in-2-yl)-N-(4-fluorobcnzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4~nuorobenzyl)-5-hydroxy-1 -methyl-2-{ 1 -|( I -oxidopyridin-2-yl)carbonyl|pyrrolidin-2-yi}-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyI)-5-hydroxy-1 -methy!-6-oxo-2-| I -(pyrazin-2-ylcarbonyl)pyrrolidin-2-yl |-! ,6-dihydropyrimidine-4-carboxamide;
2-[(4R)-3-acetyl-l,3-thiazolidin-4-yl]-N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-1.6-dihydropyrimidinc-4-carboxamide;
N-(4-nuorobenzyl)-5-hydroxy-I-melhyl-2-| l-methyl-4-(methylsulfonyl)pipcrazin-2-yI|-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-nuorobenzyl)-5-hydroxy-l-methyI-2-(4-methyIthiomorpholin-3-yl)-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-[4-nuoro-2-(mcthylsulfbnyI)benzyl]-5-hydroxy-Uinethyl-6-oxo-2-[l-(pyrazin-2-ylcarbonyI)pyrrolidin-2-yI]-l,6-dihydropyrimidinc-4-carboxamide;
2-(i-acetylpyrrolidin-2-yi)-N-(4-fluoro-2-(mcthyIsuironyI)benzyl]-5-hydroxy-l-methyl-6-oxo-I,6-dihydropyrimidine-4-carboxamidc;
2-(3-acctyI-l,3-thiazolidin-2-yl)-N-(4-fluorobcnzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
2-( I-(acetylamino)-l-melhylethyl]-N-(4-fluorobcnzyI)-5-hydroxy-l-methyl-6-oxo-l,6-dihvdropyrimidine-4-carboxamide;

2-( I -acetylpyrrolidin-2-yl)-N-(2-ethoxybenzyl)-5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidinc-4-carboxamide;
2-(4-acetyl-l-methylpiperazin-2-yI)-N-(4-fluorobcnzyl)-5-hydroxy-l-methyl-6-oxo-1.6~dihydropyrimidinc-4-carboxamide;
N-(4-fluorobenzyI)-5~hydroxy-1 -methyl-2-[ 1 -meihyl-4-(pyrazin-2-ylcarbonyl)piperazin-2-yl |-6-oxo- 1,6-dihydropyrim id inc-4-carboxamide;
2-(l-acetylpyrrolidin-2-yI)-5-hydroxy-l-methyl-N-[2-(methylthio)benzyl]-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-nuorobenzyl)-5-hydroxy-2-{l-[(lH-imidaxol-5-ylcarbonyl)amino]-l-mcthylethyl}-l-mcthyi-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
2-| l-benzoyl-4-(pyrazin-2-ylcarbonyl)piperazin-2-yl]-N-(4-fluorobenzyl)-5-hydroxy-i-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxcimide;
2-(4-benzoyl-l-mcthylpiperazin-2-yl)-N-(4-fIuorobenzyl)-5-hydroxy-I-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
2-[4-(benzyloxy)-l-(pyrazin-2-ylcarbonyl)pyrrolidin-2-yl]-N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidinc-4-carboxamide;
2-( I -acetyIpyrrolidin-2-yl)-N-(2,3-dimethoxybenzyl)-5 -hydroxy- l-methyl-6-oxo-1,6-dihydropyrimidinc-4-carboxamide;
2-( i -acetyIpyrroIidin-2-yl)-5-hydroxy-N-(2-methoxybenzyl)-l -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide;
Nl-|'l-(4-{[(4-fluorobcnzyI)amino]carbonyI}-5-hydroxy-l-melhyl-6-oxo-l,6-dihydropyrimidin-2-yl)-!~methyIethyl)-N2,N2-dimethylethancdiamidc;

2-(I-acetyIpyrroIidin-2-yl)-N-|2-(dimethylamino)benzyI]-5-hydrox> l-methyl-6-oxo-l,6-dihydropyrimidinc-4-carboxamide;
2-| (2S)-1 -acetylpyrrolidin-2-yl]-N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-earboxamide;
N-(4~lluorobenzyl)-5-hydroxy-2-f4-hydroxy-l-(pyra/.in-2-y!carbonyl)pyrrolidin-2-yI]-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamidc;
N-| l-(4-{[(4-fluorobcnzyl)amino]carbonyl}-5-hydroxy-]-mcthyl-6-oxo-l,6-dihydropyrimidin-2-yl)-l-methylethyl]imidazo[2J-b]| l,3]thiazo!e-6-carboxamide;
2-|(2S,4S)-l-acctyI-4-nuoropyrroIidin-2-ylJ-N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidinc-4-carboxamide;
N-(4-iluorobenzyl)-5-hydroxy-1-methyl-2-{l-methyl-4-[(l-methyl-1 H-imidazol-2-yI)carbonyljpiperazin-2-yl}-6-oxo-I,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-1 -methyI-2-( I -methyl-1 -{[(5-methyI-1,3,4-oxadiazol-2-yl)carbonyl]amino}ethyl)-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
Nl-J l-[4-({f4-fluoro-2-(methylsuIfonyl)benzyl]amino}carbonyl)-5-hydroxy-I-
mcthyi-6-oxo-l,6-dihydropyrimidin-2-yl]-l-methylethyI}-N2,N2-
dimethylethanediamide;
2-(4-acetyI-l,2-dimethylpiperazin-2-yl)-N-(4-fluorobcnzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-| I-(pyrimidin-4-ylcarbonyl)pyrrolidin-2-yl]-l,6-dihydropyrimidine-4-earboxamide;
N-(4-fluorobenzyl)~5-hydroxy-l-methyl-6-oxo-2-[ l-(pyrimidin-5-yIearbonyl)pyrrolidin-2-yl]-I,6-dihydropyrimidine-4-earboxamide;

N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-2-{ 1 -methyl-1 -[(1 H-pyrazol-5-yIcarbonyl)amino|ethyl}-6-oxo-I,6-dihydropyrimidine-4-carboxamide;
2-[(2R,4R)-l-acelyl-4-methoxypyrroIidin-2-yrj-N-(4-ilLiorobenzyl)o-hydroxy-l-methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide;
2-{ l-[(dimethylamino)(oxo)acetyl]pyrrolidin-2-yl}-N-(4-fluorobenzyl)-5-hydroxy-l-methyI-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-{l-|"4-({[4-fluoro-2-(mcthylsulfonyI)benzyl]amino)carbonyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidin-2-yl]-l-methyiethyl}imidazo[2, l-b][l,3]thiazole-6-carboxamide;
2-| _(2R,4R)-1 -bcnzoyI'4-iTiclhoxypyrrolidin-2-yrj-N-(4-l1uorobenzyl)-5-hydroxy-1 -meth\i-6-oxo-l,6-dihydropyrimidine-4-carboxamidc;
N-(4-(luorobenzyl)-5-hydroxy-2-[4-(isopropylsulfonyl)-l-methylpiperazin-2-yl]-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
2-[l,2-dimcthyl-4-(mcthylsulfonyi)piperazin-2-yl]-N-(4-fluorobenzy!)-5-hydroxy-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-2-[(2S,4R)-4-methoxy-l-methyIpyrrolidin-2-yl]-l-methyl-6-oxo-l,6-dihydixipyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-l-methyl-2-{l-|"(rnethylsulfonyl)acetyI]pyrroIidin-2-yl}-6-oxo-I,6-dihydropyrimidinc-4-carboxamide;
2-[(2S)-l-acetyl-4,4-difluoropyrroIidin-2-yl]-N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo- l,6-dihydropyrimidinc-4-carboxamide;
2-l(2R,4R)-l-acctyI-4-ethoxypyrrolidin-2-ylJ-N-(4-iliK)robcnzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;

2-|(2S)-4,4-difluoro-l-methylpyrrolidin-2-yij-N-(4-nuorobenzyl)-5-hydroxy-]-methyI-6-oxo-l,6-dihydropyrimidine-4-carboxamidc;
N-(2.3-dimethoxybenzyl)-5-hydroxy-1 -methyl-6-oxo-2-l 1 -(pyridazin-3-ylcarbonyl)pyrrolidin-2-y!]-I,6-dihydropyrimidinc-4-carboxamide;
N-(4-fluorobenzyI)-5-hydroxy-1 -methyl-2-( 1 -methyl-1 - {[morpholin-4-yl(oxo)acetyI]amino} cthyl)-6-oxo-1,6-dihydropyrim idine-4-carboxamide;
2-{(2R,4R)-l-f(diinethylamino)(oxo)acetyIj-4-mcthoxypyrrolidin-2-yl}-N-(4-fluorobenzyl)-5-hydroxy-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
2-((2S)-4,4-difluoro-l-(pyrazin-2-ylcarbonyI)pyrrolidin-2-ylJ-N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyI)-5-hydroxy-1 -methyl-2-{(2S,4S)-1 -methyI-4-[(mcthylsulfonyl)amino |pyrrol id in-2-yl}-6-oxo-1,6-dihydropyrim idine-4-carboxamide;
2-{l-[(dimethylamino)sulfonyi|pyrroIidin-2-yl}-N-(4-fluorobcnzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamicic;
2-{(2R,4R)-4-ethoxy-l-((methylamino)(oxo)acetyl]pyrrolidin-2-yl}-N-(4-fluorobenzyl)-5-hydroxy-l-mcthyI-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
2-|(2S)-4,4-difluoro-l-(pyridazin-3-ylcarbonyI)pyrrolidin-2-yl]-N-(4~tluorobenzyl)-5-hydroxy-]-methyl-6-oxo-K6-dihydropyrimidinc-4-carboxamide;
2-[(2S)-4,4-difluoro-l-(pyridiiv2-ylcarbonyl)pyrrolidin-2-ylj-N-(4-fluorobenzyl)-5-hydroxy-]-methyl-6-oxo-i,6-dihydropyrimidine-4-carboxamide;
2-{(2S)-l-[(dimethylamino)(oxo)acctylj-4,4-dinuoropyrrolidin-2-yl}-N-(4-fluorobenzyl)-5-hydroxy-l -mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide:

N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-2-{ 1 ~[morpholin-4-yl(oxo)acety!]pyrrolidin-2-yl)-6-oxo-l,6-dihydropyrimidine-4-carboxamidc;
2-{(2S)-l-[(dimethylamino)(oxo)acetyl]pyrrolidin-2-yI}-N-(4-fluorobenzyl)-5-hydroKy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamidc;
2-{(2S)-l-[(dimethyIamino)(oxo)acetyl]pyrrolidin-2-yl}-N-(4-fluoro-2-mcthoxybenzyl)-5-hydroxy-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
Nl-| l-(4-{[(4-fluorobcnzyl)amino]carbonyl}-5-hydroxy-l-methyl-6-oxo-l16-dihydropyrimidin-2-yl)-l-mcthylethyl]-Nl,N2,N2-lrimclhylcthanediamide;
2-((2S)-l-acetylpyrroIidin-2-y!l-N-(4-fluoro-2-methoxybenzyl)-5-hydroxy-l-methyI-6~oxo-l,6-dihydropyrimidinc-4-carboxamide;
N-(4-nuorobenzyl)-2-[(2S,4S)-4-nuoro-l-rnethylpyrrolidin-2-yI]-5-hydroxy-l-methyI-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
2-{(2S,4S)-]-[(dimcthylamino)(oxo)acetyl]-4-fluoropyrrolidin-2-yl}-N-(4-niiorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
Nl-| i-(4-{[(3-chloro-4-iluorobenzyl)amino]carbonyl}-5-hydroxy-l-mcthyl-6-oxo-K6'dihydropyrimidin-2-yl)-l-mcthylethyl]-N2,N2-dimethylethanediamide;
and pharmaceutically acceptable salts thereof.
Another aspect of the present invention is a compound selected from the group consisting of:
N-(4-nuorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-f l-(pyrazin-2-ylcarbonyI)pyrrolidin-2-yl |-1,6-dihydropyrimidine-4-carboxamide;
2~|(2S,4R)-l-benzoy]-4-hydroxypyrrolidin-2-yl]-N-(4-fluoiobenzyl)-5-hydroxy-l-methyl-6-oxo-K6-dihydropyrimidine-4-carboxamidc;

N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-2-{ 1 -((1 -oxidopyridin-2-yI)carbonyl]pyrrolidin-2-yij~6-oxo-i,6-dihydropyrimidine-4-carboxamide;,
2-( I -acetylpyrrolidin-2-yI)-N-(4-f1uorobenzyl)-5-hydroxy-1 -methyl-6-oxo-1.6-dihydropyrimidine-4-carboxamide;
2-f(2S,4R)-4-(benzyloxy)-l-(pyridin-2-ylcarbonyI)pyrrolidin-2-yl]-N-(4-fliior()benzyl)-5-hydroxy-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-1 -methyI-2-(4-methylmorpholin-3-yl)-6-oxo-1,6-dihydropyrimidine-4-carboxamide;
(0-N-(4-fluorobenzyl)-5-hydro\y-1 nriethyl-2-(4-methylmorpholin-3-yl)-6-oxo-1,6-dihydropyrimidine-4-carboxamide
(-) -N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-2-(4-mcthylmorpholin-3-yl)-6-oxo-1,6-dihydropyrimidine-4-carboxamide
N-(4-(luorobenzyl)-5-hydroxy-1 -methyl-6-oxo-2-[ 1 -(pyridin-2-ylcarbonyI)pyrroiidin-2-yl|-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyI)~5-hydroxy-1 -methyl-6-oxo-2-[ 1 -(pyridin-2-ylcarbonyl)-1,2,3,4-tctrahydroquinolin-2-yl]-1,6-dihydropyrimidine-4-carboxamide;
2-[(2S.4R)-l-benzoyl-4-(bcnzyloxy)pyrroiidin-2-yl]-N-(4-lluorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamidc;
2-[(2S,4R)-I-acetyl-4-(bcnzyIoxy)pyrroIidin-2-yl]-N-(4-fluorobenzyI)-5-hydroxy-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamidc;
N-(4-nuorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-| I-(pyridin-3-ylcarbonyl)pyrrolidin-2-yl |-1,6-dihydropyrimidinc-4-carboxamide;
N-(4-nuorobenzyI)-5-hydi'oxy-2-(l-isonicotinoylpyrrolidin-2-yl)-l-methyl--6-oxo-K6-dihydropyrimidinc-4-carboxamide;

2-( 1,4-dimethylpiperazin-2-yI)-N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-qxo-1,6-dihydropyrimidinc-4-carboxamide;
N-(4-nuorobenzyi)-5-hydroxy-1 -methyl-2-{ 1 -| (I -methyl-1 H-imidazol-2-yl)carbonyI]pyrrolidin-2-yl}-6-oxo-1,6-dihydropyrim id ine-4-carboxamide;
2-(l-benzoylpyrrolidin-2-yl)-N-(4-i1uorobenzyI)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-l-methyi-2-( l-(methylsulfonyl)pyrrolidin-2-yI|-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
2-|(4R)-3-acetyl-l,3-thiazolidin-4-ylJ-N-(4-nuorobenzyl)-5-hydroxy-l-methyl-6-oxo-1,6-dihydropyrim idinc-4-carboxamide;
2-{ l-|(ethylamino)carbonyl|pyrrolidin-2-yl}-N-(4-nuorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
2-(4-ethyl-l-methylpiperazin-2-yl)-N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-1.6-dihydropyrimidine-4-carboxamide;
2-|(2S,4R)-4-(benzyloxy)-l-methylpyrrolidin-2-yl]-N-(4-fluorobenzyl)-5-hydroxy-l-melhyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo-2-[ 1 -(pyridin-2-ylcarbonyl)-2,3-dihydro-lH-indol-2-yl]-I,6-dihydropyrimidine-4-carboxamide;
N-(4-fluorobenzyl)-5-hydroxy-1 -mcthyl-2-( 1 -methyl-1,2,3,4-tetrahydroquinolin-2-yl)-6-oxo-l,6-dihydropyrimidine-4-carboxamide;
N-(4-nuorobenzyl)-5-hydroxy-l-methyl-2-(2-mcthyl-1,2,3,4-tetrahydroisoquinoIin-3-yl)-6-oxo-I,6-dihydropyrimidine-4-carboxamide;

2-j 1 -(dimethylamino)-2-phenylethyl]-N-(4-fluoroben/.yl)-5-hydroxy-1 -methy 1-6-oxo-
l,6-dihydropyrimidine-4-carboxamidc; ;■.
2-|(dimethylamino)(phenyl)methyl]-N-(4-fluoroben/yl)-5-hydroxy-l-methy 1-6-oxo-I,6~dihydropyrimidine-4-carboxamide;
N-(2,3-dimethoxybenzyl)-5-hydroxy-l-methyl-2-(4-(morpholin-4-ylmethyl)phenyl]-6-oxo-1,6-dihydropyrimidine-4-carboxamide;
and pharmaceuticaliy acceptable salts thereof.
Other embodiments of the present invention include the following:
(a) A pharmaceutical composition comprising a compound of Formula (1) and a pharmaceutically acceptable carrier.
(b) A pharmaceutical composition which comprises the product prepared by combining (e.g., mixing) an effective amount of a compound of Formula (I) and a pharmaceutically acceptable carrier.
(c) The pharmaceutical composition of (a) or (b), further comprising a therapeutically effective amount of an HIV infection/AIDS treatment agent selected from the group consisting of HIV/AIDS antiviral agents, immunomodulators, and anti-infective agents.
(d) The pharmaceutical composition of (c), wherein the HIV infection/AIDS treatment agent is an antiviral selected from the group consisting of HIV protease inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, and nucleoside HIV reverse transcriptase inhibitors.
(e) A combination useful for inhibiting HIV integrase, for treating or preventing infection by HIV, or for preventing, treating or delaying the onset of AIDS, which is a therapeutically effective amount of a compound of Formula (I) and a therapeutically effective amount of an HIV infection/AIDS treatment agent selected from the group consisting of HIV/AIDS antiviral agents, immunomodulators. and anti-infective agents.
(i) The combination of (e), wherein the HIV infection/AIDS treatment agent is an antiviral selected from the group consisting of HIV protease inhibitors, non-nucleoside HIV reverse transcriptase inhibitors and nucleoside HIV reverse transcriptase inhibitors.

(g) A method of inhibiting HIV integrase in a subject in need thereof which comprises administering to the subject a therapeutically effective amount of a compound of Formula (I).
(h) A method of preventing or treating infection by HIV in a subject in need thereof which comprises administering to the subject a therapeutically effective amount of a compound of Formula (I).
(i) The method of (h), wherein the compound of Formula (I) is administered in combination with a therapeutically effective amount of at least one antiviral selected from the group consisting of HIV protease inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, and nucleoside HIV reverse transcriptase inhibitors.
(j) A method of preventing, treating or delaying the onset of AIDS in a subject in need thereof which comprises administering to the subject a therapeutically effective amount of a compound of Formula (I).
(k) The method of (j), wherein the compound is administered in combination with a therapeutically effective amount of at least one antiviral selected from the group consisting of HIV protease inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, and nucleoside HIV reverse transcriptase inhibitors
(I) A method of inhibiting HIV integrase in a subject in need thereof which comprises administering to the subject the pharmaceutical composition of (a), (b). (c) or (d) or the combination of (e) or (f).
(m) A method of preventing or treating infection by HIV in a subject in need thereof which comprises administering to the subject the pharmaceutical composition of (a), (b), (c) or (d) or the combination of (e) or (f).
(n) A method of preventing, treating or delaying the onset of AIDS in a subject in need thereof which comprises administering to the subject the pharmaceutical composition of (a), (b), (c) or (d) or the combination of (e) or (f).
The present invention also includes a compound of the present invention (i) for use in, (ii) for use as a medicament for. or (iii) for use in the preparation of a medicament for: (a) inhibiting HIV protease, (b) preventing or treating infection by HIV, or (c) preventing, treating or delaying the onset of AIDS. In these uses, the compounds of the present invention can optionally be employed in combination with one or more HIV/AIDS treatment agents selected from HIV/AIDS antiviral agents, anti-infective agents, and immunomodulators.

Additional embodiments of the invention include the pharmaceutical compositions, combinations and methods set forth in (a)-(n) above and the jjses set forth in the preceding paragraph, wherein the compound of the present invention employed therein is a compound of one of the embodiments, aspects, classes, subclasses, or features of the compounds described above. In all of these embodiments, the compound may optionally be used in the form of a pharmaceutical^ acceptable salt.
As used herein, the term tkC) _6 alkyl" (or "C l -C6 alkyl") means linear
or branched chain alkyl groups having from 1 to 6 carbon atoms and includes all of
the hexyl alkyl and pentyl alkyl isomers as well as n-, iso-, sec- and t-butyl, n- and isopropyl, ethyl and methyl. "C]-4 alkyl" means n-, iso-, sec- and t-butyl, n- and
isopropyl, ethyl and methyl.
The term "Co" as employed in expressions such as UCQ-6 alkyl" means
a direct covalent bond. For example, when Rl in Compound 1 is -CO-6 alkyl-O-Co-6 alkyl-Rk, then Rl is -O-Rk when both alkyl groups are Co alkyl. Similarly, when an
integer defining the presence of a certain number of atoms in a group is equal to zero, it means that the atoms adjacent thereto are connected directly by a bond. For
example, the compound of Formula (II) has T as a substituent at the 2-
position of the pyrimidinone ring, wherein s is an integer equal to zero, 1 or 2. When
s is zero, the substituent has the following structure: T
The term M-Cj-6 alkyl-" refers to a Ci to C^ linear or branched alkyl
group as just defined which is bivalent. It can alternatively be referred to as "Ci-6 alkylene" or "Ci-6 alkancdiyl". A class of alkylenes of particular interest with respect to the invention is -(CH2)l-6-- and sub-classes of particular interest include -(CH2)l-4-, -(CH2)l-3% -(CH2)l-2-, and -CH2-.
The term "C?-5 alkynyl" (or "C2-C5 alkynyl") means linear or
branched chain alkynyl groups having from 2 to 5 carbon atoms and includes all of the
pentynyl isomers as well as 1-bulynyl, 2-butynyl, 3-butvnyl. 1-propynyl, 2-propynyl, and ethynyl (or acctylenyl). Similar terms such as "C'2-3 alkynyl" have an analogous
meaning.
The term "C3-8 cycloalkyl" (or "C3-C8 cycloalkyl") means a cyclic
rinu of an alkane having three to eight total carbon atoms (i.e.. cvclooroDvL

cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, or cyclooctyt). The terms "C3-7
cycloalkyP", "C3-6 cycloalkyl", "C5-7 cycloalky!" and the like have analogous
meanings.
The term "C3-7 azacycloalkyr (or "C3-C7 azacycloalkyl") means a
saturated cyclic ring consisting of one nitrogen and from three to seven carbon atoms (i.e., azetidinyl, pyrrolidinyl, piperidinyl, or azepanyi).
The term "halogen" (or "halo'1) refers to fluorine, chlorine, bromine and iodine (alternatively referred to as fluoro, chloro, bromo, and iodo).
The term "Cj-6 haloalkyl" (which may alternatively be referred to as
"C]-Cg haloalkyl" or "halogenated C]-C6 alky I'") means a C] to Cfr linear or
branched aikyl group as defined above with one or more halogen substituents. The term "C1-4 haloalkyl" has an analogous meaning. The term "C|_6 fluoroalkyl'" has an
analogous meaning except that the halogen substituents are restricted to fluoro. Suitable fluoroalkyls include the series (CH2)0-4CT3 (i.e., trifluoromethyl, 2,2,2-
trilluoroethyl, 3,3,3-trifluoro-n-propyl, etc.).
The term "carbocycle" (and variations thereof such as "carbocyclic" or "carbocyclyl") as used herein refers to (i) a C3 to Cg monocyclic, saturated or
unsaturated ring, (ii) a C7 to C]2 bicyclic ring system, or (iii) aCn to C\^ tricyclic
ring system, wherein each ring in (ii) or (iii) is independent of or fused to the other
ring or rings and each ring is saturated or unsaturated. The carbocycle may be
attached to the rest of the molecule at any carbon atom which results in a stable
compound. The fused bicyclic carbocycles are a subset of the carbocycles; i.e., the term "fused bicyclic carbocycle" generally refers to a C7 to C]0 bicyclic ring system
in which each ring is saturated or unsaturated and two adjacent carbon atoms are shared by each of the rings in the ring system. Fused tricyclic carbocycles have an anaiogous meaning. A subset of the fused bicyclic carbocycles are those bicyclic carbocycles in which one ring is a benzene ring and the other ring is saturated or unsaturated, with attachment via any carbon atom that results in a stable compound. Representative examples of this subset include the following:

The term "aryl" refers to aromatic mono- and poly-carbocyclic ring systems, wherein the individual carbocyclic rings in the polyring systems are fused or attached to each other via a single bond. Suitable aryl groups include phenyl, naphthyl, and biphenylenyl.
The term "heterocycle" (and variations thereof such as "heterocyclic" or "heterocyclyl") broadly refers to (i) a 4- to 8-membered, saturated or unsaturated monocyclic ring, (ii) a 7- to 12-membered bicyclic ring system, or (iii) an 1 1 to 16-mcmbcrcd tricyclic ring system; wherein each ring in (ii) or (iii) is independent of or fused to the other ring or rings and each ring is saturated or unsaturated, and the monocyclic ring, bicyclic ring system, ortricyclic ring system contains one or more hcteroatoms (e.g., from I to 6 heteroatoms, or from 1 to 4 heteroatoms) selected from N, O and S and a balance of carbon atoms (the monocylic ring typically contains at least one carbon atom and the ring systems typically contain at least two carbon atoms); and wherein any one or more of the nitrogen and sulfur heteroatoms is optionally be oxidized, and any one or more of the nitrogen heteroatoms is optionally quaternizcd. The heterocyclic ring may be attached at any heteroatom or carbon atom, provided that attachment results in the creation of a stable structure. When the heterocyclic ring has substituents, it is understood that the substituents may be attached to any atom in the ring, whether a heteroatom or a carbon atom, provided that a stable chemical structure results.
Saturated heterocyclics form a subset of the heterocycles; i.e., the term "saturated heterocyclic" generally refers to a heterocycle as defined above in which the entire ring system (whether mono- or poly-cyclic) is saturated. The term "saturated heterocyclic ring" refers to a 4- to 8-membered saturated monocyclic ring which consists of carbon atoms and one or more heteroatoms selected from N, O and S. Representative examples include piperidinyl, piperazinyl, azepanyl, pyrrolidinyl, pyrazolidinyl, imidazolidinyl, oxazolidinyl, isoxazolidinyl, morpholinyl, thiomorpholinyl, thiazolidinyi, isothiazolidinyl, and tetrahydrofuryl (or tetrahydrofuranyi).
Hcteroaromatics form another subset of the heterocycles; i.e.. the term "heteroaromatic" (alternatively "'heteroaryr) generally refers to a heterocycle as

defined above in which the entire ring system (whether mono- or poly-cyclic) is an aromatic ring system. The term "heteroaromatic ring" refers a 5- or 6-membered monocyclic aromatic ring which consists of carbon atoms and one or more hcteroatoms selected from N, O and S. Representative examples of heteroaromatic rings include pyridyl, pyrrolyl, pyrazinyl, pyrimidinyL pyridazinyl, thienyl (or thiophenyl), thiazolyl, furanyl, imidazolyl, pyrazolyi, triazolyi, tetrazolyl, oxazolyl, isooxazolyl, oxadiazolyl, thiazolyl, isothiazoiyl, and Ihiadiazolyl.
Representative examples of bicyclic heterocycles include benzotriazolyl, indolyl. isoindolyl, indazolyl, indolinyl, isoindolinyl, quinoxalinyl, quinazolinyl, cinnolinyl, chromanyl, isochromanyl, tetrahydroquinolinyl, quinolinyl, tctrahydroisoquinolinyl, isoquinolinyl, 2,3-dihydrobenzofuranyl, 2,3-dihydrobenzo-

two adjacent carbon atoms.
Representative examples of tricyclic heterocycles include phenothiazinyl, carbazolyl, beta-carbolinyl, tetrahydro-beta-carboiinyl, acridinyl, phenazinyl, and phenoxazinyl.
Unless expressly stated to the contrary, an "'unsaturated" ring is a partially or fully unsaturated ring. For example, an "unsaturated monocyclic C(>
carbocycle" refers to cyclohexene, cyclohexadiene, and benzene.
Unless expressly stated to the contrary, all ranges cited herein are inclusive. For example, a heterocycle described as containing from "1 to 4 heteroatoms" means the heterocycle can contain 1, 2, 3 or 4 heteroatoms.
When any variable (e.g., Ra, Rt\ Rc, Rk, etc.) occurs more than one time in any constituent or in Formula 1 or in any other formula depicting and describing compounds of the invention, its definition on each occurrence is independent of its definition at every other occurrence. Also, combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.
The term "substituted" (e.g., as in "aryl which is optionally substituted with ont or more substituents ...*") includes mono- and poly-substitution by a named

substituent to the extent such single and multiple substitution (including multiple substitution at the same site) is chemically allowed.
The compounds of the present invention may have asymmetric centers and may occur, except when specifically noted, as mixtures of stereoisomers or as individual diastereomers, or enantiomers, with all isomeric forms being included in the present invention.
The N-substituted hydroxypyrimidinone compounds of the present invention may also occur as lautomers thereof. It is understood that the present invention includes all tautomcrs of the hydroxypyrimidinone compounds of Formula 1, both singly and in mixtures.
The compounds of the present invention are useful in the inhibition of HIV integrase, the prevention or treatment of infection by human immunodeficiency virus (HIV) and the prevention, treatment or the delay in the onset of consequent pathological conditions such as AIDS. Preventing AIDS, treating AIDS, delaying the onset of AIDS, or preventing or treating infection by HIV is defined as including, but not limited to, treatment of a wide range of states of HIV infection: AIDS, ARC (AIDS related complex), both symptomatic and asymptomatic, and actual or potential exposure to HIV. For example, the compounds of this invention are useful in treating infection by HIV after suspected past exposure to HIV by such means as blood transfusion, exchange of body fluids, bites, accidental needle stick, or exposure to patient blood during surgery.
The compounds of this invention are useful in the preparation and execution of screening assays for antiviral compounds. For example, the compounds of this invention are useful for isolating enzyme mutants, which are excellent screening tools for more powerful antiviral compounds. Furthermore, the compounds of this invention arc useful in establishing or determining the binding site of other antivirals to HIV integrase, e.g., by competitive inhibition. Thus the compounds of this invention are commercial products to be sold for these purposes.
Compounds representative of the present invention have been tested for inhibition in an assay for the strand transfer activity of integrase. The assay is conducted in accordance with Wolfe, A.L. et al., J, Virol. 1996, 70: 1424-1432, for recombinant integrase, except that: (i) the assay uses preassembled integrase strand transfer complexes; (ii) the strand transfer reaction is performed in the presence of inhibitor in 2.5 mM MgCl2 using 0.5 to 5 nM of a 3" ITFC labeled target DNA substrate as described in WO 02/30930 and (iii) strand transfer products are detected

using an alkaline phosphatase conjugated anti-FITC antibody and a chemiluminescent
alkaline phosphatase substrate. Representative compounds (e.g., the compounds set forth in Table 1 below) tested in the integrase assay demonstrated !C50's of about 5
micromolar or less.
Further description on conducting the assay using preassembled complexes is found in Hazuda et al., J. Virol. 1997, 7J_: 7005-701 1; Hazuda et al., Drug Design and Discovery 1997, J_5: 17-24; and Hazuda et al., Science 2000, 287: 646-650.
Certain compounds representative of the present invention have also
been tested in an assay for inhibition of acute HIV infection of T-iymphoid cells,
conducted in accordance with Vacca, J.P. et al., Proc. Natl. Acad. Sci. USA 1994, 9J_: 4096. These compounds demonstrated IC95's of about 20 micromolar or less.
The compounds of the present invention may be administered in the form of pharmaceutical^ acceptable salts. The term "pharmaceutically acceptable salt" refers to a salt which possesses the effectiveness of the parent compound and which is not biologically or otherwise undesirable (e.g., is neither toxic nor otherwise deleterious to the recipient thereof). Suitable salts include acid addition salts which may, for example, be formed by mixing a solution of the compound of the present invention with a solution of a pharmaceutically acceptable acid such as hydrochloric acid, sulfuric acid, acetic acid, trifluoroacetic acid, or benzoic acid. When the compounds of the invention carry an acidic moiety, suitable pharmaceutically acceptable salts thereof can include alkali metal salts (e.g., sodium or potassium salts), alkaline earth metal salts (e.g., calcium or magnesium salts), and salts formed with suitable organic ligands such as quaternary ammonium salts. Also, in the case of an acid (-COOH) or alcohol group being present, pharmaceutically acceptable esters can be employed to modify the solubility or hydrolysis characteristics of the compound.
For the purpose of preventing or treating HIV infection or preventing, treating or delaying the onset of AIDS, the compounds of the present invention may be administered orally, parenterally (including subcutaneous injections, intravenous, intramuscular, intrasternal injection or infusion techniques), by inhalation spray, or rectal ly, in the form of a unit dosage of a pharmaceutical composition containing a therapeutically effective amount of the compound and conventional non-toxic pharmaceutically-acceptable carriers, adjuvants and vehicle
The term "administration" and variants thereof (e.g., "administering" a compound) in reference to a compound of the invention mean providing the.
compound or a prodrug of the compound to the individual in need of
treatment. When a compound of the invention or a prodrug thereof is provided in
combination with one or more other active agents (e.g., antiviral agents useful for
treating HIV infection or AIDS), "administration" and its variants are each understood

to include concurrent and sequential provision of the compound or prodrug and other agents.
As used herein, the term "composition" is intended to encompass a product comprising the specified ingredients in the specified amounts, as well as any product which results, directly or indirectly, from combining the specified ingredients in the specified amounts.
By "pharmaceutical^ acceptable" is meant that the ingredients of the pharmaceutical composition must be compatible with each other and not deleterious to the recipient thereof.
The term "subject" (alternatively referred to herein as "patient") as used herein refers to an animal, preferably a mammal, most preferably a human, who has been the object of treatment, observation or experiment.
The term "therapeutically effective amount" as used herein means that amount of active compound or pharmaceutical agent that elicits the biological or medicinal response in a tissue, system, animal or human that is being sought by a researcher, veterinarian, medical doctor or other clinician, which includes alleviation of the symptoms of the disease being treated. When the active compound (i.e., active ingredient) is administered as the salt, references to the amount of active ingredient are to the free acid or free base form of the compound.
The pharmaceutical compositions may be in the form of oral ly-
administrable suspensions or tablets or capsules, nasal sprays, sterile injectible
preparations, for example, as sterile injectible aqueous or oleagenous suspensions or
suppositories. These compositions can be prepared by methods and contain excipients
which are well known in the art. Suitable methods and ingredients are described in
Remington's Pharmaceutical Sciences, 18th edition, edited by A. R. Gennaro, Mack
Publishing Co., 1990, which is herein incorporated by reference in its entirety.
The compounds of this invention can be administered orally in a dosage range of 0.001 to 1000 mg/kg of mammal (e.g.. human) body weight per day in a single dose or in divided doses. One preferred dosage range is 0.01 to 500 mg/kg body weight per day orally in a single dose or in divided doses. Another preferred doses. For oral administration, the compositions can be provided in the form of tablets or capsules containing 1.0 to 500 milligrams of the active ingredient, particularly 1,5, 10, 15,20.25,50, 75, 100, 150, 200. 250, 300, 400, and 500 milligrams of the active ingredient for the symptomatic adjustment of the dosage to the patient to be treated. 'The specific dose level and frequency of dosage for any particular patient may be varied and will depend upon a variety of factors including

the activity of the specific compound employed, the metabolic stability and length of action of that compound, the age, body weight, general health, sex, diet, mode and time of administration, rate of excretion, drug combination, the severity of the particular condition, and the host undergoing therapy.
As noted above, the present invention is also directed to use of the HIV
integrase inhibitor compounds of the present invention with one or more agents useful
in the treatment of HIV infection or AIDS. For example, the compounds of this
invention may be effectively administered, whether at periods of pre-exposure and/or
post-exposure, in combination with effective amounts of one or more of the
HIV/AIDS antivirals, imunomodulators, antiinfectives, or vaccines useful for treating
HIV infection or AIDS. Suitable antiviral agents include those listed in the following
Table:

PI — protease inhibitor
nnRTI = non-nuclcosidc reverse transcriptase inhibitor
nRTI = nucleoside reverse transcriptase inhibitor
A compound of the present invention can also be administered in combination with another HIV integrase inhibitor such as a compound described in WO 99/62513, WO 99/62520, or WO 99/62897. A compound of the present invention can also be administered in combination with a CCR5 receptor antagonist, such as a compound described in WO 99/04794, WO 99/09984, WO 99/38514, WO 00/59497, WO 00/59498, WO 00/59502, WO 00/59503, WO 00/76511, WO 00/76512, WO00/76513, WO 00/765 14, WO 00/76792, or WO 00/76793. The compounds of this invention may be effectively administered, whether at periods of pre-exposure and/or post-exposure, in combination with effective amounts of one or more HIV/AIDS antivirals, immunomodulators, antiinicctives, or vaccines useful for treating HIV infection or AIDS disclosed in the Table in WO 01/38332, which is herein incorporated by reference in its entirety.
It will be understood that the scope of combinations of the compounds of this invention with HIV/AIDS antivirals, immunomodulators, anti-infectives or vaccines is not limited to those listed above or listed in the above-referenced Table in WO 01/38332, but includes in principle any combination with any pharmaceutical composition useful for the treatment of AIDS. The HIV/AIDS antivirals and other agents will typically be employed in these combinations in their conventional dosage ranges and regimens as reported in the art, including the dosages described in the Physicians' Desk Reference, 54lh edition, Medical Economics Company, 2000. The dosage ranges for a compound of the invention in these combinations are the same as those set forth above.
Abbreviations used in the instant specification, particularly the Schemes and Examples, include the following:
AIDS " acquired immunodeficiency syndrome
ARC AIDS related complex
BOC or Boc := t-butyloxycarbonyl
Bn ~-: benzyl
Bz - benzoyl
CBZ or Cbz = carbobenzoxy (alternatively, benzyloxycarbonyl)
DMAD - dimethylacetylenedicarboxylate

DMAP r dimethylaminopyridine
DMF '-'-'- N,N-dimethylformamide
Ht ^ ethyl
LtOAc -■ ethyl acetate
FIA-MS -" How injection analysis mass spectrometi^
HIV ■■"-"■ human immunodeficiency virus
I -I PLC "" high performance liquid chromatography
m-CPBA - meta-chloroperbenzoic acid
Me - methyl
NMP :": N-methyl pyrrolidinone
NMR nuclear magnetic resonance
Ph L-~ phenyl
TFA ; trilluoroacetic acid
THF ~:z tetrahydrofuran The compounds of the present invention can be readily prepared according to the following reaction schemes and examples, or modifications thereof, using readily available starting materials and reagents. In these reactions, it is also possible to make use of variants which are themselves known to those of ordinary skill in this art, but arc not mentioned in greater detail. Furthermore, other methods for preparing compounds of the invention will be readily apparent to the person of ordinary skill in the art in light of the following reaction schemes and examples. Unless otherwise indicated, all variables are as defined above.
The compounds of the present invention can be prepared by coupling suitable substituted alkyl l-alkyI-l,6-dihydro-5-hydroxy-6-oxopyrimidine-4-carboxylates (or carboxylic acids or halides) with the appropriate amines, as represented by Scheme I. In the scheme, P is H or a protective group, typically an ester (e.g., benzoate or pivalate) that is normally removed under the conditions employed to convert the the methyl ester to the amide. The ester protective group is typically used to purify the 2-substituted-5,6 dihydroxypyrimidine-4-carboxylates after their synthesis when the unprotected product cannot be crystallized from the reaction crude and/or for synthetic reasons.

Methods for coupling carboxylic acid derivatives with amines to form carboxamides are well known in the art. Suitable methods are described, for example, in Jerry March, Advanced Organic Chemistry, 3rd edition. John Wiley & Sons, 1985, pp. 370-376. Amines of formula 1-1 can be prepared using the methods described in Richard Larock, Comprehensive Organic Transformations. VCH Publishers Inc, 1989, pp 385-438, or routine variations thereof.
Methyl l-alkyl-l,6-dihydro-5-hydroxy-6-oxopyrimidine-4-carboxylates of formula 1-2 can be prepared as shown in Scheme 2, wherein amidoxime 2-1 can be reacted with DMAD in an appropriate solvent and at a suitable temperature to give the intermediate dihydroxypyrimidine 2-2, followed by protection of the 5-hydroxy group in 2-2 with a suitable protecting agent such as benzoate or pivalate to give 2-3, and then alkylation of nitrogcn-1 to afford 1-2. This procedure is described in the literature [Culbertson et al., J Ileterocycl Chew, 1979, J_6 (7): 1423-24]. Dihydroxypyrimidine 2-2 can be isolated or directly protected to give 2-3. The alkyl group can be introduced on Ni by reaction of 2-3 with an alkylating agent in the presence of an inorganic base (e.g., cesium carbonate). If a mixture of N- and O-alkylated derivatives results, the desired N-alkylated product 1-2 can be separated by flash chromatography. Scheme 2 is exemplified in Example 1.

Scheme 2
(- ~i
Methyl l-alkyl-l,6-dihydro-5-hydroxy-6-oxopyrimidine-4-carboxyIates of formula 1-2 can be prepared as shown in Scheme 3, wherein an N-alkylamidoxime 3-1 can be reacted with dimethylacetylenedicarboxylate to give the unprotected 1-2 (P- 11). The unprotected compound can be isolated as such or it can be converted to 1-2 by reaction with a suitable protecting group. Scheme 3 is exemplified in Example 2.
Scheme 3

Amidoximes 2-1 and 3-1 are prepared from the corresponding nitriles by chemistry described herein (see Example 1, Step 1 and Example 2, Step 2). Nitriles can be prepared from carboxylic acids by various procedures known in the an.

including, for example, conversion to carboxamides by the procedure of of Pozdnev
{Tetrahedron Lett. 1989, 30: 5193) (see also, Example 6, Step 2), and dehydration of
the amide by the procedure of Waldmann {Tetrahedron 1994, 50: 11865) (see also,
Example 6, Step 3).
Compounds of the present invention of general formula 3-3 or 3-6 can
be prepared in accordance with Scheme 3, Parts 1 and 2, wherein haloderivative 3-1
or 3-4 can be synthesized by the bromination or chlorination of a suitable substrate affording a -CH2Br, -CI bCI, -CHBr-, or -CMC!- group, followed by displacement of
the halogen with a nucleophile ("Nu") such as an amine, thiol, or alcoholatc to obtain the nucleophile-substituted methyl ester intermediate 3-2 or 3-5, which need not be isolated. Elaboration of the methyl ester functionality into the carboxamide will afford the final product 5-3 or 3-6. Scheme 3 is exemplified in Example 5.
Scheme 3 - Part I

Scheme 4 depicts the preparation of compounds of the invention that contain an alkylated aliphatic amine in the substituent at the 2 position. Nitrogen alkylation is achieved via a reductive amination or alkylation. The nitrogen alkylation can be performed before formation of the amide {via 4-3) or after formation of the amide {via 4-2) depending on the substrate, with suitable deprotection as necessary. Scheme 4 is exemplified in Examples 6 to 8 below.

Compounds of the present invention with general formula 5-3 containing an acylated nitrogen or sulfonylated nitrogen in the substituent at the 2-position, can be prepared following Scheme 5. Acylation or sulfonylation of the nitrogen in the 2-substituent of the pyrimidine core provides compound 5-2, which can bo elaborated into the final amide 5-3 by reaction of a suitable amine in a polar solvent. Scheme 5 is exemplified in Examples 9 to 12 below.

The preparation of compounds that feature a carboxamide at the 2 position of the pyrimidine core can be achieved as shown in Scheme 6, wherein a starting material bearing a 2-ethyl- and a 4-methylcarboxyIate functionality (6-1) is employed. This strategy will allow the regioselective elaboration of the 4-methyl ester into the carboxamide by reaction with a suitable amine. The other ester bond in the 2 position can then be further elaborated. Scheme 6 is exemplified in Example 13 below.

Compounds of the present invention of formula 7-2 can be prepared by reaction of aldehydes or ketones 7-1 with suitable amines under reductive alkylation conditions, as shown in Scheme 7. Scheme 7 is cxcmplifed in Kxample 14 below.

In the processes for preparing compounds of the present invention set forth in the foregoing schemes and exemplified in the examples below, functional groups in various moieties and substituents may be sensitive or reactive under the reaction conditions employed and/or in the presence of the reagents employed. Such sensitivity/reactivity can interfere with the progress of the desired reaction to reduce the yield of the desired product, or possibly even preclude its formation. Accordingly, it may be necessary or desirable to protect sensitive or reactive groups on any of the molecules concerned. Protection can be achieved by means of conventional protecting groups, such as those described in Protective Groups in Organic Chemistry, ed. J.F.W. McOmie, Plenum Press, 1973 and in T.W. Greene & P.G.M. Wuts, Protective Groups in Organic Synthesis, John Wiley & Sons, 1991. The protecting groups can be removed at a convenient subsequent stage using methods known in the art. For example, in preparing the compounds of the invention it is sometimes necessary to protect one or more amino groups (e.g., amino groups present in substituents at the 2-position of the pyrimidinone ring)

with, for example, a 13oc or Cbz group or to protect hydroxy (e.g., the 5-hydroxy group on the with, for example, a benzoyl or benzyl group. The Boc group pan be removed by acid treatment (e.g., TFA) either before or after formation of the final amide at C-6 of the pyrimidinone nucleus. The Cbz and benzyl groups are typically removed by catalytic hydrogenation or under strong acid conditions, either prior to or following formation of the final amide. The benzoyl group can be removed concurrently with the formation of the final amide. Examples 6 and 12 below illustrate the use of a Boc protective group and of Boc, benzoyl and benzyl protective groups in the preparation of compounds of the invention.

The preparation of compounds that feature a bis oxalamide at the 2 position of the pyrimidine core can be achieved as shown in Scheme 8. wherein a

starling material bearing a basic nitrogen at the 2- position of the pyrimidinc carboxyamide (8-1) is employed. This strategy will allow to obtain the final compound (8-3) following two possible procedures: by simple coupling of monoamide oxalic acid to the amine (8-1) or by the acylation of the basic nitrogen of (8-1) with dimethyl oxalate to give the ester intermediate (8-2) that is converted to the final compound by heating in presence of amine in appropriate solvent. Scheme 8 is exemplified in Examples 17, 18, and 20 below.
The following examples serve only to illustrate the invention and its practice. The examples are not to be construed as limitations on the scope or spirit of the invention.
EXAMPLE I
Methyl 5-(benzoyloxy)-2-[l-(/
Step 1: Tert-butyI-2-famino(hydroxyimino)methyl]pyrrolidine-l-carboxylate

A solution of hydroxylamine hydrochloride (1.0 eq.) in MeOH was added at 0 °C to a solution of KOH (1.0 eq.) in MeOH. The resulting reaction mixture was filtered and added to a solution of/t7r/-butyl-2-cyanopyrrolidine-l-carboxylate (1.0 cq.) in methanol and stirred at 40 °C for 2 h.The solvent was removed //; vacuo and the residue treated with water; the solid was filtered and washed with a mixture of

EhO: Petroleum Ether 1:1 to afford the title compound as a white solid as a mixture ofrotamers byNMR.
'H-NMR (DMSO-6, 400 MHz) 5 8.92 (s, 1 H),5.35(s,l H), 5.15 (s, I H), 4.25 (bs, 0.5 II), 4.10 (s, 0.5 II), 3.40-3.30 (m, 1 H), 2.10-1-70 (m, 4 H), 1.40 (s, 4.5 H),1.35 (s, 4.5 H), one signal is obscured by water.
Stop J!: Methyl 5-(benzoyloxy)-2-[l-(^r/-butoxycarbonyl)pyrrolidin-2-yl|-6-
hydroxypyrimidine-4-carboxylate

A solution of the product of Step 1 (1.0 eq.) and dimethyl acetylenedicarboxylate (1.05 eq.) in CHCbwas refluxed for 3 h. The reaction mixture was concentrated and the crude product was used directly in the next step without further purification. The crude product was dissolved in xylene and refluxed for 24 h. The solvent was removed in vacuo and the crude was dissolved in pyridine. Benzoic anhydride was added (1.5 eq.). The reaction mixture was stirred at room temperature until the starting material was consumed as determined by MS analysis. The reaction mixture was concentrated, and the resulting oil was diluted with ethyl acetate and washed with IN HO solution, saturated NaHCOi solution, saturated Nad solution. The crude oil obtained after organic solvent evaporation was purified by flash chromatography to obtain the title compound as a yellow solid. 'H-NMR(CDC-13, 400 MHZ) S 12.08 (bs, 1 H), 8.18 (d, J- 7.6 Hz, 2 H), 7.64 (t, J = 7.4 Hz, 1 H), 7.50 (t, J- 7.6 Hz, 2 H), 4.80-4.60 (m, I H), 3.82 (s, 3 H), 3.60-3.50 (m, I i I), 3.40-3.20 (m, 1 H), 2.50-2.10 (m, 2 H), 2.00-1.70 (m, 2 H), 1.50 (s, 9 H). MS/w/z444(M+H)+.
StcpJV Methyl 5-(benzoyloxy)-2-| l-(/er/-butoxycarbonyl)pyrrolidin-2-yl]-l-
mcthyI-6-oxo-I,6-dihydropyrimidine-4-carboxylate To a stirred solution of the product of Step 2 (1.0 eq.) in THI\ Cs2C03
was added (1.2 eq.) followed by the addition of CH3I (2.0 eq.). The reaction was

stirred at 40°C until the starting material was consumed as determined by MS analysis. The reaction was concentrated and the residue taken up with EtQAc, washed with I N HO, saturated solution of NaHCCb and brine. The organic phase was dried over anhydrous Na;>S04, filtered and concentrated. Reaction crude showed 3.4:1 ratio N (desired product) versus O methylation. The title product was purified by flash column chromatography (EtOAc: Petroleum Ether =: 1:1) and obtained as a 1:1 mixture of rotamers by NMR.
lH-NMR(CDCI3!400MHz)5 8.12(d,y=7Hz, 2 II), 7.58 (t,J= 7 Hz, 1 11), 7.46 (t, 7= 7 Hz, 2 H), 4.97-4.95 (m, 0.5 H), 4.87-4.83 (m, 0.5 H), 3.74 (s, 1.5 H), 3.72 (s, 1.5 H), 3.63 (s, 1.5 H), 3.59 (s. 1.5 H), 3.56-3.42 (m, 1 H), 2.40-2.25 (m, 5 H), 1.41 (s, 4.5 H). 1.25 (s, 4.5 H). MS w/z458(M-i-H)'.
Also obtained was the O-methylated compound of formula:

as a mixture of rotamers by NMR. 'H-NMR (CDC13,400 MHz) 6 8.21 (d, J= 7.6 Hz, 211), 7.72 (t, J= 7.6 Hz, 111), 7.56 (t, J= 7.6 Hz, 2H), 5.10-5.05 (m, 0.3H), 5.00-4.95 (m, 0.7H), 4.01 (s, 3H), 3.87 (s, 3H), 3.80-3.60 (m, 2H), 2.50-2.40 (m, 1H), 2.15-2.00 (m, 2H), 2.00-1.85 (m, III), 1.61 (s, 2.7H), 1.40 (s, 6.3H). MSm/z458(M+H)EXAMPLE 2 Eicnzyl 2-[5-(benzoyloxy)-4-(methoxycarbonyl)-1 -methyl-6-oxo-1,6-dihydropyrimidin-2-yl|indoline-l-carboxylate

StepJj Benzyl 2-|[hydroxy(methyl)aminoj(imino)methyl]indoline-l-
carboxylale

l-Benzyloxycarbonyl-2-cyanoindoiine was added to a solution of tricthylamine (2 eq.) and MeNHOH.HCl (2 cq.) in HtOH. After stirring overnight the reaction mixture was evaporated, dissolved in KtOAc, washed with water, dried over Na2S04and evaporated to afford the title compound.
'll NMR(DMSO-d6, 340K, 300 MHz) 8 7.68 (d,./ - 8.0 Hz, 1 H), 7.41-7.30 (m, 5 11), 7.19 (t, J =7.5 Hz, 2 11), 6.99 (t, J =7.6 Hz, 1 H). 5.53 (dd, J= 5.5, 10.9 Hz, I H), 5.22 (s, 2 H), 3.62 (dd, J- 11.0, 16.6 Hz, I H), 3.33 (s, 3 H), 3.01 (dd,J-5.5 Hz, 16.6 Hz, 1 H). MSIH/Z326(M+H)'Step 2: Benzyl 2-[5-(benzoyIoxy)-4-(methoxycarbonyl)-l-methyl-6-oxo-l,6-
dihydmpyrimidi-2-yl]indoIine-l-carboxylate The product of Step 1 was dissolved in CHCI3 and dimethylacetylenediearboxylate was added dropwisc (1.2 eq.) at room temperature. After 4 h the mixture was evaporated, and the residue was dissolved in xylene and stirred at 160 °C for 2 days. The solvent was then evaporated, and the residue was dissolved in pyridine, after which (PhCO)20 (2 eq.) was added and the reaction mixture was stirred for 2 days. After evaporation, the resulting crude oil was diluted with EtOAc, washed with HC1 IN, dried over Na^SCXi and evaporated. The product was purified by flash chromatography on silica gel (F.tOAc/ petroleum ether, 1:4) to afford the title product.
1H NMR (DMSO-d6, 340 K, 400 MHz) 5 8.08 (d,./ ' 7.3 Hz, 2 H), 7.77 (L J - 7.4 Hz, 2 H), 7.62 (t, J -■ 7.6 Hz, 2 H), 7.31 -7.20 (m. 7 H). 7.00 (t, J = 7.3 Hz, 1H), 5.83 (dd. 7-4.6 Hz, 11.0 Hz, I H), 5.23-5.13 (m. 2 li). 3.76 (dd, ./= 11.1.16.6 Hz. 1 H), 3.65 (s, 3 H), 3.56 (s, 3 II), 3.27 (dd,./-4.4 Hz. 16.6 Hz, 1 II).
\A£ ,.,A SA(\ f\A+\ n*

EXAMPLE 3
A^-(4-riuorobenzyl)-5-hydiu\y-l-methyl-2-(4-methylphcnyl)-6-oxo-l,6-dihydropyrimidine-4-carboxarnide

To a stirred solution of methyl 5-[(2,2-dimelhylpropanoyI)oxy|-l-methyl-2-(4-methylphenyl)-6-oxo-l,6-dihydropyrimidine-4-carboxylate (prepared from 4-methylbenzonitrile by procedures similar to those set forth in Examples 2 or 3) in DMF 3 equivalents of 4-fluorobenzyIamine were added and mixture was stirred at 90 °C for 2 h. The title product precipitated from the cooled reaction mixture after the addition of 2 N MCI, and was collected by filtration and washed with diethyl ether. !HNMR(DMSO-d6,400MHz)5 12.45 (s, 1 H), 9.3 I (bt, .7=6.0 Hz, 1 H), 7.62 (m, 2 H), 7.40-7.32 (m, 4 II), 7.14 (t,./- 8.8 Hz, 2 H). 4.45 (d, J= 6.0 Hz, 2 H), 3.35 (s, 3 H), 2.48 (s, 3 H). MS/w/z368(M+H)EXAMPLE 4 A^-(4-fluorobenzyl)"5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide

Step 1: 4,5-Dihydroxy-6-(methoxycarbonyI)pyrimidine-2-carboxylic acid

2-l:thc)\ycarbonyI-4,5-Dihydroxy-6-(melhoxycarbonyI)pyrimidine [obtained from ethyl amino(hydroxyimino)ethanoate (Branco, P.S. et al, Tetrahedron 1992, 40: 6335) by procedures similar to those set forth in Example 1] was suspended in dioxane/TTIF 2:1 and IN NaOH was added. After 20 min the mixture was acidified with IN f ICI solution, concentrated and filtered to give the title product. 'lI-NMRCDMSO-d, 400 MHz) 5 13.10 (bs, 1 H), 11.11 (bs, 1 H), 3.82 (s, 3 H). MS m/z 2\3 (M-ll).
Step 2: Methyl 5,6-dihydroxypyrimidine-4-carboxyiate

A solution of the product of Step I in HC1 IN solution was stirred for 6 hours at 90°C. Reaction mixture was filtered and the solid washed with HCI IN. Evaporation of the filtrate afforded the title product as a solid. !H NMR (DMSO-d6, 300 K, 400 MHz) 5 7.75 (s, I H), 3.82 (s, 3 H). ,3C NMR (DMSO-d6, 300 K, 400MHz)5 165.66, 158.20, 147.14, 139.00, 127.85,52.16.
Step 3: Methyl 5-|(2,2-dimethylpropanoyl)oxy]-6-hydroxypyrimidine-4-
carboxylate

Pivaloyi chloride I.I eq. was added to a solution of the product of Step 2 in pyridine, and the mixture was heated to 40°C for 10 minutes. HPLC showed the complete conversion of starting material. The reaction mixture was concentrated, the resulting oil was diluted with ethyl acetate and washed with 1 N MCI solution. The title product was obtained as a brown solid after evaporation of the organic phase and trituration with diethyl ether.
'll NMR (DMSO-dr,, 400 MHz) 5 13.35 (s,l H), 8.18 (s, 1 II), 3.85 (s, 3 H),1.28 (s, 9 H).
Slep._4: Methyl 5-|(2,2-dimethylpropanoyl)oxy]-l-methyI-6-oxo-I,6-
dihyclropyrimidine-4-carboxylatc

Dimethyl sulfate (1.5 eq.) was added to a solution of the product of Step 3 (1 eq.) in THF containing cesium carbonate (1.5 eq.). The reaction was carried out at 50°C for thirty minutes. The solvent was evaporated and the resulting oil was dissolved in ethyl acetate, washed with IN HC1 solution. The crude title compound was recovered as yellow solid and used in the next step without purification. 'II NMR (DMSO-d6, 400 MHz) 5 8.43 (s,l H), 3.81 (s, 3 H), 3.45 (s, 3 H)J .30 (s, 9 H).
Steji_5: A^-(4-fluorobenzyI)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-
4-carboxamide
4-Fluorobenzylamine (3 eq.) was added to a solution of the crude product of Step 4 in DMF and the reaction mixture was heated to 90°C for one hour. The title compound was obtained by RP-HPLC (Cis, eluting with water and acetonitrile containing 0.1 % rfFA).
]H NMR(DMSO-d6,400MHz)5 12.5 (s,I H), 9.54 (t../- 6.2 Hz, 1 II), 8.05 (s, 1 H), 7.36 (dd, ./= 6.2, 8.4 Hz, 2 H), 7.14 (t, J= 8.4 Hz, 2 H), 4,45 (d, J = 6.2 Hz, 2 11), 3.44 (sj H).

MS/H/Z276(M-H)EXAMPLE 5 N-(4-I'1uorobenzyl)-5-hydroxy-l-melhyI-2-[4-(morpholin-4-ylmethyl)phenyI]-6-oxo-l,6-dihydropyrimidine-4-carboxamide

Step 1: Methyl 2-|4-(bromornethyI)phenylJ-5-l(2,2-dimethylpropanoyl)oxy]-l-
methyl-6-oxo-I,6-dihydropyrimidine~4-carboxylate

To a vigorously boiling solution of methyl 5-[(2,2-dimclhylpropanoyl)oxy]-I-methyl-2-(4-methyIphenyI)-6-oxo-l,6-dihydropyrimidine-4-carboxylate in carbon tetrachloride N-bromosuccinimide (1 eq.) and benzoyl peroxide (0.05 eq.) were added as dry powders. After 4 hr the mixture was allowed to reach room temperature and the precipitated succinimide was filtered off. The filtrate was evaporated under vacuum and the solid residue was used as such. 'H NMR (DMSO-dr,, 400 Ml Ix) S 7.68-7.57 (ITU 4 H), 4.77 (s, 2 H), 3.80 (s, 3 H), 3.27 (s, 3 H), 1.30 (s, 9 11).

Steg_2: N-(4-I;luorobcn/yl)-5-hydroxy-l-methyl-2-[4-(morphoIin-4-
ylmethyI)phenyi|-6-oxo-l,6-dihydropyrimidine-4-carboxamide A THF solution of methyl 2-[4-(bromomcthyl)phenylJ-5-[(2,2-dimcthylpropanoyl)oxy]-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxylate was reacted with 4 eq. of morpholine for 0.5 h at room temperature. After evaporation of volatiles, the oily residue was taken into DMF and treated with 3 eq. of 4-fluorobenzylamine at 90°C for 2 h. Title product was isolated as its trifluoroacetate salt by RP-HPLC (CI 8,water/acctonitrile with 1 % of TFA as eluant). 1H-NMR(DMSO-d6.400MH/)8 12.45 (s, 1 H), 10 (bs, 1 H), 9.3 1 (bt, 1 H), 7.74 (m, 2 11), 7.62 (m, 2 11), 7.35 (m, 2 II), 7.14 (t, J-8.8 Hz, 2 H), 4.54-4.38 (m, 4 H), 4.1-3.9 (m, 2 H), 3.9-3.7 (m, 2 H), 3.68-3.51 (m, 2 H), 3.31 (s, 3 H), 3.2-3.1 (m, 2 H). MS: m/z 453 (M+H)HXAMPLE6
N-(4-nuorobenzyI)-5-hydroxy-l-methyl-2-(4-methyImorpholin-3-yl)-6-oxo-l,6-dihydropyrimidine-4-carboxamide

Step 1: 4-(/^r/"Butoxycarbonyl)morpholine-3-carboxylic acid
(
To a vigorously stirred solution of 3-morpholinecarboxylic acid and triethylamine (1.11 cq.) in MeOU (1.4 M) at 50 °C was added di-t-butyl dicarbonate (2 cq.). Stirring was continued at 50 °C for 5 min and at room temperature overnight. -- The reaction mixture was then concentrated to obtain an oily residue and suspended

between EtOAc (500 ml) and saturated NaUC03 (500 ml). The organic layer was extracted with saturated NaHCCh (2x250 ml) and 112() (250 ml). Combined aqueous layers were brought to pi I =: 2.0 with 3 M HC1 and immediately extracted with EtOAc (2x500 ml). The combined organic layers were washed with dilute HCI, dried, filtered and evaporated to give the title compound as a pale yellow oil, a 1:1 mixture of rotamers by NMR.
5 'II NMR (400 MHz, DMSO-d6) 12.93 (bs, 1 H), 4.32 (s, 0.5 H), 4.29 (s, 0.5 H), 4.2-4.1 (m, 1 H), 3.83-3.74 (m, I II), 3.58-3.52 (m, 2 H), 3.36-3.31 (m, 1 H), 3.16(t, JH 1.4 Hz, 0.5 H). 3.00 (t, J-1 1.4 Hz, 0.5 H). 1.40 (s, 4.5 H), 1.36 (s, 4.5 H). MS//7/z232(M+H)Step 2: /er/-Butyl 3-(aminocarbonyl)morpholinc-4-carboxyIate

To a stirred solution of the compound prepared in Step 1 (1 eq.), pyridine (0.6 eq.) and di-/-butyl dicarbonate (1.3 eq.) in dioxane (0.6 M), NH4HCO3 (1.26 eq.) was added and the mixture was stirred at room temperature for 20 hours. Mixture was concentrated, taken up in BtOAc and washed with water and brine. Organics were dried over Na2S04 and evaporated giving the title product as an oil which crystallized at room temperature.
1H-NMR(DMSO-d6.300MHz)5 7.35(bs, 1 H), 7.06 (bs, 1 H), 4.15 (bs, 2 H), 3.76 (bs, I H), 3.57-3.51 (m, 2 H), 3.28 (m, 1 II), 3.18 (m, 1 H), 1.36 (s, 9 H). MSA/;/Z231 (M+H)'.
Step.3: ^r/-Liutyl 3-cyanomorpholine-4-carboxylate

A solution of the product of Step 2 (I eq.) and triethylamine (2.1 eq.) in CH2CI2 (0.1 M) was cooled to 0 °C and trifluoroacetic anhydride (1.1 eq.) added dropwise under nitrogen. Stirring was continued 3.5 hours more at room temperature and volatilcs removed in vacuo. Residues taken in ElOAc were washed with water, brine and dried over Na2S04. Evaporation gave the title compound as a brown solid. '11 NMR (DMSO-d6, 400 MHz) 5 5.04 (d, J = 2.7 Hz, 1 H), 3.96 (d, 7=12.2 Hz, 1 H), 3.86 (dd,7- 11.5, 2.6 Hz, 1 H), 3.69 (d, 7=12.4 Hz, 1 H), 3.56 (dd,7 = 12.2, 3.2 Hz, 1 H),3.40(td,7 = 11.9,2.89 Hz, 1 H), 2.97 (m, 1 II), 1.43(s,9H). MS/w/z213(M+H)Step 4: /er/-Butyl 3-[(Z)-amino(hydroxyimino)methyl]morphoIine-4-
carboxylate

A solution of of the product of Step 3 (1 eq.), hydroxylamine hydrochloride (1.4 cq.) and triethylamine (1.7 eq.) in HtOH (0.5 M) was re fluxed under nitrogen for 5 hours. Mixture was concentrated and residues taken up in EtOAc and washed with water and brine. Combined organics were dried over Na2S04 and evaporated giving the title compound as a yellow solid.
!I I NMR (DMSO-d6, 400 MHz) 8 9.16 (bs, 1 H), 5.32 (bs, 2 H), 4.30 (bs, 1 H), 4.08 (d, 7- 11.6 Hz, 1 H), 3.75 (d, 7= 6.8 Hz, 1 H), 3.50-3.33 (m, 4 H), 1.38 (s, 9 H). MS: m/z246(M+H)Ste|2..5: DimcthyI-2-({2-amino-2-[4-(/er/-butoxycarbonyl)morphoIin-3-
yl]ethenyl}oxy)but-2-enedioate

A solution of the product of Step 4 (1 eq.) and dimethyiacetylencdicarboxylate (1.2 eq.) in CHCI3 was refluxed for 1 hour under nitrogen and solution concentrated. Residue was purified by flash chromatography on silica gel, cluents petroleum ether/EtOAc 7:3 -> 1:1, to give the desired product as a mixture of two isomers H/Z (76:14).
!l 1 NMR (DMSO-dft, 400 MHz, 300K) 5 6.60 and 6.20 (2 bs, 2 H), 5.58 and 5.41 (2s, 1 II), 4.36 (bs, 1 II), 4.04 (bs, 1 H), 3.8 (bs, 1 H), 3.76 and 3.72 (2 s, 3 H), 3.63 and 3.58 (2 s, 3 H), 3.53 (td,./- 13.6, 3.7 Hz, 1 H), 3.44 (t, J- 10.4 Hz, 1 H), 3.31 (m, 2 11), (s, 9 11). MS/w/z388(M+H)St^E_6- /er/-Butyl-3-[4,5-dihydroxy-6-(methoxycarbonyl)pyrimidin-2-
yl]morpholine-4-carboxylate

The adducts of Step 5 were refluxed in xylenes for 24 hours. Then the reaction was cooled down and concentrated in vacuo. Ethyl ether was added until precipitation of a solid that was filtered, washed with ethyl ether and dried to give the title pyrimidinc as an orange solid.
'HNMR(DMSO-d6, 400 MHz, 340 K) 8 4.62 (s, HI). 4.15 (d, J-12 Hz, 111). 3.84 (bs. Ill), 3.82 (s, 3H), 3.70 (dd. J= 12.3, 4 Hz, I H). 3.61 (dd, Jr= 12.2,3.8 Hz, ] H), 3.56(1, J- 13 Hz, III), 3.43 (tdj= 11.5, 3.4 Hz, HI). 1.35 (s,9H).

MS m/z 356 (M i-\l)Step 7: /^r/-Butyl-3-f5-(benzoyloxy)-4-hydroxy-6-
(methoxycarbonyl)pyrimidin-2-yl]morpholine-4-carboxylatc

The pyrimidine from Step 6 in dry pyridine (0.2 M), was treated with ben/.oic anhydride (2 eq.) overnight at room temperature. The mixture was evaporated, taken in EtOAc and washed with HCI 1N, NaHCC>3 and brine. Organics were dried over Na^S04, and filtered, evaporated and purified by flash chromatography on silica gel, cluents EtOAc/Petroleum Ether: 7/3. "H NMR (DMSO-dr,, 300 MHz, 340K) 5 13.3 (bs, 1 H), 8.07 (d, J = 7.5 Hz, 2 H), 7.76 (t, J =7.5 Hz, 1 II), 7.61 (t, J= 7.5 Hz, 2 H), 4.73 (s, 1 H), 4.22 (d,y = 12.4 Hz, 1 11), 3.86 (d, J- II.OHz, 1H), 3.78 (dd, J- 12.4,3.9 Hz, 1 H), 3.73 (s, 3 H), 3.58 (t, y- 13.9 Hz, 2 H), 3.47 (td, J = 10.7, 3.6, 1 H), 1.36 (s. 9 H). MS w/z 600 (M-i-H)*.

The pyrimidine product of Step 7 in dry THF (0.6 M) was treated with cesium carbonate (1.5 eq.) and dimethyl sulfate (1.5 eq.) at 50 °C for 1 hour. Solvent

was removed in vacuo and residue taken in EtOAc, washed with HCI IN and brine. Organics were dried over Na2SO^, filtered and evaporated to obtain a crude which was purified by flash chromatography on silica gel, (elucnts BtOAc/PetroIeum Ether: 3/7) to separate the two compounds 8A and 8B (ratio 8A/8B 1/0.85).
An alternative route was also employed as follows: The pyrimidine product of Step 7 was added to a suspension of LiH (1.1 eq) in dioxane at room temperature. The mixture was aged 45 min at 38 °C and was then cooled to room temperature. Dimethylsulfate (1.3 eq) was added and the mixture was warmed to 38 °C (4h) and 56 °C (4h). The reaction mixture was cooled to 16 °C and glacial acetic acid (0.1 eq) was added, followed by water and EtOAc. The aqueous layer was separated and extracted with EtOAc. The combined organic layer was dried (Na2S04) and concentrated to an oil, which was chromatographed through silica gel, eluting with 50-55% EtOAc/hexanes to separated compound 8A from 8B. The fractions were evaporated to a foamy solid. This solid was dissolved in ether and re-evaporated to foamy solid that could be scraped out easily. This solid was dried in a vacuum oven overnight at 40 °C to afford 8B as a pale yellow solid. The ratio of 8A/8B is variable with this route, from 1:4 to 1:12.
/cv*/-Butyl-3-[5-(benzoyloxy)-4-methoxy-6-(methoxycarbonyl)pyrimidin-2-yl]
rnorpholine-4-carboxylate (8A).
'll NMR (300 MHz, DMSO-d6+TFA, 330K) 5 8.10 (d, J=7.9 Hz, 2 H), 7.77 (t, J=7.3
Hz. 1 H),7.61 (t, J-7.4Hz,2H),4.94(bs, 1H), 4.50 (d, J-l 1.6 Hz, 1H), 4.0 (s, 3H),
3.85-3.81 (m, 2 II), 3.76 (s, 3 H), 3.66 (d, J-10.4 Hz, 1H), 3.49-3.45 (m, 2 11), 1.35
(bs, 9 H).
MS w//z474(M + H)*".
/er/-Fiutyl-3-[5-(benzoyloxy)-4-(methoxycarbonyl)-!-methyl-6-oxo-l,6-dihydropyrimidin-2-yl]morpholine-4-carboxyiate (8B).
'H NMR (DMSO-d6, 400 MHz, 330K,) 5 8.09 (d, ./■-= 7.3 Hz, 2 H), 7.77 (t, J = 7.5 Hz. 1 H),7.62(t,y-7.8Hz,2H),5.08(d,y-3.4Hz, 1 H).4.21 (±J= 12.3 Hz, 1 H), 3.95-3.85 (m, 3 11), 3.76 (s, 3 H), 3.58 (s, 3 H), 3.55-3.50 (m, 2 H), 1.34 (s, 9 H). MS////z474(M-f H)Step 9: tert-Butyl-3'(4-{[(4-fluorobenzyl)amino|carbonyl}-5-hydroxy-l-
mcthyI-6-OKO-l,6-dihydropyrimidin-2-yl|-morpholine-4-carboxylate

The methyl ester 8B in dry MeOH was treated with 4-fluorobcnzylaminc (2.5 eq.) at reflux for 2 hours. Solvent was removed in vacuo and residue triturated with Et.->() to obtain the title product.
'llNMR(300MH/., DMSO-d6, 320K)8 11.95(bs, I 11), 8.32 (t, J= 6.0 Hz, 1 H), 7.39-7.35 (m, 2 H), 7.19-7.13 (m, 2 H), 4.96 (dd,./-4.25, 2.42 Hz, 1 H), 4.62 (dd, J= 14.9, 6.95 Hz, 111), 4.49 (dd, J= 14.9, 5.83 Hz, III), 4.16 (dd, J= 12.2, 2.0 Hz, 1H), 3.87-3.79 (m, 211), 3.70-3.64 (m, HI), 3.55-3.45 (m, 5H), 1.23 (s, 9H). MSm/z463 (M+M)+.
Step 10: N-(4-nuorobenzyl)-5-hydroxy-1 -methyl-2-morpholin-3-yl-6-o.\o-1,6-
dihyclropyrimidine-4-carboxamide

The compound from Step 9 was treated with a mixture of dichloromethane/TFA (2/1) for 1 hour at room temperature. Organics were removed in vacuo to give the title compound as a solid.
'11 NMR(300 MHz, DMSO-dr„ 300 K) 5 9.45 (bs, 1 H), 7.39-7.36 (m, 2 H), 7.19-7.15 (m, 2 H), 4.93 (d,.7-9.2 Hz, 1 H), 4.64 (dd../- 15.4, 6.7 Hz, 1 H), 4.55 (dd, 7-15.4, 6.2 Hz, 1 II), 4.35 (d,./= 12.8 Hz, 1 II), 4.08 (d,7- 12.6 Hz. I H), 3.77 (t, J = 12.4 Hz, 1 H), 3.55 (s, 3 H), 3.55-3.46 (m, 2 H), 3.40-3.34 (m, 1 H). MS /»/z363(M + H)+.

Step 11: N-(4-nuorobcnzyl)-5-hydroxy-l-mcthyl-2-(4-methyImorpholin-3-yl)-6-
oxo-l,6-dihydropyrimidine-4-carboxamide
The compound from Step 10 was dissolved in MeOH and treated with triethylamine (1 eq.), sodium acetate (1.6 eq.), formaldehyde 37% w/w aq. soin. (3 eq.), and sodium cyanoborohydride (1.43 eq.). The mixture was left stirring at room temperature for 1 hour. The reaction mixture was concentrated and the title compound was obtained by RP-IIPLC purification (C|«, eluting with water and acetonitrile containing 0.1 % TFA), as its trifluoroacetate salt.
'H NMR (400 MHz, l)MSO-d6■♦TFA) 5 12.33 (bs, 1 II), 10.05 (bs, 1 H), 9.48 (t, J = 6.4Ilz, 1 H), 7.35-7.33 (m. 2 II), 7.15-7.12 (m, 2 11), 4.98 (d, ./ = 8.8 Hz, 1 H), 4.57 (d,./-6.4Hz, 2H). 4.36(d,./- 12.7 Hz, 1 H), 4.13 (d.7- 12.4 Hz, 1 H), 3.77 (t, 7 = 12.5 Hz, 1 H), 3.69 (d,./ 12.8 Hz, 1 H), 3.54 (s, 3 H), 3.48-3.41 (m, 2 H), 2.83 (s, 3
H).
MS wi/z 377 (M-H I) N-(4-lluorobenzyl)-5-hydroxy-l-methyl-2-(4-methylmorpholin-3-yl)-6-oxo-l,6-dihydropyrimidine-4-earboxamide has been resolved into its enantiomers by semi preparative chiral UPLC using the following conditions:
Solvents: a mixture of 1:1 0.2%TFA in Hexanes : EtOH
Column: chiralpak AS column, 250 x 46 mm at 1 .Oml/min, collected by
absorbtion at 260 nM The first eluate is the (f) enatiomer (MeOH, c - 0.24, 25C): fa]D=(+) 55.42. The second eluate is the (-) enantiomer (MeOH, c^0.215, 25C) [a]D- (-) 51.63.
EXAMPLE 7 2-(4-ethyI-l-methyIpiperazin-2-yl)-//-(4-fluorobenzyl)-5-hydroxy-l-methyI-6-oxo-I,6-dihydropyrimidine-4-carboxarnide

Step 1: Methyl l-methyl-2-(4-/eA7-butoxycarbonylpiperazin-2-y!))-5-
benzoyloxy-6-oxo-l,6-dihydropyrimidine-4-carboxylate

Methyl l-methyl-2-(4-/er/-butoxycarbonyl-l-ben/yloxycarbonyIpipcrazin-2-yi))-5-bcnzoyloxy-6-oxo-l,6-dihydropyrimidine-4-carboxylate (prepared from 1-[(ben/.yioxy)carbonyI|-4-(/er/-butoxycarbonyl)pipera/,ine-2-carboxylic acid (Bigge et al, Tetrahedron Lett. 1989, 3_0: 5193) by procedures similar to those set forth in Examples 2 or 3 in combination with a deprotection step) was dissolved in MeOH and hydrogenated at atm pressure on 10% Pd/C for 1 hour. The crude title product was obtained after filtration and evaporation.
Step 2: N-(4-fIuorobcn/.yl) l-methyl-2-(4-/er/-butoxycarbony!piperazin-2-yl))-
5-hydroxy-6-oxo-l,6-dihydropyrimidine-4-carboxamide

The crude product from Step 1 was dissolved in MeOH and 4-fluorobenzylamine (3.5 eq.) added. After being relluxed overnight, the precipitate was filtered and washed with Ct20 to afford the title product.
Step 3: N-(4~fluorobenzyl) l-methyl-2-(4-/^/7-butoxycarbonyl-l-
methylpiperazin-2-yi))-5-hydroxy-6-oxo-l,6-dih)drop>rimidine-4-carboxamide

The solid product from Step 2 was dissolved in MeOH and NaCNBH3 (1.4 eq.), AcONa (1.6 eq.), IICH0 37%(1 eq.) were added. The reaction mixture was stirred at room temperature for 2 days, and then evaporated to afford the crude title product.
'II NMR (DMSOd6 f TI;A, 340K, 400MHz) 5 7.40-7.35 (m, 2H), 7.18-7.10 (m, 2H), 4.83 (d, J- 7.3 Hz, IH). 4.59 (d, J - 6.3 Hz, 2H), 4.41 (d, J - 14.9 Hz, IH), 4.20-4.10 (m, 1H), 3.75-3.60 (m, IH), 3.54 (s, 3H), 3.38-3.25 (m, 2H), 3.15-3.05 (m, 1H), 2.85 (s. 311), 1.45 (s, 911). MS (Elf) m/z - 476 (M+H)S.^ep_4: Ar-(4-fluorobenzyI)-5-hydroxy-l-methyl-2-(l-methylpiperazin-2-yI)-6-
oxo-I,6-dihydropyrimidine-4-carboxamide

The crude product from Step 3 was stirred in CH2CI2/TFA (1:1) for 2 hours to remove
the Boc protective group from the piperazinyl nitrogen.
'H NMR (DMSOd6, 340K, 400MHz) 5 12.25 (bs, 111), 9.03 (bs, IH), 7.42-7.35 (m,
211), 7.20-7.10 (m, 211), 4.62-4.45 (m, 2H), 4.14-4.09 (m, IH), 3.62 (s. 3H), 3.62-3.52
(m, IH), 3.48-3.32 (m, IH), 3.25-3.15 (m, IH), 3.15-3.05 (m, 2H), 2.44-2.32 (m, IH),
2.34 (s, 3H).
MS(El+)n//z = 376(M+H)'Step 5 : 2-(4-ethyl-1-methylpiperazin-2-yl)-A'-(4-fluorobenzyI)-5-hydroxy-1 -
methyl-6-oxo-l,6-dihydropyrimidinc-4-carbo.\amide

Triethylamine (2 eq.). NaCNBH3 (1.4 eq.), AcONa (1.6 eq.) and CH3CHO (1 eq.)
were added to a methanolic solution of the crude product obtained in step 4. The
reaction was stirred at room temperature for 1 hour. The title product was obtained as
its trifluroacelate salt by preparative RP-HPLC purification (CI8, gradient of
CH3CN/H2O + O.OI %TFA).
'H NMR (DMSO-d6 i TFA, 300 MM/.) 8 9.40 (l J- 5.9 Hz, 1 H), 7.34 (t, J= 8.02
Hz. 2 H), 7.14 (t,./ - 8.7 11/, 2 II), 5.00 (d,./-9.9 Hz, 1 H), 4.54 (d, 7= 6.1 Hz, 2 H),
4.04-3.82 (m, 3 H), 3.55-3.43 (m, 4 H), 3.30-3.22 (m, 4 H), 2.87 (s, 3 H), 1.21 (t, y =
7.14 Hz, 3 H).
MS m/z 404 (MM\)EXAMPLE 7B
Step 1: A^-(4-fluorobenzyI)-5-hydroxy-2-[4-(isopropylsulfonyl)-l-
methylpiperazin-2-yl]-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide

4-fluorobenzyl 2-(1.2-dimethylpiperazin-2-yl) -5-hydroxy- 1-methyl -6-oxo- 1,6-dihydropyrimidine-4-carboxylate , obtained during the preparation of the compound in example 7 step 4, was dissolved in THF/NaOH 2N (1:1) followed by the addition of iPrSC^CI (4 eq). After being stirred at room temperature overnight, further addition of iPrSChCl (2.4 eq) and NaOH 2N (2.4 eq) were made to complete the reaction. After 3 hours NaOH 2N (10 eq) was added and the reaction mixture was stirred for 10 minutes at room temperature. The title product was isolated by preparative HPLC (Column C18, gradient of CH3CN/H20 + 0.01 %TFA).
'H NMR (DMSOdftT TFA, 300K, 300MHz) 5 9.48 (bt, J =-■ 6.5 Hz,lH), 7.39-7.35 (m, 211). 7.7.22-7.12 (m„ 211), 4.96 (d, J = 8.4 Hz, 1H), 4.57 (d, J = 6.3 Hz, 211), 4.23 (d, J = 14.4 Hz, HI), 3.96 (d, J - 10.8 Hz, 1H), 3.76 (d, J - 10.2 Hz, 1H), 3.53 (s, 3H), 3.50-3.35 (m, 3H), 3.23-3.15 (m, HI), 2.87 (s, 311), 1.25 (d, J - 6.9 Hz, 6H).

MS: m/z 482 (M+H)EXAMPLE 8 A/-(4-nuorobenzyI)"5-hydroxy-l-methyl-2-(l-mcthyIpipericiiii-2-yl)-6-oxo-l,6--dihydropyrimidine-4-carboxamidc

Methyl 5-(bcnzoyloxy)-1 -methyl-6-oxo-2-piperidin-2-yl-1,6-dihydropyrimidinc-4-carboxylate (prepared from l-(benzyloxycarbonyl)piperidine-2-carboxylic acid by procedures similar to those set forth in Examples 1 or 2 in combination with a deprotcction step) was suspended in THF and treated with 3 eq. of triethylamine and 3 eq. of methyl iodide at 40 °C. After stirring for 5 h, THF was evaporated and residue poured into EtOAc and washed with brine. Organic phase was dried (Na^SC^), filtered and concentrated under reduced pressure. The oily residue was taken into EtOAc and treated with 3 eq. of 4-fluorobenzylamine at 90 °C for 0.5 h. The title product was isolated as its trifluoroacctic salt by preparative RP-HPLC (CI 8, 5 ^iM, acetonitrile/water containing 0.1% TFA as eluant). ,HNMR(DMSO-dft,400MHz)8 12.28 (bs, 1 H), 9.50(bt, I H), 9.31 (bs, 1 H), 7.37 (dd, J = 5.6 Hz, 8.4 Hz, 2 H), 7.18 (t, J = 8.8 Hz, 2H), 4.8-4.6 (m, 1 II), 4.57 (d, J = 6.4 Hz, 2 H), 3.70-3.60 (m, I 11), 3.50 (s, 3 H), 3.4-3.3 (m, 1 H), 2.78 (bs, 3 H), 2.4-2.3 (m, 1 H), 1.92-1.46 (m, 511). MS/w/z375(M+H)"EXAMPLE 9 2-( I -AcetyIpyrrolidin-2-yl)-A/-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide

Methyl-5-(bcnzoyloxy)-2-[l-(/cr/-butoxycarbonyl)pyrroIidin-2-yl]-6-hydroxypyrimidine -4-carboxyIate was treated with TFAiCH^Cb (3:7) at 0 °C. The solution was warmed to room temperature and the progress of the reaction was monitored by MS analysis. After lh the reaction was complete and the solvent was removed under reduced pressure using a rotatory evaporator. The title product was precipitated with Et20 and collected by filtration.
!H-NMR(CDCI3,400MHz)8 8.17(d,J=7.4Hz, 2 H), 7.67 (t, J = 7.6 Hz, 1 H), 7.52 (t, J= 7.6 Hz, 2 H), 5.45 (dd, J= 7.6, 6.7 Hz, 1 II), 3.82 (s, 3 H), 3.66 (s, 3 H), 3.61 (t, .7= 7.0 Hz, 2 11), 2.78-2.69 (m, 1 H), 2.40-2.00 (m, 3 H). MS/w/*358(M+H)+.
Sicj"?_2- 2-(l-Acetylpyrrolidin-2-yl)-A^-(4-[luorobcnzyl)-5-hydroxy-l-methyI-6-
oxo-l,6-dihydropyrimidine-4-carboxamide To a stirred solution of the product of Step I (1.0 eq.) in CIICI3, trielhylamine (3.0 eq.) was added followed by the addition of acetyl chloride (1.5 eq.). The reaction was stirred at room temperature until the starting material was consumed as determined by MS analysis. The reaction mixture was concentrated and the crude product was used directly in the subsequent step without further purification.

A solution of the crude product from above (1.0 eq.) in NMP was treated with 4-fluorobenzylamine (2.0 eq.). The solution was stirred at reflux until the reactants were consumed as determined by MS analysis. The title compound was obtained by RP-HPLC purification (Cis, eluting with water and acetonitrile containing 0.1 % trifluoroacetic acid) as a 4:1 mixture of rotamers by NMR.
'll-NMR (DMSO-d6, 400 MHz) 5 12.11 (bs, 1 H), 8.49 (t, .7=6.2 Hz, 0.8 H), 8.30 (t, y=--6.2 Hz? 0.2 H), 7.4-7.3 (m, 2 II), 7.15 (t, J-8.8 Hz, 2 M), 5.22 (dd, J=$A 3.2 Hz, 0.2 H). 5.02 (dd, .7-8.0, 3.2 I Iz, 0.8 H), 4.60-4.47 (m, 2 H), 3.95-3.85 (m, 0.8 H), 3.80-3.70 (m, 0.2 H), 3.59-3.57 (m, 0.8 H), 3.55 (s, 2.4 H), 3.52 (s, 0.6 H), 3.43-3.37 (m, 0.2 H), 2.40-1.7 (m, 4 H), 2.5 (s, 2.4 H), 1.75 (s, 0.8 H). MSw/z389(M+H)+.
EXAMPLE 10 2-(l-benzoyI-2,3-dihvdro-l//-indol-2-yl)-A/r-(4-lluorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide

Step I: Methyl 2-(2,3-dihydro-1//-indol-2-yl)-1 -methyl-5-benzoy!oxy-6-oxo-
l,6-dihydropyrimidine-4-carboxyIate
^^

BenzvI 2-[ 5-(bcnzoyioxy)-4-(methoxyearbonyl)-1 -methyl-6-oxo-1 ?6-dihydropyHmidi-2-yI|indoIinc-l-carboxyIate was dissolved in EtOAc and

hydrogenated at atmospheric pressure on 10% Pd/C overnight. The crude title product was obtained after filtration and evaporation
Step 2: Methyl 2-(l-benzoyl-2,3-dihydro-l//-indol-2-yl)-5-benzoyloxy-l-
methyI-6-oxo-l,6-dihydropyrimidine-4-carboxylate

THF was added to the crude product of Step 1, followed by pyridine (2 cq.) and PhCOCI (I eq.). After being stirred at room temperature overnight, the reaction mixture was evaporated to give the crude title product.
Stee_3: 2-(l-benzoyI-2,3-dihydro-l//-indol-2-yl)-yV-(4-tluorobenzyl)-5-
hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide The crude product of Step 2 was dissolved in MeOH and 4-
fluorobenzylaminc (3.5 eq.) added. The solution was stirred at 60 °C over night. The
title product was obtained by preparative RP-HPLC (CI8, gradient of CH3CN/H2O +
0.01 %TFA).
!HNMR(DMSO-d6 i TFA, 340 K, 400 MHz) 5 7.75-7.80 (m, 1 H), 7.45-6.97 (m, 13
H). 5.77(dd,y= 10, 3.6Ilz, 1 H), 4.35-4.50 (m, 2 11), 3.72 (dd, J = 16, 10 Hz, 1 H),
3.35 (s, 3 H),3.16(dd,J- 16, 3.6 Hz, 1 H).
MS m/z 499 (M+H)EXAMPLE 1 1 Ar-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-[ l-(pyridin-2-ylcarbonyl)-l,2,3,4-tetrahydroquinolin-2-yl]-l,6-dihydropyrimidine-4-carboxamide

Benzyl 2-|5-(bcnzoyloxy)-4-(methoxycarbonyI)-1 -methyl-6-oxo-1,6-dihydropyrimidi-2-yI|-l,2,3,4-tetrahydroquinoline-l-carboxylate (prepared from tclrahydroquinoline-2-carboxylic acid (RobI et al, Tetrahedron Letters 1995, 36: 1593) by protection of the nitrogen and following procedures similar to those set forth in Examples 1 or 2 in combination with a deprotection step) was dissolved in EtOAc and hydrogenated at atmospheric pressure on 10% Pd/C at room temperature overnight. The title product was obtained as the residue after filtration and evaporation of the organic solvent.
Sjep_2: Methyl 5-benzoyloxy-!-methyl-6-oxo-2-| l-(pyridin-2-ylcarbonyl)-
l,2,3,4-tetrahydroquinolin-2-yl]-l,6-dihydropyrimidine-4-carboxylate

The residue of Step 1 was dissolved in dichloromethane. Pyridine, picolinoyl chloride hydrochloride and a catalytic amount of DMAP were added. A further addition of the reactants was made alter two hours. After evaporation of the solvent, the residue was diluted with EtOAc, the organic phase washed with water, dried (Na2S04) and evaporated to afford the title product.
Step 3: A^-(4-fluorobenzyl)-5-hydroxy-I-methyl-6-oxo-2-[l-(pyridin-2-
ylcarbonyl)-l,2,3,4-tetrahydroquinolin-2-yl]-l,6-dihydropyrimidine-4-carboxamide
The residue of Step 2 was dissolved in DMF and 4-fluorobenzylamine (3 eq.) was added. The reaction mixture was stirred at 90°C for 1 h. The title compound was purified by preparative HPLC and isolated as its trifluoroacetic salt (CI 8, gradient of CH3CN/H20 f 0.01% TFA).
lH-NMR(DMSO-d6+TFA,400MHz,340K)5 8.35(d,y=4.2Hz, 1 H),7.81 (t,V = 7.4 Hz, I H), 7.54 (bt. 1 II), 7.49 (d, J= 7.7 Hz, 1 H), 7.37 (dd, J = 5.2 Hz, 7.0 Hz, 1 H), 7.25-7.22 (m, 2 II), 7.17-7.09 (in, 3 H), 6.90 (t, J = 7.3 Hz, 1 H), 6.62 (t,./- 7.3 Hz. I H), 6.43 (bs, 1 H), 5.74 (t, 7-7.6 Hz, 1 H), 4.42 (dd, ^=6.4 Hz, 14.8 Hz,lH), 4.32(dd, .7=6.4 Hz, 14.8 Hz, 1 H), 3.65 (s, 3 H), 2.80-2.70 (m, 3 H), 1.85-1.75 (m, 1 H). MS/w/z514(M+H)f.
EXAMPLE 12 2-\ (2SAR)-\ -benzoyl-4-hydroxypyrrolidin-2-yI]-iV-(4-nuorobenzyI)-5-hydrpxy-l-methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide

Methyl 2-f(25,4/?)-1 -tert-butyloxycarbonyl-4-(benzyIoxy)pyrrolidin-2-yl|-5-(benzoyloxy)-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxylate [obtained from N-Boc-O-benzyl-L-hydroxyproline using chemistry similar to those set forth in Examples 1 or 2; the stereochemistry of products of Steps 1 to 3 is based on that of starting material] was dissolved in dichloromethane (0.03 M), followed by addition of an excess of TFA. The mixture was stirred at room temperature for 1 hour. The solvent was evaporated in vacuo. To the residue dissolved in pyridine, benzoic anhydride (2 eq.) was added. The mixture was stirred at room temperature for 5 hours. Pyridine was evaporated in vacuo and the residue dissolved in EtOAc was washed with HC1 (1M), saturated aqueous NaHC03 and brine, dried on Na2S(>4, filtered and evaporated in vacuo to give the title product as a yellow solid.
'U NMR (DMSO-d6, 400 MHz, 330 K) 5 8.07 (d, J- 7.6 Hz, 2 H), 7.77 (t, .7-7.3 Hz, H), 7.62 (t, 7=7.74 I Iz, 2 11), 7.52-7.49 (m, 5 H), 7.33-7.30 (m, 5 H), 5.47 (bt, 1 H), 4.53 (d,J= 12.1 Hz, i H), 4.44 (d. J-12.0 Hz. 1 H),4.36(bs. I H), 3.87-3.84 (m, 1

H), 3.76(s, 3 H), 3.73 (s, 3 H), 3.57 (d, 7=11.2 Hz, 1 11)2.70 (t, 7=12.2 Hz, I H), 2.31-2.28 (m, 1 H).
SICJL.2: 2-|(2.V,47e)-Nbenzoyl-4-(benzyloxy)pyrrolidin-2-yl]-A^-(4-
nuorobenzyl)-5-hydroxy-l-methyi-6-oxo-l,6-dihydropyrimidine-4-carboxamide

The compound of Step 1 was dissolved in methanol and 4-fluorobenzylamine (5 eq.) was added. The mixture was refluxed overnight. After cooling, the reaction mixture was filtered and washed with ethyl ether to obtain the title product as a white solid.
'HNMR (DMSO-d6,400MHz, 300 K) 5 12.15 (s, 1 11), 9.00 (br t, lH),7.48(d, .7-7.6 Hz, 2 H) 7.41-7.20 (m, 10 H), 7.12 (t,./= 8.8 Hz, 2H), 5.27 (t, J= 8Hz, 1 H), 4.63 (dd, J= 14.9, 7.3 Hz, 1 H), 4.56-4.38 (m, 2 H), 4.26 (bs, 1 H) 4.25 (d, 7=11.4 Hz, 2 H) 3.68 (s, 3 H), 3.52 (d, 7= 11.2 Hz, 1 H), 2.66-2.63 (m, 1 H), 2,26-2.20 (m, 1 H). MS/w/z557(M+H)Step 3: 2-1X25,4/?)-] -bcnzoyl-4-hydroxypyrrolidin-2-yl]-A^-(4-fiuorobenzyl)-5-
hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide The title compound of Step 2 was dissolved in AcOH and 10% Pd/C
(10% weight) was added. The mixture was stirred under Hsat atmosphere overnight.
Pd/C was filtered, AcOl I evaporated in vacuo, and the resulting title compound was
washed with methanol.
'H NMR(DMSO-d(i, 400 MHz) S 12.1 (s, 1 H), 9 (bt, 1 H), 7.51-7.47 (m, 3 11), 7.41-
7.33 (m, 4 H) 7.11 (t, 7= 8.8 Hz, 2 H), 5.27 (t, 7= 8 Hz, I H), 5.08 (d, 7=3.2 Hz, 1 H),

4.63 (dd, 7=14.8 Hz, 7.3 Hz, I H), 4.43-4.39 (m, 2 II), 4.20 (d, J- 7.4 Hz, 1 H), 3.67 (s. 3 H), 2.41-2.36 (m, I II). 2.2-2.1 (m, I H). MS w/z467(M-H-I)EXAMPLE 13
yW-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-oxo-yV^-(pyridin-2-ylmcthyI)-1.6-dihydropyrimidine-2,4-dicarboxamide

2-Ethyl 4-methyl 5-[(2,2-dimethylpropanoyl)oxy]-1 -methyl-6-oxo-1,6-dihydropyrimidine-2,4-dicarboxylate (made by protection and alkylation of the starting material of Example 4, Step I using procedures similar to those set forth in Examples I or 2) was dissolved in DME, 4-fluorobenzyIamine (3.1 eq.) was added and the mixture was stirred at 90 °C overnight. After concentration of the solvent, the residue was taken into EtOAc, washed with 1 N HO, dried over Na2SC>4 and evaporated to obtain crude A^-(4-fluorobenzyl)-2-ethoxycarbonyM-methyl-5-hydroxy-6-oxo-l,6-dihydropyrimidine-4-carboxamide. To this crude product was added 2-picolylamine (8 eq.), and the reaction was stirred at 90 °C overnight. The title product was obtained as its trifluoroacetic salt by preparative RP-HPLC purification (CI8 gradient of CH3CN/H20 f- 0.01% TFA).
!H NMR (DMSO-d6, 300K, 400 MHz) 5 12.70 (bs, 1 H), 9.75-9.65 (m, 2 H), 8.56 (d, 7==4.4Hz, 1 H), 7.90-7.80 (m, 1 H), 7.44 (d, J= 8.0 Hz, 1 H), 7.40-7.35 (m, 3 H), 7.17 (t, J -■= 9.2, 2 H), 4.60 (d, J - 6.0 Hz, 2 H), 4.54 (d, J - 6.0 Hz, 2 H), 3.67 (s, 3H). MS/v//z4I2(M-HI)EXAMPLE 14 2-[2-(4-benzoylpiperazin-l-yl)elhyI]-A^-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-L6-dihydropyrimidine-4-carboxamide

Methyl 2-(2,2-dimethoxyethyl)-5-benzoyIoxy-l-methyl-6-oxo-I,6-dihydropyrimidine-4-earboxylate (1.0 eq.) (prepared from 3,3-dimethoxypropionitrile by procedure similar to those set forth in Examples 1 or 2) in dry MeOH was treated with 4-fluorobenzyl amine (2.5 eq.) at reflux for 2 hours. Solvent was removed in vacuo and residue triturated with Et20 to obtain the title product. !H NMR (DMSO-d6, 300K, 400 MHz) 5: 9.80 (br s, III), 7.41-7.38 (m, 2H), 7.15 (t, J = 8.7 Hz, 2H), 5.04 (br s, IH), 4.47 (d, J = 6.2 Hz, 2H), 3.46 (s, 3H), 3.28 (s, 6H), 3.01 (d,J = 5.5Hz,2H). MS: w/z366(M-H)-f
Stcp 2: N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-2-(2-oxoethyl)-l,6-
dihydropyrimidine-4-carboxamide

The product of Step 1 was treated with a mixture HC1 IN/IT IF for 1 hour at 40 °C. Organics were removed in vacuo and residue extracted in DCM, dried over Na2SC)4 and concentrated to give the title compound as a foam which was immediately reacted in the following reductive amination. MS: m/z 320 (M HI-H)--h
Step 3: 2-[2-(4-ben/oylpiperazin-l-yl)ethyIj-Ar-(4-fluorobenzyl)-5-hydroxy-l-
methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide The product of Step 2 was dissolved in MeOI-f and treated with sodium acetate (1.6 eq.), 1-benzoylpiperazine (2 eq.), and sodium cyanoborohydride (1.43 cq.). The mixture was left stirring at room temperature for 1 hour. The reaction mixture was concentrated and the title compound was obtained by RP-HPLC purification ( Cis, eluting with water and acetonitrile containing 0.1 % TFA). IHNMR(CDCl3+TFA,273K,600MHz)8: 10.431 (br s, I H), 8.38 (t, J - 5.7 Hz, 1H), 7.61 (t, J = 6.4 Hz, 1H), 7.52 (t, J = 7.7 Hz, 2H), 7.41 (d, J = 7.4 Hz, 2H), 7.28 (2H, overlapped by CMCI3), 7.07 (t, J - 8.5 Hz, 2H), 4.97 (d, J - 14 Hz, 1H), 4.63 (d, J - 5.7 Hz, 2H), 4.10 (d, J = 14 Hz, 1H), 3.93 (d, J - 1 1.9 Hz, 1H), 3.82-3.74 (m, 4H), 3.61 (s,3H), 3.47(t, J= 12.6 Hz, 1H), 3.41 (br s, 211), 3.29-3-26 (m, 1H), 3.15-3.14 (m, HI). MS: /w/z494(M + H)+.
EXAMPLE 15
A/-(4-t1uorobenzyl)-5-hydroxy-l-(2-hydroxy-3-morpholin-4-ylpropyl)-6-oxo-l,6-dihydropyrimidine-4-earboxamide

Methyl 5-j(2,2-dimethylpropanoyl)oxy]-6-hydroxy-1,6-dihydropyrimidinc-4-carboxylate (see Example 4, Step 3) was dissolved in THF, then allyl bromide (2 eq.) and CS2CO3 (2 eq.) were added. The reaction mixture was rcfluxed for 2h, then evaporated. The residue was diluted with EtOAc, washed with IN MCI, dried (Na2S04) and the solvent evaporated. The product was purified by flash chromatography on silica gel eluting with a gradient of petroleum ether/EtOAc. !H-NMR (DMSO-d6, 400 MM/, 300K) 8 8.47 (s, Ml), 5.99-5.92 (m, 1H), 5.25-5.14 (m, 2M), 4.58 (d, J = 5.5 Hz, 211), 3.82 (s, 3H), 1.28 (s, 9H).
Sl£R_2: yV-(4-tluorobenzyl)-5-hydroxy-l-(2-hydroxy-3-morpholin-4-ylpropyl)-
6-oxo-l,6-dihydropyrimidine-4-carboxamide
2a. The compound of Step 1 was dissolved in dichloroethane and m-CPBA was added (5 eq.). The reaction mixture was refluxed until the starting material was completely consumed, then evaporated. MS m/z 311 (M+H)*.
2b. Crude material from step 2a was dissolved in MeOM and morpholine (6 eq.) was added. The reaction mixture was refluxed for 3h, then evaporated. MS (Elf) m/z 398 (M+H)+.
2c. Crude material from step 2b was dissolved in DMF and 4-fluorobenzylamine (3 eq.) was added. The reaction mixture was stirred at 90 °C for

3h. The title compound was obtained as its trifluoroacetate salt by RP-HPLC
purification (gradient of CMjCN/H20 + 0.01% TEA).
'll-NMR (DMSO-d6 +TFA, 400 MHz, 340K) o 9.27 (bt, III), 7.94 (s, 1H), 7.40-7.36
(m, 211), 7.15-7.11 (m, 211), 4.48 (d, J= 6.4 Hz, 2H), 4.30-4.36, (m, 1H), 4.09 (dd, J=
13.6, 4.0 Hz, 1H), 3.91-3.86 (m. 5H), 3.34-3.30 (m, 5H), 3.18 (dd, J= 13.6 ,4.0 Hz,
111).
MSw/z407(M+H)EXAMPLE 16 2-|(2S,4S)-l-acetyI-4-nuoropyrrolidin-2-yl]-N-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo- 1.6-dihvdropvrimidine-4-carboxamide
l-benzyl-2-methyl(2S,4R) 4-hydroxypyrrolidine-l,2 dicarboxylate in
dichloromethane was added dropwise to a solution, precooled to -78 °C, oi"N,N-
diethylaminosulfur trifluoride (1.0 eq.) in dichloromethane. The reaction was stirred
while the temperature was allowed to increase to 25 °C. The solvent was concentrated
under vacuum and the crude was purified by flash chromatography (eluent: petroleum
ether: EtOAc = 1:1) to give the title compound.
'H NMR (CDC13, 300 MHz, 300 K) 8 7.42-7.30 (m, 5H), 5.35-5.10 (m, 3H), 4.65 (d,
J-9.6 Hz, 0.5H), 4.57 (d, J- 9.4Hz, 0.5H), 3.99-3.62 (m, 211), 3.79 (s, 1.5H), 3.68 (s,
1.5H). 2.62-2.29 (m,2H).
MS:m/z282(MMl)'.

Step 2: (4S)-l-[(Benzyloxy)carbonyl]-4-fluoro-L-proline
.. /■
l-Bcnzyl-2-methyl-(2S,4S)-4-fluoropynx)lidine-l,2-dicarboxylate dissolved in methanol was treated with NaOH IN (2 eq.) and the reaction mixture was stirred at 50 °C for 3 hours. Alter concentration of the solvent, HC1 IN was added until pH=l and the aqueous layer was extracted three times with dichloromethane. The organic phase was washed with brine, dried over Na2SO;j and filtered to give, after concentration, title compound.
'llNMR (CDCI3, 400 MHz, 300 K) 5 7.45-7.30 (m, 5H), 5.33-5.18 (m, 3H), 4.70-4.60 (bm, IH), 4.00-3.65 (m, 211), 2.85-2.25 (m, 2H). MS:m/z268(M+H)+.
Step 3: Benzyl-(2S,4S)-2-aminocarbonyl-4-(luoropyrrolidine-l-carboxylate

A stirred solution of (4S)-l-[(Bcnzyloxy)carbonylJ-4-fiuoro-L-proline in dioxane was
treated with pyridine (0.7 eq.) and B0C2O (1.3 eq.), then ammonium bicarbonate (1.26
eq.) was added and the mixture was stirred at room temperature for 15 hours.
Dioxane was concentrated and the residue was taken up in ethyl acetate, washed with
1 N MCI and brine, dried over Na2SC>4 to give, after filtration and concentration, title
compound.
{l 1 NMR (DMSO-d6, 400 MHz, 340 K) § 7.40-7.28 (m, 511), 5.25 (dt. JM_r-- 53.6 Hz, J
= 4.5 Hz, 1H), 5.13-5.06 (m, 211), 4.28 (d, J= 9.6Hz, 1H), 3.80-3.63 (m. 2H), 2.45-
2.21 (m, 2H).
MS:m/z267(M-H-l)*.

Step 4: Benzyl-(2S,4S)-2-cyano-4-fluoropyrrolidine-!-carboxylate

Bcnzyl-(2S,4S)-2-aminocarbonyl-4-nuoropyrroIidine-]-carboxylate in
dichloromethane was treated al 0 °C with Et3N (2.1 eq.) and trifluoroacetic anhydride
was added dropwise.
The reaetion mixture was stirred at 0 °C for 0.5 hour and 10 minutes at room
temperature. Then, it was diluted with dichloromethane, washed with HCI IN and
brine, dried over Na2SO.| and filtered to give, after concentration, title compound.
'li NMR (DMSO-dr„ 400 MHz, 340 K) 5 7.42-7.30 (m, 5H), 5.40 (dbt, JH_|.-= 52.3 Hz,
HI). 5.20 (d, JH2.7 Hz, HI), 5.16 (d, J- 12.7 Hz, III), 4.94 (d, J= 8.4Hz. 1 H), 3.68-
3.56 (m, 211), 2.63-2.41(m, 211).
MS: m/z 249 (M+H)'Step_rV Benzyl-(2S,4S)-2-[amino(hydroxyimino)methyl]-4-fluoropyrrolidine-
I-carboxylate

BenzyI-(2S,4S)-2-cyano-4-fluoropyrroiidine~l-carboxylate dissolved in absolute ethanol was treated with triethyl amine (1.5eq.) and hydroxylamine hydrochloride (1.3 cq.).
The reaction mixture was stirred at 50 °C for 3 hours and then the solvent was removed under reduced pressure. The residue was partitioned between water and dichloromethane and the aqueous layer was extracted with dichloromethane three times. The organic phase was dried over Na2SO.j and filtered. The solid obtained by concentration was then recrystallized from MeOH to give title compound.

'H NIMR (DMSO-dft. 400 MH/, 300 K) 5 9.10 (bs, III), 7.40-7.25 (m, 5H), 5.35-5.15 (m, 3H), 5.07 (m, 211), 4.43 (d. J = 9.1 Hz, 1H), 3.72-3.56 (m. 2H), 2.45-2.20(m, 2H). MS: m/z282(M+lir.
Stcp..6j. Dimcthyl-2-{[(amino-{(2S,4S)-l-[(benzyloxy)carbonyl]-4-
fluoropyrrolidin-2-yl} methyl idenc)amino]oxy}but-2-enedioatc
/"*/"* ft A _
BcnzyI-(2S,4S)-2-[amino(hydroxyimino)methyl]-4-nuoropyrrolidine-I-carboxylate in
chloroform was treated with dimethylacetylene dicarboxylate for 3 hours at 60 °C.
The chloroform was then concentrated to give the title compound as a 8:2 mixture of
isomers.
'II NMR (DMSO-d(1. 400 MHz, 300 K) 5 7.45-7.25 (m, 5H), 6.51 (bs, 1.6 H), 6.14
(bs, 0.4 H), 5.64 (s, 0.8H), 5.61 (s, 0.2 H), 5.30 (dt, J».F= 53.9 Hz, J= 4.6 Hz, 1H),
5.15-5.04 (m, 2H), 4.51 (t, J-8.8 Hz, 0.8H), 4.44 (bt, 0.4H), 3.85-3.48 (m, 8H), 2.67-
2.23 (m, 2H).
MS:m/z424(M+H)T.
Step 7: Methyl-2-{(2S,4S)-l-[(benzyloxy)carbonyl]-4-fluoropyrroIidin-2-yl}-
5,6-dihydroxypyrimidine-4-carboxylate

Dimethyl-2-{[(amino-{(2S,4S)-l-[(benzyloxy)carbon>T|-4- fluoropyrrolidin-2-yl}methylidene)amino]oxy}but-2-enedioate was refluxcd for 6 hours in ortho-xylene.

The reaction mixture was then cooled down to room temperature and petroleum ether was added. A light brown solid precipitated to give after filtration title compound, that was not purified furthermore, but used as such in the following reaction.
SlepJL Methyl-5-(benzoyloxy)-2-{(2S,4S)-l-((benzyloxy)carbonyl|-4-
fluoropyrrolidin-2-yl}-6-hydroxypyrimidine-4-carboxylate

Methyl-2-{(2S,4S)-l-[(ben/yloxy)carbonylJ-4-nuoropyrrolidin-2-yl}-5,6-dihydroxypyrimidine-4-carboxylate in pyridine was treated with benzoic anhydride (1.3 eq.) and the reaction mixture was stirred at room temperature overnight. Pyridine was concentrated and the residue was taken up in ethyl acetate and washed with HC1 IN and brine. The organic phase was dried over Na2S04 and filtered to give after concentration a crude that was purified by Hash chromatography , (eluent: petroleum ether: ethyl acetate- 1:1) to give title compound.
'II NMR (DMSO-d6, 400 MHz, 300 K) 5 13.50 (bs, 1H), 8.09 (d, J=7.7Hz, 2H), 7.80 (t, J- 7.35 Hz, 1H), 7.64 (t, J=7.8 Hz, 211), 7.45-7.15 (m, 5H), 5.36 (dbt, JH-r=54 Hz, 111), 5.14 (m, 2H),5.02-4.93 (m, 1H), 3.95-3.60 (m, 211), 3.76 (s, 3H), 2.80-2.36 (m, 211). MS:m/z496(M+H)+.
Step 9 : Methyl-5-(benzoyloxy)-2-{(2S,4S)-l-[(benzyloxy)carbonylJ-4-
fluoropyrrolidin-2-yI}-l-methyl-6-oxo-1.6-dihydropyrimidine-4-carboxylate .

Melhyl-5-(benzoyI()xy)-2-{(2S,4S)-l-[(bcnzyloxy)carbonyl|-4-fluoropyrroiidin-2-yl}-6-hydroxypyriinidinc-4-carboxylate, dissolved in dry dioxane, was added to a suspension of lithium hydride (1.2 eq.) in dry dioxane. The reaction mixture was stirred at 38 °C for 45 minutes and then cooled down to room temperature. Dimethyl sulfate (1.3 eq.) was added and the mixture was heated to 58 °C and stirred at this temperature for 3 hours. The reaction mixture was then cooled down and glacial acetic acid (0.2 eq.) was added, followed by water and ethyl acetate. The aqueous layer was separated and extracted with ethyl acetate; the organic phase was dried over Na2S04 and filtered to give, after concentration, a crude that was purified by flash chromatography (clucnt petroleum ether: ethyl acetate from 4:6 to 2:8) to give the title compound as a 4.6:5.4 mixture of rotamers by NMR.
'I-I NMR (DMSO-d6, 400 MHz, 300 K) 5 8.08 (d, J-7.5 Hz, 2H), 7.79 (t. J- 7.3 Hz, 111). 7.63 (t, J=7.5 Hz, 2H)S 7.37-7.11 (m, 5H), 5.48-5.38 (m, 2H), 5.20 (d, J= 12.8 Hz. 0.46H), 5.12 (d, J-11.8 Hz, 0.54H), 5.10 (d, J=I2.5 Hz, 0.54H), 4.92 (d. J=12.8 Hz, 0.46H), 4.00-3.75 (m. 2H), 3.72 (s, 3H), 3.59 (s, 1.6H), 3.52 (s, 1.4H), 2.90-2.65 (m, 211). MS:m/z5I0(IVMlf.
Step 1.0: Mcthyl-2-j(2S,4S)-1 -acetyi-4-fluoropyrrolidin-2-yl]-5-(benzoyloxy)-6-
hydroxypyrimidine-4-carboxylate.

Methyl-5-(benzoylo\y)-2-{(2S,4S)-l-[(benzyIoxy)carbonyI|-4-fluoropyrrolidin-2-yl}-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxylate. dissolved in ethyl acetate was treated with Pd/C 10% (10%w/w) and acetic anhydride (1 eq.) and submitted under H2 atmosphere at room temperature. The reaction mixture was stirred at room temperature for 18 hours and then the suspension was filtered over celite to give the title compound as a 7:3 mixture of rotamers by NMR.
]H NMR (DMSO-d6, 400 MHz, 300 K) 5 8.07 (m, 2H), 7.78 (m, 1H), 7.62 (m, 2H), 5.75-5.26 (m, 2H), 4.13-3.60 (m, 2H), 3.72 (s, 3H), 3.59 (s, 3H), 2.79-2.36 (m, 2H), 2.03 (s, 2.1 H), 1.87 (s, 0.9U). MS:m/z418(MHI)Stcp_.LL: 2-((2S>4S)-l-acetyl-4-fluoropyrrolidin-2-yl]-N-(4-fluorobenzy))-5-
hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide.
Methyl-2-[(2S,4S)-l-acetyl-4-fluoropyrroIidin-2-yl]-5-(benzoyIoxy)-6-hydroxypyrimidine-4-carboxylate was dissolved in MeOH (0.12 N) and treated with 4-F-benzylamine (3 eq.) in a sealed tube. The reaction mixture was stirred at 65 °C for 18 hours, then it was cooled down. The solvent was evaporated and the residue was washed with ethyl ether several times to obtain a solid that was recrystallized from ethanol and washed again with ethyl ether to give the title compound as a 7.3:2.7 mixture of rotamers by NMR.
'il NMR (DMSO-d6, 500 MHz, 300 K) 5 12.01 (bs, I H). 8.52 (t, J = 6.3 Hz, 0.7H), 8.34 (t, J = 6.3 Hz, 0.311), 7.34-7.29 (m, 2H), 7.18-7.12 (m, 2H), 5.39 (dbt, JH-F=54.3 Hz. 0.7H), 5.29 (dt, J[M- 54.2 Hz, J-4.4 Hz, 0.3 II), 5.38 (d, J=8.9 Hz, 0.3H), 5.18

(dd, J-9.2 and 1.6 Hz, 0.7H), 4.55-4.47 (m, 2H), 4.20-3.78 (m, 2H), 3.51 (s, 2.1H), 3.50(s, 0.9H), 2.75-2.54 (m, 1H), 2.47-2.27 (m, 1H), 2.00 (s, 2.1 H), 1.81 (s. 0.9H). MS: m/z 407 (M+M)+.
EXAMPLE 17
2-{(2.S',4/^)-l-[(diiTiethylamino)(oxo)acetyl]-4-methoxypyrrolidin-2-yl}-AA-(4-fliiorobenzyi)-5-hydroxy-l-mcthyl-6-oxo-I,6-dihydropyrimidine-4-carboxamide

Step I: (4/?)-1 -|(Benzyloxy)carbonyl]-4-mcthoxy-L-proline
^■^ la/lb
Synthesized following the procedure reported on Journal of Medicinal Chemistry 1988,31,875-885.
Step 2: Benzyl-(2.V,4y?)-2-cyano-4-methoxypyrroIidine-l-carboxylate

To compound (4y?)-l-[(I3enzyioxy)carbonylJ-4-mcthoxy-L-prolinc dissolved in dioxane, Hoc anhydride (1.3 eq), NH4HCO3 (1.26 eq.) and pyridine were added. The mixture was stirred overnight at room temperature. Dioxane was removed in vacuo

and the residue, dissolved in ethyl acetate, was washed with HC1 IN, saturated aqueous NaHC03 and brine, dried over Na2S04, filtered and concentrated,in vacuo to get the primary amide. The crude product was dissolved in dichioromethane and tricthylamine (2.1 eq,) was added. The mixture was cooled down to 0° C and trifiuoroacetic anhydride (1.1 cq.) was added. After I hour the dichioromethane solution was diluted and washed with HC1 IN, saturated aqueous NaHCC>3 and brine, dried over Na2SO.j, filtered and evaporated in vacuo. The compound was purified by flash chromatography on silica gel (eluent ethyl acetate: petroleum ether = 20%:80%) as a 4:6 mixture of rotamers by NMR.
'II NMR (DMSO-d6. 400 MHz, 300 K) 5 7.45-7.3 (nru 5H), 5.20 (d, J-12 Hz, 0.4H), 5.14 (s, 1.211), 5.12 (d, J- 12 Hz, 0.4H), 4.75 (t, J- 7 Hz, 0.4H), 4.64 (t, J 7.8 Hz, 0.611), 4.02 (bs, 111), 3.6-3.45 (m, 2H), 3.21 (s, 311), 2.45-2.40 (partially under DMSO)(m, 1H), 2.40-2.25 (m, 1H).
St^P. 3: Benzyl-(2.,4/0-2-famino(hydroxyimino)methylJ-4methoxypyrrolidine
-1-carboxylate
To benzyl-(25,,4/?)-2-cyano-4-methoxypyrrolidine- 1-carboxylate, dissolved in ethanol (0.4 M), hydroxylamine hydrochloride (1.3 eq.) and tricthylamine (1.5 eq.) were added. The mixture was stirred at 40°C for 4 hours then at room temperature overnight. The mixture was concentrated in vacuo and the residue dissolved in ethyl acetate washed with brine, dried over Na2S04, filtered and concentrated to give title compound.
!I1 NMR (DMSO-d(1, 400 MHz, 300 K) 5 9.05 (bs, 1H), 7.45-7.25 (m, 5H). 5.4 (bs, 211). 5.10 (d, J- 13 Hz, HI), 5.03 (d, J=13 Hz, 1H), 4.26 (t, J= 7.4 Hz, 111), 3.97 (bs, HI). 3.63-3.45 (m, 211), 3.22 (s, 3H) 2.3-2.03 (m, 211).

Step 4: Uimcthyl-2-{|(amino-{(2 mcthoxypyrrolidin-2-yI} methyl idene)amino]oxy}but-2-enedjoate

7o benzyl-(2iS',47^)-2-[amino(hydroxyimino)methyl]-4methoxypyrroIidine -I-carboxylate, dissolved in chloroform, dimethyl acetylendicarboxylate (1.1 eq.) was added. The mixture was refluxed for 1 hour and left stirring at 40° C overnight. The chloroform was removed in vacuo and the crude product purified by flash chromatography on silica gel (eluent ethyl acetate: petroleum ether = 40: 60). Two isomers were present in ratio 7:3.
1II NMR (DMSO-d6, 400 Mil/, 300 K) 8 7.40-7.23 (m, 5H), 6.7-6.55 (2bs, 1.4 H), 6.35-6.2 (bs, 0.6H). 5.61 (s, 0.7H), 5.59 (s, 0.3M), 5.10 (d, J=13 Hz, 0.7H), 5.08 (s, 0.611), 5.02 (d, JH3 Hz, 0.7H), 4.30-4.20 (m, HI), 3.97 (bs, 1H), 3.78 (s, 2.IH), 3.73 (s, 0.9H), 3.62 (s, 0.9H), 3.59 (s, 2.1H), 3.65-3.50 (m, 2H), 3.22 (s, 3H), 2.37-2.23 (m, 1H), 2.10-1.95 (m, 1H).
Step 5: Methyl 5-(bcn/oyloxy)-2-{(25',4/0-l-[(benzyloxy)carbonyl]-4-
methoxypyrrolidin-2-yl}-6-hydroxypyrimidine-4-carboxylate

Dimethyl-2- {[(amino- {(2SAK)- l-[(ben/yloxy)carbonylJ-4-methoxypyrrolidin-2-yl}mcthylLdene)amino]oxy}but-2-enedioate were dissolved in xylene and the solution

stirred at 150°C for 3 hours and at room temperature overnight. Xylene was concentrated in vacuo. To the crude compound, dissolved in pyridine, benzoic anhydride (1.3 eq.) was added and the reaction mixture was stirred at room temperature overnight. The solution was concentrated in vacuo and the crude dissolved in ethyl acetate washed with 1 N HO, saturated aqueous NaHCOi and brine, dried on Na^SO^ filtered and evaporated in vacuo. The crude product was purified by flash chromatography on silica gel (eluent ethyl acetate: petroleum ether = 10:90) and showed a 1:1 mixture of rotamers by NMR.
jH NMR (DMSO-d6, 400 MHz, 300 K) S 13.5 (s, 1H), 8.09 (t, J- 7.0 Hz, 2H), 7.82-7.75 (m, 1H), 7.66-7.61 (m, 211), 7.40-7.25 (m, 4 H), 7.12-7.06 (m, lH),5.10(s, 1H), 5.09 (d, J- 12.5 Hz, 0.5H), 4.88 (d, J= 12.5 Hz, 0.5H), 4.66 (dd, J 16.2 and 8.0 Hz, 111), 4.10-4.00 (m, 1H), 3.74 (s, 3H), 3.75-3.60 (m, 211), 3.25 (s, 3H), 2.45-2.40 (partially under DMSO) (m, IH), 2.13-2.03 (m, 111).
Stcp._6: Methyl-5-(benzoyloxy)-2-{(25,4y^)-l-[(benzyloxy)carbonyl]-4-
methoxypyrrolidin-2-yl} -1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxylate

To methyl 5-(ben7.oyloxy)-2-{(25;47?)-l-[(benzylox\)carbonyl]-4-methoxypyrrolidin-2~yI}~6-hydroxypyrimidinc-4-carboxylate, dissolved in dioxane, LiH (1.4 eq.) was added and the reaction mixture stirred at 38° C for 40 minutes. The temperature was raised to 60°C and dimethyl sulphate (1.3 eq.) was added dropwise. After two hours the reaction mixture was cooled down to 0°C and HC1 I N was added to quench the reaction. The reaction mixture was extracted with ethyl acetate and the organic phase washed with HC1 IN, saturated aqueous NaHCCb and brine, dried on Na2SO.i, filtered and concentrated in vacuo. The desired product was isolated by flash chromatography

on silica gel (eluent ethyl acetate: petroleum ether = 30:70) as a 1:1 mixture of rotamers by NMR:
'11 NMR (DMSO-d 7.66-7.61 (m, 2H), 7.38-7.22 (m, 4H), 7.08-7.02 (m, 1H), 5.18-5.12 (m, 111), 5.13 (d,
J= 13.1 Hz, 0.5H), 5.07 (d, J= 13.1 Hz, 0.5H), 5.06 (d, J= 12.4 Hz, 0.5H), 4.84 (d, J=
12.4 Hz, 0.5H), 4.08-4.17 (m. 1H), 3.73 (s, 3H), 3.75-3.55 (m, 2H), 3.65 (s, 1.5H),
3.44 (s, 1.5H), 3.26 (s, 311), 2.62-2.52 (partially under DMSO) (m, 1H), 2.30-2.15 (m,
1H).
MS: tn/z 522 (M+H)"
Step 7: Benzyl-(2tS',4/?)-2-(4-{[(4-fluorobenzyl)aminojcarbonyl}-5-hydroxy-l-
methyl-6-oxo-l,6-dihydropyrimidin-2-yl)-4-methoxypyrrolidine-l-carboxylate

To methyl-5-(benzoy!oxy)-2-{(2.S\4/?)-l-[(benzyloxy)carbonyl]-4-methoxypyrrolidin-2-yl}-l-methyl-6-oxo-1.6-dihydropyrimidine-4-carboxylate,dissolved in methanol, 4-F-benzylamine (3 eq.) was added. The reaction mixture was stirred at reflux overnight. Methanol was removed in vacuo and the residue triturated with ethyl ether to give the title product as a 4:6 mixture of rotamers by NMR:
'll NMR (DMSO-dr, + TFA, 400 MHz, 300 K) 5 14.0 (bs, 1H), 8.92 (t, J = 6.4 Hz, 0.4H), 8.73 (t, J = 5.9 Hz, 0.6H), 7.35-7.25 (m, 4H), 7.20-7.05 (m, 4H), 6.93 (d, J= 7.5 Hz, 1H), 5.09-4.95 (m, HI), 5.09 (d, J= 12.3 Hz, 0.6H), 4.75 (d, J= 12.3 Hz. 0.6H), 5.05 (d, J= 13 Hz, 0.4H), 4.98 (d, J= 13 Hz, 0.4H), 4.52-4.43 (m, 211), 4.12-4.06 (bm, 0.411), 4.06-4.02 (bm, 0.611), 3.87 (dd, J= 11.5 and 4.5Hz, 0.4H), 3.84 (dd, J - 12 and 2.7Hz, 0.6H), 3.65-3.55 (m, ll-I),3.59(s, 1.2H), 3.41 (s. 1.8H), 3.25 (s, 311). 2.45-2.40 (partially under DMSO) (m, 1H), 2.30-2.15 (m, 1H). MS: m/z511 (MHI)'

StepJJ: A^-(4-nuorobenzyl)-5-hydroxy-2-|(2.S;4/0-4-methoxypyrroWdin-2-yl]-
l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide

Bcn/yl-(2.S\4/?)-2-(4-{[(4-i1uon)bcnzyl)amino]carbonyl}-5-hydroxy-l-rnethyI-6-oxo-1.6-dihydropyrimidin-2-yl)-4-methoxypyrrolidine-l-carboxylate was dissolved in methanol and Pd/C I0%wt (14%w/\v) was added. The mixture was stirred under H2 atmosphere at room temperature. After 2 hours the reaction mixture was filtered and methanol was removed in vacuo to give title compound.
*H NMR (DMSO-d6-fTFA, 400 MHz, 300 K) 5 12.58 (bs, 1H), 10.16 (bs, 1H), 9.74 (t, J= 6.3 Hz, 1H), 8.90 (bs, 111), 7.36 (dd, J - 8.5 and 5.7 Hz, 2H), 7,19 (t, J= 8.8 Hz, 2H), 5.01 (bs, IH), 4.50-4.60 (m, 2H), 4.19 (bs, IH), 3.55-3.45 (m, 1H), 3.47 (s, 3H), 3.45-3.35 (m, IH), 3.32 (s, 3H), 2.74 (dd, J= 13.9 and 7.5 Hz, IH), 2.17-2.10 (m, IH). MS:m/z377(M+H)'f
Step 9: 2-{(2(V,4/^)-l-[(dimethylamino)(oxo)acctyl]-4-methoxypyrrolidin-2-
yI}-A'-(4-fluorobcnzyl)-5-hydroxy-l-melhyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide
To JV-(4-fluorobenzyl)-5-hydroxy-2-[(25,4/?)-4-methoxypyrrolidin-2-yI]-l-methyl-6-oxo-1,6-dihydropyrimidine-4-carboxamide, triethylamine (1 eq.) was added. The reaction mixture was cooled down to 0°C and methyl chlorooxoacetate (3 eq.) was added. After 1 hour the reaction mixture was concentrated and a big excess of dimelhylamine 2M in II IF (30 eq.) was added The reaction mixture was concentrated and the desired compound was isolated by HPLC purification (Waters, Symmetry CJS,

5um, 19x50mm eluting with water and acetonitrile containing 0.1% trifluoroacetic
acid) as a 2:8 mixture of rotamcrs by NMR:
'H NMR (DMSO-d6, 400 MHz, 340 K) 5 11.9 (bs, HI). 8.99 (bs, 0.8H), 8.85 (bs,
0.2H), 7.40-7.30 (m, 2H), 7.14 (t, J= 8.8 Hz, 2H), 5.21 (t, J= 7.5 Hz, iH), 4.54 (dd, J=
14.9 and 6.7 Hz, 111), 4.45 (dd, J = 14.9 and 6.4 Hz, HI), 4.10 (bs, IH), 3.91 (dd, J =
11.6 and 4.6 Hz, 0.2H), 3.79 (dd, J= 11.2 and 4.4 Hz, 0.8H), 3.60-3.50 (m, 1 H), 3.58
(s, 2.4H), 3.48 (s, 0.6H), 3.29 (s, 0.6H), 3.27 (s, 2.4H), 2.87 (s, 2.4H), 2.81 (s, 2.4H),
2.64 (s, 0.6H), 2.57 (s, 0.6H), 2.70-2.50 (m, IH), 2.30-2.20 (m, 0.8H), 2.20-2.10 (m,
0.211).
MS:m/z476(M+H)+
EXAMPLE 18
N]-\ l-(4-{[(4-fluorobenzyl)amino]carbonyl}-5-hydroxy-l-methyl-6-oxo-l,6-dihyclropyrimidin-2-yl)-l-]nethyicthylJ-A^ ,;V"-dimcthylethancdiamide (11).

Organic Synthesis Coll. Vol.II pg 29
Acetone cyanohydrin was diluted with MeOU (approx. 3 mmol/mL). The solution was cooled and saturated with ammonia gas, and the reaction mixture was allowed to stand for one day. The excess of ammonia and methyl alcohol were evaporated by rotary evaporation. Residue consisted in the title product.
Step 2: Benzyl 1 -cyano-1 -methylethylcarbamate

To a suspension of 2-amino-2-methyIpropanenitrile in water an equimolar amount of Na2C03 and a slight excess (1.1 eq) of benzylchloroformate were added, with an external cooling. Reaction mixture was stirred o/n at room temperature, extracted in EtOAc and the organic phase was washed with Nal ICOjss, dried (Na2S04), filtered and concentrated. Product was obtained as a white solid.
'll-NMR (CDCI3) S 7.48-7.33 (bs, 5 H), 5.15 (s, 2 11), 4.98 (bs, 1 H). 1.68 (s, 6 H); 13C-NMR(CDC13)S 153.33, 13.81, 127.81, 127.63, 127.55, 120.64,66.56,46.19, 26.67; MS(M+1)/I//J219.
Step 3: Benzyl 2-amino-2-(hydroxyimino)-l.l-dimcthylethylcarbamate.

Hydroxylamine hydrochloride in methanol was added to an equimolar stirred solution of potassium hydroxide in methanol. The mixture was stirred for 15 min and the precipitated potassium chloride was removed by filtration. The filtrate was added to an equimolar amount of the nitrile and the solution stirred overnight at 40 °C, then cooled to room temperature and concentrated. The resulting residue was triturated with water and the white solid, after drying under vacuum, consists mainly in the title product.
'II-NMR(DMSO) 59.12 (bs, 1 H), 7.48 (bs, 5 H), 7.08 (bs. I H), 5.33 (bs, 2 H), 4.98 (s, 2 11), 1.39 (s, 6 1 f): MS (Mi I) m/z 252.

Step 4: Methyl 2-( l-{[(benzyIoxy)carbonyl]amino}-l-methylethyI)-5,6-
dihydroxypyrimidine-4-carboxylate.

Benzyl 2-amino-2-(hydraxyimino)-l,l-dimethylethylcarbamate was suspended in chloroform and treated with 1.2 eq of dimethylacetylcnedicarboxylate and reaction was refluxed overnight. Alter cooling at room temperature, volatiles were evaporated and the residue was taken into xylene and heated at 145 °C for 48 h. The reaction mixture was stirred at room temperature overnight to allow the precipitation of the product (5) as a light brown solid. This solid was collected by filtration and washed with diethyl ether.
'H-NIMRCDMSCOS 12.54 (S, I H), 10.21 (s, 1 H), 7.44 (bs, 1 H), 7.30 (bs, 5 H), 4.95 (s, 2 H), 3.80 (s, 3 H), 1.47 (s, 6 H); MS (M+l) m/z 362.
-Si£lL5: Methyl 5-(benzoyloxy)-2-(l-{[(bcnzyloxy)carbonyI]amino}-l-
methylethyl)-6-hydroxypyrimidine-4-carboxylate.

To a stirred solution of methyl 2-(l-{[(benzyloxy)carbonyl]amino}-l-methylethyI)-5,6-dihydroxypyrimidine-4-carboxyIate in pyridine. 1.1 eq of benzoic anhydride were added and stirring prolonged at room temperature over night. Pyridine was evaporated and residue was taken in eihyl acetate and washed with 1 N HC1 and brine. Organic layer was separated, dried (Na2S04), filtered and concentrated by rotary evaporation and residue was purified by Hash column chromatography (Si02, petroleum ether/ethyl acetate 60/40 v/v as eluant). Collection and evaporation of appropriate fractions afforded title product.

lH-NMR(CDCI3)5 12.2 (bs, 1 II), 8.15 (d, J= 7.4 Hz, 2 H), 7.65 (t, J = 7.4 Hz, 1 H), 7.50 (t, 7 = 7.5 Hz, 2 H), 7.32 (bs, 5 H), 5.54 (bs, 1 11), 5.05 (s, 2 H), 3.82 (s. 3 H), 1.67 (s, 6 H); MS (M+l) m/z 466.
Step 6: Methyl 5-(benzoyloxy)-2-(l-{[(benzyloxy)carbonyl]amino}-l-
mcthylethyl)-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxylate
To a stirred solution of Lif I (1.1 eq) in dioxane, methyl 5-(benzoyIoxy)-2-(l-{[(benzyloxy)carbonyl]amino}-l-methylethyl)-6-hydroxypyrimidine-4-carboxylate was added and the mixture was stirred at 38 °C for 45 min. After cooling down to room temperature, dimethylsulfate (1.3 eq) was added and reaction mixture was heated at 60 °C for 2 h. Mixture was then cooled to room temperature, dioxane evaporated and residue was purified by flash chromatography, eluting with 65/55 v/v petroleum ether/ethyl acetate. Collection and evaporation of appropriate fractions afforded the title product.
lH-NMR(CDCl3)5 8.19(d,7=7.3 Hz, 2 H), 7.65 (t, .7- 7.3 Hz, 1 H), 7.51 (t, .7=7.6 Hz, 2 H), 7.33 (bs, 5 II), 5.63 (bs, 1 H), 5.03 (s, 2 H). 3.80 (s, 3 H), 3.63 (bs, 3 H), 1.72 (s, 6 H); MS (M+l) m/z 480.
Step._8: Benzyl l-(4-{[(4-fluorobenzyl)aminoJearbonyl}-5-hydroxy-l-methyl-
6-oxo-l,6-dihydropyrimidin-2-yI)-l-methylethyIcarbamate.

To a mcthanolic solution of methyl 5-(benzoyloxy)-2-(l-{[(bcnzyloxy)carbonyl]amino}-l-methyIethyl)-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxylate,/)-fluoro benzylamine (3 cq) was added and mixture was refluxed over nighl. After evaporation of methanol, residue was taken in BtOAc, washed with IN I1C1 and brine, dried (Na2S04), filtered and evaporated to obtain the title product.
'll-NMR(CDCl3)8 I1.9(bs, 1 H), 7.79 (bt, 1 H), 7.35-7.29 (m, 7 II), 7.07 (t, y = 8.6 Hz, 2 H), 5.27 (bs, 1 H), 5.02 (bs, 2 H), 4.58 (d, J- 6.2 Hz, 2 H), 3.67 (s. 3 H), 1.70 (s,6H);MS(M+l)m/z469.
S]ej2_9: 2-( 1 -amino-1 -mcthyIethyl)-//-(4-fluorobenzyl)-5-hydroxy-1 -methyl-6-
oxo-l,6-dihydropyrimidine-4-carboxamide.

A mcthanolic solution of Benzyl l-(4-{[(4-fluorobenzyl)amino]carbonyl}-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidin-2-yl)-Nmethylethylcarbamate was stirred over night under a hydrogen atmosphere in the presence of catalytic 10% Pd/C. Catalyst was then filtered oft"through celite, and the filtrate was concentrated. Product was obtained after trituration with ethyl ether.
'H-NMR(DMSO)8 12.31 (bs, 1 H), 9.68 (bt, J-6.6 Hz, 1 H), 8.60 (bs, 2 H), 7.43 (dd, J = 8.4 Hz, J = 5.7 Hz, 2 H), 7.20 (t, y = 8.8 Hz, 2 H), 4.54 (d, J 6.6 1 iz, 2 H), 3.56 (s, 3 H), 1.73 (s, 6 II); MS (M+l) m/z 335.
Step 10: Methyl {[l-(4-{[.(4-fluorobcnxyl)amino]carbonyI}-5-hydroxy-I-
methyl-6-oxo-l,6-dihydropyrimidin-2-yl)-l-methylethyI]amino}(oxo)acetate.

To a stirred mixture of 2-(l-amino-l-methyIethyl)-A^-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide (4) and triethyl amine (3 eq) in chloroform, methyl chlorooxoacetate (1.5 eq) was added with an external cooling. Finished the addition, the ice bath was removed and the mixture was stirred at room temperature for 3h. Reaction mixture was then partitioned between chloroform and IN IICI. Organic layer was separated, washed with brine, dried (Na2SC>4), filtered and concentrated to obtain title product.
'H-NMR (DMSO) 5 12.2 (bs, 1 H), 9.47 (s, 1 II), 9.04 (t, 7= 6.3 Hz, 1 H), 7.38 (dd, J-8.4 Hz, 7=5.7 Hz, 2 11), 7.16 (t, 7=8.8 Hz, 2 H), 4.50 (d, 7= 6.3 Hz, 2 H), 3.78 (s, 3 H), 3.45 (s, 3 11), 1.67 (s, 6 H); MS (M+l) m/z 421.
Step 11: N] -[ 1 -(4- {[ (4-fluorobenzyl)amino]carbonyl} -5-hydroxy-1 -methyl-6-
oxo~l,6-dihydropyrimidin-2-yl)-I-methylethyI]-A/' ,N -dimethylethanediamide (11).
Methyl {[ 1 -(4-{[(4-fluorobenzyl)amino]carbonyl} -5-hydroxy-1 -methyl-6-oxo-1,6-dihydropyrimidin-2-yl)-l-methylethyl]amino}(oxo)acetate was refluxed in an excess of 2 M solution of dimethylamine in THF for 2 h. Reaction mixture was cooled to room temperature, evaporated and residue was purified by RP HPLC (CI8, water/acetonitrile containing 0.1% of trifluoroacetic acid as eluant). Collection and lyophilization of appropriate fractions afforded the title product. ,H-NMR(DMSO)8 12.19 (s, 1 H), 9.32 (s, 1 H), 9.06 (t, 7= 6.4 Hz, 1 H), 7.40 (dd, 7 -8.5 Hz, 7= 5.7 Hz, 2 H), 7.18 (t, 7= 8.8 Hz, 2 11), 4.51 (d, 7 = 6.4 Hz, 2 H), 3.55 (s, 3 11), 2.93 (s, 3 H), 2.87 (s, 3 H), 1.68 (s, 6 H); 13C-NMR (DMSO) 5 168.23, 163.76, 163.09, 161.20 (d, 7= 96.4 Hz), 158.46, 151.90, 145.49, 134.77, 129.40 (d, 7 - 3.2 Hz). 124.29, 115.05 (d, 7= 8.5 Hz), 56.50, 41.51, 35.46, 33.42, 32.68, 26.85; MS (Mr 1) m/z 434; MS (M+l) m/z 434.

EXAMPLE 19
Step 1: Af-(4-fluorobenzyl)-5-hydroxy-1 -mcthyl-2-( I -methyl-1 -{[(5-methyl-
1,3,4-oxadiazol-2-yl)carbonyl]amino) ethyl)-6-oxo-1,6-dihydropyrimidine-4-carboxamide

A solution of S-methyl-l^^-oxadiazoIe^-carboxylic acid was treated with 1.9 equivalents of oxalyl chloride and a few drops of anhydrous A'.Af-dimethylformamide. After 1 h, mixture was concentrated, residue was triturated with /-z-hexane and directly added to an equimolar solution of 2-(l -amino-1 -methylethyI)-jV-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-K6-dihydropyrimidinc-4-carboxamide (described in step 9, example 18) in acctonitrile. Tricthyl amine (3 eq) was added to the mixture and the reaction was stirred overnight at room temperature. Title product was isolated by prep RP HPLC (CI8, acetonitrile/water containing 0.1% of trifluoroacetic acid as eluant). 1H-NMR(DMSO)8 12.2 (bs, I H), 9.84 (s, 1 H), 9.05 (t, J - 6.5 Hz , 1 H),7.38(dd,J = 8.4 Hz, 7- 5.6 Hz, 2 11), 7.17 (t, J= 8.8 Hz, 2 H), 4.50 (d, J= 6.5 Hz, 2 11), 2.56 (s, 3 H), 1.74 (s, 6 H), one methyl signal obscured by water, MS(M+1)/M/Z445.
EXAMPLE 20
2-{(2,ST)-l-|(dimethylamino)(oxo)acelyr]-4,4-difluoropyrrolidin-2-yl}-iV-(4-fluorobenzyl)-5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide

A solution of dimethyl sulfoxide (2.1 eq) in dry dichloromethane was added dropwise to a stirred solution of oxalyl chloride (1.01 eq) in dry dichloromethane (1.25 N) at-78 °C under N2 atmosphere. After 15 min, a solution of the commercially available 1-benzyl-2-methyl-(2LS\4#)-4-hydroxypyrrolidine-1,2-dicarboxylate in dry dichloromethane was added slowly, and stirring was continued for 30 min at -78 °C. Alter addition of triethylaminc (5 eq), the mixture was gradually warmed up to room temperature. The mixture was quenched with water and aqueous layer was separated and extracted with dichloromethane. The extract was washed with brine and dried over Na2SC>4. Concentration of the solvent in vacuo gave a residue, which was purified by flash cromatography (ethyl acetate:petroleum ether = 3:7) to give title product as a yellow oil.
"H NMR (DMSO-de+TFA, 400 MHz, 330 K) 5 7.40-7.32 (m, 5H), 5.20-5.09 (m, 2H), 4.79 (d, J = 9.7 Hz, 1H), 3.95 (d, J = 17.9 Hz, HI), 3.78 (d, J - 17.9 Hz, 1H), 3.64 (s, 311), 3.13 (dd, J- 18.7 and 10.6, 1H), 2.62 (dd, J = 18.7 and 2.7 Hz, 1H). MS: m/z278(M+H)+
Step 2: 1-Benzyl 2-methyl (2,Sr)-4,4-difluoropyrrolidine-l,2-dicarboxylate

A solution of l-benzyl-2-mcthyl-(25)-4-oxopyrrolidine-l,2-dicarboxylate in dichloromethane was slowly added to a solution of diethylaminosulfur fluoride in dichloromethane precooled to - 78 °C. The reaction mixture was warmed to room temperature and mixed with cold water. The organic layer was separated, washed with water, dried over Na2S04 and evaporated to give title compound as a yellow oil. 'II NMR (DMSO-d6, 400 MHz, 330K) 8 7.40-7.32 (m, 5H), 5.16-5.12 (m, 211), 4.63 (br s, 1H), 3.96-3.80 (m, 2H), 3.65 (s, 3H), 3.15-2.86 (m, 1H), 2.56-2.45 (partially under DMSO) (m, 111).
I9F NMR 'll-l9F dec (DMSO-d6, 400 MHz, 330 K) 8 - 98.13 (d, J = 223.7 Hz) + -98.72 (d, J = 223.6 Hz) (rotamera), -101.38 (d, J == 190.7 Hz)+ -102.00 (d, J = 191.3 Hz) (rotamer b) (2F). MS m/z 300 (M + 11)+.
Step 3: l-[(Benzyloxy)carbonyl]-4,4-difluoro-L-proline

A solution of 1-benzyl 2-methyl (2S)-4,4-difluoropyrrolidine-l,2-dicarboxylate in methanol was refluxed with 2N NaOH (2 eq) for 2 hours. Methanol was removed and pH adjusted to 1 with 3 N HC1 obtaining a suspension which was extracted several times with ethyl acetate. Combined organics were dried overNa2S04 and evaporated to give title product as a dark brown oil.
*II NMR(DMSO-dr,,400MHz,330K)5 12.96 (brs, 111), 7.36-7.31 (m, 511), 5.11 (s, 2H).4.50(bs, 1H), 3.91-3.80 (m, 2H), 3.01-2.82 (m. 111), 2.56-2.41 (partially under DMSO)(m, 1H). MS: m/z284(M-H)Step 4; BenzyI-(2S)-2-aminocarbonyi-4,4-difiuoropyrrolidine-l-carboxylate

To a stirred solution of l-[(bcn/yloxy)carbonyl]-4,4-dinuoro-L-proline, pyridine (0.6
eq.) and di-t-butyl dicarbonate (1.3 eq) in dioxane, ammonium bicarbonate (1.26 eq)
was added and the mixture was stirred at room temperature for 20 hours. Dioxane was
concentrated and the residue dissolved in ethyl acetate and washed with HC1 1 N,
saturated aqueous NaHCC^ and brine, dried over Na2S04, filtered and evaporated in
vacuo to obtain a yellow oil.
Two sets of signals, two con formers (ratio 1:1) were present.
'II NMR (DMSO-d6,400 MHz, 300 K) 5 7.56 (d, J - 15.4 Hz, 1H), 7.39-7.34 (m,
5H), 7.17 (d, J - 19.3 Hz, 1H), 5.10-5.08 (m, 211), 4.42 (dd, J = 9.3 and 4.7, 0.5 H),
4.34 (dd, J - 9.2 and 4.6 Hz, 0.5 H), 3.92-3.73 (m, 211), 2.90-2.72 (m, 1H), 2.43-2.30
(m, 111).
MS:m/z285(M+H)Step 5: Benzyl-(2.V)-2-cyano-4,4-difluoropyrrolidine-l-carboxylate

A solution of benzyl-(2S)-2-aminocarbonyl-4,4-difiuoropyrrolidine-l-carboxylate and triethylamine (2.1 eq.) in dichloromethane was cooled to 0°C and trifluoroacetic anhydride (1.1 eq.) was added dropwise under nitrogen. Stirring was continued for 1 hour allowing the mixture to reach room temperature. Volatiles removed in vacuo and residue taken up in ethyl acetate, washed with HC1 IN, brine and dried over Na2S04. Evaporation gave title compound as brown oil.
'H NMR (DMSO-d Stej3_6: Benz.yl-(25)-2-famino(hydroxyimino)methyl]-4,4-difluoropyrrolidine-
1-carboxylate

A solution of benzyI-(2.S)-2-cyano~4,4-difluoropyrrolidine-l -carboxylate,
hydroxylamine hydrochloride (1.4 eq.) and triethylamine (1.7 eq.) in ethanol was
refluxcd under nitrogen for 5 hours. Mixture was concentrated and residues taken up
in ethyl acetate and washed with water and brine. Combined organics were dried over
Na2SC>4 and evaporated to give title compound as a foam.
!H NMR (DMSO-dG, 300 MHz, 330 K) 8 9.12 (bs, HI), 7.38-7.34 (m, 5H), 5.36 (bs,
2H), 5.13 (dj - 14.4 Hz, 1H) + 5.09 (d, J - 14.4 Hz, I H), 4.56 (dd, J = 8.6 and 4.9
Hz, 1H), 4.07-3.76 (m, 211), 2.80-2.71 (m 1H), 2.60-2.51 (partially under DMSO) (m,
1H).
MS:m/z300(M+H)+.
Step_7: Dimethyl-2-{f(amino-{(2lSr)-l-[(benzyloxy)carbonyl]-4,4-
difluoropyrrolidin-2-yl}methylidene)amino]oxy}but-2-enedioate
F

A solution of benzyi-(25)-2-[amino(hydroxyimino)methyl]-4,4-difluoropyrrolidine-l-carboxylate and dimethylacetylcndicarboxylate (1.2 eq.) in chloroform was refluxed for 1 hour under nitrogen and the solution was concentrated. Residue was purified by flash chromatography on silica gel, (eluent: petroleum ethercthyl acetate = 7.5:2.5), to give the desired product as a 3:1 mixture of two isomers by 'H NMR. 'H NMR (DMSO-d6, 300 MHz, 330 K) 5 7.45 -7.25 (m, 5H), 6.63 (bs, 1.5H), 6.30 (bs, 0.5H), 5.62 (s, 0.7511), 5.60 (s, 0.25H), 5.13 (s, 211), 4.58 (dd, J = 9.1 and 4.9 Hz) + 4.57 (dd, partially overlapped) (1H), 3.96-3.86 (m, 2H), 3.79 (s, 2.2H), 3.74 (s, 0.8H), 3.66 (s, 0.8H), 3.61(s, 2.2H), 2.93-2.81(m, 1H), 2.56-2.43 (partially under DMSO)(m, 1H). MS:m/z442(M+H)+.

Step_8: Methyl-2-{(2S)-l-[(benzyloxy)carbonyiJ-4,4-difluoropyrrolidin-2-yl}-
5,6-dihydroxypyrimidine-4-carboxylale

A solution ofdimethyl-2-{[(amino-{(2tS>l-[(benzyIoxy)carbonyl]-4,4-dinuoropyrroIidin-2-yI}methylidene)amino]oxy}bul-2-enedioate in o-xylene was re fluxed for 6 hours. Then the reaction was cooled down and concentrated at rotavapor. Ethyl ether was added until precipitation of a solid that was filtered, washed with other ethyl ether and dried to give the title pyrimidine as a brown solid. Two sets of signals, two rotamers (ratio 1:1) were present.
'11 NMR (DMSO-d6, 400 MHz, 300 K) S 12.97 (s, 1H). 10.38 (s, 1H), 7.40-7.29 (m, 311), 7.22-7.15 (m, 1H); 7.10-7.05 (m, 1H), 5.12 (d, J - 12.6 Hz, 0.5H) 5.10 (s, 1H), 4.89 (d, J = 12.6 Hz, 0.5H), 4.86-4.72 (m, 1H), 4.10 3.86 (m, 2H), 3.81 (s, 3H), 2.90-2.85 (m, 1H), 2.64-2.53 (partially under DMSO) (m, 111). MS:m/z410(M+H)+.
Step 9: Methyl 5-(benzoyloxy)-2-{(2i>!-[(benzyloxy)carbonyl]-4,4-
diiluoropyrrolidin-2-yl}-6-hydroxypyrimidine-4-carboxylate

Mcthyl-2-{(25)-l-[(benzyloxy)carbonyI]-4,4-dilluorop\rrolidin-2-yl}-5,6-. dihydroxypyrimidine-4-carboxylate in dry pyridine was treated with benzoic anhydride (2 eq.) overnight at room temperature.
The mixture was evaporated, taken up in ethyl acetate and washed with HC1 IN and brine. Organics were dried over Na2S04, filtered and evaporated to obtain an oil which was purified by flash chromatography on silica gel (eluent: ethyl acetate:petroleum ether = 7:3).

!H NMR (DMSO-d6, 300 MHz, 330 K) 8 13.51 (bs, 1H), 8.10 (d, J - 7.6 Hz, 2H), 7.79 (t, J - 7.1 Hz, 1H), 7.64 (t, J = 7.6 Hz, 2H), 7.33-7.17 (m, 5H), 5.13 (s, 2H), 4.99 (t, J - 7.3 Hz, 1H), 4.09-3.97 (rn, 2H), 3.77 (s, 3H), 3.02-2.99 (m, 2H). MS:m/z514(M+H)+.
Step 10: MethyI-5^(benzoyloxy)-2-{(2iS)-l-i(benzyloxy)carbonyl]-4,4-
difluoropyrrolidin-2-yl}-l-methyi-6-oxo-l,6-dihydropyrimidine-4-carboxylate
I
Methyl 5-(benzoyloxy)-2-{(2iS>l-[(benzyloxy)carbonylJ-4,4-difluoropyrrolidin-2-yl}-6-hydroxypyrimidine-4-carboxylate dissolved in dry 1,4-dioxane was added to a suspension of Lill (1.4 eq.) in dioxane. The mixture was stirred at 38° C for 45 minutes and then cooled down to room temperature. Dimethyl sulphate (1.3 eq.) was added and the mixture was warmed to 58 °C for 1 hour. The reaction mixture was cooled down to 16 °C and glacial acetic acid (0.1 eq) was added, followed by water and ethyl acetate. The combined organic layers were dried (Na2SC>4), filtered and concentrated to an oil which was cromatographed through silica gel (eluent: ethyl acetate:petroleum ether^3:7) to give the desired compound as a 1:1 mixture of two rotamers bv ]H NMR
'H NMR (DMSO-de, 300 MHz, 300 K) 5 8.11-8.08 (m. 2H), 7.80 (t, J= 7.7 Hz, 1H), 7.67 - 7.65 (m, 2H), 7.36-7.10 (m, 5H), 5.50 (dd, J = 9.2 and 4.7 Hz, 1H), 5.22 (d, J = 12.9 Hz, 0.5H), 5.14 4.95 (m, 1H), 4.93 (d, J = 12.3 Hz, 0.5H), 4.16-3.79 (m, 2H), 3.74 (s, 3H), 3.61 (s,1.5H), 3.45 (s,1.5H), 3.25-3.11 (m, 1H), 2.89-2.74 (m. 1H). MS: m/z 528 (NM-H)+.
Step ..J.I: Benzyl-(2.S)-4,4-difluoro-2-(4-{[(4-fluorobenzyl)amino]carbonyl}-5-
hydroxy-1 -methyl-6-oxo-l ,6-dihydropyrimidin-2-yl)pyrrolidine-1 -carboxylate

Methyl-5-(benzoyIoxy)-2-{(2^-l-[(benzyloxy)carbonyI|-4,4-difluoropyrrolidin-2-yl}-l-mcthyl-6-oxo-l,6-dihydropyrimidine-4-carboxylatc in dry MeOH was treated with 4-fiuorobenzyl amine (2.5 eq.) at reflux for 2 hours. Solvent was removed in vacuo and the residue was taken up in ethyl acetate, washed with HC1 IN, brine, dried over Na^SOa- The filtrate was concentrated in vacuo and triturated with ethyl ether to obtain the title compound as a 1.5:1 mixture of two rotamers by NMR. 'll NMR (DMSO-de-iTFA, 300 MHz, 300 K) 5 8.92 (bt, 0.4H), 8.69 (bt, 0.6H), 7.36-7.31 (m, 411), 7.20 -7.09 (m, 4H), 6.97 (dJ - 7.2 Hz, 1II), 5.34-5.25 (m, 1H), 5.14 (d, J = 12.4 Hz, 0.411 ), 5.07-4.99 (m, 1.2H), 4.81 (d, J - 12.2 Hz, 0.4H), 4.51-4.48 (m, 211), 4.38-4.21 (m, 1H), 4.07-3.96 (m, 1H), 3.59 (s, 1.2H),3.48 (s, 1.8H), 3.05-2.95 (m, 1H), 2.78-2.68(m, 1H). MS:m/z517(M+H)Step 12: (2.S,)-4,4-difluoro-2-(4-{[(4-fiuorobcnzyl)amino]carbonyl}-5-hydroxy-
1 -methyl-6-oxo-1,6-dihydropyrimidin-2-yl)pyrrolidinium trifluoroacetate

A solution of benzyl-(2.V)-4,4-difiuoro-2-(4-{f(4-fluorobenzyl)amino]carbonyl}-5-hydroxy-l-methyi-6-oxo-l,6-dihydropyrimidin-2-yl)pyrrolidine-l-carboxylate in MeOH was treated with Pd/C 10%wt (10% w/w) for 3 hours at room temperature under H2 atmosphere. The mixture was filtrated over a celite pad, concentrated in vacuo and treated with trifiuoroacetic acid (10 eq.). The acid in excess was removed in vacuo to obtain title product as a pale yellow solid after trituration with ethyl ether.

'H NMR (DMS0-d6+TFA, 300 MHz, 340K) S 9.60 (bt, 1H), 7.39 (t, J = 8 Hz, 2H), 7.17 (t, J - 8,8 Hz, 211), 5.35 (t, J = 8.4 Hz, HI), 4.62 (dd, J - 15.3 and 6.6;-Hz, 1H), 4.55 (dd, J - 15.2 and 6.3 Hz, 1H), 4.05--3.87 (m, 2H), 3.48 (s, 3H), 3.30-3.14 (m, 1H), 2.96-2.78 (m, 1H). MS: m/z 383 (M+H)+.
Step 13: 2-{(26>l-|(dimethylamino)(oxo)acctyll-4,4-difluoropyrrolidin-2-yl}-
A^-(4-nuorobenzyl)-5~hydroxy-l-methy!-6-oxo-l,6-dihydropyrimidine-4-carboxamide
A solution of (2iS,)-4,4-diiluoro-2-(4-{[(4-nuorobenzyl)aminoJcarbonyl}-5-hydroxy-l-methyI-6-oxo-l,6-dihydropyrimidin-2-yl)pyrrolidinium trifluoroacetate in chloroform and triethylamine (1.01 eq.) was treated with methyl chlorooxacetate (2 eq.) at 0 °C. The mixture was allowed to reach room temperature for 2 hours. Dimethylamine (30 eq.) was added at room temperature and the mixture left stirring over night. The mixture was concentrated in vacuo and purified by preparative HPLC (Column: Cis, eiuent: acetonitrile and water containing 0.1 % trifluoroacetic acid). To obtain the title product two rotamers (ratio 4:1) were found in 11 NMR.
Hi NMR (DMSO-d6+TFA, 300 MHz, 300 K) 5 9.23 (t, J = 6.5 Hz, 0.8H), 9.10 (bt, 0.2H), 7.34 - 7.31 (m, 2H), 7.11 (t, J - 8.8 Hz, 2H), 5.48 (dd, J = 8.9 and 5.7 Hz, 1H), 4.53 (dd, J = 15.0 and 6.7 Hz, 1H), 4.42 (dd, J = 15.0 and 6.2 Hz, 1H), 4.24-4.16 (m, 111), 4.05-4.02 (t, J = 11.8 Hz, 1H), 3.52 (s, 2.4H), 3.45 (s, 0.6H), 3.15-3.04 (m, 1.6H), 2.84 (s, 2.411), 2.80 (s. 2.4H), 2.79 - 2.65 (m, 0.4H), 2.63 (s, 0.6H), 2.57 (s, 0.6H). MS:m/z482(M+H)+.
EXAMPLE 21 * 2-|l,2-dimethyl-4-(methylsulfonyl)piperazin-2-yI]-A/-(4-fluorobenzyl)-5-hydroxy-l-
methyI-6-oxo-l,6-dihydropyrimidine-4-carboxamide

To a cooled (-75 °C) solution of LDA 2M in heptane/THF (1.5 eq) in THF, a solution of 1 -[(benzyloxy)carbonyl|-4-(/er/-butoxycarbonyl)piperazine-2-carboxylic acid (Bigge et al, Tetrahedron Lett. 1989, 30: 5193) in THF was added dropwise at -75°C. After being stirred for 1 hour at -75 °C, Mel (1.5 eq) was added. After 2 hours at -75 °C the reaction mixture was left warming to r.t., evaporated, diluted with AcOEt, washed with NaHC03, water, brine and dried over Na2S04. The crude was purified by flash chromatography on silica gel (petroleum ether/AcOEt, 85:15) to obtain the title compound .
1II NMR (DMSOd6, 340K, 300MHz) 5 7.45-7.30 (m, 5H), 5.19 (AA' system, J = 13 Hz, 2H), 4.05 (d, J = 14 Hz, 1H), 3.87-3.78 (m, HI), 3.66 (d, J = 14 Hz, 1H), 3.62-3.35 (m, 3H), 1.66 (s, 3H), 1.45 (s, 9H). MS: m/z 360 (M+H)+.
Step_2: 1-benzyl 4-/e/7-hutyl 2-[(Z)-amino({[(lA>3-methoxy-l-
(methoxycarbonyl)-3-oxoprop-l-enyr]oxy}imino)methyl]-2-methyl piperazine-l,4-dicarboxylate.

A solution of 1-benzyl 4-/eri~buty\ 2-cyano-2-methylpiperazine-l,4-dicarboxylate in EtOIl was added to a solution of Et3N (3.2 eq) and NU20I1 HCI (3 eq) in EtOH. The mixture was stirred 2 hr at 40 °C. After evaporation of the solvent, the residue was diluted with AcOEl, washed with water, dried over Na2S04, filtered and concentrated. The residue was further dissolved in chloroform and dimethylacetylenedicarboxylate (1.5 cq) added to the stirred solution. Reaction was refluxed over night. The mixture was evaporated and the residue was purified by flash chromatography on silica gel (petroleum ether/AcOEt, 65:35) affording the title compound as mixuture of isomers in 3.5:1 ratio.
!H NMR (DMSOd6, 340K? 300MHz). Two sets of signals were observed due to the presence of the geometric isomers: 5 7.48-7.25 (m, 5H), 6.31( bs, 1.56 H), 6.01 (bs, 0.44 H), 5.63 ( s,0.78 H), 5.55 (s, 0.22 H), 5.12-5.02 (m, 2H), 3.85-3.60 (m, 9H), 3.60-3.45 (m,2H), 3.45-3.31 (m, 1H), 1.51 (s, 2.4H), 1.45 (s, 0.66 H), 1.41 (s, 9H). MS:m/z535(M+H)+.
^tcp_3: 1 -benzyl 4-(ert-buty\ 2-[5-(benzoyloxy)-4-hydroxy-6-
(methoxycarbonyl) pyrimidin-2-yl]-2-methylpiperazine-l,4-dicarboxylate

1-benzyl 4-/m-butyl 2-[(Z)-amino({[(l£)-3-methoxy-l-(methoxycarbonyl)-3-oxoprop-l-enyl]oxy}imino)methyl]-2-methylpipcrazine-L4-dicarboxylate was

dissolved in xylene and stirred at 155 °C for 8h. After evaporation of the solvent, the residue was dissolved in pyridine and benzoic anhydride (1.5 eq) was added. The reaction mixture was stirred at room temperature over night, then pyridine was evaporated. The residue was diluted with AcOEt, the organic phase washed with HC1 IN, dried (Na2S04) and evaporated. The title product was obtained by flash chromatography (cluent: petroleum ether/AcOEt 70/30).
!H-NMR (DMSOd6, 340K, 400MHz) 8 12.96 (bs, 1H), 8.07 (d, J=12 Hz, 2 H), 7.76 (t, .7-7.6 Hz, HI), 7.62 (t, ,7-7.6 Hz, 2H), 7.37-7.22 (m, 5H), 5.03 (s, 2H), 3.96 (dt ,7,-13.6 Hz, J2==5.8!lz, 111), 3.80-3.52 (m, 7H), 3.47-3.40 (m, 1H), 1.65 (s, 3H), 1.35 (s, 911). MS:m/z607(MHI)Step 4: 1-benzyl 4-/er/-butyl 2-[5-(benzoyloxy)-4-(methoxycarbonyl)-l-
methyl-6-oxo-l,6-dihydropyrimidin-2-yl]-2-methylpiperazine»l,4-dicarboxylate.

1-Benzyl 4-/er/-butyI 2-|"5-(benzoyloxy)-4-hydroxy-6-(methoxycarbonyl) pyrimidin-2-yl]-2-methylpiperazine-l,4-dicarboxyIate was added to a suspension of LiH (1.1 eq) in dioxane (7 ml/mmol) at room temperature. The mixture was stirred at 40 °C for 45 min. then dimethylsulfalc (1.3 eq) was added and the temperature was raised to 60 °C. After 1 h glacial acetic acid (0.1 eq) was added to the reaction mixture, followed by water (7 ml/mmol) and EtOAc (7 ml/mmol). The aqueous layer was separated and extracted with EtOAc. The combined organic layers were dried (Na2SC>4) and concentrated. The crude was purified by flash chromatography on silica gel

(AcOEt/petroleum ether, 1:4) to separate the title compound A from B (ratio A/B
1.3/1).
A: 'll NMR (CD3CN, 320K, 300MHz) 5 8.18 (d, ,/=7.2 Hz, 2H), 7.80 (t, .7=7.5 Hz,
1H), 7.63 (t, .7=7.8 Hz, 2H), 7.45-7.22 (m, 5H), 5.08 (AA' system, J = 12 Hz, 2H),
4.18-3.88 (m, 3M), 3.81 (s, 3H), 3.68-3.46 (m, 5H, at 3.58 (s)), 3.40-3.22 (m, 1H),
1.75 (s,3H), 1.49 (s,9H).
MS:m/z621 (M+H)+.
Stejl-5: Methyl 5-(benzoyloxy)-2-|4-(/er/-buloxycarbonyl)-2-methylpiperazin-
2-yl ]-1 -methyl-6-oxo-1,6-dihydropyrimidine-4-carboxylate

1 -Benzyl 4~/er/-butyl 2-[5-(benzoyloxy)-4-(mcthoxycarbonyl)-l-methyl-6-oxo-l,6-dihydropyrimidin-2-yt]--2-methylpiperazine-l,4-dicarboxylatc was dissolved in AcOEt (20 rnl/mmol) and hydrogenated at atm pressure on 10% (w/w) Pd/C over night. After filtration of the catalyst, solvent was evaporated to give crude product. 'H NMR (DMSOd6 4 TFA, 340K, 400MHz) 8 8.08 (d, J - 7.1 Hz, 2H), 7.787 (t, J = 7.4 Hz, 1H), 7.63 (t, J -7.8 Hz, 2H), 4.30 (d, J - 15.2 Hz, III), 3.90-3.50 (m, 10H), 3.35-3.25 (m, 1H), l.81(s,3H), 1.37 (s, 911). MS (EI+) m/z 487 (M+H)+.
Step_6: 2-|l,2-dimethyl-4-(methylsulfonyl)pipeaizin-2-yl]-/V-(4-fluorobenzyl)-
5-hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxamide .
Crude methyl 5-(benzoyloxy)-2-[4-(/er/-butoxycar.bonyi)-2-methylpiperazin-2-yl]-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxylate was dissolved in MeOH,/> fluorobenzylamine (3.0 eq) was added and the mixture was refluxed over night. Evaporation of the solvent afforded crude product. MS:m/z476(M+H)*.

Crude obtained in the previous step was dissolved in MeOH (20 ml/mmol) and
NaCNBH3 (2.8 eq), AcONa (3.2 eq) and HCHO 37 % in H20 (4eq) were added. The
reaction mixture was stirred at room temperature over night, evaporated and the crude
solid (4-fluorobenzyI 2-[4-(/er/-butoxycarbonyl)-l,2-dimethylpiperazin-2-yl|-5-
hydroxy-l-methyl-6-oxo-l,6-dihydropyrimidine-4-carboxylate) obtained washed with
Et20.
MS(BI+)w/z490(jM+-H)f.
Deprotection of Boc group was carried out in DCM/TFA (1:1, 10 ml/mmol) for 1
hour.
MS (1:1+) m/z 390 (M+H)+. The crude product was dissolved in DCM , Et3N (3.3 eq)
and MeS02Ci (2.6 eq) were added and the reaction was stirred at room temperature
over night. The reaction mixture was evaporated and the crude residue purified by
preparative HPLC (CI8, gradient of CH3CN/H20 + 0.01% TFA) to obtain the title
product.
'II NMR (CD3CN + TFA, 320K, 400MHz) 8 8.51 (bs, IH), 7.46-7.36 (m, 2H), 7.15-7.10 (m, 2H), 4.64 (d, J - 6.4 Hz, 2H), 4.04 (dd, J, - 14.4 Hz, J2 - 2.2 Hz, IH), 3.88-3.80 (m, IH), 3.68 (dt, J, - 13.6 Hz, J2 - 3.3 Hz, 111), 3.61 (s, 3H), 3.60-3.50 (m, IH) 3.42-3.3 l(m, 2H), 2.94 (s, 3H), 2.81 (s, 3H), 1.92 (s, 311). MS:m/z468(M+H)+.
Tables 1 and 2 below list compounds of the present invention which have been prepared. The tables provide the structure and name of each compound, the mass of its molecular ion plus 1 (M+) or molecular ion minus 1 (M~) as determined via F1A-MS. and the synthetic scheme employed to prepare the compound. When the compound was prepared as a salt, the identity of the salt is included with the compound name. The synthetic scheme identified as "1*" in Table 1 is identical to Scheme 1 above, except for an additional deprotection step to remove Boc, Cbz, or benzyl present in the 2-substituent in the pyrimidinone ring.

While the foregoing specification teaches the principles of the present invention, with examples provided for the purpose of illustration, the practice of the invention encompasses all of the usual variations, adaptations and/or modifications that come within the scope of the following claims.

I/WE CLAIM:
1. A compound of Formula (I):
wherein
Rl is
(1) -H,
(2) -C1-6 alkyl, which is optionally substituted with one or more
substituents each of which is independently halogen, -OH, -CN, -O-C1-6 alkyl, -O-C1-6 haloalkyl, -C(0)Ra, -CC>2Ra, -SRa, -Sl=0)Ra, -N(RaRb), -C(=0)-Co-6 alkyl-N(RaRb), N(Ra)-C(O)-C0-6 alkyl-N(RbRc), -S02Ra, -N(Ra)S02Rb, -S02N(RaRb),

(i) the alkyl is optionally substituted with one or more substituents each of which is independently halogen, -OH, -CN, -0-C]_6 alkyl, -0-C1-6 haloalkyl, -N(RaRb), -N(Ra)C02Rb, -N(Ra)C(=0)-Co-6 alkyl-N(RbRc), or -N(Ra)-C2-6 alkyl-OH with the proviso that the -OH is not attached to the carbon
alpha to N(Ra); and (ii) the alkyl is optionally mono-substituted with -Rs, -C1-6
alkyl-Rs, -N(Ra)-C(=O)-C0-6 alkyl-Rs, -N(Ra)-Co-6 alkyURs, -O-CO-6 alkyl-Rs, or -N(Ra)-C(-O)--C0-6 alkyl-RS; wherein Rs is
(a) aryl which is optionally substituted with one or

more substituents each of which is independently halogen, -OH, -C1-6 alkyl, -Cj-6 alkyl-ORa, -C1-6 haloalkyl,-0-C1-6 alky I, -O-C1-6 haloalkyl, methylcnedioxy attached to two adjacent carbon atoms, or aryl;
(b) a 4- to 8- membered saturated heterocyclic ring
containing from 1 to 4 heteroatoms independently selected
from N, O and S; wherein the saturated heterocyclic ring is
optionally substituted with one or more substituents each of which is independently halogen, -C1 _6 alkyl, -C1 -6 alkyl-ORa, -C1-6 haloalkyl, -0-C]-6 alkyl, -0-C|_6 haloalkyl, -C(=0)Ra -C02Ra, -C(=0)-Co-6 alkyl-N(RaRb), -S02Ra, oxo, aryl, or -C1-6 alkyl-aryl; or
(c) a 5- to 7-membered heteroaromatic ring
containing from 1 to 4 heteroatoms independently selected
from N, O and S; wherein the heteroaromatic ring is optionally
substituted with one or more substituents each of which is independently halogen, -C1-6 alkyl, -C1-6 alkyl-ORa, -C 1-6
haloalkyl, -0-C[_6 alkyl, -O-Ci-6 haloalkyl, oxo, or aryl;
(5) -Co-6 alkyl-O-Co-6 alkyl-Rk,
(6) -Co-6 alkyl-S(0)n-Co-6 alkyl-Rk
(7) -O-C1-6 alkyORk,
(8) -O-C1-6 alkyl-O-C i -6 alkyl-Rk,
(9) -0-C|-6alkyl-S(0)nRk
(10) -Co-6 alkyi-N(Ra)-Rk,
(11) -Co-6 alkyl-N(Ra)-C1-6 alkyl-Rk,
(12) -Co-6 a!kyl-N(Ra)-C1-6 alkyl-ORk,
(13) -Co-6 alkyl-C(-0)-Rk,
(14) -Co-6 alkyl-C(-0)N(Ra)-Co-6 alkyl-Rk,
(15) -Co-6 alkyl-N(Ra)C(=0)-Co-6 alkyl-Rk,
(16) -Co-6 alkyI-N(Ra)C(=0)-0-Co-6 alkyl-Rk, or
(17) -Co-6 aIkyl-N(Ra)C(=0)C(=O)Rk;
R- is -C1-6 al'kyl which is optionally substituted with one or more substituents each of which is independently

(1) halogen,
(2) -OH,
(3) -CN,
(4) -0-C1-6 alkyl,
(5) -0-C1-6aloalkyl,
(6) -C(K))Ra,
(7) -C02Ra
(8) -SRa
(9) -S(=0)Ra
(10) -N(RaRb),
(11) -C(=0)N(RaRb),
(12) -N(Ra)-C(=0)-C 1 -6 alkyl-N(RbRC),
(13) -S02Ra
(14) -N(Ra)S02Rb,
(15) -S02N(RaRb),
(16) -N(Ra)-C(Rb)K),
(17) -C3-8cycloalkyl,
(18) aryl, wherein the aryl is optionally substituted with one or more
substituents each of which is independently halogen, -C1-6 alkyl,
, -C;1 -6 haloalkyL -O-C1-6 alkyl, -O-C1-6 haloalkyl, -Co-6 alkyl-N(RaRb), or -C1_6 alkyl substituted with a 5- or 6-
membered saturated heterocyclic ring containing from 1 to 4
heteroatoms independently selected from N, O and S;
wherein the saturated heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -C1-6
alkyl, oxo, or a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; or
(19) a 5- to 8-membered monocyclic heterocycle which is saturated
or unsaturated and contains from 1 to 4 heteroatoms independently selected from N, O and S; wherein the heterocycle is optionally substituted with one or more substituents each of which is independently -Cl-6 alkyl, -0-C|-6 alkyl, oxo, phenyl, or naphthyl;
with the proviso that none of the following substituents is attached to the

carbon atom in the -C1-6 alkyl group that is attached to the ring nitrogen: halogen, -OH, -O-C1-6 alky!, -0-C1-6 haloalkyl, -SRa, -S(-0)Ra, or -N(Ra)-C(Rb)-0;
R3 is -II or-C1-6 alkyl;
R4 is((2) C|_6 alkyl which is optionally substituted with one or more
substituents each of which is independently halogen, -OH, O-C1-6 alkyl, -O-C1-6 haloalkyl, -NO2, -N(RaRb), -C(0)Ra, -C02Ra, -SRa, -S(---C)Ra, -S02Ra, or -N(Ra)C02Rb,
(3) C\-(y alkyl which is optionally substituted with one or more
substituents each of which is independently halogen, -OH, or 0-C]_4
alkyl, and which is substituted with 1 or 2 substituents each of which is independently:
(i) C3-8 cycloalkyl,
(ii) aryl,
(iii) a fused bicyclic carbocycle consisting of a benzene ring fused to a C5-7 cycloalkyl,
(iv) a 5- or 6-membered saturated heterocyclic ring
containing from 1 to 4 heteroatoms independently selected from N, O and S,
(v) a 5- or 6-membered heteroaromatic ring containing
from I to 4 heteroatoms independently selected from N, O and S, or
(vi) a 9- or 10-membered fused bicyclic heterocycle
containing from 1 to 4 heteroatoms independently selected from N, O and S, wherein at least one of the
rings is aromatic,
(4) C2-5 alkynyl optionally substituted with aryl,
(5) C3-8 cycloalkyl optionally substituted with aryl,
(6) aryl.
(7) a fused bicyclic carbocycle consisting of a benzene ring fused to a

C5-7 cycloalkyl,
(8) a 5- or 6-mcmbered saturated heterocyclic ring containing frorp 1 to 4 heteroatoms independently selected from N, O and S,
(9) a 5- or 6-mcmbered heteroaromatic ring containing from I to 4 heteroatoms independently selected from N, O and S, or
(10) a 9- or 10-membcred fused bicyclic heterocycle containing from 1 to 4 heteroatoms independently selected from N, O and S, wherein at least one of the rings is aromatic;
wherein
each aryl in (3)(ii) or the aryl in (4), (5) or (6) or each fused carbocycle in (3)(iii) or the fused carbocycle in (7) is optionally
substituted with one or more substituents each of which is independently halogen, -OH, -C]-6 alky!, -C]-6 alkyl-ORa, ~C|_6 haloalkyl, -O-C1-6 alky I, -0-C]-6 haloaikyl, -CN, -NO2, -N(RaRb), -C1-6 alkyl-N(RaRb), -C(0)N(RaRb), -C(=0)Ra, -CC>2Ra, -Ci-6 alkyl-C02Ra, -OC02Ra, -SRa, -S(0)Ra -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), -N(Ra)C(=0)Rb, -N(Ra)C02Rb, -C1-6 alkyl-N(Ra)CC)2Rb, aryl, -Ci-6 alkyl-aryl, -O-aryl, or -Co-6 alkyl-het wherein hct is a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, and het is
optionally fused with a benzene ring, and is optionally substituted with one or more substituents each of which is independently -C1-6 alkyl,
-C1-6 haloalkyl, -0-C]-6 alkyl, -O-Cl-6 haloalkyl, oxo, or -C02Ra;
each saturated heterocyclic ring in (3)(iv) or the saturated
heterocyclic ring in (8) is optionally substituted with one or more substituents each of which is independently halogen, -C1-6 alkyl, -C1-6 haloalkyl, -O-C1-6 alkyl, -O-C1--6 haloalkyl, oxo, aryl, or a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms
independently selected from N, O and S; and
each heteroaromatic ring in (3)(v) or the heteroaromatic ring in (9) or each fused bicyclic heterocycle in (3)(vi) or the fused bicyclic heterocycle in (10) is optionally substituted with one or more substituents each of which is independently halogen, -C1_6 alky-Ci-6 haloalkyl, -0-C1_6 alkyl, -O-C1-6 haloalkyl, oxo, aryl, or-C]-6l, alkyl-aryl;

or alternatively R3 and R4 together with the N to which both are attached form a C3-7
i
azacycloalkyl which is optionally substituted with one or more substituents each of which is independently -C1-6 alkyl or oxo;
each Ra, Rb, Rc, and Rd is independently -H or -C1-6 alkyl;
Rk is carbocycle or heterocycle, wherein the carbocycle or heterocyele is optionally substituted with one or more substituents each of which is independently
(1) halogen,
(2) -OH,
(3) -CN,
(4) -C1-6 alkyl, which is optionally substituted with one or more
substituents each of which is independently halogen, -OH, -CN, -O-C1-6 alkyl, -O-C1-6 haloalkyl. -C(=0)Ra, -C02Ra. -SRa, -S(=0)Ra, -N(RaRb), -C(=O)-(CH2)0-2N(RaRb), N(Ra)-C(=O)-(CH2)0-2N(RbRc), -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(RbH),
(5) -O-C1-6 alkyl, which is optionally substituted with one or more
substituents each of which is independently halogen, -OH, -CN, -O-C1-6 alkyl, -O-C1-6 haloalkyl, -C(=0)Ra, -C02Ra, -SRa,
-S(=0)Ra -N(RaRb), -C(=O)-(CH2)0-2N(RaRb), N(Ra)-C(-O)-(CH2)0-2N(RbRC), -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), 0r -N(Ra)-C(Rb)=0,
(6) -NO2,
(7) oxo,
(8) -C(=0)Ra
(9) -C02Ra,
(10) -SRa
(11) -S(=0)Ra,
(12) -N(RaRb),
(13) -C(=0)N(RaRb),
(14) -C(==0)-C 1 -6 alkyl-N(RaRb),

(15) -N(Rii)C(K))Rb
(16) -S02Ra
(17) -S02N(RaRb),
(18) -N(Ra)S02Rb,
(19) -Rm.
(20) -C i -6 alkyl-Rm, wherein the alkyl is optionally substituted with
one or more substituents each of which is independently halogen, -OH, -CN, -C1-6 haloalkyl, -O-C1-6 alkyl, -O-C1-6 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb). -N(Ra)CC)2Rb, -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=o,
(21) -Co-6 alkyl-N(Ra)-Co-6 alkyl-Rm,
(22) -Co-6 alkyl-O-Co-6 alkyl-Rm,
(23) -Co-6 alkyl-S-Co-6 alkyl-Rm,
(24) -Co-6 alkyi-C(K))-Co-6 alkyl-Rm,
(25) -C(=0)-0-Co-6 alkyl-Rm,
(26) -C(-0)N(Ra)-Co-6 alkyl-Rm,
(27) -N(Ra)C(=())-Rm,
(28) -N(Ra)C(= 0)-C 1 -6 alkyl-Rm, wherein the alkyl is optionally
substituted with one or more substituents each of which is independently halogen, -OH, -CN, -Cl-6 haloalkyl, -O-C1-6 alkyl, -O-C1-6 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra -N(RaRb), -N(Ra)C02Rb, -S02Ra -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=0,
(29) -N(Ra)-C(=0)-N(Rb)-Co-6 alkyl-Rm,
(30) -N(Ra)-C(~-0)-0-Co-6 alkyl-Rm,
(31) -N(Ra)-C(-0)-N(Rb)-S02-Co-6 alkyl-Rm,
(32) -C(K))-C(-0)-N(RaRb),
(33) -C(=0)-C 1 -6 alkyl-S02Ra, or
(34) -C(=0)-C(=0)Rm;
carbocycle in Rk is (i) a C3 to Cs monocyclic, saturated or unsaturated ring, (ii) a C7 to C|2 bicyclic ring system, or (iii) a C11 to C16 tricyclic ring system, wherein each
ring in (ii) or (iii) is independent of or fused to the other ring or.-rings and each ring is

saturated or unsaturated;
heterocycle in Rk is (i) a 4- to 8-membered, saturated or unsaturated monocyclic ring, (ii) a 7- to 12-membered bicyclic ring system, or (iii) an 11 to 16-membered tricyclic ring system; wherein each ring in (ii) or (iii) is independent of or fused to the other ring or rings and each ring is saturated or unsaturated; the monocyclic ring, bicyclic ring system, or tricyclic ring system contains from 1 to 6 heteroatoms selected from N, O and S and a balance of carbon atoms; and wherein any one or more of the nitrogen and sulfur heteroatoms is optionally be oxidized, and any one or more of the nitrogen heteroatoms is optionally quaternized;
each Rm is independently C3-8 cycloalkyl; aryl; a 5- to 8-membered monocyclic
heterocycle which is saturated or unsaturated and contains from 1 to 4 heteroatoms independently selected from N, O and S; or a 9- to 10-membered bicyclic heterocycle which is saturated or unsaturated and contains from 1 to 4 heteroatoms independently selected from N, O and S; wherein any one or more of the nitrogen and sulfur heteroatoms in the heterocycle or bicyclic heterocycle is optionally oxidized and any one or more of the nitrogen heteroatoms is optionally quaternized; and wherein
the cycloalkyl or the aryl defined in Rm optionally substituted with one or more substituents each of which is independently halogen, -C1-6 alkyl
optionally substituted with -0-C1-4 alkyl, -C1-6 haloalkyl, -OC1-6 alkyl, -O-C1-6 haloalkyl, -N(RaRb), aryl, or -C1-6 alkyl-aryl; and
the monocyclic or bicyclic heterocycle defined in Rm is optionally substituted with one or more substituents each of which is independently halogen, -C1-6 alkyl, -C1-6 haloalkyl, -O-C1-6 alkyl, -O-C1-6 haloalkyl, oxo, aryl, -C1-6 alkyl-aryl, -C(=0)-aryl, -C02-aryl, -CO2-CI-6 alkyl-aryl, a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, or a 5- or .6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; and
each n is independently an integer equal to zero, 1 or 2;
or a pharmaceutical!)' acceptable salt thereof.

2. The compound according to claim 1, wherein R1 is:
(1) -H,
(2) -Cl-4 alkyl, which is optionally substituted with from I to 4
substituents each of which is independently halogen, -OH, -CN, -O-Ci-4 alkyl, -O-Cj-4 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb), -C(-0)-C()-4 alkyl-N(RaRb), N(Ra)-C( -S02N(RaRb), _N(Ra)-C(-0)Rb, -N(Ra)C(=0)Rk,
or -N(Ra)C(=O)C(=0)N(RbRc)
(3) -Rk
(4) -Ci_4 alkyl-Rk, wherein:
(i) the alkyl is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -OH, -CN, -0-C]_4
alkyl, -O-C1-4 haloalkyl, -N(RaRb), -N(Ra)C02Rb, -N(Ra)C(-0)-Co-4 alkyl-N(RbRc), or -N(Ra)-(CH2)2-4-OH; and (ii) the alkyl is optionally mono-substituted with -Rs,
-N(Ra)-C(=0)-Co-4 alkyl-Rs, -N(Ra)-Co-4 alkyl-Rs, -0-C()-4 alkyl-Rs, or -N(Ra)-C(0)-C()-4 alkyl-RS; wherein Rs is
(a) aryl which is optionally substituted with from 1
to 3 substituents each of which is independently halogen, -OH,
-C1-4 alkyl, -Cl-4 alkyl-ORa, -C|_4 haloalkyl, -O-C1-4 alkyl,
-O-C1-4 haloalkyl, methylcnedioxy attached to two adjacent
carbon atoms, or phenyl;
(b) a 5- or 6-membered heteroaromatic ring
containing from 1 to 4 heteroatoms independently selected
from N, O and S; wherein the heteroaromatic ring is optionally
substituted with from 1 to 3 substituents each of which is independently halogen, -C1_4 alkyl, -C1--4 alkyl-ORa, -C1_4
haloalkyl, -O-C1-4 alkyl, -0-C1-4 haloalkyl, oxo, or phenyl; or

(c) a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 hetcroatoms independently selected from N, O and S; wherein the saturated heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C1-4 alkyl, -C1-4 alkyl-ORa, -C1_4 haioalkyl, -O-C]-4 alkyl, -0-C|_4 haloalkyl, -C(-0)Ra, -C02Ra, -C(=0)-C()-4 alkyl-N(RaRb), -S02Ra, oxo, or phenyl, or (5) -(CH2)0-3-C(-O)N(Ra)-(CH2)0-3-Rk;
or a pharmaceutically acceptable salt thereof.
3. The compound according to claim 2, wherein R' is:
(1) -H,
(2) -C1-4 alkyl, which is optionally substituted with from 1 to 3
substituents each of which is independently halogen, -O-Cj-4 alkyl,
-O-C1-4 haloalkyl, -C(=0)Ra -CO2Ra, -N(RaRb), or
(3) -Rk,
(4) -(CH?)l-4-Rk, wherein:
(i) the -(CH2)l-4- moiety is optionally substituted with 1 or 2
substituents each of which is independently halogen, -OH, -O-C1-4 alkyl, -0-C1_4 haloalkyl, or -N(RaRb); and
(ii) the -(CH2)l-4- moiety is optionally mono-substituted with -Rs
or -N(Ra)-(CH2)l-2-Rs; wherein Rs is
(a) phenyl which is optionally substituted with from
1 to 3 substituents each of which is independently halogen, -C i -4 alkyl, -C l .4 alkyl-ORa, -C1-.4 haloalkyl, -O-C1.4 alkyl,
or -O-C 1 -4 haloalkyl; or
(b) a 5- or 6-membered heteroaromatic ring
containing from 1 to 4 heteroatoms independently selected
from N, O and S; wherein the heteroaromatic ring is optionally.

substituted with from 1 to 3 substituents each of which is independently halogen, -C1.4 alkyl, -C | -4 alkyl-ORa, -C1-4 haloalkyl, -0-C1_4 alkyl, or -O-C1-4 haloalkyl; or
(c) a 5- or 6-membered saturated heterocyclic ring
containing from 1 to 4 heteroatoms independently selected
from N, O and S; wherein the saturated heterocyclic ring is
optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C1-4 alkyl, -C1_4 alkyl-ORa,
-C0_4 haloalkyl, -O-C1-4 alkyl, -O-C1.4 haloalkyl, -C(K))Ra
or -C02Ra,
(5) -C(-O)N(Ra)-(CH2)0-3-Rk,
(6) -C(ClI3)2N(Ra)C(=0)Rb?
(7) -C(CM3)2N(Ra)C(-0)Rk, or
(8) -C(CII3)2N(Ka)C(=0)C(-0)N(RbRc);
or a pharmaceutical^ acceptable salt thereof.
4. The compound according to claim 1, wherein
Rk is C3-8 cycloalkyl; aryl selected from phenyl and naphthyl; a bicyclic carbocycle
selected from indanyl and tetrahydronaphthyl; a 5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S; or a bicyclic heterocyele which is a benzene ring fused to a 5- or 6-membered saturated or unsaturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected from N, O and S;
wherein the cycloalkyl, aryl, bicyclic carbocycle, saturated heterocyclic ring, heteroaromatic ring, or bicyclic heterocyele is optionally substituted with from 1 to 4 substituents each of which is independently
(1) halogen,
(2) -OH,
(3) -CN,
(4) -C1-4 haloalkyl,
(5) -C1_4 alkyl, which is optionally substituted with from 1 to 3

substituents each of which is independently -OH, -CN(, -O-Cj-4 alkyi, -O-C1.4 haloalkyl, -C(=0)Ra, -C02Ra,-SRa, -S(=0)Ra, -N(RaRb), -C(=O)-(CH2)0-2N(RaRb),
N(Ra)-C(=O)-(CH2)0-2N(RbRC),-SO2Ra, -N(Ra)S02Rb, -S02N(RaRb), 0r -N(Ra)-C(Rb)=0,
(6) -O-C1_4 haloalkyl
(7) -O-C 1-4 alkyl, which is optionally substituted with from 1 to 3
substituents each of which is independently -OH, -CN, -O-Cl-6 alkyl, -O-C1 -6 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb), -C(=O)-(CH2)0-2N(RaRb), N(Ra)-C(=O)-(CH2)0-2N(RbRC),-SO2Ra -N(Ra)S02Rb, -S02N(RaRb), or-N(Ra)-C(Rb)=0,
(8) -N02,
(9) oxo,
(10) -C(0)Ra,
(11) -C02Ra,
(12) -SRa,
(13) -S(=0)Ra,
(14) -N(RaRb),
(15) -C(=0)N(RaRb),
(16) -C(=0)-C 1 -6 alkyl-N(RaRb),
(17) -N(R3)C(=0)Rb,
(18) -S02Ra,

(18) -S02N(RaRb),
(19) -N(Ra)S02Rb,
(20) -Rm,
(21) -Ci_4alkyl-Rm,
(22) -(CH2)0-2-N(Ra)-(CH2)0-2-Rm.
(23) -(CH2)0-2-O-(CH2)0-2-Rm,
(24) -(CH2)0-2-S-(CH2)0-2-Rm,
(25) -(CH2)0-2-C(=O)-(CH2)0-2-Rm.
(26) -C(-O)-O-(CH2)0-2-Rm,
(27) -C(-0)N(Ra)-Rm, Gr

(28) -C(0)-C(=0)N(RaRb); or a pharmaceuticaliy acceptable salt thereof.
5. The compound according to claim 4, wherein
each Rm is independently C3-7 cycloalkyl; aryl selected from phenyl and naphthyl; a
5- or 6-membered saturated heterocyclic ring containing from 1 to 4 heteroatoms
independently selected from N, O and S; a 5- or 6-membered heteroaromatic ring
containing from 1 to 4 heteroatoms independently selected from N, O and S, wherein
any N is optionally oxidized to form an N-oxide; or a bicyclic heterocycle which is a
benzene ring fused to a 5- or 6-membered, saturated or unsaturated heterocyclic ring
containing from 1 to 3 heteroatoms selected from N, O and S; wherein
the cycloalkyl or the aryl defined in Rm is optionally substituted with from 1 to 4 substiluents each of which is independently halogen, -C|-4 alkyl,
-C1-4 haloalkyl, -O-CM alkyl, -OC1_4 haloalkyl, -N(RaRb), phenyl, or
-(CH2)l-2-phenyl;
the saturated heterocyclic ring defined in Rm is optionally substituted with from I to 4 substituents each of which is independently -C1_4 alkyl
optionally substituted with -O-C1-4 alkyl, -C1.4 haloalkyl, -0-C1_4 alkyl,
-O-C1-4 haloalkyl, oxo, phenyl, -(CH2)l-2-phenyl, -C(=0)-phenyl,
-C02-phenyI, -C02-(CH2)l-2-phenyl, a 5- or 6-membered saturated
heterocyclic ring containing from 1 to 4 heteroatoms independently selected
from N, O and S, or a 5- or 6-membered heteroaromatic ring containing from
1 to 4 heteroatoms independently selected from N, O and S; and
the heteroaromatic ring or the bicyclic heterocycle defined in Rm is
optionally substituted with from 1 to 4 substituents each of which is independently halogen, -C 1.4 alkyl, -C1-4 haloalkyl, -O-Ci-4 alkyl, -O-Ci-4
haloalkyl, oxo, phenyl, or -(CH2)l-2-phenyl;
or a pharmaceutical]}' acceptable salt thereof.
6. The compound according to claim 4, wherein Rk is phenyl; a 5-
or 6-membered saturated heterocyclic ring containing 1 or 2 heteroatoms selected

from I or 2 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; a 5- or 6-membered heteroaromatic ring containing 1 or 2 hcteroatoms selected from 1 or 2 N atoms, 0 or 1 O atoms, and 0 or I S atoms; or a bicyclic heterocycle which is a benzene ring fused to a 5- or 6-membered saturated heterocyclic ring containing 1 or 2 nitrogen atoms; wherein:
(a) the phenyl, the saturated heterocyclic ring, heteroaromatic ring, or bicyclic heterocycle is optionally substituted with from 1 to 3 substituents each of which is independently
(1) fluoro,
(2) chloro,
(3) bromo,
(4) -OH
(5) -CF3,
(6) -C1-4 alkyl, which is optionally substituted with 1 or 2 substituents each of which is independently -OH, -CN, -0-C]_4 alkyl, -OCF3, -N(RaRb), -C(=0)N(RaRb), or N(Ra)-C(-O)-(CH2)0-2N(RbRC),
(7) -OCF3,
(8) -O-C1-4 alkyl
(9) -C(0)Ra,
(10) -C02Ra,
(11) -SRa,
(12) -SRa,
(13) -N(RaRb),
(14) -C(0)N(RaRb),
(15) -C(=0)-(CH2) 1 -2-N(RaRb),
(16) -N(Ra)C(=0)Rb, or
(17) -S02Ra;
(b) the phenyl is optionally mono-substituted with
(1) -(CH2)l-2-Rm,or
(2) -(CIl2)0-2-N(Ra)-(CH2)0-2-Rm;and
(c) the saturated heterocyclic ring, heteroaromatic ring, or bicyclic
heterocycle is optionally mono- or di-substituted with
(1) oxo

(2) -(CH2)l-2-Rm,
(3) -0-(CH2)l-2-Rm, or
(4) -(CH2)0-|-C(-OHCH2)0-2-Rm; or a pharmaceutically acceptable salt thereof.
7. The compound according to claim 6, wherein
each Rm is independently cyclopropyl; phenyl; a 5- or 6-membered saturated
heterocyclic ring selected from pyrrolidinyl, imidazolidinyl, pyrazolidinyl, piperidinyl,
piperazinyl, and morphoiinyl; or a 5- or 6-membered heteroaromatic ring selected
from thienyl, pyridyl optionally in the form of an N-oxide, imidazolyl, pyrrolyl,
pyrazolyl, thiazolyl, isothiazolyl, oxazolyl, isooxazolyl, oxadiazolyl, thiadiazolyl,
pyrazinyl, pyrimidinyl, triazolyl, tetrazolyl, furanyl, and pyridazinyl; wherein
the cyclopropyl is unsubstituted;
the phenyl is optionally substituted with from I to 3 substituents each of which is independently halogen, -Ci_4 alkyl, -CF3, -O-Ci-4 alkyl, -OCF3,
or -N(RaRb);
the saturated heterocyclic ring is optionally substituted with 1 or 2 substituents each of which is independently -C]-4 alkyl, -CF3, -0-C]_4 alkyl,
-OCF3, oxo, phenyl, -(^H2)|-2-phenyl, -C0 -C02-CH2-phenyl;and
the heteroaromatic ring is optionally substituted with 1 or 2 substituents each of which is independently -Ci-4 alkyl, -CF3, -O-C1-.4 alkyl,
-OCF3, oxo, phenyl, or -(CIl2)]-2-phenyl;
or a pharmaceutically acceptable salt thereof.
8. The compound according to claim 1, wherein R2 is:
(1) -C1-6 alkyl,
(2) -C1-6 alkyl substituted with -N(RaRb), with the proviso that -N(RaRb) is not attached to the carbon atom in the -C1 -6 alkyl group that is
attached to the ring nitrogen,
(3) -C]-6 alkyl substituted with phenyl, wherein the phenyl is:

(a) optionally substituted with from 1 to 4 substitupnts each
of which is independently halogen, -Cl-4 aikyl, -Ci-4
haloalkyl, -0-C|-4 alkyl, -O-C1-4 haloalkyl, or -C0-4 alkyl-N(RaRb); and
(b) optionally mono-substituted with -C1-4 alkyl
substituted with a 5- or 6-rnembered saturated heterocyclic ring
containing from 1 to 3 heteroatoms selected from 1 or 2 N
atoms, 0 or 1 O atoms, and 0 or 1 S atoms;
wherein the heterocyclic ring is optionally substituted
with from 1 to 3 substituents each of which is independently -C|_6 alkyl, oxo, or a 5- or 6-membered heteroaromatic ring
containing from 1 to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atom, and 0 or 1 S atom; or
(4) -C1-6 alkyl optionally substituted with -OH and substituted with a 5-
or 6-membered saturated monocyclic heterocycle which contains from I to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heterocycle is optionally substituted with from 1 to 4 substituents each of which is independently -C1-6 alkyl, -O-C1-6 alkyl, oxo, or phenyl; or
(5) -C1_6 alkyl substituted with a 5- or 6-membered heteroaromatic ring
which contains from 1 to 3 heteroatoms selected from 1 to 3 N atoms,
0 or 1 O atoms, and 0 or 1 S atoms; wherein the heteroaromatic ring is
optionally substituted with from I to 4 substituents each of which is
independently-C1-6 alkyl, -O-C1-6 alkyl, oxo, or phenyl;
or a pharmaceutically acceptable salt thereof.
9. The compound according to claim 8, wherein R2 is methyl; or a
. pharmaceutically acceptable salt thereof,
10. The compound according to claim 1, wherein
R3 is -H or -C]_4 alkyl; or a pharmaceutically acceptable salt thereof.

11. The compound according to claim 10, wherein R3 is -H or methyl; or a pharmaceuticaily acceptable salt thereof.
12. The compound according to claim 11, wherein R3 is -H; or a pharmaceuticaily acceptable salt thereof.
13. The compound according to claim 1, wherein R.4 is Cj-4 alkyl
substituted with an aryl, which is optionally substituted with from 1 to 4 substituents each of which is independently halogen, -OH, -C1-4 alkyl, -C]-4 alkyl-ORa, -C]-4 haloalkyl, -0-C1_4 alkyl, -O-Cj-4 haloalkyl. -CN, -NO2, -N(RaRb), -CM alkyl-N(RaRb), -C(-0)N(RaRb), -C(=0)Ra -C02Ra, -CM alkyl-C02Ra, -OC02Ra, -SRa, -S(==0)Ra, -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), -N(Ra)C(=0)Rb, -N(Ra)C02Rb, -CM alkyI-N(Ra)C02Rb, methylenedioxy attached to two adjacent ring carbon atoms, phenyl, -CM alkyl-phenyl, -O-phenyl, or -(CH2)0-2-het;
wherein het is a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, and het is optionally fused with a benzene ring, and is optionally substituted with 1 or 2 substituents each of which is independently -C1-4 alkyl, -C1_4 haloalkyl, -O-C1-4 alkyl, -0-C1_4 haloalkyl, or-C02Ra;
or a pharmaceuticaily acceptable salt thereof.
14. The compound according to claim 13, wherein R4 is
-CH2-phenyI, wherein the phenyl is optionally substituted with from 1 to 3
substituents each of which is independently fluoro, bromo, chloro, -OH, -Ci_4 alkyl,
-Ci_4 fluoroalkyl, -O-Ci-4 alkyl, -O-Cj-4 fluoroalkyl, -(CH2)1-2-N(RaRb), -S02Ra,
-(CH2)0-2-CO2Ra, -(CH2)0-2-N(Ra)CO2Rb, -NO2, -SRa, -N(RaRb) or phenyl; and
each Ra and Rb is independently is H or -C1-_4 alkyl;
or a pharmaceuticaily acceptable salt thereof.
15. The compound according to claim 14, wherein R4 is

-CI l2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents, each of which is independently -F, -Br, -CI, -OH, -C1-4 alkyl, -C1-4 fluoroalkyl, -0-C|_4 alkyl, -SO2-C1-4 alkyl, -S-C1-4 alkyl, -N(CH3)2, OZ-O-CM
fluoroalkyl;
or a pharmaceutically acceptable salt thereof.
16. The compound according to claim 15, wherein R4 is
/>fluorobenzyl or 2,3-dimethoxybenzyI;
or a pharmaceutically acceptable salt thereof.
17. The compound according to claim 1, wherein:
Rl is-Rk;
Rk is phenyl which is
(a) optionally substituted with from I to 3 substituents each of
which is independently:
(1) halogen,
(2) -C]-6 alkyl, which is optionally substituted with 1 or 2
substituents each of which is independently -O-C] -6 alkyl, -O-C1-6 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb), -C(=O)-(CH2)0-2N(RaRb), N(Ra)-C(=O)-(CH2)0-2N(RbRc),-S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=o,
(3) -C1-6 haloalkyl,
(4) -O-C1-6 haloalkyl,
(5) -C(=0)Ra,
(6) -C02Ra,
(7) -C(=0)N(RaRb), or
(8) -C(=0)-Ci-6 alkyl-N(RaRb); and
(b) optionally mono-substituted with
(1) -C1_4alkyl-Rm, or
(2) -Co-4 alkyl-N(Ra)-CQ-4 alkyl-R™;

wherein Rm is aryl selected from phenyl and naphthyl; a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected*from N, O and S; or a 5- or 6-membercd heteroaromatic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; wherein
the aryl defined in R™ is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C]-4 alkyl, -CF3, -O-C1-4 alkyl. -OCF3, or -N(RaRb);
the saturated heterocyclic ring defined in Rm is optionally substituted with from I to 3 substituents each of which is independently -C]-4 alkyl or
oxo, and is additionally optionally mono-substituted with phenyl, -(CH2)l-2-phenyl, -C(0)-phenyl, -CC>2-phenyl, -C02-(CH2)l-2-phenyl, or a
5- or 6-membered heteroaromatic ring containing from I to 3 heteroatoms independently selected from N, O and S; and
the heteroaromatic ring defined in Rm is optionally substituted with 1 or 2 substituents each of which is independently -C]-4 alkyl or oxo;
or a pharmaceutically acceptable salt thereof.
18. The compound according to claim 17, wherein R2 is methyl; R3 is -H;
R4 is:
(1) -CH2-phenyl, wherein the phenyl is optionally substituted with
from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -Cj-4 alkyl, -Ci_4 fluoroalkyl, -O-Ci-4 alkyl, -O-C1-4 fluoroalkyl, -(CH2)l-2-N(RaRb), -SC)2Ra, -(CH2)0-2-CO2Ra, -(CH2)0-2-N(Ra)CO2Rb, -N02, -SRa, -N(RaRb) or phenyl; or
(2) a fused bicyclic carbocycle selected from

each Ra and Rb is independently is H or -Ci-4 alkyl;
or a pharmaceuticalty acceptable salt thereof.
19. The compound according to claim 18, wherein R4 is
4-fluorobenzyl or 2,3-dimethoxybenzyl;
or a pharmaceutically acceptable salt thereof.
20. A compound of Formula (II):

wherein
Qis:
(1) methyl which is optionally substituted with 1 or 2 of-O-Ci-4 alkyl,
(2) phenyl which is optionally substituted with from 1 to 3 substituents
each of which is independently -F, -CI, Br, -Cl-4 alkyl. -CF3, -O-Cj-4
alkyl, -OCF3, methylenedioxy attached to two adjacent carbon atoms,
or phenyl, or
(3) a 5- or 6-mcmbcrcd saturated heterocyclic ring containing from 1 to 3
heteroatoms independently selected from N, O and S; wherein the saturated
heterocyclic ring is optionally substituted with 1 or 2 substituents each

of which is independently -F, -CI, -Br, -C1.4 alkyl, oxo, phenyl, or
-C(-0)-phenyI; ;
T is:
(1) -H,
(2) -OH,
(3) methyl or ethyl, optionally substituted with -OH or -O-Ci-4 alkyl,
(4) -O-C1-4 alkyl
(5) -N(RaRb),
(6) -N(Ra)-(CH2)2-OH,
(7) -N(Ra)-C02Rb,
(8) -N(Ra)-C(=0)-(CH2)l-2-N(RaRb),
(9) -Rs,
(10) -(CH2)l-2-Rs,or
(11) -(CH2)0-2-N(Ra)-(CH2)0-3-Rs;
Rs is:
(1) phenyl optionally substituted with from 1 to 4 substituents each of which is independently halogen, -Cl-4 alkyl, -C1.4 alkyl-ORa, -Ci_4 haloalkyl, -O-C)-4 alkyl, -O-C1-4 haloalkyl, or -N(RaRb);
(2) a 5- or 6-membered saturated heterocyclic ring containing from
1 to 3 heteroatoms independently selected from N, O and S; which is
optionally substituted with from 1 to 4 substituents each of which is independently -C1.4 alkyl, -Cl-4 alkyl-ORa, -Cl-4 haloalkyl, -O-C'1-4 alkyl,
-O-C 1-4 haloalkyl, -C(=0)Ra, oxo, phenyl, or -CH2-phenyl; or
(3) a 5- or 6-membered heteroaromatic ring containing from 1 to 3
heteroatoms independently selected from N, O and S; which is optionally substituted with from 1 to 4 substituents each of which is independently -C1-4
alkyl, -C1-4 alkyl-ORa, _C1_4 haloalkyl, -O-C].4 alkyl, -O-C-4 haloalkyl, or1 oxo;
R2 is

(1) -C|-4 alkyl,
(2) -C l -4 alkyl substituted with -N(RaRb), with the proviso that -N(RaRb)
r
is not attached to the carbon atom in the -C1-4 alkyl group that is
attached to the ring nitrogen, or
(3) -C1-4 alkyl substituted with a 5- or 6-membered saturated monocyclic
heterocyclic which contains from 1 to 3 heteroatoms selected from 1 to
3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the saturated
heterocycle is optionally substituted with from 1 to 4 substituents each of which is independently a -C1-4 alkyl;
R3 is-H or-C1-4 alkyl;
R4 is -CH2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 substituents each of which is independently fluoro, bromo, chloro, -OH, -CM alkyl, -C1-4-fluoroalkyl, -O-C1-4 alkyl, -O-CM fluoroalkyl, -(CH2)l-2-N(RaRb), -S02Ra, -(CH2)0-2-CO2Ra, -(CH2)0-2-N(Ra)CO2Rb, -N02, -SRa, -N(RaRb) 0r phenyl;
each Ra and Rb is independently -H or -C1-4 alkyl; and
s is an integer equal to zero, 1, or 2;
or a pharmaceutically acceptable salt thereof.
21. The compound according to claim 20, wherein Q is phenyl;
Tis:
(1) -H,
(2) -N(RaRb),
(3) a 5- or 6-mcmbered saturated heterocyclic ring containing from 1 to 3 heteroatoms independently selected from N, O and S; which is optionally substituted with 1 or 2 substituents each of which is independently -C1-4 alkyl or -C(=0)RA. or

(4) -N(Ra)-(CH2)l-2-heteroaromatic, wherein the heteroaromatic is a 5- or 6-membcred ring containing 1 or 2 N atoms;
R2 is methyl;
R3 is-H; and
R4 is -CH2-phenyI, wherein the phenyl is optionally substituted with 1 or 2 substituents each of which is independently -F, -CI, -Br, -Cj-4 alkyl, -CF3, -O-C1-4 alkyl, -SO2CH3, -SCH3, -N(CI!3)2 or-OCF3;
each Ra and Rb is independently -H, methyl or ethyl; and
s is an integer equal to zero or 1;
or a pharmaceutically acceptable salt thereof.
22. The compound according to claim 1, wherein
Rl is-Rk;
Rk is (i) a 5- or 6-membered saturated heterocyclic ring containing from 0 to I oxygen atoms and from I to 3 nitrogen atoms or (ii) a bicyclic heterocycle which is a benzene ring fused to a 5- or 6-membered saturated heterocyclic ring containing from 0 to 1 oxygen atoms and from 1 to 3 nitrogen atoms;
wherein the saturated heterocyclic ring or bicyclic heterocycle is
optionally substituted with from 1 to 3 substituents each of which is independently
(1) -C1_4 alkyl, which is optionally substituted with from 1 to 4
substituents each of which is independently halogen, -O-C1-4 alkyl, -O-C1-4 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb), -C(=O)-(CH2)0-2N(RaRb),
N(Ra)-C(=O)-(CH2)0-2N(RbRC),.S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or-N(Ra)-C(Rb)=Of
(2) -OH,

(3) -C(=0)Ra,
(4) -C02Ra,
(5) -C(K))N(RaRb),
(6) -C(=0)-C 1 -6 alkyl-N(RaRb),
(7) -SRa,
(8) -S(-C))Ra
(9) -S02Ra,
(10) -N(RaRb),
(11) -Rm,
(12) -C1-4 alkyl-Rm, wherein the alkyl is optionally substituted with
from 1 to 4 substituents each of which is independently halogen, -OH, -CN, -C]-4 haloalkyl, -O-C1.4 alkyl, -O-C1-4 haloalkyl, -C(=0)Ra, -C02Ra, -SRa, -S(=0)Ra, -N(RaRb), -N(Ra)CC>2Rb, -S02Ra, -N(Ra)S02Rb, -S02N(RaRb), or -N(Ra)-C(Rb)=0,
(13) -Co-4 alkyl-N(Ra)-Co-4 alkyl-Rm,
(14) -Co-4 alkyl-O-Co-4 alkyl-Rm,
(15) -Co-4 alkyl-S-CO-4 alkyl-Rm,
(16) -Co-4 alkyl-C(=0)-Co-4 alkyl-Rm,
(17) -C(=0)-0-Co-4 alkyl-Rm, 0r
(18) -C(=0)N(Ra)-Co-4 alkyl-Rm;
wherein each Rm is independently -C3-6 cycloalkyl; aryl selected from phenyl and
naphthyl; a 5- or 6-mcmbered saturated heterocyclic ring containing from 1 to 3
heteroatoms independently selected from N, O and S; or a 5- or 6-membered
heteroaromatic ring containing from 1 to 3 heteroatoms independently selected from
N, O and S, wherein any N is optionally oxidized to form an N-oxide; wherein
the aryl is optionally substituted with from 1 to 3 substituents each of which is independently halogen, -C]-4 alkyl, -CF3, -O-Ci-4 alkyl, -OCF3, or
-N(RaRb);
the saturated heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -C1.4 alkyl or oxo, and is
additionally optionally mono-substituted with phenyl, -(CH2)l-2-phenyl,
-C(=0)-phenyl, -C02-phenyl, or -C02-(CH2)l-2-phenyl; and

the heteroaromatic ring is optionally substituted with 1 or 2 substituents each of which is independently halogen, -C1-4 alkyl, or oxo;
or a pharmaceutically acceptable salt thereof.
23. The compound according to claim 22, wherein

R8is:
(1) -H,
(2) -C | -4 alkyl, which is optionally substituted with 1 or 2
substituents each of which is independently -OH, -O-C i .4 alkyl, -OCF3, -C(=0)Ra -C()2Ra, -SRa -N(RaRb), or -C(-0)N(RaRb),
(3) -C(=0)Ra.
(4) -CC)2Ra.
(5) -C(-0)N(RaRb),
(6) -C(=0)-(CH2) 1.2-N(RaRb>;

(7) -S()2Ra,
(8) -(CU2)l-2-Rm,
(9) -(CH2)0-2-C(=O)-(CH2)0-2-Rm-
(10) -C(=O)-O-(CH2)0-2-Rm, or
(11) -C(=O)N(Ra)-(CH2)0-2-Rnn;
RlO is-H, -OH, -C i .4 alkyl, -O-Ci-4 alky!, -N(RaRb), or -0-(CH2)l-2-Rm ;
Rl2 is
(1) -H,
(2) -C | _4 alkyl, which is optionally substituted with 1 or 2
subslituents each of which is independently-OH, -O-C1.4 alkyl, -OCF3, -C(=0)Ra -Co2Ra, -SRa, -N(RaRb), 0r -C(=0)N(R3Rb),
(3) -C(=0)Ra,
(4) -C02R3,
(5) -C(=O)-(CH2)l-2-N(RaRb),0r
(6) -S02Ra;
R2 is methyl;
R3 is -H or methyl;
R4 is -CH2-phenyl, wherein the phenyl is optionally substituted with from 1 to 3 subslituents each of which is independently fluoro, bromo, chloro, -OH, -C1-4 alkyl,
-C1-4 fluoroalkyl, -O-C1.4 alkyl, -O-C1-4 fluoroalkyl, -(CH2)l-2-N(RaRb), -S02Ra
-(CH2)0-2-CO2Ra, -(Cll2)0-2-N(Ra)CO2Rb, -NO2, -SRa, -N(RaRb) or phenyl; and
each Ra and Rb is independently -H or -C1.4 alkyl; or a pharmaceutically acceptable salt thereof.
24. The compound according to claim 1, which is a compound of

Formula (III):
wherein R2 is:
(1) -C 1 -6 alkyl,
(2) -C1-6 alky! substituted with -N(RaRb), with the proviso that -N(RaRb)
is not attached to the carbon atom in the -C1-6alkyl group that is
attached to the ring nitrogen,
(3) -C1-6 alkyl substituted with phenyl which is:
(a) optionally substituted with from 1 to 4
substituents each of which is independently halogen, -Cl-4
alkyl, -C1_4 haloalkyl, -0-C|-4 alkyl, -O-C1-4 haloalkyl, or -Co-6 alkyl-N(RaRb); and
(b) optionally mono-substituted with -C]-4 alkyl
substituted with a 5- or 6-membered saturated heterocyclic ring containing from 1 to 3 hetcroatoms selected from 1 or 2 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms;
wherein the heterocyclic ring is optionally substituted with from 1 to 3 substituents each of which is independently -C]-6 alkyl, oxo, or a 5- or 6-mcmbered heteroaromatic ring
containing from 1 to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atom, and 0 or 1 S atom;
(4) -C]-6 alkyl optionally substituted with -OH and substituted with a 5-
or 6-membered saturated monocyclic heterocycle which contains from 1 to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atoms, and 0 or 1 S atoms; wherein the heterocycle is optionally substituted with from 1 to 4 substituents each of which is independently-C1-6 alkyl, -O-C1-6 alkyl, oxo, or phenyl; or
(5) -C1-6 alkyl substituted with a 5- or 6-membered heteroaromatic ring
which contains from 1 to 3 heteroatoms selected from 1 to 3 N atoms,

0 or 1 O atoms, and 0 or 1 S atoms; wherein the heteroaromatic ring is
optionally substituted with from 1 to 4 substituents each of whjch is independently -C1_6 alkyl, -0-C|-6 alkyl, oxo, or phenyl;
or a pharmaceutically acceptable salt thereof.
25. The compound according to claim 24, wherein
R2 is:
(1) -C1-4 alkyl,
(2) -(CH2)2-3-N(RaRb),
(3) -(Cll2)|-3-phenyl, wherein the phenyl is:
(a) optionally substituted with from 1 to 3
substituents each of which is independently fluoro, chloro, bromo, -C1-4 alkyl, -CF3, -O-C1-4 alkyl, -O-CF3, or
-(CM2)l-3-N(RaRb);and
(b) optionally mono-substituted with
-(CI l2)l-3-saturated heterocycle which is a 5- or 6-membered
saturated heterocyclic ring containing from 1 to 3 heteroatoms
selected from 1 or 2 N atoms, 0 or 1 O atoms, and 0 or 1 S
atoms, wherein the heterocyclic ring is optionally substituted
with from 1 to 3 substituents each of which is independently -C1 -4 alkyl or pyridyl;
(4) -(CH2) 1-3-sauced heterocycle, wherein the -(CH2)l-3- moiety is
optionally substituted with an -OH and the saturated heterocycle is a 5-
or 6-membered saturated monocyclic heterocycle which contains from
1 to 3 heteroatoms selected from 1 to 3 N atoms, 0 or 1 O atoms, and 0
or 1 S atoms; wherein the heterocycle is optionally substituted with from 1 to 3 substituents each of which is independently a -Cl_4 alkyl;
or
(5) -(Cll2)l-3-pyridyI;
R3 is -H or methyl;

31. A pharmaceutical composition, which comprises an effective amount of the compound according to claim 28, or a pharmaceutical^ accqptable salt thereof, and a pharmaceutically acceptable carrier.
31. A pharmaceutical composition comprising a therapeutically
effective amount of a compound.according to claim 1, or a pharmaceutically
acceptable salt thereof, and a pharmaceutically acceptable carrier.
32. A pharmaceutical composition, which comprises the product
prepared by combining an effective amount of a compound according to claim 1, or a
pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

Documents:

868-chenp-2004-abstract.pdf

868-chenp-2004-assignement.pdf

868-chenp-2004-claims.pdf

868-chenp-2004-correspondnece-others.pdf

868-chenp-2004-correspondnece-po.pdf

868-chenp-2004-description(complete).pdf

868-chenp-2004-form 1.pdf

868-chenp-2004-form 13.pdf

868-chenp-2004-form 26.pdf

868-chenp-2004-form 3.pdf

868-chenp-2004-form 5.pdf

868-chenp-2004-pct.pdf

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Patent Number

212400

Indian Patent Application Number

868/CHENP/2004

PG Journal Number

07/2008

Publication Date

15-Feb-2008

Grant Date

03-Dec-2007

Date of Filing

23-Apr-2004

Name of Patentee

M/S. ISTITUTO DI RICERCHE DI BIOLOGIA MOLECOLARE P. ANGELETTI, SPA

Applicant Address

VIA PONTINA KM 30,600 ,I-00040 POMEZIA (ROME),

Inventors:

#	Inventor's Name	Inventor's Address
1	CRESCENZYL, BENEDETTA	VIA PONTINA K 30,600 ,I-00040 POMEZIA (ROME),
2	GARDELLI, CRISTINA	VIA PONTINA K 30,600 ,I-00040 POMEZIA (ROME),
3	MURAGLIA, ESTER	VIA PONTINA K 30,600 ,I-00040 POMEZIA (ROME),
4	NIZI, EMNAUELA	VIA PONTINA K 30,600 ,I-00040 POMEZIA (ROME),
5	OR VIETO,FEDERICA	VIA PONTINA K 30,600 ,I-00040 POMEZIA (ROME),
6	PACE, PAOLA	VIA PONTINA K 30,600 ,I-00040 POMEZIA (ROME),
7	PESCATORE, GIOVANNA	VIA PONTINA K 30,600 ,I-00040 POMEZIA (ROME),
8	PETROCCHI, ALESSIA	VIA PONTINA K 30,600 ,I-00040 POMEZIA (ROME),
9	POMA , MARCO	VIA PONTINA K 30,600 ,I-00040 POMEZIA (ROME),
10	ROWLEY, MICHAEL	VIA PONTINA K 30,600 ,I-00040 POMEZIA (ROME),
11	SCARPELLI, RITA	VIA PONTINA K 30,600 ,I-00040 POMEZIA (ROME),
12	SUMMA, VINCENZO	VIA PONTINA K 30,600 ,I-00040 POMEZIA (ROME),

PCT International Classification Number

A61K 31/515

PCT International Application Number

PCT/GB02/04753

PCT International Filing date

2002-10-21

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	60/362,191	2002-03-06	U.S.A.
2	60/339,568	2001-10-26	U.S.A.