Title of Invention	"AN ADAMANTANE COMPOUND"
Abstract	A compound of general formual wherein m represents 1, 2 or 3; each R independently represents a hydrogen or halogen atom; A represents C(O)NH or NHC(O); Ar represents a group X represents a bond, an oxygen atom or a group CO, CH2, OCH2, NR5 , CH2NR5 , CONR5 or S(O)n; n is 0, 1 or 2; one of R2 and R3 represents a halogen, nitro, amino or a C1-C6 alkyl, and the other of R2 and R3 represents a hydrogen atom; either R4 represents a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and optionally an oxygen atom, the heterocyclic ring system being optionally substituted by one or more substituents independently selected from fluorine atoms, hydroxyl, carboxyl, cyano, C1-C6 alkyl, C1-C6 hydroxyalkyl, -NR6R7, -(CH2)rNR6R7 and -CONR6R7, or R represents a 3- to 8-membered saturated carbocyclic ring system substituted by one or more substituents independently selected from -NR6 R7 , -(CH2)rNR6 R7 and -CONR R , the ring system being optionally further substituted by one or more substituents independently selected from fluorine atoms, hydroxyl and C1-C6 alkyl; r is 1,2, 3,4, 5 or 6; R5 represents a hydrogen atom or a C1-C6 alkyl or C3-C8 cycloalkyl group; R6 and R7 each independently represent a hydrogen atom or a C1-C6 alkyl, C2-C6 hydroxyalkyl or C3-C8 cycloalkyl group, or R6 and R7 together with the nitrogen atom to which they are attached form a 3- to 8-membered saturated heterocyclic ring; with the provisos that, (a) when A represents C(O)NH and R4 represents an unsubstituted 3- to 8-membered saturated aliphatic heterocyclic ring system containing one nitrogen atom, then X is other than a bond, and (b) when A represents C(0)NH and X represents a group CH2 or OCH2 then R4 does not represent an unsubstituted imidazolyl, unsubstituted morpholinyl, unsubstituted piperidinyl or unsubstituted pyrrolidinyl group, and (c) when A represents NHC(O) and R4 represents an unsubstituted 3- to 8-membered saturated aliphatic heterocyclic ring system containing one nitrogen atom, then X is other than a bond, and (d) when A represents NHC(O) and X represents OCH2 then R4 does not represent an unsubstituted 1-piperidinyl or unsubstituted 1-pyrrolidinyl group; or a pharmaceutically acceptable salt or solvate thereof.

Title of Invention

"AN ADAMANTANE COMPOUND"

Abstract

A compound of general formual wherein m represents 1, 2 or 3; each R independently represents a hydrogen or halogen atom; A represents C(O)NH or NHC(O); Ar represents a group X represents a bond, an oxygen atom or a group CO, CH2, OCH2, NR5 , CH2NR5 , CONR5 or S(O)n; n is 0, 1 or 2; one of R2 and R3 represents a halogen, nitro, amino or a C1-C6 alkyl, and the other of R2 and R3 represents a hydrogen atom; either R4 represents a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and optionally an oxygen atom, the heterocyclic ring system being optionally substituted by one or more substituents independently selected from fluorine atoms, hydroxyl, carboxyl, cyano, C1-C6 alkyl, C1-C6 hydroxyalkyl, -NR6R7, -(CH2)rNR6R7 and -CONR6R7, or R represents a 3- to 8-membered saturated carbocyclic ring system substituted by one or more substituents independently selected from -NR6 R7 , -(CH2)rNR6 R7 and -CONR R , the ring system being optionally further substituted by one or more substituents independently selected from fluorine atoms, hydroxyl and C1-C6 alkyl; r is 1,2, 3,4, 5 or 6; R5 represents a hydrogen atom or a C1-C6 alkyl or C3-C8 cycloalkyl group; R6 and R7 each independently represent a hydrogen atom or a C1-C6 alkyl, C2-C6 hydroxyalkyl or C3-C8 cycloalkyl group, or R6 and R7 together with the nitrogen atom to which they are attached form a 3- to 8-membered saturated heterocyclic ring; with the provisos that, (a) when A represents C(O)NH and R4 represents an unsubstituted 3- to 8-membered saturated aliphatic heterocyclic ring system containing one nitrogen atom, then X is other than a bond, and (b) when A represents C(0)NH and X represents a group CH2 or OCH2 then R4 does not represent an unsubstituted imidazolyl, unsubstituted morpholinyl, unsubstituted piperidinyl or unsubstituted pyrrolidinyl group, and (c) when A represents NHC(O) and R4 represents an unsubstituted 3- to 8-membered saturated aliphatic heterocyclic ring system containing one nitrogen atom, then X is other than a bond, and (d) when A represents NHC(O) and X represents OCH2 then R4 does not represent an unsubstituted 1-piperidinyl or unsubstituted 1-pyrrolidinyl group; or a pharmaceutically acceptable salt or solvate thereof.

Full Text	FORM 2 THE PATENTS ACT 1970 [39 OF 1970] & THE PATENTS RULES, 2003 COMPLETE SPECIFICATION [See Section 10; rule 13] "AN ADAMANTANE COMPOUND" ASTRAZENECA AB, a Swedish company of S-151 85 Sodertalje, Sweden The following specification particularly describes the invention and the manner in which it is to be performed: ADAMANTANE DERIVATIVES The present invention relates to adamantane derivatives, a process for their preparation, pharmaceutical compositions containing them, a process for preparing the pharmaceutical compositions, and their use in therapy. Adamantane derivatives are known in the art, e.g. from WO 95/04720 for use as astrin and cholecystokinin receptor ligands, from Chem. Abs. (1977), Volume 86, No. 13 36: 89560d) for use as analgesics, and from US-A-3 464 998 as antibiotics. The P2X7 receptor (previously known as P2Z receptor), which is a ligand-gated ion channel, is present on a variety of cell types, largely those known to be involved in the uflammatory/immune process, specifically, macrophages, mast cells and lymphocytes A and B). Activation of the P2X7 receptor by extracellular nucleotides, in particular denosine triphosphate, leads to the release of interleukin-113 (IL-1β) and giant cell formation (macrophages/microglial cells), degranulation (mast cells) and proliferation (T cells), apoptosis and L-selectin shedding (lymphocytes). P2X7 receptors are also located a antigen-presenting cells (APC), keratinocytes, salivary acinar cells (parotid cells), spatocytes and mesangial cells. It would be desirable to make compounds effective as P2X7 receptor antagonists for be in the treatment of inflammatory, immune or cardiovascular diseases, in the aetiologies which the P2X7 receptor may play a role. In accordance with the present invention, there is therefore provided a compound of general formula wherein m represents I, 2 or 3, preferably 1 or 2; each R independently represents a hydrogen or halogen (e.g. fluorine, chlorine, bromine or iodine) atom, preferably a hydrogen atom; A represents C(0)NH or, preferably, NHC(O); AT represents a group X represents a bond, an oxygen atom or a group CO, (CH2)1-6. CH=, (CH2)1-6O, O(CH2)1-6 O(CH2)2-6O, O(CH2)2-3O(CH2)1-3, CR'(OH), (CH2)1-3O(CH2)1-3, (CH2)1-3O(CH2)2-3O, NR5. (CH2)1-6NR5, NR5(CH2)1-6, (CH2)1-3NR5(CH2)1-3. O(CH2)2-6NR5, O(CH2)2-3NR5(CH2)1-3, (CH2)1-3NR5(CH2)2-3O, NR5(CH2)2-6O, NR5(CH2)2-3O(CH2)1-3. CONR5, NR5CO, s(O)n, s(O)nCH2, CH2s(O)n, SO2NR5 or NR5SO2; n is 0,1 or 2; R'represents a hydrogen atom or a C1-C5 alkyl, preferably methyl, group; one of R2 and R3 represents a halogen, cyano, nitro, amino, hydroxyl, or a group selected from (i) C1-C6 alkyl optionally substituted by at least one C3-C6 cycloalkyl, (ii) C3-C8 cycloalkyl, (iii) C1-C6 alkyloxy optionally substituted by at least one C3-C6 cycloalkyl, and (iv) C3-C8 cycloalkyloxy, each of these groups being optionally substituted by one or more fluorine atoms, and the other of R2 and R3 represents a hydrogen or halogen atom; either R4 represents a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and optionally an oxygen atom, the heterocyclic ring system being optionally substituted by one or more substituents independently selected from fluorine atoms, hydroxyl, carboxyl, cyano, C1-C6 alkyl. C1-C6 hydroxyalkyl, -NR6R7, -(CH2)rNR6R7 and -CONR6R7, or R4 represents a 3- to 8-membered saturated carbocyclic ring system substituted by one or more substituents independently selected from -NR6 R7 , -(CH2)rNR6 R7 and -CONR6 R 7 , the ring system being optionally further substituted by one or more substituents independently selected from fluorine atoms, hydroxyl and C1-C6 alkyl; r is 1, 2, 3,4, 5 or 6; R5 represents a hydrogen atom or a C1-C6 alkyl or C3-C8 cycloalkyl group; R6 and R7 each independently represent a hydrogen atom or a C1-C6 alkyl, C2-C5 hydroxyalkyl or C3-C8 cycloalkyl group, or R and R together with the nitrogen atom to which they are attached form a 3- to 8-membered saturated heterocyclic ring; with the provisos that, (a) when A represents C(O)NH and R4 represents an unsubstituted 3- to 8-membered saturated aliphatic heterocyclic ring system containing one nitrogen atom, men X is other than a bond, and (b) when A represents C(O)NH and X represents a group (CH2)1-6 or O(CH2)1-6, then R4 does not represent an unsubstituted imidazolyl, unsubstituted morpholinyl, unsubstituted piperidinyl or unsubstituted pyrrolidinyl group, and (c) when A represents NHC(O) and R4 represents an unsubstituted 3- to 8-membered saturated aliphatic heterocyclic ring system containing one nitrogen atom, then X is other than a bond, and (d) when A represents NHC(O) and X represents O(CH2)1-6, NH(CH2)1-6 or SCH2, then R4 does not represent an unsubstituted 1-piperidinyl or unsubstituted 1-pyrrolidinyl group, and (e) when A represents NHC(O) and X represents O(CH2)2-3NH(CH2)2, then R4 does not represent an imidazolyl group; or a pharmaceutically acceptable salt or solvate thereof. In the context of the present specification, unless otherwise indicated, an alkyl substituent or alkyl moiety in a substituent group may be linear or branched. Examples of alkyl groups/moieties containing up to 6 carbon atoms include methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl and hexyl. When one of R2 and R3 represents a C1-C6 alkyl/C1-C6 alkyloxy optionally substituted by at least one C3-C6 cycloalkyl, it should be understood that one or both of the alkyl and cycloalkyl moieties may be optionally substituted by fluorine atoms. In relation to R4 , a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and optionally an oxygen atom may be a monocyclic or bicyclic ring system. Further in relation to R4 , a 3- to 8-membered saturated carbocyclic ring system may be a monocyclic or bicyclic ring system. When R6 or R7 represents a C2-C6 hydroxyalkyl in the substituent NR6R7, -(CH2)rNR6R7 or -CONR6R7, it will be appreciated that the hydroxyl group will not be bonded to the same carbon atom as the nitrogen atom. When R and R together with the nitrogen atom to which they are attached form a 3- to 8-membered saturated heterocyclic ring, the ring obtained is moncyclic. Preferably X represents a bond, an oxygen atom or a group CO, (CH2)1-6, CH=, O(CH2)1-6, O(CH2)2-6O, O(CH2)2-3O(CH2)1-3. CR'(OH), NR5, (CH2)1-6NR5, CONR5, S(O)n or S(O)nCH2- One of R2 and R3 represents a halogen (e.g. fluorine, chlorine, bromine or iodine), cyano, nitro, amino, hydroxyl, or a group selected from (i) C1-C6 alkyl, preferably C1-C4 alkyl, optionally substituted by at least one (e.g. 1, 2 or 3) C3-C6 cycloalkyl (i.e. cyclopropyl, cydobutyl, cyclopentyl or cyclohexyl), (ii) C3-C8 cycloalkyl (e.g. cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl), (iii) C1-C6 alkyloxy, preferably C1-C4 alkyloxy, optionally substituted by at least one (e.g. 1, 2 or 3) C3-C6 cycloalkyl (i.e. cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl), and (iv) C3-C8 cycloalkyloxy (e.g. cyclopropyloxy, cyclobutyloxy, cyclopentyloxy or cyclohexyloxy), each of these groups being optionally substituted by one or more (e.g. 1, 2, 3 or 4) fluorine atoms, and die other of R2 and R3 represents a hydrogen or halogen (e.g. fluorine, chlorine, bromine or iodine) atom. Preferably, one of R2 and R3 represents a halogen (especially chlorine or bromine) atom or a nitro, amino or C1-C6 alkyl (especially methyl or ethyl) group and the other of R2 and R3 represents a hydrogen atom. R4 may represent a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and optionally an oxygen atom, the heterocyclic ring system being optionally substituted by one or more (e.g. 1, 2,3 or 4) substituents independently selected from fluorine atoms, hydroxyl, carboxyl, cyano, C1-C6 alkyl, preferably C1-C4 alkyl, C1 -C6 hydroxyalkyl, preferably C1-C4 hydroxyalkyl, -NR6R7, -(CH2)rNR6R7 and -CONR6R7. The 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system in the group R4 may be a monocyclic ring system such as pyrrolidinyl (e.g. 1-pyrrolidinyl, 2- pyrrolidinyl or 3-pyrrolidinyl), piperidinyi (e.g. 1-piperidinyl, 2-piperidinyI, 3-piperidinyl or 4-piperidinyl), 4-piperiden-3-yl, piperazinyl (e.g. 1-piperazinyl), homopiperazinyl, Alternatively, R4 may represent a 3- to 8-membered saturated carbocyclic ring system substituted by one or more (e.g. 1, 2 or 3) substituents independently selected from NR6 R7 , -(CH2)rNR6 R7 and -CONR6R7, the ring system being optionally further substituted by one or more (e.g. 1, 2, 3 or 4) substituents independently selected from fluorine atoms, hydroxyl and C1-C6 alkyl, preferably C1-C4 alkyl. The 3- to 8-membered saturated carbocyclic ring in the group R is preferably a monocyclic ring system such as a cyclopentyl or cyclohexyl ring. When X represents a bond or a group CO, (CH2)1-6, O(CH2)2-6. O(CH2)2-3O(CH2)2-3, (CH2)1-3O(CH2)2-3. NR5(CH2)2-6, (CH2)1-3NR5(CH2)2-3, O(CH2)2-3NR5(CH2)2-3, NR5(CH2)2-3O(CH2)2-3, NR5CO, SO2 or NR5SO2, R4 preferably represents a group: When X represents an oxygen or sulphur atom or a group CH=, (CH2)1-6O, OCH2, O(CH2)2-6O, O(CH2)2-3OCH2, CROH, (CH2)1-3OCH2, (CH2)1-3O(CH2)2-3O, NR5, (CH2)1-6NR5, O(CH2)2-6NR5, NR5CH2, (CH2)1-3NR5CH2, O(CH2)2-3NR5CH2. (CH2)1-3NR5(CH2)2-3O, NR5(CH2)2-6O, NR5(CH2)2-3OCH2, CONR5, SO, S(O)nCH2, CH2S(O)n or SO2NR5 , R4 preferably represents a group: R represents a hydrogen atom, or a C1-C6, preferably C1-C4, alkyl (e.g. methyl, ethyl, propyl, butyl, pentyl or hexyl) or C3-C8, preferably C3-C6, cycloalkyl (e.g. cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl) group. R6 and R7 each independently represent a hydrogen atom, or a C1-C6, preferably C1-C4, alkyl (e.g. methyl, ethyl, propyl, butyl, pentyl or hexyl), C2-C6 hydroxyalkyl or C3-C8, preferably C3-C6, cycloalkyl (e.g. cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl) group, or R and R together with the nitrogen atom to which they are attached form a 3- to 8-membered, preferably 3- to 6-membered, saturated heterocyclic ring such as a pyrrolidinyl or piperidinyl ring. Preferred compounds of the invention include: 2-Nitro-3-piperazin-1 -yl-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, 2-Amino-3-piperazin-l-yl -N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, dihydrochloride salt, 2-Chloro-3-piperazin-l-yl -N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, 2-Chloro-5-piperazin-1 -yl -N-(tricyclo[3.3.1.1 3.7]dec-l-ylmethyl)-benzamide, 2-Chloro-5-(hexahydro-1H-1,4-diazepin-1 -yl)-N-(tricyclo[3.3.1.13.7]dec-1 -y imethyl)- benzamide, hydrochloride salt, 5-(4-Arnino-l-piperidinyl)-2-chloro-N-(tricyclo(3.3.1.13.7]dec-l-ylmethyl)- benzamidc, hydrochloride salt, (+/-)-5-(3-Amino-1-pyrrolidinyl)-2-chloro-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)- benzamide, hydrochloride salt, 2-Chloro-5-piperazin-l-ylmethyl-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-[(hexahydro-1H-1,4-diazepin-1 -yl)methyl] -N-(tricyclo[3.3.1.13.7]dec-1 - ylmethyl)-benzamide, hydrochloride salt, 5-[(4-Amino-l-piperidinyl)methyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, hydrochloride salt, 5-[(3-Amino-l-pyrTolidinyl)methyI]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, hydrochloride salt, 2-Chloro-5-(4-piperidinyloxy)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt, (R)-2-Chloro-5-(2-pyrrolidinylmethoxy)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt, (S)-2-Chloro-5-{2-pyrrolidinylmethoxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, hydrochloride salt, 2-Chloro-5-(3-piperidinylmethoxy)-N-(tricyclo[3.3.1.13.7]dec-1-ylmethyl)- benzamide, hydrochloride salt, cis-5-[(4-Aminocyclohexyl)oxy]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)- benzamide, hydrochloride salt, 2-Methyl-5-( 1 -piperazinylmethyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-( 1-piperazinylmethyl)-N-(2-tricyclo[3.3.1.13.7]dec-1-ylethyl)-benzamide, hydrochloride salt, (+/-)-2-Chloro-5-(3-pyrrolidinyloxy)-N-(tricyclo[3.3.1.13.7]dec- l-yimethyl}-benzamide, hydrochloride salt, (+/-)-2-Chloro-5-(3-piperidinyloxyhN-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt, trans-5-[(4-Aminocyclohexyl)oxy]-2-chloro-N-(tricyclo[3.3.1.13.7]dec- 1-yimethy!)-benzamide, cis-(+/-)-5-[(3-Aminocyclopentyl)oxy]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamidc, (S,S)-2-Chloro-5-(2,5-diazabicyclo[2.2.1 ]hept-2-yl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylrnethyl)-benzamide, hydrochloride salt, 2-Chloro-5-(2-methyl-1 -piperazinyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt, (4y-)-2-Chloro-5-(3-pyrrolidinylamino)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-bcnzamide, hydrochloride salt, (+/-)-5-(3-Amino-1 -pipericiinyl)-2-chloro-N-(tricycIo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, (+/-)-2-Chloro-5-(3-piperidinylamino)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, 2-Chloro-5-[hexahydropymjlo[3,4-c]pyrrol-2(lH)-yl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, N-[2-methyI-5-(4-piperidinyloxy)phenyl]-tricyclo[3.3.1.13.7]decane-1 -acetamide, hydrochloride salt, NT-[2-chloro-5-(4-piperidinyloxy)phenyl]-tricyclo[3.3.1.13.7]decane-l-acetamide, hydrochloride salt, 2-Chloro-5-[(4-piperidinyl^mino)methyl]-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)- benzamide, dihydrochloride salt, 5-[[[4-(Aminomethyl)cyclohexyl]amino]rnethyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec- l-ylmethyl)-benzamide, dihydrochloride salt, 5-[[(4-Aminocyclohexyl)amino]methyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l- ylmediyl)-benzamide, dihydrochloride salt, 5-[(l-Azabicyclo[2.2.2]oct-3-ylamino)methyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-yimethyl)-benzamide, N-(4-(3-Aminopyrrolidin-1 -yl)-2-methylphenyl]-2-(tricyclo[3.3.1.1 3.7]dec-1 - yl)acetamide, dihydrochloride salt, N-(2-Methyl-4-piperazin-l-ylphenyl)-2-(tricyclo[3.3.1.13.7]dec-l-yl)acetamide, dihydrochloride salt, cis-4-(3-Amino-cyclopentyloxy)-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)- benzamide, hydrochloride salt, 2-Chloro-4-(4-piperidinyloxy)-N-(tricyclo[3.3.1.13,7]dec-l-ylraethyl)-benzamide, hydrochloride salt, (+/-)-2-Chloro-4-(pyrrolidin-3-yloxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, 2-Chloro-4-(piperidin-3-yloxy)- N-(tricyclo[3.3.1.13.7] dec-1-yimethyO-benzamide, hydrochloride salt, 2-Chloro-4-(4-piperazin-1 -yI)-N-(tricyclo[3.3.1.13.7]dec-1 -yimethyO-benzamide, hydrochloride salt, 2-Chloro-4-(3-pyrrolidinyIamino)-N-(tricyclo(3.3.1.13.7]dec-1-yimethyO-benzamide, hydrochloride salt, 2-Chloro-4-(hexahydro-lH-l,4-diazepin-l-yl)-N-(tricyclo[3.3.1.13.7]dec-l- ylmethyl)-benzamide, hydrochloride salt, (±)-5-[(3-Amino-l-piperidinyl)methyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l- ylmethyO-benzamide, hydrochloride salt, 2-Chloro-5-(2,5-diazabicyclo[2.2.1 ]hept-2-ylmethyl)-N-(tricyclo(3.3.1.13.7]dec-1 - yimethyl)-benzamide, hydrochloride salt, 2-Chloro-5-{9-oxa-3,7-diazabicyclo[3.3.1]non-3-ylmethyl)-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-(3,7-diazabicydo[3.3.1 }non-3-yimethyO-N-(tricyclo[3.3.1.13.7]dec-l -yimethyO-benzamide, hydrochloride salt. trans-2-Chloro-5-[[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]inethyl]-N- tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt, cis-2-Chloro-5-[(hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)methyl]-N- tricyclo[3.3.1.13.7]dec-l -yimethyl)-benzamide, hydrochloride salt, 2-Chloro-5-(4-piperidinyiidenernethyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)- lenzamide, hydrochloride salt, 2-Chloro-5-(4-piperidinylmethyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, ydrochloride salt, 2-Chloro-5-(4-hydroxy-piperidin-4-yl)-N-(tricyclo [3.3.1.13.7]dec-1 -ylmethyl)- benzamide, hydrochloride salt, 2-Chloro-5-(l,2,3,6-tetrahydro-pyridin-4-yl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyi)-benzamide, hydrochloride salt, 2-Ethyl-5-piperazin-1 -ylmethyl -N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-(piperidin-4-ylsulfanyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, hydrochloride salt, 2-Chloro-5-(piperidin-4-ylsulfmyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)- benzamide, 2-Chloro-5-(piperidin-4-ylsulfonyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, hydrochloride salt, 2-Chloro-5-(piperidin-4-ylmethylsulfanyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, hydrochloride salt, 2-Chloro-5-(piperidin-4-ylmethanesulfonyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)- benzamide, hydrochloride salt, 2-Chloro-5-(piperazine-1 -carbonyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)- benzamide, hydrochloride salt, 2-Chloro-5-([ 1,4]diazepane-1 -carbonyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)- snzamide, hydrochloride salt, 4-Chloro-N^piperidin-4-yl-)-N2-(tricyclo[3.3. 1.13.7]dec-1 -ylmethyl)- ophthalamide, hydrochloride salt, 2-Chloro-5-{hydroxy-4-piperidinylmethyl)-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethy])-benzamide, hydrochloride salt, (±)-2-Chloro-5-(hydroxy-3-piperidinylmethyl)-N-(tricyc]o[3.3.1.13.7]dec-1 -methyl)-benzamide, hydrochloride salt, 2-Bromo-5-piperazin-1 -ylmethyl-N-(tricyclof3.3.3.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-[2-( 1 -piperaziny l)ethyl ]-N-(tricyclo [3.3.1.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-[2-(2,5-diazabicycIo[2.2.1 ]hept-2-yl)ethyl]-N-(tricyclo[3.3.1. l3.7]dec-1 -lmethyl)-benzamide, hydrochloride salt, 5-[2-(4-Amino-1 -piperidinyl)ethyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-enzamide, hydrochloride salt, 2-Chloro-5-[2-(3-piperidinylamino)ethyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-enzamide, dihydrochloride salt, 5-[2-(3-Amino-1 -piperidinyl)ethyI]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-enzamide, hydrochloride salt, 2-Chloro-5-[2-{3-pyrrolidinylamino)ethyl]-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-enzamide, dihydrochloride salt, 5-[2-[(3R)-3-Aminopyrrolidinyl]ethyl]-2-chloro-N-(tricyclo[3.3.1.1I3.7]dec-1-[methyl)-benzamide, hydrochloride salt, 2-Chloro-5-[2-[2-(hydroxymethyl)-1 -piperazinyl]ethyl]-N-(tricyclo[3.3.1.13.7]dec-1 -[methyl)-benzamide, hydrochloride salt, 2-Chloro-5-(hexahydro-1H-1,4-diazepin-1 -yl)-N-(2-tricyclo[3.3.1. l3.7]dec-1 -ylethyl)-snzamide, hydrochloride salt, (+/-)-5-(3-Amino- l-pyrrolidinyl)-2-chloro-N-(2-tricyclo[3.3.1.13.7]dec-1 -ylethyl)-benzamide, hydrochloride salt, 2-Chloro-5-(4-piperidinylcarbonyI)-N-(tricyclo[3.3.1.13.7]dec-1-ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-[1 -hydroxy-1 -(4-piperidinyl)ethyl]-N-(tricycio[3.3.1.13.7]dec-1 -ylmethyl)-snzamide, hydrochloride salt, 2-Chloro-5-[2-( 1 -piperazinyl)ethoxy)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-[2-(4-piperidinyl)ethoxy)-N-(tricyclo[3.3.1. l3.7]dec-l-yimethyl)-benzamide, hydrochloride salt, 2-Chloro-5-[2-(4-piperidinyloxy)ethoxy)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-[2-[2-(l-piperazinyl)ethoxy]ethoxy]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyi)-benzamide, hydrochloride salt, 2-Chloro-5-[(5,6-dihydro-1 (4H)-pyrimidmyl)methy\]-N-(tricyclo[33.l. l3.7]dec-1 -ylmethyl)-benzamide, 2-Chloro-5-[[4-[(2-hydroxyethyl)amino]-l-pipcridinyl]methyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt, 2-Chioro-5-[[4-hydroxy-4-[[( 1 -methylethyl)amino]methyI]-1 -piperidinyljmethyl]-N-(tricyclo[3.3.1. l3.7]dec-1-ylmethyl)-benzamide, 2-Chloro-5-[( 1,2,3,6-tetrahydro-3-pyridinyl)methyl]-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)- benzamide, hydrochloride salt, 2-Chloro-5-(3-piperidinylmethyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)- benzamide, acetate salt, 2-bromo-5-[[4-[(2-hydroxyethyl)amino]-l-piperidinyl]methyl]-A/-(tricyclo[3.3.1.13.7] dec-1-ylmethyl-benzamide, and 2-Chloro-5-[(E)-3-piperidinylidenemethyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide. The present invention further provides a process for the preparation of a compound of formula (I) as defined above which comprises: (i) when X represents a CH2 group, R4 represents a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and optionally an oxygen atom, the heterocyclic ring system being optionally substituted by one or more substituents independently selected from fluorine atoms, hydroxyl, carboxyl, wherein one of R10 and R11 represents a hydrogen atom and the other of R10 and R11 represents a group -CH2L1 in which L represents a leaving group (e.g. a halogen atom) and m, A, R1 , R2 and R3 are as defined in formula (I), with a compound of general formula R4'-H (III) in the presence of a base (e.g. diisopropylethylamine), wherein R4' represents a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and optionally an oxygen atom, the heterocyclic ring system being optionally substituted by one or more substituents independently selected from fluorine atoms, hydroxyl, carboxyl, cyano, C1-C6 alkyl, C1-C6 hydroxyalkyl, -NR6 R7 , -(CH2)rNR R and -CONR R and wherein R and R are as defined in formula (I); or (ii) when X represents an oxygen atom or a group 0(CH2h-6, 0(CH2h-60. 0(CH2)2-30(CH2)i.3, 0(CH2)2-6NR5 or 0(CH2)2-3NR5(CH2)i.3, reacting a compound of general formula 12 13 12 13 wherein one of R and R represents a hydrogen atom and the other of R and R 12 3 represents a hydroxyl group and m. A, R , R and R are as defined in formula (I), with a compound of general formula wherein Y represents a bond or a group (CH2)i-6, 0(02)2-6. (012)1-30(02)2-3, NR5(02)2-6 or (OJ2)i-3NR5(CH2)2-3 and R4 is as defined in formula (I), in the presence of 1,1 -(azodicarbonyl)dipiperidine and tributylphosphine (under conditions of the Mitsunohu reaction: Tetrahedron Lett. (1993), 34, 1639); or (iii) when X represents a bond, an oxygen atom or a group 0(02) 1-6. 0(02)2-60, 0(CH2)2.30(O2)i.3, NR5, NR5(CH2),.6, NR5(CH2)2-60 or NR (02)2-30(02)1.3 and A is NHC(O), reacting a compound of general formula 14 15 4 14 15 wherein one of R and R represents a group -X'-R and the other of R and R represents a hydrogen atom, X'represents a bond, an oxygen atom or a group 0(O2)i-6, 0(O2)2-60, 0(O2)2-30(O2)i-3, NR5. NR5(02)i-6, NR5(O2)2-60 or 5 2 NR (02)2-30(02)1.3, L represents a leaving group (e.g. a hydroxy! or chloride leaving "> 3 4 5 group) and R~, R , R and R are as defined in formula (I), with a compound of general formula wherein m and R are as defined in formula (I), optionally in the presence of a coupling agent (e.g. 1,1 '-carbonyldiimidazole); or (iv) when X represents a bond, an oxygen atom or a group 0(CH2)i-6, 0(CH2)2.60? 0(CH2)2-30(CH2)i-3, NR5, NR5(CH2),.6l NR5(CH2)2-60 or 5 NR (CH2)2-30(CH2)]-3 and A is C(0)NH, reacting a compound of general formula 2 3 14 15 wherein R and R are as defined in formula (I) and R and R are as defined in formula (VI) in (iii) above, with a compound of general formula wherein m and R are.as defined in formula (I), in the presence of a base (e.g. diuopropyiamine); or (v) when X represents a bond or a group NR , NR (CH2)i.6, NR5(CH2)2-60 or NR (CH2)2-30(CH2) 1.3, reacting a compound of general formula wherein one of R and R represents a leaving group, L .such as a halogen atom and the other of R and R represents a hydrogen atom and m, A, R , R and R are as defined in formula (I), with a compound of general formula R4-Z (XI) wherein Z represents a hydrogen atom or a group NHR , (CH2)i-6NHR , 0(CH2)2-6NHR5 or a group (CH2)i-30(CH2)2-3NHR5 and R4 and R5 are as defined in formula (I), optionally in the presence of a palladium catalyst (e.g. palladium acetate), a phosphine ligand (e.g. BINAP) and a base (e.g. cesium carbonate); or (vi) when X represents a group CHiO, reacting a compound of formula (H) as defined in (i) above with a compound of formula (V) as defined in (ii) above wherein Y represents a bond, in the presence of a base (e.g. sodium hydride) or in the presence of a metal salt (e.g. silver trifluoromethanesulfonate); or (vii) when X represents a group CHbNR , reacting a compound of formula (II) as defined in (i) above with a compound of formula (XI) as defined in (v) above wherein Z represents a group NHR ; or (viii) when X represents a group CH20(CH2) 1.3 or CH20(CH2)2-30, reacting a compound of formula (H) as defined in (i) above with a compound of formula (V) as defined m (ii) above wherein Y represents a group (CH2)i_3 or 0(CH2)2-3> m the presence of a base (e.g. sodium hydride) or in the presence of a metal salt (e.g. silver trifluoromethanesulfonate); or (ix) when X represents a group CH3NR CH2 or CH2NR5 (02)2.3 O reacting a compound of formula (II) as defined in (i) above with a compound of formula (XI) as 5 5 defined m (v) above wherein Z represents a group CH2NHR or 0(CH2)2-3NHR ; or 4 (x) when X represents a group CHT and R represents an unsubstituted 4- to 6-membered saturated aliphatic heterocyclic ring system containing one nitrogen atom, reacting a compound of formula (II) as defined in (i) above, with a compound of general formula wherein s and t independently represent 1 or 2; or 18 19 4 18 19 wherein one of R and R represents a group -X"-R and the other of R and R represents a hydrogen atom, X" represents a group CO, CONR , NR CO, SO2, 5 5 4 NR SO2 or SO2NR , L represents a leaving group (e.g. a hydroxyl or chloride leaving 2 3 4 5 group) and R , R , R and R are as defined in formula (I), with a compound of formula (VII) as defined in (iii) above, optionally in the presence of a coupling agent (e.g. 1,1 '-carbonyIdiimidazole); or (xii) when X represents a group CO, CONR5, NR5CO, S02, NR5S02 or 5 SO2NR and A is C(0)NH, reacting a compound of general formula I 2 3 18 19 wherein R and R are as defined in formula (I) and R and R are as defined in formula (XHI) in (xi) above, with a compound of formula (DC) as defined in (iv) above, in the presence of a base (e.g. diisopropylamine); or (xiii) when X represents a sulfur atom, reacting a compound of formula (X) as defined in (v) above, with an organolithium reagent such as n-butyllithium (e.g. at -70 °C) and then witii a compound of general formula 4 wherein Tol represents a tolyl group (4-memylphenyl) and R is as defined in formula (I); or (xiv) when X represents a CHOH or CH2 group, reacting a compound of formula (X) as defined in (v) above, with an organolithium reagent (e.g. methyllithium/t-butyllithium or n-butyllithium at -70 °C) and then with a compound of general formula wherein R is as defined in formula (I), optionally followed by a reduction reaction, e.g. with methyloxalylchloride and triethylamine followed by tributyltin hydride in the presence of azobiswobutyronitrile; or (xv) when X represents a bond, reacting a compound of formula (X) as defined in (v) above, with an organolithium reagent such as n-butyllithium (e.g. at -70 °C) and then with a compound of general formula wherein R is as defined in formula (I), optionally followed by a reduction reaction, e.g. with methyloxalylchloride and triethylamine followed by tributyltin hydride in the presence of azobiswobutyronitrile; (xvi) when X represents a group SO, oxidising a corresponding compound of formula (I) in which X represents a sulphur atom (e.g. using, as oxidising agent, 3-chloroperoxybenzoic acid or potassium peroxymonosulphate (commercially sold under the trade mark "OXONE")); or (xvii) when X represents a group SCHb, reacting a compound of formula (X) as defined in (v) above, witJi an organolithium reagent (e.g. memyllithium and/or t-butyllithium at -70 °C) and then with a compound of general formula 4 wherein R is as defined in formula (I); or - (xviii) when X represents a group SOCHi or SO2CH2, oxidising a corresponding compound of formula (I) in which X represents a group SCH2 (e.g. using, as oxidising agent, 3-chloroperoxybenzoic acid or potassium peroxymonosulphate (commercially sold under the trade mark "OXONE")); or (xix) when X represents a group CH=, reacting a compound of formula (II) as defined in (i) above with trimethyl phophite and then with a compound of formula (XVII) as defined in (xv) above in the presence of a base (e.g. lithium diisopropylamide); or (xx) when X represents a group (CH2)i-6. reacting a compound of general formula 20 21 herein one of R and R represents a group CHO or a group (CH^uCHO and the 20 21 12 3 her of R and R represents a hydrogen atom, and m, A, R , R and R are as defined 4 4 formula (I), with a compound of general formula (XX), R -H, wherein R is as defined fonnula (I), in the presence of a reducing agent (e.g. sodium triacetoxyborohydride, in a itable solvent such as dichloroethane); or (xxi) when X represents a group (CH2)i-6NR5, (CH2)i-3NR3(CH2)i.3 or !H2)i-3NR (CH^oO. reacting a compound of formula (XIX) as defined in (xx) above, 4 ith a compound of general formula (XXI), R Z', wherein Z' represents a group HR5, (CH2)i-3NHR5, 0(CH2)2-3NHR5 and R4 and R5 are as defined in formula (I), in e presence of a reducing agent (e.g. sodium triacetoxyborohydride, in a suitable solvent ch as dichloroethane); or (xxii) when X represents a group (CH2)i.30(CH2)i-3 or (CH^ioOtCH^O, acting a compound of formula (XK) as defined in (xx) above in which one of R20 and :1 represents a group CHO or a group (CH2)i-2CHO and the other of R20 and R21 presents a hydrogen atom, with a reducing agent (such as sodium borohydride), followed reaction with a compound of general formula (XXII), R -E, wherein E represents a aup (CH2)i-3L or 0(CH2)2-3L , L is a leaving group (such as a halogen atom or a 4 Iphonate ester group, e.g. p-toluenesulphonate) and R is as defined in fonnula (I), in the ssence of a base (such as sodium hydride); or (xxiii) when X represents a group (CHi)i-6, reacting a compound of formula (II) as defined in (i) above with trimethylphosphite and then with a compound of formula (XVI) as defined in (xiv) above, a compound of formula (XVII) as defined in (xv) above or a 4 4 compound of general formula (XVIA), R (CHJJMCHO in which R is as defined in formula (I), in the presence of a base (e.g. lithium diisopropylamide), followed by a reduction reaction (for example, with hydrogen and a platinum oxide catalyst); or (xxiv) when X represents a group (CH2)2-60, reacting a compound of general formula wherein one of R22 and R23 represents a group (CH2)2-6L6 and the other of R20 and R21 represents a hydrogen atom, L6 represents a leaving group (e.g. a halogen atom or a sulphonate ester group such as p-toluenesulphonate) and m. A, R\ R2 and R3 are as defined in formula (I), witii a compound of formula (V) as defined in (ii) above in which Y represents a bond; or (xxv) when X represents a group CR'(OH) in which R' is a CpCe alkyl group, oxidising a corresponding compound of formula (I) in which X represents CH(OH) (e.g. using the oxidant dimethylsulphoxide/oxalyl chloride), followed by reaction with a Ci-C* alkyllithium reagent; or (xxvi) when X represents a group CH2S, reacting a compound of formula (II) as defined in (i) above with a compound of general formula (XXIV), R4-SH, wherein R4 is as defined in formula (I), in the presence of a base (e.g. sodium hydride); or (xxvii) when X represents a group CH2SO or CH2S02, oxidising a corresponding compound of formula (I) in which X represents a group CH2S (e.g. using, as oxidising agent, 3-chloroperoxybenzoic acid or potassium peroxymonosulphate (commercially sold under the trade mark "OXONE")); or (xxviii) when X represents a group CH2 and R4 represents a 3-piperidinyl or 2-piperazinyI group, reacting a compound of formula (II) as defined in (i) above with a reagent formed by combining pyridine or pyrazine with an aluminium hydride reagent (e.g. lithium aluminium hydride), followed by a reduction reaction (e.g. with hydrogen and a platinum catalyst); or (xxix) when X represents a group CH= and R4 represents a 3-piperidinyl group, reacting a compound of general formula wherein one of R24 and R25 represents an aldehyde group -CHO, and the other of R24 and j 25 R represents a hydrogen atom and m, A, R , R and R are as defined in formula (I), with 2,3,4,5-tetrahydropyridine (BuU.Chem.Soc.Jpn. 1983, 56, 3199), followed by a reduction reaction (e.g. with sodium borohydride in a protic solvent such as methanol); or (xxx) when X represents a bond, NR5 or NR5(CH2),. vherein one of R26 and R27 represents a pyridyl, pyrazinyl, NR5-pyridyl, NR5-pyrazinyl, >IR5(CH2) t.6-pyridyl or NR5(CH2)t^-pyrazinyl group and the other of R26 and R27 epresents a hydrogen atom, and m, A, R1, R2 and R3 are as defined in formula (I), with a ource of hydrogen and a hydrogenation catalyst (such as platinum oxide); or » (xxxi) when X represents a group CH20(CH2) 1.3 or CH20(CH2)2.30 and A is ■IHQO), reacting a compound of general formula /herein one of R28 and R29 represents a group -Xw-R and the other of R28 and R29 epresents a hydrogen atom, X™ represents a group CH20(CH2)i-3 or CH20(CH2)2-30, 7 represents a leaving group (e.g. a hydroxyl or chloride leaving group) and R2, R3 and R4 re as defined in formula (I), with a compound of formula (VII) as defined in (iii) above, prionally in the presence of a coupling agent (e.g. l,l'-carbonyldiimidazoIe); or (xxxii) when X represents a group CH20(CH2)i-3 or CH20(CH2)2.30 and A is '(O)NH, reacting a compound of general formula 2 3 28 29 wherein R and R are as defined in formula (I) and R and R are as defined in formula (XXVII) in (xxxi) above, with a compound of formula (JX) as defined in (iv) above, in the presence of a base (e.g. diisopropylamine); and optionally after (i), (ii), (iii), (iv), (v), (vi), (vii), (viii), (ix), (x), (xi), (xii), (xiii), (xiv), (xv), (xvi), (xvii), (xviii), (xix), (xx), (xxi), (xxii), (xxiii), (xxiv), (xxv), (xxvi), (xxvii), (xxviii), (xxix), (xxx), (xxxi) or (xxxii) converting the compound of formula (I) to a further compound of formula (I) and, if desired, forming a pharmaceutically acceptable salt or solvate of the compound of formula (I). The processes of the invention may conveniently be carried out in a solvent, e.g. an organic solvent such as dichloromethane, dichloroethane, tetrahydrofuran, dioxane, xylene or dimethylformamide, at a temperature, e.g. in the range from 0 to 200 °C, preferably in the range from 0 to 150 °C. Compounds of formula (H) in which A is NHC(O) may be prepared by reacting a compound of general formula wherein L represents a leaving group (e.g. a hydroxyl or chloride leaving group) and R , R , R and R are as defined in formula (II), with a compound of formula (VI!) as defined above, optionally in the presence of a coupling agent (e.g. 1,1-carbonyidiimidazole). Compounds of formula (XXX) in which one of R and R represents a hydrogen atom and the other of R andR represents a group-CH2L and L1 represents a bromine atom can be prepared by reacting a compound of general formula wherein one of R and R represents a hydrogen atom and the other of R and R 2 3 represents a methyl group and R and R are as defined in formula (I), with N-bromosuccinimide and catalytic azobisijobutyronitrile or dibenzoylperoxide, optionally followed by chlorination with oxalyl chloride and catalytic dimethylformamide or with thionyl chloride. Compounds of formula (II) in which A is C(0)NH and L represents, for example, a bromine atom may be prepared by reacting a compound of general formula 2 3 30 31 wherein R and R are as defined in formula (I) and R and R are as defined in formula (XXXI) above, with a compound of formula (IX) as defined above, in the presence of a base (e.g. diwopropylethylamine), followed by reaction with N-bromosuccinimide and catalytic azobiswobutyronitrile or dibenzoylperoxide. Compounds of formula (tV)in which A is NHC(O) may be prepared in an analogous manner to compounds of formula (II) in which A is NHC(O), using instead of the intermediate compound of formula (XXX), an intermediate compound of general formula 11 2 wherein L represents a leaving group (e.g. a hydroxyl or chloride leaving group) and R , R3, R12 and R13 are as defined in formula (IV). Compounds of formula (IV) in which A is C(0)NH may be prepared by reacting a compound of general formula wherein R2, R3, R12 and R13 are as defined in formula (IV), with a compound of formula (K) as defined above, optionally in the presence of a base (e.g. ditropropylethylamine). Compounds of formula (Vl) can be prepared by reacting a compound of general formula ■39 33 34 wherein R represents a hydrogen atom or a C j -Q alkyl group, one of R and R represents a leaving group, L12, $uch as a halogen atom (e.g. bromine or iodine) or a 33 34 trifraorometiianesutfonate group ^ & && ^ ■ ^ ^ wpwswfts ^ hT&rcfgti* ttssHi, and R2 and R3 are as defined in formula (VI), with a compound of general formula wherein X' and R are as defined in formula (VI), in the presence of a palladium catalyst (e.g. palladium acetate), a phosphine ligand (e.g. BINAP) and a base (e.g. cesium :arbonate) (1996 J. Am. Chem. Soc, 7215-6; 1997 J. Am. Chem. Soc, 3395), followed by a hydrolysis reaction (e.g. with sodium hydroxide) and optionally a chlorination reaction (e.g. with oxalyl chloride and catalytic dimethyl? ormamide or with thlonyl chloride). Compounds of formula (Vlfl) may conveniently be prepared by reacting a compound Df formula (VI) in which L represents a hydroxy! group with diphenyiphosphoryl azide in Jie presence of a base such as triethylamine. Compounds of formula (X) in which A is NHC(O) may be prepared in an analogous nanner to compounds of formula (H) in which A is NHC(O), using instead of the ntermediate compound of formula (XXX), an intermediate compound of general formula n 2 vherein L represents a leaving group (e.g. a hydroxyl or chloride leaving group) and R , I3, R16 and R17 are as defined in formula (X). Compounds of formula (X) in which A is C(0)NH may be prepared in an analogous nanner to compounds of formula (TV) in which A is C(0)NH, using instead of the ntermediate compound of formula (XXXW), an intermediate compound of general ormula wherein R", R , R and R are as defined in formula (X). Compounds of formula (XII) can be prepared as described in Syn. Lett. (1998) 379-380. 5 Compounds of formula (XIH) in which X" represents a group CO, CONR , SO2 or SO2NR can be prepared by reacting a compound of general formula wherein one of R andR represents a group COL orS02L and the other of R and R represents a hydrogen atom, L represents a leaving group (e.g. a halogen atom),v" 37 2 3- R represents a hydrogen atom or a C\~C$ alky I group, and R and R are as defined in formula (XIII), with a compound of formula (XXXVI) in which X' represents a bond or a group NR , in the presence of a base such as diwoprbpylethylamine and catalytic dimethylaminopyridine, followed by a hydrolysis reaction (e.g. sodium hydroxide) and, optionally, a chlorination reaction (e.g. with oxalyl chloride and catalytic dimethylformamide or with thionyl chloride). Compounds of formula (XM) in which X" represents a group represents a group NR3CO or NR5S02can be prepared by reacting a compound of general formula 38 39 5 38 39 wherein one of R and R represents a group NHR and the other of R and R represents a hydrogen atom, R is as defined for compound (XXXEC), and R2 and R3 are as defined in formula (XIII), with a compound general formula (XLI), R -J, wherein 4 J represents a group COC1 or S02C1 and R is as defined in formula (I), in the presence of a base such as diwopropylethylamine. Compounds of formula (XIV) may conveniently be prepared by reacting a compound of formula (XIII) in which L4 represents a hydroxyl group with diphenylphosphoryl azide in the presence of a base such as triethylamine. Compounds of formula (XIX) in which one of R20 and R21 represents a group (CH2)i.5CHO and the other of R20 and R21 represents a hydrogen atom can be prepared by oxidising a compound of general formula wherein one of R40 and R41 represents a group (CH2)2-60H and the other of R40 and R41 represents a hydrogen atom, and m, A, R1, R2 and R3 are as defined in formula (I), using as the oxidising agent, for example, Dess Martin Periodinane reagent. Compounds of formula (XL.TI) in which one of R40 and R41 represents a group (CH2)20H and the other of R40 and R41 represents a hydrogen atom can be prepared from a compound of general formula (X) as defined above, an organolithium reagent such as methyllithium (at -70 °C) followed by n-butyllithium (at -70 °C), and then treatment with ethylene oxide. Compounds of formula (XIII) in which one of R40 and R41 represents a group (CH^OH and the other of R40 and R41 represents a hydrogen atom can be prepared by reacting a compound of general formula (X) as defined above with a compound of general formula in the presence of a palladium catalyst such as tetrakis(triphenylphosphine)palladium(0), followed by reduction with, for example, hydrogen and a platinum oxide catalyst. Compounds of formula (XIX) in which one of R20 and R21 represents a group CHO and the other of R20 and R21 represents a hydrogen atom (which are equivalent to compounds of formula (XXV)) can be prepared from a compound of general formula (X) as defined above, with an organolithium reagent such as methyllithium (at -70 °C) followed by n-butyllithium (at -70 °C) and then with dimethylformamide. Compounds of formula (XXTII) in which L represents an iodine atom or p-toluenesulphonyloxy group may be prepared by reacting a compound of formula (XLH) as defined above with iodine/triphenylphosphine/imidazole or with a sulphonyl chloride such as p-toiuenesulphonyl chloride, in the presence of a base such as diisopropylethylamine. 26 27 Compounds of formula (XXVI) in which one of R and R represents a pyridyl or 9fi 97 pyrazinyl group and the other of R and R represents a hydrogen atom can be prepared from a compound of formula (X) as defined above by reaction with a pyridyl or pyrazinyl boronic acid in the presence of a palladium catalyst such as tetrakis(triphenylphosphine)palladium(0). 9rt 97 Compounds of formula (XXVT) in which one of R and R represents a NR5-pyridyl, NR -pyrazinyl, NR (CH2) ^-pyridyl or NR (CH2)i-6-pyrazinyl group and 26 27 the other of R and R represents a hydrogen atom can be prepared from a compound of formula (X) as defined above by reaction with a compound NHR pyridyl, NHR'pyraziny], NHR"(CH2)i.6-pyridy' or NHR'fCH^i-a-pyrazinyl, in the presence of a palladium catalyst (e.g. palladium acetate), a phosphine ligand (e.g. BINAP) and a base (e.g. cesium carbonate). Compounds of formulae (HI), (V), (VII), (K), (XI), (XV), (XVI), (XVIA), (XVII), (xvin), (xx), (xxi), (xxn), (xxiv), (xxvn), (xxvni), (XXXD, (xxxn), (xxxm), (XXXIV), (XXXV), (XXXVI), (XXXVH), (XXXVUO, (XXXIX), (XL), (XLI), (XLS) and fxl.TTT) are either commercially available, are well known in the literature or may be prepared easily using known techniques. Compounds of formula (D can be convened into further compounds of formula (I) using standard procedures. For example, compounds of formula (I) in which one of R and R represents a nitro group can be converted to compounds of formula (I) in which one of 2 3 R and R represents an amino group by reduction using iron powder and ammonium chloride in ethanol/water under reflux conditions. The latter compounds can in turn be 2 3 converted into compounds of formula (I) in which one of R and R represents a halogen atom, e.g. chlorine, by diazotization (e.g. with sodium nitrite) and reaction with copper chloride. Compounds of formula (I) in which R or R represents a hydrogen atom can be converted to compounds of formula (I) in which R or R represents a C j -Cg alkyl, C2-C6 hydroxyalkyl, C3-C8 cycloalkyl or a 3- to 8-membered saturated heterocyclic ring by standard chemical procedures. It will be appreciated by those skilled in the art that in the processes of the present invention certain functional groups such as hydroxyl or amino groups in the starting reagents or intermediate compounds may need to be protected by protecting groups. Thus, the preparation of the compounds of formula (I) may involve, at an appropriate stage, the removal of one or more protecting groups. The protection and deprotection of functional groups is described in Protective Groups in Organic Chemistry', edited by J.W.F. McOmie, Plenum Press (1973) and Protective Groups in Organic Synthesis', 2nd edition, T.W. Greene and P.G.M. Wuts, Wiley-Interscience (1991). The compounds of formula (I) above may be converted to a pharmaceutically acceptable salt or solvate thereof, preferably an acid addition salt such as a hydrochloride, hydrobromide, phosphate, acetate, fumarate, maleate, tartrate, citrate, oxalate, methanesuiphonate orp-toluenesulphonate, or an alkali metal salt such as a sodium or potassium salt. Certain compounds of formula (I) are capable of existing in stereoisomeric forms. It will be understood that the invention encompasses all geometric and optical isomers of the compounds of formula (I) and mixtures thereof including racemates. Tautomers and mixtures thereof also form an aspect of the present invention. The compounds of the present invention are advantageous in that they possess pharmacological activity. They are therefore indicated as pharmaceuticals for use in the treatment of rheumatoid arthritis, osteoarthritis, psoriasis, allergic dermatitis, asthma, chronic obstructive pulmonary disease (COPD), hyperresponsiveness of the airway, septic shock, glomerulonephritis, irritable bowel disease, Crohn's disease, ulcerative colitis, atherosclerosis, growth and metastases of malignant cells, myoblastic leukaemia, diabetes, Alzheimer's disease, meningitis, osteoporosis, burn injury, ischaemic heart disease, stroke and varicose veins. Accordingly, the present invention provides a compound of formula (I), or a phannaceutically acceptable salt or solvate mereof, as hereinbefore defined for use in therapy. In anouier aspect, the invention provides the use of a compound of formula (I), or a pharmaceutically acceptable salt or solvate thereof, as hereinbefore defined in the manufacture of a medicament for use in therapy. In the context of the present specification, the term "therapy" also includes "prophylaxis" unless there are specific indications to the contrary. The terras "therapeutic" and "therapeutically" should be construed accordingly. The invention further provides a method of effecting immunosuppression (e.g. in the treatment of rheumatoid arthritis, irritable bowel disease, atherosclerosis or psoriasis) which comprises administering a therapeutically effective amount of a compound of formula (I), or a pharmaceutically acceptable salt or solvate thereof, as hereinbefore defined to a patient. The invention also provides a method of treating an obstructive airways disease (e.g. asthma or COPD) which comprises administering to a paitient a therapeutically effective amount of a compound of formula (I), or a pharmaceutically acceptable salt or solvate thereof, as hereinbefore defined to a patient. For the above-mentioned therapeutic uses the dosage administered will, of course, /ary with the compound employed, the mode of administration, the treatment desired and he disorder indicated. The daily dosage of the compound of formula (I)/sait/soIvate ^active ingredient) may be in the range from 0.001 mg/kg to 30 mg/kg. The compounds of formula (I) and pharmaceutically acceptable salts and solvates hereof may be used on their own but will generally be administered in the form of a iharmaceutical composition in which the formula (I) compound/salt/solvate (active ngredient) is in association with a pharmaceutically acceptable adjuvant, diluent or carrier. Depending on the mode of administration, the pharmaceutical composition will preferably :omprise from 0.05 to 99 %w (per cent by weight), more preferably from 0.10 to 70 %w, >f active ingredient, and, from 1 to 99.95 %w, more preferably from 30 to 99.90 %w, of a )hannaceutically acceptable adjuvant, diluent or carrier, all percentages by weight being >ased on total composition. Thus, the present invention also provides a pharmaceutical composition comprising a compound of formula (I), or a pharmaceuticaily acceptable salt or solvate thereof, as hereinbefore defined in association with a pharmaceuticaily acceptable adjuvant, diluent or carrier. The invention further provides a process for the preparation of a pharmaceutical composition of the invention which comprises mixing a compound of formula (I), or a pharmaceuticaily acceptable salt or solvate thereof, as hereinbefore defined with a pharmaceuticaily acceptable adjuvant, diluent or carrier. The pharmaceutical composition of the invention may be administered topically (e.g. to the lung and/or airways or to the skin) in the form of solutions, suspensions, heptafiuoroalkane aerosols and dry powder formulations; or systemically, e.g. by oral administration in the form of tablets, capsules, syrups, powders or granules, or by parenteral administration in the form of solutions or suspensions, or by subcutaneous administration or by rectal administration in the form of suppositories or transdermally. The present invention will now be further explained by reference to the following illustrative examples. To a suspension of 3-chloro-2-nitrobenzoic acid (2.68 g) in dichloromethane (10 ml) at 0°C was added oxaiyi chloride (3 ml) and dimethylformamide (1 drop). The resulting mixture was stirred at room temperature under a nitrogen atmosphere for 1 hour, then concentrated under reduced pressure to yield a solid. The solid was dissolved in dichloromethane (10 ml) and cooled to 0°C. A solution of 1-adamantanemediylamine (2.19g) and iV.A'-dii.sopropylethylamine (II ml) in dichloromethane (10 ml) was added portion-wise and the resulting solution allowed to stir at room temperature under a nitrogen atmosphere for 2h. The reaction mixture was poured into water and the organic phase separated and washed wim 2N hydrochloric acid, 10% aqueous sodium hydroxide and saturated brine. The organic phase was then dried over sodium sulfate, filtered and concentrated under reduced pressure and the resulting solid re-crystallized from iso-propanol to afford the subtitle compound as a solid (3.52 g). MS (APCI +ve) 349 (M+H)+ 'H NMR (DMSO-d6) 5 8.74 (1H, t); 7.89 (1H, m); 7.75-7.69 (2H, m); 2.91 (2H, d), 1.93 (3H, bs); 1.64 (6H, dd); 1.47 (6H, d) b) 3-(4-{ 1,1-dimethylethyl }oxycarbony!]-piperazin-l -yl>2-nitro-Ar- 3 7 (tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide 3 7 A mixture of 3-chloro-2-mtro-/V-(tricyclo [3.3.1.1 ' ]dec-1 -ylmethyl)-benzamide (2.80 g, Example la) and piperazine-1-carboxylic acid, tert-buty\ ester (7.47 g) in dry dimethyl sulfoxide (10 ml) was heated at 120°C under a nitrogen atmosphere for 24h. The cooled reaction mixture was diluted with water and extracted tiirice with ethyl acetate. The combined extracts were washed with water, dried over sodium sulfate, filtered, and the filtrate concentrated under reduced pressure to give a solid. Purification by chromatography over silica gel, during wim M-c-hexane/ethyi acetate (2:1) gave me subtitle compound as a solid (3.8 g). MS (APCI +ve) 499 (M+H)+ 'H NMR (DMSO-dg) 5 8.55 (1H, t); 7.62-7.59 (2H. m); 7.43 (1H, dd); 3.38 (4H, bt); 2.90-2.84 (6H, m), 1.93 (3H, bs); 1.63 (6H, dd); 1.47 (6H, d); 1.41 (9H, s) 3 7 c) 2-Nitro-3-piperazin-l-yI WV-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide A solution of 3-(4- {1,1 -dimethyiethyl} oxycarbonylj-piperazin-1 -yl)-2-nitro-/V- (tricyclo [3.3.1.1 ' ] dec-l-ylmethyl)-benzamide (0.58 g, Example lb) and hydrochloric acid (6.4 ml, 4N in dioxane) in tetrahydrofuran (20 ml) was stirred at room temperature under a nitrogen atmosphere for 18h. The reaction mixture was concentrated under reduced pressure and the residue dissolved in water, made basic with solid sodium bicarbonate and extracted with dichloromethane three times. The combined organic extracts were dried over magnesium sulfate, filtered and the filtrate concentrated under reduce pressure to give a solid. Purification by chromatography over silica gel, eluting with 10% methanol in dichloromethane afforded the title compound as a solid (0.165 g). MS (APCI +ve) 399 (M+H)+ H NMR (DMSO-dfi) 5 8.52 (1H, t); 7.59 (1H, t); 7.51 (1H d); 7.35 (1H, d); 2.88 (2H, d); 2.81 (4H, m); 2.37 (4H, m); 1.93 (3H, bs); 1.67 (3H, d); 1.60 (3H, d); 1.47 (6H, s) Example 2 3 7 2-Amkio-3-piperazin-l-yI -iV-(tricyclo[3J.l.l ' ]dec-l-ylmethyl>benzamide, dihydrocfaloride salt a) 2-Amino-3-(4-{l,l-dimethylethyl}oxycarbonyl]-piperaziii-l-yI)-A/'- 37 (tricyclt{3J.l.l ' ]dec-l-ylmethyl)-benzaraide A suspension of 3-(4-{ 1,1 -dimethyiethyl}oxycarbonyl]-piperazin-1 -yl)-2-nitro-iV- (tricyclo [3.3.1.13' ] dec-l-ylmethyl)-benzamide (3.8 g, Example lb), iron powder (2.13 g) and ammonium chloride (2.04 g) in 2:1 ethanol/water (90 ml) was heated at reflux, under a nitrogen atmosphere, for 2h. The cooled reaction mixture was filtered and the filtrate partitioned between water and ethyl acetate. The organic layer was separated and washed with water twice further, dried over magnesium sulfate, filtered and the filtrate concentrated under reduced pressure to give a residue. Purification of the residue by chromatography over silica gel, eluting with 20% ethyl acetate in trohexane, yielded the subtitle compound as a solid (2.27 g). MS (APCI+ve) 469 (M+H)+ 3 7 b) 2-Amino-3-piperazin-l-yl-A^-(tricyclo[3«3.1.1 ' ]dec-l-ylmethyl)-benzamide, dihydrochJoride salt Prepared as described in Example lc) using 2-amino-3-(4-{ 1,1-dimethyl ethyl} 3 7 oxycarbonyl]-piperazin-l-yl)-/v"-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.2 g, Example 2a) and hydrochloric acid (5 ml, 4N in dioxane). The reaction mixture was concentrated under reduced pressure to give a solid which when triturated with diethyl sther gave the title compound as a solid (0.2 g). MS(APCI+ve) 369(M-2HC1)+ 'HNMR (DMSO-d6) 5 9.16 (2H, bs); 8.14 (IH, t); 7.37 (IH, d); 7.07 (IH, d); 6.64 (IH, t); 3.27 (4H, bs); 2.98 (4H, bs); 2.95 (2H, d); 1.93 (3H, bs); 1.67 (3H, d); 1.59 (3H, d); 1.48 ;6H, s). Example 3 3 7 J-Chloro-3-piperazin-l-yl -AKtricycIo[3.3.1.1 ]dec-l-yimethyl)-benzamide a) 2-Chloro-3-(4-{l,l-dimetbylethyl}oxycarbonyl]-piperazin-l-yI)-A^-(tricycio[3.3.1.13,7]dec-l-ylmethyI)-benzamide To a solution of 2-amino-3-(4-{ l,l-dimethyIethyl}oxycarbonyi]-piperazin-l-yJ)-/V-(tricycio[3.3.1.1 ]dec-l-ylmethyl)-benzamide (lg„ Example 2a) in tetrahydrofuran (23 ml) was added 1M aqueous hydrochloric acid (2.78 ml) and water (10 ml). The solution was cooled to 0°C and sodium nitrite (1.91 g) added portion-wise, whilst maintaining the internal temperature below 5°C. After stirring at 0-5°C for 0.5h, a pre-cooled suspension of copper (I) chloride (10.58 g) and copper (II) chloride in water (20ml) was added portion-wise to the pale yellow suspension. The mixture was stirred at 0°C for 0.5h then at room temperature for 0.5h. The reaction mixture was poured into a mixture of water and dichloromethane and 1/1 : 0.88 ammonia/water was added until the aqueous phase was homogeneous. The layers were separated and the aqueous phase extracted twice further with dichloromethane. The combined organic extracts were washed with l/l : 0.88 ammonia/water until the aqueous layer was colourless, dried over sodium sulfate, filtered and concentrated under reduced pressure to yield an oil. Purification by chromatography on silica gel, eluting with 20-35% ethyl acetate/jjo-hexane gave the subtitle compound as a solid (0.45 g). MS (APCI +ve) 388 (M-BOC)+ H NMR (DMSO-de) 8 8.27 (ltf, t); 7.32 (1H, t); 7.19 (1H, d); 7.04 (1H, d); 3.48 (4H, m); 2.93-2.91 (6H, m); 1.94 (3H, bs); 1.64 (3H, d); 1.59 (3H, d); 1.52 (6H, s); 1.43 (?H, s). 37 b) 2-Chloro-3-piperazin-l-yl -iV-(tricyclo[3.3.1.1 ' ]dec-J.-ylmethyI)-benzamide To a solution of 2-Chloro'3-(4-{ l,l-dimethylethyl}oxycarbonyl]-piperazin-l-yl)-iV- (tricyclo[3.3.1.1 ]dec-l-ylmethyl)-benzamide (0.45 g, Example 3a) in dichloromethane (10 ml) was added trifluoroacetic acid (5 ml). After stirring at room temperature under a nitrogen atmosphere the reaction mixture was concentrated under reduced pressure to give a gum. The gum was partitioned between water and dichloromethane and made basic with solid sodium bicarbonate. The layers were separated and the aqueous layer extracted twice further with dichloromethane. The combined organic extracts were washed twice with water, saturated brine then dried over magnesium sulfate, filtered and the filtrate concentrated under reduced pressure to give a foam. The foam was purified by normal phase HPLC (0-20% ethanol/dichloromethane) and chromatography over silica gel, eiuting 10% methanol in dichloromethane, to afford the title compound as a foam (0.05 g). MS (APCI +ve) 388/90 (M+H)+ 'H NMR (DMSO-d6) 5 8.24 (1H, t); 7.31 (1H, t); 7.15 (1H, d); 7.00 (1H, d); 2.96-2.87 (10H, m); 1.93 (3H, bs); 1.67 (3H, d); 1.59 (3H, d); 1.52 (6H, s). 37 a) 2-ChIoro-5-nitro-Ar-(tricyclo[33.1.1 ' ]dec-l-ylmethyl)-benzamide To a solution of 2-chloro-5-nitrobenzoic acid (1.22g) in N, JV-dirnethylformamide (1.5 ml) was added carbonyldiimidazole (1.0 g). The resulting reaction mixture was stirred for 2.5h and then 1-adamantanemethylamine (l.Og) was added. After 14h the reaction mixture was partitioned between ethyl acetate and water and the organic layer was separated, washed with water and brine and then dried over sodium sulphate (Na2S04). The organic layer was concentrated under reduced pressure to give a residue which was purified by silica gel chromatography (eiuting with 3-10% methanol in dichloromediane) to yield the subtitle compound as a yellow solid (1.7 g). MS (APCI +ve) 348/350 (M+H)+ H NMR (CDC13) 5 8.53 (1H, d), 8.2 (1H, dd), 7.6 (1H, d), 6.2 (1H, bs), 3.2 (2H, d), 2.0(3H,bs), 1.8(12H,m) b) 5-Amino-2-chloro-/V-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyf)-benzaniide A solution of the nitro compound from Example 4a, (0.50 g) and ammonium chloride (0.5g) were dissolved in 50% aqueous ethanol. Iron powder (0.5g) was added and the mixture stirred at reflux temperature for 3 hr before being cooled and solids removed by filtration. The modier liquors were treated with 10% sodium hydroxide solution and the product extracted into ethyl acetate. The organic solution was washed with brine, dried over sodium sulphate (Na2SC>4) and concentrated to give a residue which was purified by silica gel chromatography to give the title compound as a white solid (0.4g). MS (APCI+ve) 319/21 (M+H)+ !HNMR (DMSO-de) 8 8.14 (1H, t); 7.03 (1H, dd); 6.56 (2H, m); 5.36 (2H, s); : 2.89 (2H, d); 1.95 (3H, s); 1.7 (12H, m) 37 c) 2-Chloro-5-Piperazin-l-yl -/V-(tricyclo[3.3.3H ' ]dec-l-ylmethyl)-benzamide 3 7 To a solution of 5-aniino-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (1.00 g, Example 4b) in xylene (20 ml) was added Z7i.s-(2-chloroethyl)amine hydrochloride salt (0.620g). The mixture was heated at 150°C for 12h (a dark solution is obtained). The cold solution was washed with 2M HC1, the aqueous layer washed with ethyl acetate then basified with sodium bicarbonate and extracted twice with dichloromethane. The organic layer was dried over magnesium sulfate, filtered and the filtrate concentrated under reduced pressure to give "a foam. The crude material was purified on silica gel (0-10% ethanol/dichloromethane), to afford the title compound as a white solid (0.90 g). MS (APCI+ve) 388/90 (M+H)+ 'H NMR (DMSO-de) 5 8.22 (1H, t); 7.22 (1H, d); 6.96 (1H, dd); 6.84 (1H, d); 3.50-3.20 (7H, m); 3.00-2.90 (2H, t); 2.91 (2H, d); 1.94 (3H, bs); 1.67 (3H, d); 1.59 (3H, d); 1.52 (6H, s). a) 4-[4-Chloro-3-(ethoxycarbonyl)phenyl]hexahydro-l^-l,4-diazepine-l-carboxylic acid, 1,1-dimethylethyl ester ' A mixture of 5-bromo-2~chloro-benzoic acid, ethyl ester (0.50 g), hexahydro-1//-1,4-diazepine-1-carboxylic acid, 1,1-dimethylethyl ester (0.46 g), cesium carbonate (0.86 g), palladium (21) acetate (8.5 mg) and (R)-BINAP (35 mg) in toluene (3 ml) was heated at 100 °C for 14h in a pressure vessel flushed with nitrogen. The cooled reaction mixture was poured into water and extracted (3 times) with ethyl acetate. The combined organic extracts were washed with saturated sodium chloride solution and men dried over magnesium sulfate. Evaporation under reduced pressure gave an oil which was purified by chromatography over silica gel, eluting with 20% ethyl acetate in iyo-hexane to yield the subtitle compound as an oil (0.21 g). MS (APCI +ve) 282/284 (M-BOC)+ b) 4-(3-Carboxy-4-chlorophenyl)hexahydro-lff-l,4-dia2epine-l-carboxylic acid, 1,1- dimethylethyl ester A suspension of 4-[4-chloro-3-(ethoxycarbonyl)phenyl]hexahydro- IH-1,4-diazepine-1-carboxyiic acid, 1,1-dimethyiethyi ester (Example 5a, 0.2 lg), lithium hydroxide monohydrate (1.05ml of 3M solution in water) in 1:1 ethanol/water (7 ml) was stirred at room temperature for 14h. More lithium hydroxide monohydrate (0.55ml of 3M solution in water) was added followed by tetrahydrofuran (1 ml). The resulting solution was stirred for 4h at room temperature then poured into water and extracted with diethyl ether. The aqueous phase was separated, acidified with 2M hydrochloric acid and then extracted with dichloromethane three times. The combined dichloromethane layers were dried over magnesium sulfate and evaporated under reduced pressure to yield the subtitle compound as a glass. MS (APCI +ve) 298/300 (M-'Bu)+ 37 c) Hexahydro-4-[4-methyl-3-[[(tricyclo[3.3.1.1 ' ]dec-l-yImethyl)aminojcarbonyl]- phenyI]l.ff-l,4-diazepine-l-carboxylic acid, 1,1-dimethylethyl ester A solution of 4-(3-carboxy-4-chlorophenyOhexahydro-1H-1,4-diazepine-1 -carboxylic acid, 1,1-dimethylethyl ester (Example 5b, 0.10 g) and N,N'-carbonyldiimidazole (0.045 g) in dimethylformamide (3 ml) was stirred at room temperature for 2h. 1-Adamantanemethylamine (0.050 ml) was then added and stirring continued for 14h. The reaction mixture was poured into water and extracted with ethyl acetate three times. The ethyl acetate layers were combined and washed with 2M hydrochloric acid, 10% aqueous sodium hydroxide and brine, then dried over magnesium sulfate and concentrated under reduced pressure. Purification by chromatography on silica gel, eluting with 20-30% ethyl acetate in wo-hexane, gave the subtitle product as a gum which crystallised on standing. MS (APCI +ve) 502/504 (M+H)+ d) 2-Chloro-S-(hexahydro-Lff-l,4-diazepin-l-yl)-iV-(tricyclo[3J.l.l3'7]dec-l- ylmethyl)- benzamide, hydrochloride salt 3 7 Hexahydro-4-[4-methyl-3-[[(tricyclo[3.3.1.1 ' ]dec-l-ylrnethyl)ammo]carbonyl]- phenyl]-lfM ,4-diazepine-1-carboxylic acid, 1,1-dimethylethyl ester(from Example 5c) was dissolved in methanol (5 ml) and hydrochloric acid (0.5ml of a 4N solution in dioxane) was added. After stirring at room temperature for 14h, the mixture was evaporated to 2/3 original volume under reduced pressure. Diethyl ether was gradually added to the solution and the resulting precipitate collected by filtration, washed with diethyl ether and dried in vacuo to afford the title compound as a solid (0.027 g) MS (APCI +ve) 402/404 (M+H)+ 'HNMR (DMSO-d6) 6 9.11 (2H, bs); 8.18 (lH,t); 7.24 (1H, d); 6.81 (1H, dd); 6.71 (1H, d); 3.71 (2H, t); 3.50 (2H,t); 3.19 (2H, bs); 2.93 (2H, bs); 2.92 (2Hf d); 2.08 (2H, m); 1.94 (3H, bs); 1.67 (3H, d); 1.59 (3H, bs); 1.52 (6H, s) a) 2-Chloro-5-[4-[[(l,l-dunethylethoxy)carbonyl]amino]-l-piperidinyl]-benzoic acid, ethyl ester Prepared as described in Example 5a) using 5-bromo-2-chloro-benzoic acid, ethyl ester (0.50 g), 4-piperidinyl-carbamic acid, 1,1 -dimethylethyl ester (0.46 g), cesium carbonate (0.86 g), palladium (H) acetate (8.5 mg) and (R)-BINAP (35 mg) and toluene (3 ml) to afford the subtitle compound as an oil (0.17 g). MS (APCI +ve) 383/385 (M+H)+ b) 2-Chloro-5-[4-([(l,l-dimethyIethoxy)carbonyI]aniino]-l •piperidinyl]- benzoic acid Prepared as described in example 5b) using 2-chloro-5-[4-[[(l,l-dimethylethoxy)-carbonyi]aminoJ-1 -piperidinylJ-benzoic acid, ethyl ester (Example 6a, 0.17 g), lithium r hydroxide monohydrate (0.88 ml of a 3M solution in water), 1:1 ethanol/water (7 ml) and tetrahydrofuran (1ml) to give the subtitle compound as a solid (0.14 g). MS (APCI +ve) 354/356 (M+H)+ c) [l-[4-Chloro-3-[[(tricydo[3J.l.l3'7]dec-l-ylmethyl)aniino]carbonyl]phenyl]-4- piperidinyl]-carbamic acid, 1,1-dimethylethyi ester Prepared as described in Example 5c) using 2-chloro-5-[4-[[( 1,1-dimethylethoxy)carbonyl]amino]-l-piperidinyl]- benzoic acid (Example 6b, 0.065 g), N,N'-carbonyldiimidazole (0.030 g), 1-adamantanemethylamine (0.032 ml) and dimethylformamide (3 ml) to give die subtitle compound as a solid. MS (APCI +ve) 501/503 (M+H)+ d) 5-(4-Aniino-l-piperidinyI)-2-chloro-A^-(tricyclo[3J.l.l3'7]dec-l-ylmethyl)- benzamide, hydrochloride salt . Prepared as described in example 5d) above using [l-[4-chloro-3- 3 7 [[(tricyclo[3.3.1.1 ' ]dec-l-ylmemyl)amino]carbonyl]phenyl]-4-piperidinyl]-carbamic acid, 1,1-dimeth.ylethyl ester (Example 6c), hydrochloric acid (0.5ml of a 4N solution in dioxane) and methanol (10 ml). The mixture was heated at reflux for 15 min. to complete the reaction. After evaporation to two-thirds of the original volume, a solid crystallised on standing which was collected by filtration and dried in vacuo to give the title compound as a solid (0.025 g). MS (APCI +ve) 402/404 (M-HC1)+ 'H NMR (DMSO-d6) 8 8.23 (1H, t); 8.11 (IH,bs); 7.28 (1H, d); 7.03 (1H, dd); 6.94 ;iH. s); 3.74 (2H, d); 3.20 (1H, m); 2,91 (2H, d); 2.83 (2H, t); 1.98 (2H, bs); 1.94 (3H, bs); 1.69-1.58 (8H,m); 1.52 (6H,s) Example 7 -Hr-)-5-(3-Amino-l-pyrrolidinyl)-2-chloro-A'-(tricyclo[3.3.1.13'7]dec-l-ylmethyl)- i) (+/-)-2-Chloro-5-[3-[[(l,l-dimethylethoxy)carbonyl]aniino]-l-pyrrolidinyl]-lenzoic acid, ethyl ester Prepared as described in Example 5a) using 5-bromo-2-cbloro-benzoic acid, ethyl stcr (0.50 g), 3-pyrrolidinyI-carbamic acid 1,1-dimediylethyl ester (0.42 g), cesium arbonate (0.86 g), palladium (II) acetate (21 mg) and (R)-BINAP (88 mg) and toluene 3 ml) to afford the subtitle compound as an oil (0.25 g). AS (APCI +ve) 311/313 (M-BOC)+ 0 (+/-)-2-Chloro-5-[3-[[(l,l-dimethylethoxy)carbonyl]amino]-l-pyrrolidinyi]-tenzotc acid Prepared as described in Example 5b) using (+/-)-2-chloro-5-[3-[[(l,l-[imethylethoxy)carbonyl]aminoj-l-pyrrolidinyl]- benzoic acid, ethyl ester (Example 7a, l.25g), lithium hydroxide monohydrate (1.36ml of a 3M solution in water), 1:1 thanol/water (7 ml) and tetrahydrofuran (1ml) to give the subtide compound as a solid 0.23 g). MS (APGI +ve) 284/286 (M-BOC)+ c) (+/-)-[l-[4-chloro-3-[[(tricyclo[3J.1.13,7]dec-l-ylmethyi)amino]carbonyI]phenyI]- 3-pyrToUdinyl]-carbamic acid, 1,1-dimethylethyl ester Prepared as described in Example 5c) using (+/-)-2-chloro-5-[3-[[(l,l-dimethylethoxy)carbonyl]amino]-l-pyrrolidinyl]- benzoic acid (Example 7b, 0.070g), N,N'-carbonyldiimidazole (0.033 g), 1-adamantanemethylamine (0.036 ml) and dimethylformamide (3 ml) to give the subtitle compound as a gum. MS (APCI +ve) 487/489 (M+H)+ d) (+/-)-5K3-Amino-l-pyrrolidinyl)-2-chloro-A^-(tricyclo[33.1.13'7]dec-l-yImethyI)- benzamide, hydrochloride salt Prepared as described in example 5d) above using (+/-)-[ l-[4-chloro-3- 3 7 [[(tricyclo[3.3.1.1' ]dec-1 -ylmethyl)amino]carbonyl]phenyl]-3-pyrroIidinyl]-carbamic icid, 1,1-dimethylethyl ester (Example 7c), hydrochloric acid (0.5ml of a 4N solution in lioxane) and methanol (5 ml). Evaporation under reduced pressure gave a solid on trirtuation wim diemyl ether. Recrystallisation from methanol/diethyl ether gave the title rompound as a solid (0.030 g). MS (APCI +ve) 388/390 (M+H)+ lH NMR (DMSO-dg) 5 8.24 (3H, bs); 8.20 (1H, t); 7.25 (1H, d); 6.61 (1H, dd); 6.51 ;iH, d); 3.94 (1H, m); 3.55-3.32 (2H, m); 3.29 (2H, m); 2.92 (2H, d); 2.37-2.27 (1H, m); U3-2.05 (1H, m); 1.94 (3H, bs); 1.68(3H, d); 1.59 (3H, d); 1.52 (6H, s) a) 5-Bromomethyl-2-chloro-ben2oic acid To a stirred solution of 2-chloro-5-methyl-benzoic acid (25g) in chloroform (500ml) at 50°C was added N-bromosuccinimide (27.40g). The flask was purged with nitrogen and azobistsobutyronitrile (0.10g) added in one portion. The solution was heated at reflux for lh. Further azobiswobutyronitrile (0. lOg) was added and the mixture heated a further 3h. The solution was concentrated in vacuo, redissolved in diethyl ether and filtered to remove insoluble succinimide. The ether solution was washed widi 2N aqueos hydrochloric acid solution followed by brine then dried over magnesium sulphate. The solution was concentrated to a volume of 150ml then diluted with isohexane. After further partial concentration crystallization started. The mixture was allowed to stand in an ice-bam for lh. The resulting crystals were filtered, washed with isohexane and dried in vacuo to give the subtitle compound (17g). b)5-Bromomethyl-2-chIoro-A^-(tricyclo[3.3.1.13,7]dec-l-yImethyl)-benzaniide To a stirred solution of 5-bromomethyl-2-chloro-benzoic acid (Example 8a, 12.4g) in dichloromethane (250ml) and dimethylformamide (0.12ml) at 0°C was added oxalyl chloride (8.7ml). The cooling bath ws removed and the solution allowed to warm to room temperature. Once gas evolution had ceased the solution was concentrated in vacuo. The residue was redissolved in dichloromethane (300ml), cooled to 0°C and treated with dzuopropyleraylamine (12.4 ml) and adamantylmethylamine (7.54ml). After 15min. at 0°C the solution was poured into diethyl ether (1L) and washed with IN aqueous hydrochloric acid followed by brine. The organics were dried over magnesium sulphate and concentrated in vacuo to give the title compound as a white powder (19g) MS (APCI +ve) 396/398 (M+H)+ 'H NMR (DMSO-d6) 5 8.39 (1H, t); 7.50-7.40 (2H, m); 4.74 (2H, s); 2.92 (2H, d); 2.50 (3H, s); 1.94 (3H, bs); 1.67 (3H, d); 1.59 (3H, d); 1.52 (6H, s). c) 2-Chloro-5-(4-[{l,l- (tricyclo[3J.l.l3'7]dec-l-yImethyl)-ben2amide, 3 7 A mixture of 5-bromomethyl-2-chloro-A^-(tricyclo[3.3.1.1' ]dec-1 -ylmethyl)- benzamide (Example 8b, 0.130g), 1-terrbutyloxycarbonylpiperazine (0.074g) and dilsopropylethylamine (6.3 ml) in dimethylformamide (3 ml) was heated at 60°C for 3h. The mixture was diluted with water (10 ml) and extracted with ethyl acetate (3 x 10 ml). The organic layer was dried over magnesium sulfate, filtered and the filtrate concentrated under reduced pressure. The crude material was purified on a silica gel eluting with dichloromethane/ethanol (0-20% gradient) to afford the title compound as a white foam (0.112g). MS (APCI +ve) MW 502/504 (M+H)+ JH NMR (DMSO-dfi) 5 8.28 (1H, t); 7.40 (1H, d); 7.32 (1H, dd); 7.29 (1H, d); 3.74 (2H, s); 3.28 (4H, t); 2.90 (2H, d); 2.31 (4H, t); 1.92 (3H, bs); 1.70-1.50 (6H, m); 1.59 (6H, d); 1.37 (9H, s). d) 2-Chloro-5-piperazm-l-yImethyl -AKtricycto[33.1.13'7]dec-l-ylmethyl)- benzamide, hydrochloride salt 2-Chloro-5-(4-[ {1,1 -dimethylethyl} oxycarbonyl]-piperazin-1 -yl)methyl -N- 3 7 (tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide, (Example 8c, 0.080g) was dissolved in methanol (3ml), 4N HC1 in dioxane (1ml) was added and the mixture stirred at room temperature for 1.5h. The solvent was removed under vacuum and the resulting solid was triturated with ether to afford the title compound as a white powder (0.062g). MS (APCI +ve) MW 402/404 (M+H)+ 'H NMR (DMSO-dg) 5 8.30 (IH, t); 7.63 (2H, bs); 7.55 (IH, d); 4.33 (IH, bs); 4.05 (4H, m); 3.50-3.00 (4H, m); 3.50-3.40 (IH, m); 2.92 (2H, d); 1.92 (3H, bs); 1.70-1.50 (6H,m); 1.57 (6H, bs). According to the procedure described in Example 8, the following compounds were prepared. MS (APCI +ve) MW 416/418 (M+H)+ 'H NMR (DMSO-de) 8 11.62 (bs, IH), 9.57 (bs, IH); 9.30 (bs, IH); 8.34 (IH, t); 7.80-7.60 (2H, m); 7.59 (IH, d); 4.50-4.30 (bs, 2H); 3.80-3.00 (m, 8H); 2.94 (2H, d); 2.25-2.10 (m, 2H); 1.94 (3H, bs); 1.66 (3H, d); 1.58 (3H, d); 1.54 (6H, s). Example 10 5-[(4-Amino-l-pip€ridinyI)methyI]-2-chIoro-iV-(tricyclo[3.3.1.13'7]dec-l-ylmethyI)-benzamide, hydrochloride salt MS (APCI +ve) MW 416/418 (M+H)+ 'H NMR (DMSO-de) 5 8.35 (1H, t); 8.30 (2H, bs); 7.66 (1H, d); 7.65 (1H, s); 7.59 (1H, d); 428 (d, 2H); 3.65-3.18 (m, 4H); 3.10-2.90 (1H, m); 2.95 (2H, d); 2.15-2.05 (2H, m); 2.05-1.90 (1H, m); 1.94 (3H, bs); 1.68 (3H, d); 1.61 (3H, d); 1.54 (6H, s). MS (APCI +ve) MW 402/404 (M+H)+ lH NMR (DMSO-de) 5 8.56 (1H, bs); 8.42 (2H, bs); 8.35 (1H, t); 7.66 (2H, bs); 7.59 (1H, d); 4.60-4.40 (m, 2H); 4.20-3.00 (m, 5H); 2.94 (2H, d); 2.35-1.95 (m, 2H); 1.95 (3H, bs); 1.68 (3H, d); 1.61 (3H, d); 1.54 (6H, s). a) 2-Chloro-5-hydroxy-Ar-(tricycIo[3.3.1.13,7]dec-l-ylmethyl)-benzamide To a solution of 2-chloro-5-hydroxybenzoic acid (3.12g) in ACiV-dimethylformamide (50 ml) was added l.T-carbonyldiimidazole (3.0 g). The resulting reaction mixture was stirred for 2.5h and then 1-adamantanemethylamine (3.0g) was added. Stirring was continued for 14h . The reaction mixture was partitioned between ethyl acetate and water and the organic layer was separated, washed with water and brine and then dried over sodium sulphate (Na2SC>4). The organic layer was concentrated under reduced pressure to give a residue which was purified by silica gel chromatography (eluting with 3-10% methanol in dichloromethane) to yield the subtitle compound as a white solid (0.15 g). MS (APCI+ve) 319/321 (M+H)+ H NMR pMSO-de) 5 9.85(lH,s), 8.25 (1H, t), 7.24(1H, d), 6.76-6.82(2H, m), 2.90 (2H,d), 1.93(3H, s), 1.67 (3H, d), 1.57 (3H, d), 1.51 (6H, s) 37 b) 2-Cblbro-5-(4-piperidinyloxy)-iV-(tricyclo[3J.l.l ' ]dec-l-ylmethyl)-benzamide, hydrochloride salt 3 7 To a solution of 2-chloro-5-hydroxy-iV-(tricyclo [3.3.1.1 ' ]dec-1 -methyl)-benzamide (0.20 g, Example 12a), 4-hydroxy-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0,19 g) and tributylphosphine (0.23 ml) in dry tetrahydrofuran (6 ml) ,was added 1-[[(1- piperidinylcarbonyl)azo]carbonyl]-piperidine (0.24 g). The orange solution was heated at 60°C under a nitrogen atmosphere for 2h. At this point additional 4-hydroxy-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.19 g), tnbutylphosphine (0.23 ml) and l-[[(l-piperidinylcarbonyl)azo]carbonyl]- piperidine (0.24 g) were added.. Heating was continued and the process described above repeated until reaction was complete as judged by LC/MS. The cooled reaction mixture was diluted with diethyl ether then filtered. The Filtrate was concentrated and purified by normal phase HPLC (0-2% methanol/ dichloromethane) followed by chromatography on silica gel (0-2% medianol/ dichloromethane) to give the t-butyloxycarbonyl (BOC)-protected compound as a colourless foam. The foam was dissolved in methanol (5 ml) and 4N hydrochloric acid in dioxane (0.25 ml) added. The solution was stirred at room temperature under a nitrogen atmosphere until the reaction was complete as judged by LC/MS. Evaporation of solvent followed by trituration witfi diethyl ether gave the title compound as a colourless solid (0.15 g). MS (APa+ve) 417/419 (M+H)+ lH NMR (DMSO-dg) 5 8.65 (2H, bs); 8.30 (IH, t); 7.39 (IH, d); 7.07 (IH, dd); 6.99 (IH, d); 4.72-4.67 (IH, m); 3.21 (2H, bm); 3.07 (2H, bm); 2.92 (2H, d); 2.12-2.07 (2H, m); 1.94 (3H, bs); 1.88-1.80 (2H, m); 1.67 (3H, d); 1.59 (3H, d); 1.52 (6H, s) Preparcd as described in Example 12b using 2-chloro-5-hydroxy-JV-(tricyclo[3.3.1.13'7]dec-l-methyl)-benzamide (0.20 g, Example 12a), N-tBOC-D-prolinoI (0.19 g) and tributylphosphine (0.23 ml), dry tetrahydrofuran (6 ml) and 1-[[(1-piperidinylcarbonyl)azo]carbonyi]- piperidine (0.24 g) to obtain the butyloxycarbonyl (BOC)-protected compound, followed by treatment with 4N hydrochloric acid in dioxane (0.4 ml) and methanol (5 ml) to yield the title compound as colourless solid (0.14 g) MS (APCI+ve) 403/405 (M+H)+ 'HNMR (CD3OD) 5-8.45 (1H, bt); 7.46 (1H, d); 7.14-7.10 (2H, m); 4.41 (1H, dd); 4.18 (1H, t); 4.10-4.04 (1H, m); 3.41 (2H, t); 3.10 (2H, m); 2.36-2.28 (1H, m); 2.25-2.08 (2H, d); 2.03 (3H, s); 2.00-1.90 (1H, m); 1.83 (3H, m); 1.74 (3H, d); 1.68 (6H, s) Prepared as described in Example 12b using 2-chloro-5-hydroxy-iV-(tricyclo[3.3.1.13,7]dec-l-methyl)-benzamide (0.20 g- Example 12a), N-tBOC-L-prolinol (0.19 g) and tributylphosphine (0.23 ml), dry tetrahydrofuran (6 ml) and 1-[[(1-piperidinylcarbonyl)azo]carbonyl]- piperidine (0.24 g) to obtain the t-butyloxycarbonyl (BOC)-protected compound, followed by treatment with 4N hydrochloric acid in dioxane (0 J ml) and methanol (5 ml) to yield the title compound as colourless solid (0.07 g) MS (APQ+ve) 403/405 (M+H)+ 'HNMR (CD3OD) 5 8.45 (1H, bt); 7.46 (1H, d); 7.14-7.10 (2H, m); 4.41 (1H, dd); 4.18 (1H, t); 4.104.04 (1H, m); 3.41 (2H, t); 3.10 (2H, m); 2.36-2.28 (lH,m); 2.25-2.08 (2H, d); 2.03 (3H, s); 2.00-1.90 (1H, m); 1.83 (3H, m); 1.74 (3H, d); 1.68 (6H, s) Prepared as described in Example 12b using 2-chloro-5-hydroxy-N-Cricyclo[3.3.1.13,7]dec-l-methyI)-benzamide (0.20 g- Example 12a), i-piperidinemethanol (0.20 g) and tributylphosphine (0.23 ml), dry tetrahydrofuran (6 ml) nd l-([(l-piperidinylcarbonyl)azo]carbonyI]- piperidine (0.24 g) to obtain the t-•utyloxycarbonyJ (BOC)-protected compound. This compound was treated with 4N ydrochloric acid in dioxane (0.5 ml) and methanol (5 ml) to yield the title compound as olourless solid (0.09 g), AS (APCI +ve) 417/19 (M+H)+ H NMR (DMSO-d6) 8 8.34 (2H, bs); 8.29 (1H, t); 7.38 (1H, d); 7.01 (1H, dd); 6.93 1H, d); 3.99-3.95 (1H, m); 3.91-3.87 (1H, m); 3.34 (1H, m); 3.23 (1H, bd); 2.92 (2H, d); L82-2.71 (2H, m); 2.22 (1H, m); 1.94 (3H, s); 1.82 (2H, d); 1.72-1.66 (4H, m); 1.59 3H, d); 1.52 (6H, s); 1.39-1.32 (1H, m) ilxample 16 3 7 is-5-[(4-Aminocyclohexyl)oxy]-2-chloro-N-(tricyclo[3J.l.l ' ]dec-l-ylmethyl)- lenzamide, hydrochloride salt Prepared as described in Example 12b using 2-chloro-5-hydroxy-N- 3 7 (tricyclo[3.3.1.1 ' ]dec-l-methyl)-benzamide (0.20 g, Example 12a), trans-4-amino- cyclohexanol (0.20 g) and tributylphosphine (0.23 ml), dry tetrahydrofuran (6 ml) and l-[[(l-piperidinylcarbonyl)azo]carbonyl]- piperidine (0.24 g) to obtain the t-butyloxycarbonyl (BOC)-protected compound. This compound was treated with 4N hydrochloric acid in dioxane (0.5 ml) and methanol (5 ml) to yield the title compound as colourless solid (0.065 g). MS (APCI +ve) 417/19 BP 417 H NMR (DMSO-d6) 8 8.30 (IH, t); 7.97 (3H, bs); 7.38 (IH, d); 7.02 (IH, dd); 6.92 (IH, d); 4.62 (IH, bs); 3.11 (IH, bs); 2.92 (2H, d); 1.94 (5H, s); 1.76-1.58 (12H, m); 1.52 (6H,s). Example 17 37 2-MethyI-5-(l-piperazinylmethyl)-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide, hydrochloride salt To a solution of 2-bromo-5-(4-[{ l,l-dimethylethyl}oxycarbonyl]-piperazin-l-1)methyl -N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.20g, Example 65b) and etrakis(triphenylphosphine)palladium(0) (2mg) in dry toluene (6 ml) was added etramethyltin (0.2ml). The solution was heated at 130°C in a sealed tube for 18hrs. The :ooled reaction mixmre was evaporated and the residue was treated with 10% KF solution a acetone and stirred for 45min. The mixmre was concentrated and chromatographed on ilica gel (isohexane men 60% ethyl acetate/ 40% isohexane) to give the -butyloxycarbonyl (BOC)-protected compound as a colourless oil. The oil was dissolved n methanol (2 ml) and 4N hydrochloric acid in dioxane (1 ml) added. The solution was tirred at room temperature under a nitrogen atmosphere until the reaction was complete as ndged by LC/MS. Evaporation of solvent followed by trituration with diethyl etiier gave tie title compound as a colourless solid (0.03 g). AS (APCI +ve) 382 (M+H)+ HNMR (CD3OD) 57.61 (1H, s); 7.55(1H, d); 7.39 (1H, d); 4.45 (2H, s); 3.67-3.46 8H, bm); 3.08 (2H, s); 2.45 (3H, s); 1.99(3H, s); 1.78 (3H, d); 1.71 (3H, d); 1.62 (6H, s) Example 18 l-OUoro-5-(l-piperazinylinethyl)-N-(2-tricyclo[3J.l.l3'73dec-l-ylethyl)-benzaiiiide, lydrochloride salt 3 7 a) 5-(bromomethyI)-2-chloro-N-(2-tricyclo[3.3.1.1 ' ]dec-l-ylethyl)-benzamide To a solution of 2-chloro-5-(bromomethyl)-benzoic acid (1.0 g) in dichloromethane (25ml) at 0°C was added dimethylformamide (0.05ml) followed by oxaiyl chloride (0.52 ml). The reaction was allowed to warm to room temperature and stirred for 30min. The volatiles were removed under vacuum and the residue dried under high vacuum. The acylchloride was dissolved in dichloromethane (20 ml) and added to a solution of 2-adamantanethylamine hydrochloride salt (0.95g) in dichloromethane (20ml) and diisopropylethylamine (2 ml) at 0°C. The reaction was allowed to warm to room temperature and stirred for 2h. The organics were washed with water (20ml) then saturated aqueous ammonium chloride solution and the organic layer dried over magnesium sulfate then filtered. The filtrate was concentrated under reduced pressure to a solid. The crude material was recrystallised from dichloromethane/hexane to afford the subtitle compound as,a white solid (1.3 g). b) 4-[[4-OdoroO-[[(2-tricyclo[33JJ3'7]dec4-ylethyl)ainino]carbonyl]- phenyl]methyl]-l-piperazinecarboxylic acid, 1,1-dimethylethyl ester 3 7 Arnixture5-(bromomethyl)-2-chloro-N-(2-tncyclo[3.3.1.1 ' ]dec-l-ylethyl)- benzamide (Example 18a, 0.35g), l-tertbutyloxycarbonylpiperazine (0.213g), potassium carbonate (0.20g) and potassium iodide (10 mg) in acetone (5 ml) was heated at 60°C for 2h. The acetone was removed under vacuum, the residue taken into dichlorometane and the solid removed by filtration. The crude material was purified on a silica gel eluting with dichloromethane/ethanol (0-10% gradient) to afford the subtitle compound as a white foam (0.383g). MS (APCI +ve) MW 516/518 (M+H)+ !H NMR (CDC13) 8 7.63 (1H, bs); 7.34 (2H, bs); 6.09 (1H, bs); 3.60-3.30 (8H, m); 2.50-2.30 (4H, bs); 1.97 (3H, bs); 1.72 (3H, d); 1.68 (3H, d); 1.56 (6H, bs); 1.44 (9H, s); 1.50-1.35 (2H,m) c) 2-Chloro-5-(l-piperazinyImethyl)-N-(2-tricyclo[3.3.1.13'7]dec-l-ylethyl)- benzamide, hydrochloride salt 3 7 4-[[4-chloro-3-[[(2-tricyclo[3.3.1.1 ' ]dec-l-ylethyl)amino]carbonyl]phenyl]methyl]- 1-piperazinecarboxylic acid, 1,1-dimetfiylethyl ester, (Example 18b, 0.270g) was dissolved in methanol (3ml), 4N HC1 in dioxane (2ml) was added and the mixture stirred for 14h at room temperature. The solvent was removed under vacuum and the resulting solid was triturated with ether to afford the title compound as a white powder (0.207g). MS (APCI +ve) MW 416/418 (M+H)+ !H NMR (CD3OD) 5 7.69 (1H, s); 7.66 (1H, d); 7.60 (1H, d); 4.86 (2H, s); 3.70-3.50 (8H, m); 3.50-3.35 (2H, m); 1.98 (3H, bs); 1.78 (3H, d); 1.70 (3H, d); 1.62 (6H, bs); 1.50-1.35 (2H,m). Prepared as described in Example 12b using 2-chloro-5-hydroxy-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.155 g, Example 12a), tributylphosphine (0.23 ml), (+/-)-3-hydroxy-l-pyrrolidinecarboxylic acid , 1,1-dimethylethyl ester (0.19 g), l-[[(l-piperidinylcarbonyl)azo]carbonyl]-piperidine (0.24 g) and dry tetrahydrofuran (10 ml) to give the t-butyloxycarbonyl (BOC)-protected compound as a colourless foam. This compound was treated with 4N hydrochloric acid in dioxane (0.5 ml) and methanol (5 ml) to yield the title compound as a colourless solid (0.075 g). MS (APCI+ve) 389/391 (M+H)+ !H NMR (CD3OD) 5 8.42 (1H, bt); 7.42 (1H, d); 7.09-7.03 (2H, m); 5.23 (1H, bm); 3.59-3.41 (4H, m); 3.07 (2H, d); 2.36-2.30 (2H, m); 1.99 (3H, bs); 1.79 (3H, d); 1.70 (3H,d);1.63(6H,d) Prepared as described in Example 12b using 2-chloro-5-hydroxy-N- 3 7 (tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.15 g, Example 12a), tributylphosphine (2 x 0.18 ml), 3-hydroxy-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester (2 x 0.14 g), l-[[(l-piperidinylcarbonyl)azo]carbonyl]-piperidine (2 x 0.18 g) and dry tetrahydrofuran (6 ml) to give the t-butyloxycarbonyl (BOC)-protected compound as a colourless foam. This compound was treated with 4N hydrochloric acid in dioxane (0.25 ml) and memanol (5 ml) to yield the title compound as a colourless foam (0.042 g). MS (APCI+ve) 403/405 (M+H)+ H NMR (CD3OD) 5 8.42 (IH, t); 7.41 (IH, d); 7.14-7.10 (2H, m); 4.82 (IH, bm); 3.51 3.39 (IH, m); 3.38 (2H, m); 3.20-3.17 (IH, m); 3.06 (2H. d); 2.10-2.04 (2H, m); 2.00 (3H, bs); 1.94-1.89 (IH, m); 1.84-1.68 (7H, d); 1.64 (6H, d) Example 21 37 trans-5-[(4-Aminocyclohexyl)oxy]-2-chIoro-N-(tricycIo[3.3.1.1 ' ]dec«l-ylmethyl)- benzamide Prepared as described in Example 12b using 2-chloro-5-hydroxy-N- 3 7 (tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.15 g, Example 12a), tributylphosphine (3 x 0,18 ml), cis- 0.15 g), l-[[(l-piperidinylcarbonyl)azo]carbonyl]-piperidine (3 x 0.18 g) and dry tetrahydrofuran (6 ml) to give the t-butyloxycarbonyl (BOQ-protected compound as a colourless foam. This compound was treated with 4N hydrochloric acid in dioxane (0.5 ml) and methanol (3 ml) to yield the tide compound as a colourless foam (0.080 g). MS (APCI+ve) 417/419 (M+H)+ ^NMR (CD3OD) 8 8.38 (IH, t); 7.34 (IH, d); 6.98 (IH, dd); 6.96 (IH, d); 4.30 (IH, m); 3.17 (IH, m); 3.04 (2H, d); 2.22 (2H, bm); 2.09 (2H, m); 1.98 (3H, bs); 1.77 (3H, d); 1.68 (3H, d); 1.62 (6H, s); 1.55 (4H, m) Example 22 cis-(+/-)-S-[(3-Aminocyclopentyl)oxy]-2-chloro-N-(tricyclo[3.3.1.13' ]dec-l-ylmethyl)- benzamide Prepared as described in Example 12b using 2-chloro-5-hydroxy-N- 3 7 (tricyclo[3.3.1.1 * ]dec-l-ylmethyl)-benzamide (0.20 g, Example 12a), tributylphosphine (0.24 ml), trans-(+/-H3-hydroxycyclopentyl)-carbarnic acid, 1,1-dimethylemyl ester (0.19 g), l-[[(l-piperidinylcarbonyl)azo]carbonyl]-piperidine (0.24 g) and dry tetrahydrofuran (3 ml) to give the t-butytoxycarbonyl (BOC)-protected compound as a colourless foam. This compound was treated with 4N hydrochloric acid in dioxane (0.5 ml) and methanol (5 ml) to yield the title compound as a colourless foam (0.15 g). MS (APCI+ve) 403/405 (M+H)+ lH NMR (CD3OD) 5 7.36 (1H, d); 7.02-6.98 (2H, m); 4.94-4.90 (1H, m); 3.75-3.68 [lH, m); 3.04 (2H, s); 2.55 (1H, m); 2.24-2.17 (1H, m); 2.09-2.03 (2H, m); 1.98-1.86 ;5H, m); 1.76 (3H, d); 1.68 (3H, d); 1.62 (6H, d) Example 23 :S^)-2-Chloro-5-(2^-diazabicyclo[2^.1]hept-2-yl)-N-(tricycIo[33.1.13'7]dec-l-rlmethyO-benzamide, hydrochloride salt 37 a) 5-Bromo-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide Prepared as in Example la from 5-bromo~2-chlorobenzoic acid (7.17g), oxalyl chloride (5.3ml), dichloromethane (150ml), dimethylformamide (0.05ml), diisopropylethylamine (6ml) and adamantylmethylamine (5ml) to give the subtitle compound as white colourless needles (7.3g). MS (APCI-ve) 382/384 (M-H)+ b) (S^)^CbJoro-5-(2^-diazabicyclo[2^.1]hept-2-yl)-N-(tricyclo[3J.l.l3'7]dec-l- ylmethyl)-benzamide, hydrochloride salt 37 A mixture of 5-bromo-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (1.70 g, Example 23a), 2,5-diazabicyclo[2.2.1]heptane-2-carboxylic acid, 1,1-dimethylethyl ester (1.06 g), cesium carbonate (2.20 g), (R)-(+)-2,2'-bis(diphenylphosphino)-l,r- biriaphthyl ((R>(+)-BINAP, 0.20 g), and palladium (ID acetate (0.050 g) in dry toluene (10 ml) was heated at 100°C under nitrogen for 24h. The cooled reaction mixture was filtered, washing the residue with ethyl acetate. The filtrate was washed with water and brine, dried (MgS04) and evaporated under reduced pressure to give an orange oil. The oil was purified by chromatography on silica gel, eluting with 0.5% methanol/dichloromethane to yield the r-butyloxycarbonyl (BOC) protected compound as a colourless foam. The foam was dissolved in methanol (20 ml) and 4N hydrochloric acid in dioxane (2.5 ml) added. The solution was stirred at room temperature until reaction was complete (LCMS). The solution was then evaporated under reduced pressure and the residue triturated with diethyl ether to afford the title compound as an off-white solid (0.92 g). MS (APCI+ve) 400/402 (M-HC1)+ 2H NMR (CD3OD) 8 8.32 (1H, t); 7.30 (1H, d); 6.77-3.70 (2H, m); 4.69 (1H, s); 4.50 (1H, s); 3.73 (1H, dd); 3.67 (2ft s); 3.06 (2H, d); 2.30 (1H, bd); 2.06 (1H, bd); 1.99 (3H, bs); 1.78 (3H, d); 1.70 (3H, d); 1.64 (6H, s); 1.55 (4H, m) Methanol peak masks other H signal. Prepared as described in Example 23 above from 5-btomo-2-chioto-N-(tricyclo[3.3.1.13'7]dec-l-ylmethyl)-benzamide (0.30 g, Example 23a), 3-methyl-l-piperazinecarboxylic acid, 1,1 -dimethylethyl ester (0.20 g), cesium carbonate (0.36 g), (R)-(+)-2,2'-bis(diphenylphosphino)-l,l'-bmaphthyl ((R)-(+)-BINAP,0.036 g), palladium (H) acetate (0.009 g) and dry toluene (10 ml) to yield the t-butyloxycarbonyl (BOC)-protected compound. This compound was treated with 4N hydrochloric acid in dioxane (0.5 ml) and methanol (5 ml) to yield the title compound as a solid (0.025 g). MS (APCI+ve) 402/404 (M-HC1)+ JH NMR (CD3OD) 8 8.40 (1H, t); 7.37 (1H, d); 7.11 (1H, dd); 7.07 (1H, d); 4.00-3.96 (1H, m); 3.43-3.39 (3H, m); 3.28-3.19 (3H, m); 3.06 (2H, d); 1.98 (3H, bs); 1.77 (3H, d); 1.70 (3H, d); 1.63 (6H, s); 1.10 (3H, d). Prepared as described in Example 23 above from 5-bromo-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.30 g, Example 23a), 3-amino-l-pyrrolidinecarboxylic acid, 1,1-dimethyIethyl ester (0.18 g), cesium carbonate (0.36 g), (R)-BINAP (0.036 g), anhydrous toluene (3 ml) and palladium (II) acetate (0.009 g); the mixture was heated for 14h in a pressure vessel flushed with nitrogen. Additional (R)-BINAP (0.036 g) and palladium (H) acetate (0.009 g) were added and heating continued for a further 24h. The cooled reaction mixture was poured into water and extracted witii ethyl acetate three times. The organic fractions were combined and washed with water then brine, and dried (MgSC>4). Evaporation under reduced pressure gave an oil which was purified by normal phase HPLC (0-5% methanol/dichloromethane) to yield the t-butyloxycarbonyl (BOC)- protected compound as a colourless foam. The foam was dissolved in methanol (5 ml) and 4N hydrochloric acid in dioxane (0.5 ml) added. The solution was stirred at room temperature under a nitrogen atmosphere until the reaction was complete as judged by LCMS. Evaporation followed by trituration witli diethyl ether and methanol yielded the title compound as an off-white solid/foam (0.040 g). MS (APCI +ve) 388/390 (M-HCl)-f- lH NMR (CD3OD) 6 8.20 (1H, bt); 7.12 (IE, d); 6.63-6.60 (2H, m); 4.76-4.08 (1H, m): 3.43-3.38 (2H, m); 3.35-3.28 (1H, m); 3.25 (1H, m); 2.94 (2H, s); 2.31-2.22 (1H, m); 2.01-1.94 (1H, m); 1.89 (3H, bs), 1.67 (3H, d); 1.60 (3H, d); 1.53 (6H, s) Example 26 (+/-)-5-(3-Amino-l-piperidinyI)-2-chIoro-N-(tricyclor3.3.1.13'7]dec-l-ylmethyI)- benzamide Prepared as described in Example 23 above from 5-bromo-2-chloro-N- 3 7 ktricycIo(3.3.1.1 ' ]dec-l-ylmetfiyl)-benzamide (0.20 g, Example 23a), 3-piperidinyl- carbamic acid, 1,1-dimethylethyl ester (0.12 g), cesium carbonate (0.24 g), (R)-(+)-2,2'- bis(diphenylphosphino)-l,r-binaphthyl ((R)-(+)-BINAP, 0.024 g), palladium (II) acetate (0.006 g) and dry toluene (3 ml) to yield the t-butoxycarbonyl (BOC)-protected compound. The t-butoxycarbonyl (BOC)-protected compound was dissolved in methanol (5 ml) and hydrochloric acid (0.5 ml of a 4N solution in dioxane). After stirring at room temperature for 24h the mixture was evaporated and the residue partitioned between ethyl acetate and saturated sodium bicarbonate. The layers were separated and the aqueous phase acidified with 2M hydrochloric acid and extracted with ethyl acetate. The organic phase was dried over magnesium sulfate and then evaporated under reduced pressure to give a gum. Purification by chormatography on silica gel, eluting with 4-10% methanol in dichloromethane/aqueous ammonia afforded the title compound as a solid (0.036 g). MS (APCI+ve) 402/404 (M+H)+ H NMR (CD3OD) 5 7.25 (1H, d); 7.00 (1H, dd); 6.96 (1H, d); 3.59 (1H, dd); 3.48-3.45 (1H, m); 3.04 (2H, d); 2.91-2.85 (1H, m); 2.82-2.75 (1H, m); 2.58 (1HT dd); 1.98-1.93 (4H, m); 1.85-1.75 (3H, d); 1.70-1.62 (10H, d); 1.34-1.25 (1H, d). Prepared as described in Example 23 above from 5-bromo-2-chloro-N-(tricyclo[3.3.1.13,7]dec-l-yImethyl)-benzamide (0.30 g, Example 23a), 3-amino-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.19 g), cesium carbonate (0.36 g), (R)-(+)-2^'-bis(diphenylphosphino)-l,l'-binaphthyl ((R)-(+)-BINAP, 0.036 g), palladium (II) acetate (0.008 g) and dry toluene (3 ml) to yield the t-butyloxycarbonyl (BOC)-protected compound. This compound was treated with methanol (5 ml) and hydrochloric acid (0.5 ml of a 4 M solution in dioxane) followed by an acid/base work-up. Purification by chromatography on silica gel, eluting with 4-10% methanol in dichloromethane/aqueous ammonia afforded the title compound as a solid (0.008 g). MS (APCI+ve) 402/404 (M+H)+ ]H NMR (CD3OD) 8 7.14 (1H, d); 6.68-6.65 (2H, m); 3.47-3.40 (1H, m); 3.25 (1H, m); 3.05-3.02 (3H, m); 2.72-2.65 (1H, m); 2.52-2.47 (1H, m); 2.08-2.04 (1H, m); 1.97 (3H, bs); 1.89-1.82 (1H, m); 1.77 (3H, d); 1.70-1.62 (10H, d); 1.50-1.40 (1H, m). Prepared as described in Example 23 above from 5-bromo-2-chloro-N- 3 7 (tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.15 g, Example 23a), hexahydro- pvrrolo[3,4-c]pyrrole-2(lH)-carboxylic acid, 1,1-dimethylethyl ester (0.17 g), cesium carbonate (0.33 g), (R)-(+)-2,2'-bis(diphenylphosphino)-l,r-binaphthyl ((R)-(+)-BINAP, 0.018 g), palladium (II) acetate (0.004 g) and dry toluene (2 ml) to yield the t- butyloxycarbonyl (BOC)-protected compound. This compound was treated with methanol (5 ml) and hydrochloric acid (0.5 ml of a 4 M solution in dioxane) followed by an acid/base work-up. Trituration of the residue with dichloromethane afforded the title compound as a solid (0.020 g). MS (APCI+ve) 414/4I6(M+H)+ 'HNMR(CD3OD) 5 8.17 (IH, t); 7.20 (IH, d); 6.63 (IH, dd); 6.54 (IH, d); 3.36 (2H, m); 3.02 (2H, dd); 2.95-2.90 (4H, m); 2.80 (2H, m); 2.60 (2H, dd)); 1.94 (3H, bs); 1.67 (3H, d); 1.59 (3H,d); 1.52 (6H,d). Prepared as described in Example 12b using N-(5-hydroxy-2-methylphenyl)-tricyclo[3.3.1.13'7]decane-I-acetamide (0.51 g, Example 12, WO 99/29660), tributylphosphine (0.64 ml), l-[[(l-piperidinylcarbonyl)azo]carbonyl]-piperidine (0.65 g), 4-hydroxy-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.52 g) and dry tetrahydrofuran (10 ml) to give the t-butyloxycarbonyi (BOC) protected compound as a colourless solid. This compound was treated with 4N hydrochloric acid in dioxane (0.5 ml) and methanol (5 ml) to yield the title compound as a colourless solid (0.13 g). MS (APCI+ve) 383 (M-HCD+ H NMR (CD3OD) 5 7.19 (IH, d); 7.12 (IH, d); 6.83 (IH, dd); 4.71-4.$6 (IH, m); 3.46-3.40 (2H, m); 3.28-3.22 (2H, m); 2.25 (3H, s); 2.21 (IH, s); 2.21-2.14 (2H, m); 2.11-2.04 (5H,m); 1.84-1.73 (12H,m). Prepared as described in Example 12b using N-(2-chloro-5-hydroxyphenyI)-tricyclo[3.3.1.13,7]decane-l-acetamide (0.25 g, Example 28, WO 99/29660), tributylphosphine (0.29 ml), l-[[(l-piperidinylcarbonyl)azo]carbonyl]-piperidine (0.30 g), 4-hydroxy-l-piperidinecarboxylic acid, 1,1-dimethylethyi ester (0.24 g) and dry tetrahydroruran (10 ml) to give the t-butyloxycarbonyl (BOC) protected compound as a colourless solid. This compound was treated with 4N hydrochloric acid in dioxane (1 ml) and methanol (20 ml) to yield the title compound as a colourless solid (0.08 g). MS (APd+ve) 375/377 (M-HC1)+ !HNMR (CD3OD) 8 7.55 (1H, d); 7.41 (1H, d); 6.88 (1H, dd); 4.76-4.70 (1H, m); 3.48-3.39 (2H, m); 3.30-3.22 (2H, m); 2.25 (2H, s); 2.22-2.16 (2H, m); 2.14-2.03 (2H, m); 1.84-1.72 (12am). 3 7 a) 2-Chloro-5-formyl-N-(tricyclo[33.1.1 ' ] dec-l-ylmethyl)-benzamide 3 7 A solution of 5-bromo-2-chloro-N-(tricyclo[3.3.1.1' ]dec-l -ylmethyl)-benzamide (3.25 g, Example 23a) in anhydrous tetrahydrofuran (150 ml) was cooled to -78°C under a nitrogen atmosphere. A solution of methyllithium (1.4M in diethyl ether, 6.1 ml) was added over 2min. The mixture was stirred at -78°C for lOmin, then a solution tert-butyllithium (1.7M in pentane, 10.0 ml) was added dropwise. The mixture was stirred at -78°C for a further lOmin, then dimethylformamide (1.0 ml) was added. The resulting solution was stirred at -78°C for 30min., quenched with saturated aqueous ammonium chloride solution (100 ml) and extracted with ethyl acetate. The combined extracts were dried over anhydrous magnesium sulfate, filtered, and the filtrate concentrated under reduced pressure to give the subtitle compound as a solid (2.76 g). MS (APCI +vc) 332 (M+H)+ !HNMR (DMSO-d6) 8 10.04 (1H, s); 8,49 (1H, t); 7.96-7.91 (2H, m); 7.74 (1H, d); 2.96 (2H, d), 1.95 (3H, s); 1.64 (6H, AB); 1.53 (6H, d). b) 4-[4-CWoro-3-[(tricycIo[3J.l.l3'7]dec-l-ylmethyI)amino]carbonyl] phenyI]methyl]ainrao]-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester 2-Chloro-5-formyl-N-(tricyclo [3.3.1.13'7] dec-l-ylmethyl)-benzamide (0.270 g, Example 31a) and 3-amino-l-pyrrolidinecarboxylic acid, 1,1-dimethylethyl ester (0.325 g, Journal of Medicinal Chemistry, 1998,41(22), 4273-4278) were dissolved in 1,2-dichloroethane (30 ml), under a nitrogen atmosphere. Sodium triacetoxyborohydride (0.24 g) was added and the mixture was stirred for 14h at room temperature. Water and dichloromethane were added and the layers were partitioned. The organic extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by HPLC eluting with a gradient of 0-10% of ethanol in dichloromethane, then by chromatography over silica gel eluting with ethyl acetate : iso-hexane (1:1) then ethyl acetate : ethanol (98:2) to give the subtitle compound as a colourless oil (0.158 g). MS (APCI +ve) 516 (M+H)+ c) 2-Chloro-5-[(4-piperidinylamino)methyl]-N-(tricyclo[3J.l.l3'7]dec-l-ylmethyl)- benzamide, dihydrochioride salt 3 7 Prepared from 4-[[[4-chloro-3-[[(tricyclo[3.3.1.1 ' ]dec-l-ylmethyI)amino]carbonyl] phenyl]methyl]amino]-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.158 g, Example 31b) methanol (3 ml) and 4N hydrochloric acid solution in dioxane (2 ml). Solvents were removed under reduced pressure and the residue was triturated with ethyl acetate, iso-hexane and diethyl ether to give the title compound as a white solid (0.126 g). MS (APCI +ve) 416 (M+H-2HC1H !HNMR (CD3OD) 5 8.47 (1H, t); 7.62-7.56 (3H, m), 4.33 (2H, s); 3.58-3.55 (3H, m); 3.12 (2H, t); 3.07 (2H, d); 2,44 (2H, d); 2.03-1.92 (5H, m); 1.73 (6H, q); 1.63 (6H, d). a) [[4-[[[4-Chloro-3-[[(tricyclo[3J.l.l3'7]dec-l-ylmethyl)amino]carhonyl] phenyJ]methyl]amino]cyclohexyl]methyI]-carbamic acid, 1,1-dimelhyiethyi ester Prepared according to the method described in Example 3 lb from 2-chloro-5-formyi-N-(tricyclo [3.3.1.13,7] dec-l-ylmethyl)-benzamide (0.30 g, Example 31a), [(4-aminocyclohexyl)methyI]-carbamic acid, 1,1-dimethylethyI ester (0.207 g, WO 97/32882), sodium triacetoxyborohydride (0.135 g) and 1,2-dichloroemane (10 ml). The residue was purified by chromatography over silica gel eluting with ethyl acetate : iso-hexane (1:1) then ethyl acetate : ethanol (9:1) to give the subtitle compound as a colourless oil (0.26 g). MS (APCI +ve) 544 (M+H)+ b) 5-[[[4-(Aminomethyl)cyclohexyl]aniino3methyI]-2-chloro-N- 37 (tricyclo[33.1.1 ' ]dec-l-ylmethyl)-benzamide, dihydrochloride salt Prepared from [[4-[[[4-chloro-3-[[(tricyclo[3.3.1.13'7]dec-1 - ylmethyl)amino]carbonyl] phenyl]methyl]amino]cyclohexyl]methyl]-carbamic acid, 1,1- dimethylethyl ester (0.26 g, Example 32a) methanol (5 ml) and 4N hydrochloric acid solution in dioxane (2 ml). Solvents were removed under reduced pressure and the residue was triturated widi diethyl ether to give the title compound as a white powder (0.191 g). MS (APCI +ve) 444 (M+H-2HC1)+ H NMR (CD3OD) 8 7.60-7.58 (3H, m), 4.29 (2H, s); 3.28-3.12 (1H, m); 3.09 (2H, s); 2.84 (2H, d); 2.31 (2H, bd); 2.00 (5H, bs); 1.75 (6H, q); 1.65 (6H, d); 1.71-1.65 (1H, m); 1.63-1.44 (2H, m); 1.31-1.12 (2H, m). Example 33 3 7 5-[[(4-Aminocyclohexy0amino]niethyl]-2-chloro-N-(tricydo[3.3.1.1 ' ]dec-l- ylmethyl)-benzamide, dihydrochloride salt a) [4-[[[4-chloro-3-[[(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)amino]carbonyi]phenyl]- methyI]amino]cycIohexyI]-carbamic acid, 1,1-dimethylethyI ester Prepared according to the method described in Example 3 lb from 2-chloro-5-formyl-N-(tncyclo [3.3.l.l3'7] dec-l-ylmethyl)-benzamide (0.30 g, Example 31a), (4-aminocyclohexyl)-carbamic acid, 1,1-dimethylethyl ester (0.194 g, Journal of Organic Chemistry, 1996, 61(25), 8811-8818), sodium triacetoxyborohydride (0.135 g) and 1,2-dichloroethane (10 ml). The residue was purified by chromatography over silica gel eluting with ethyl acetate: iso-hexane (1:1) then ethyl acetate : ethanol (95:5) to give the subtitle compound as a colourless oil (0.24 g). MS (APCI+ve) 530 (M+H)+ 37 b) 5-[[(4-Aminocyclohexyl)amino]methyl]-2-chloro-N-(tricyclo[3-3.1.1 ' ]dec-l- ylmethyl)-benzamide, dihydrochloride salt Prepared from [4-{[[4-chloro-3-[[(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)amino]carbonyl]phenyl] methyl]amino]cyclohexyl]-carbamic acid, 1,1-dimethylethyl ester (0.26 g, Example 33a), methanol (5 ml) and 4N hydrochloric acid solution in dioxane (1 ml). Solvents were removed under reduced pressure and the residue was triturated with diethyl ether to give the title compound as a white powder (0.190 g). MS {APCI +ve) 430 (M+H-2HC1)+ HNMR (CD3OD) 5 7.61-7.59 (3H, m), 4.30 (2H, s); 3.28-3.11 (2H, m); 3.08 (2H, s); 2.40-2J32 (2H, m); 2.21-2.17 (2H, m); 2.00 (3H, s); 1.74 (6H, q); 1.64 (6H, d); 1.63-1.48 (4am). Example 34 5-[(l-Azabicyclo[2.2.2]oct-3-yIamino)methyI]-2-chloro-N-(tricycIof3.3.1.13'7]dec-l-ylmethyO-benzamide Prepared according to the method described in Example 31b from 2-chloro-5-formyl-V-(tricyclo [3.3.1.l3,7]dec-l-ylmethyl)-benzamide (0.30 g, Example 3 la), l-azabicyclo[2.2.2]octan-3-amine dihydrochloride salt (0.18 g), sodium riacetoxyborohydride (0.135 g) and 1,2-dichloroethane (10 ml). The residue was purified >y chromatography over silica gel eluting with ethyl acetate : iso-hexane (1:1) followed by sthyl acetate: ethanol (95:5). Repurification by chromatography over silica gel eluting vith dichloromethane : methanol (95:5) then (9:1) gave the title compound as a white gum 0.013 g). rfS (APCI +ve) 442 (M+H)+ H NMR (CDC13) 5 7.68 (1H, d); 7.39 (1H, d); 7.31 (1H, dd); 6.41 (1H, t); 3.75 (2H, s); 5.42-3.31 (2H, ra); 3.25-3.09 (6H, m); 2.94 (1H, d); 2.38-2.23 (2H, m); 2.22-2.14 (1H, m); L01 (3H, s); 1.92-1.83 (2H, m); 1.69 (6H, q); 1.59 (6H, d). Example 35 H4^3-AjninopyiToUdin-l-yl)-2-methylphenyl]-2-(tricyclo[3^.1.13,7]dec-l-rl)acetamide, dihydrochloride salt a) [l-(3-Methyl-4-nitrophenyl)-pyrroIidin-3-yl]-carbamic acid tert-butyl ester 4-Fluoro-2-methyl-l-nitrobenzene (1 g), pyrrolidin-3-ylcarbamic acid tert-butyl ester (1.2 g), potassium carbonate (1.79 g) and dimethyl sulfoxide (10 ml) were heated together at 80°C under nitrogen for 15h. The mixture was then cooled, diluted with ethyl acetate (200 ml), washed with 2N aqueous hydrochloric acid (200 ml), dried (MgSC>4) then concentrated. Purification of the residue by silica gel chromatography (eluting with 20% ethyl acetate in isohexane) gave the subtitle compound (1.744 g). XH NMR (DMSO-d6) 5 8.03 - 8.00 (1H, d), 7.28 -7.21 (1H, br d), 6.51 - 6.47 (2H, m), 4.20 - 4.12 (1H, br m), 3.61 - 3.16 (4H, m), 2.56 (3H, s), 2.20 - 2.08 (1H, m), 1.98 -1.85 (lH,m), 1.39(9H,s). b) [l-(4-Amino-3-methylphenyl)-pyrTolidin-3-yI]-carbamic acid tert-butyl ester [l-(3-Methyl-4-nitrophenyl)-pyrroIidin-3-yl]-carbamic acid tert-butyl ester (1.744 g, Example 35a), iron powder (1.52 g), ammonium chloride (1.45 g), ethanol (50 ml) and water (50 ml) were refluxed together under nitrogen for 2h. The mixture was cooled and the iron was filtered off. Water (200 ml) was added to the residue and the product extracted into ethyl acetate (3 x 200 ml), dried (MgSC>4), and concentrated to give the subtitle compound (1.56 g). H NMR (CDC13) 6.65 (1H, br s), 6.38 (2H, br m), 4.80 (1H, m), 4.33 (2H, br m), 3.60 2.80 (5H, m), 2.31 - 2.17 (4ft m), 1.92 - 1.82 (1H, m), 1.45 (9H, br s).- c) {l-[4-(2-(tricycIo[3.3.1.1 '7]dec-l-yI)acetyiamino)-3-methylphenyI]-pyrroIidin-3- yl}-carbamic acid tert-butyl ester To a solution of adamantan-1-yl-acetic acid (0.46g) in dichloromethane (10ml) at 0°C was added dimethylformamide (0.1ml) followed by oxalyl chloride (2.50 ml). The reaction was allowed to warm to room temperature and stirred for 30min.. The volatiles were removed under vacuum and the residue dried under high vacuum. The residue was dissolved in dichloromethane (10ml) and added to a solution of [l-(4-amino-3-methylphenyl)-pyrrolidin-3-yl]-carbamic acid tert-butyl ester (0.70g, Example 35b) in dichloromethane (10ml) and triethylamine (0.8 ml) at 0°C. The reaction was allowed to warm to room temperature and stirred for 3h. The solution was washed with 2N aqueous hydrochloric acid (20ml), then brine (20 ml) and the organic layer dried over magnesium sulfate then filtered. The filtrate was concentrated under reduced pressure. The crude material was purified by silica gel chromatography (eluting with 1% methanol in dichloromethane) to yield the subtitle compound(l. lg). MS (APCI +ve) MW 468 (M+H)+ H NMR (DMSO-d6) 5 8.86 (IH, s); 7.01 - 6.98 (IH, d); 7.18 - 7.14 (IH, br d); 6.33 - 6.27 (3H, m); 4.15 - 4.04 (IH, m); 3.42 - 3.15 (3H, m); 3.00 - 2.97 (IH, m); 2.12 (3H, s); 2.00 (2H, s); 1.99 - 1.80 (5H, m); 1.70 -1.61 (12H, m); 1.39 (9H, s). d) N44-(3-AniinopyrroUdiii-l-yl)-2-methylphenyl]-2.(tricyclot3^.1.13i7]dec-l- yOacetamide, dihydrochloride salt 37 {l-[4-(2-(tricycIo[3.3 • I • 1 ' Jdec-1 -yI)acetyIamino)-3-methylphenyI]-pyrroIidin-3- yl}-carbamic acid tert-butyl ester (0.20 g, Example 35c) was dissolved in methanol (5 ml) and hydrochloric acid (0.5ml of a 4N solution in dioxane) was added. After stirring at room temperature for 14h, me mixture was evaporated to 2/3 original volume under reduced pressure. Diethyl ether was gradually added to me solution and the resulting precipitate collected by filtration, washed with diethyl ether and dried in vacuo to afford the title compound as a solid (0.15 g) MS (APCI +ve) 368 (M+H)+ !HNMR (DMS0-d6) 5 8.92 (1H, s); 8.21 (2H,br s); 7.07 - 7.04 (1H, d); 6.41 - 6.35 (2H, m); 3.91 (1H, br m); 3.50 - 3.39 (2H, m); 3.29 - 3.20 (2H, m); 2.37 - 2.27 (2H, m); 2.14 (3H, s); 2.02 (2H, s); 1.94 (3H, s); 1.70 - 1.58 (12H, m). a) 4-(3-MethyI-4-nitrophenyI)piperazine-l-carboxyIic acid tert-butyl ester 4-FIuoro-2-methyl-l -nitrobenzene (2 g), piperazine-1-carboxyiic acid tert-butyl ester (4.8 g), potassium carbonate (3.57 g) and dimethyl sulfoxide (20 ml) were heated together at 80 °C under nitrogen for 15h. The mixture was then cooled, diluted with ethyl acetate (200 ml), washed with 2N aqueous hydrochloric acid (200 ml), dried (MgSO,), and concentrated to give the subtitle compound (4.10g). MS (APCI+ve) 321 (M)+ H NMR (DMSO-d6) 5 8.02 - 7.98 (1H, d), 6.89 - 6.86 (2H, m), 3.45 (8H, s), 2.55 (3H, s), 1.42 (9H,s). b) 4-(4-Amino-3-methylphenyl)piperazine-l-carboxylic acid tert-butyl ester 4-(3-Memyl-4-nitrophenyl)piperazine-l-carboxylic acid tert-butyl ester (2 g, Example 36a), iron powder (1.74 g), ammonium chloride (1.67 g), ethanol (50 ml) and water (50 ml) were refluxed together under nitrogen for 2h. The mixture was cooled and the iron was filtered off. Water (200 mi) was added to the residue and the product xtracted into ethyl acetate (3 x 200 ml), dried (MgSO,), and concentrated to give the abtide compound (1.22 g). H NMR (DMSO-d6) 5 6.62 - 6.52 (3H, m), 4.38 (2H, s), 3.41 (4H, br s), 2.83 (4H, br s), .02 (3H, s), 1.41 (9H,s). 37 I 4-[4- irboxylic acid tert-butyl ester To a solution of adamantan-1-yl-acetic acid (0.40g) in dichloromethane (10ml) at 'C was added dimethylformamide (0.1ml) followed by oxalyl chloride (2.00 ml). The action was allowed to warm to room temperature and stirred for 30min.. The volatiles ere removed under vacuum and the residue dried under high vacuum. The residue was ssolved in dichloromethane (10ml) and added to a solution of 4-(4-amino-3-ethylphenyl)piperazine-l-caroxylic acid tert-butyl ester (0.60g, Example 36b) in chloromethane (10ml) and triethylamine (0.7 ml) at 0°C. The reaction was allowed to arm to room temperature and stirred for 3h. The solution was washed witii 2N aqueous fdrochloric acid (20ml), then brine (20 ml) and the organic layer dried over magnesium tlfate'then filtered. The filtrate was concentrated under reduced pressure. The crude aterial was was purified by silica gel chromatography (eluting with 1% methanol in chloromethane) to yield the subtitle compound(0.42g). S (APC1 +ve) MW 468 (M+H)+ INMR (DMSO-d6) 8 8.96 (1H, s); 7.14 - 7.11 (1H, d); 6.79 - 6.72 (2H, m); 3.47 - 3.40 H, m); 3.20 - 3.00 (4H, m); 2.14 (3H, s); 2.03 (2H, s); 1.94 (3H, br s); 1.70 -1.56 2H,m);1.42(9H,s). i N-(2-MethyM-piperazin-l-ylphenyl)-2-(tricyclo[3.3.1.1 ]dec-l-yl)acetamide, hydrochloride salt 3 7 4-[4-(2-(tricycIo[3.3.1.1' Jdec-1 -yi)acety{amino)-3-methyIphenyiJ-piperazine-1 - rboxylic acid tert-butyl ester (0.05 g, Example 36c) was dissolved in methanol (2 ml) and hydrochloric acid (0.5ml of a 4N solution in dioxane) was added. After stirring at room temperature for 14h, the mixture was evaporated to 2/3 original volume under reduced pressure. Diethyl ether was gradually added to the solution and the resulting precipitate collected by filtration, washed with diethyl ether and dried in vacuo to afford the title compound as a solid (0.043 g) MS (APCI +ve) 368 (M+H)+ lKNMR (DMSO-d6) 5 9.01 (3H, brs); 7.18 - 7.15 (IH, d); 6.84 - 6.82 (IH, d); 6.79 - 6.76 (IH, dd); 3.31 - 3.29 (4H, m); 3.28 - 3.16 (4H, m); 2.16 (3H, s); 2.04 (2H, s); 1.94 (3H, br s); 1.69-1.58 (12H,m). 3 7 a) 2-Chloro-4-hydroxy-N-(tricyclo[33.1.1 ' ]dec-l-ylmethyl)-benzamide To a solution of 2-chloro-4-hydroxybenzoic acid (3.30 g) in dimetiiylformamide (20 ml) was added l,r-carbonyldiimidazole (3.30 g). The reaction mixture was stirred for 2.5h and men I-adamantanemediylamine (3.4 ml) was added. After 14h the reaction mixture was partitioned between ethyl acetate and 2N aqueous hydrochloric acid and the organic layer was separated, washed with water then brine and dried (MgSO,). The organic layer was concentrated under reduced pressure to give a residue which was purified by silica gel chromatography (eluting with 10 - 70% ethyl acetate in dichloromethane) to yield a wnite solid wnicn was inmraied witn emyi acetate to yieia tne suotitie compound as a white solid (3.6 g). MS (APCI +ve) 320/322 (M+H)+ H NMR (DMSO-d6) 5 10.12 (1H, s), 8.10 - 8.06 (1H, t), 7.27 - 7.24 (1H, d), 6.81 (1H, d), 6.77 - 6.73 (1H, dd), 2.91 - 2.88 (2H,d), 1.93 (3H, br s), 1.69 -1.56 (6H, br q), 1.50 (6H, br s). 3 7 b) cis-4-(3-Amino-cyclopentyloxy)-2-chloro-N-(tricycIo[3.3.1.1 ' ]dec-l-ylmethyl)- benzamide, hydrochloride salt 3 7 To a solution of 2-chloro-4-hydroxy-N-(tricyclo[3.3.1.1 ' ]dec-1 -ylmethyl)- benzamide (0.20 g, Example 37a), rro7W-(3-hydroxycyclopentyl)-carbamic acid, tert-butyl ester (0.19 g) and tributylphospbirie (0.23 ml) in dry tetrahydrofuran (6 ml) was added l-[[(l-piperidinylcarbonyl)azo]carbonyl]-piperidine (0.24 g). The orange solution was heated at 60°C under a nitrogen atmosphere for 2h. Additional trans- (3-hydroxycyclopentyl)-carbamic acid, terf-butyl ester (0.19 g), tnbutylphosphine (0.23 ml) and l-[[(l-piperidinylcarbonyl)azo]carbonyl]- piperidine (0.24 g) were added. Heating was continued and the process described above repeated until reaction was judged complete as judged by LC/MS. The cooled reaction mixture was diluted with diethyl ether then filtered. The filtrate was concentrated and purified by chromatography on silica gel (25 - 33% ethyl acetate/ hexane) to give the t-butyloxycarbonyl (BOC)-protected compound as a colourless foam. The foam was dissolved in methanol (5 ml) and 4N hydrochloric acid in dioxane (0.25 ml) added. The solution was stirred at room temperature under a nitrogen atmosphere until the reaction was complete as judged by LC/MS. Evaporation of solvent followed by trituration with diethyl ether gave the title compound as a colourless solid (0.24 g). MS (APCI+ve) 403/405 (M+H)+ H NMR (DMS0-d6) 5 8.18 (1H, t); 7.96 (2H, br s); 7.37 - 7.34 (IH, d); 7.05 (1H, m); 6.97 - 6.94 (IH, m); 4.87 (IH, br m); 3.72 - 3.40 (2H, m); 2.93 - 2.90 (2H, d); 2.04 -1.51 (19H, m); 1.22 (2H, m). 3 7 To a solution of 2-chloro-4-hydroxy-N-(tricyclo[3.3.1.1 ' ]dec-l-methyl)-benzamide (0.20 gf Example 37a), 4-hydroxy-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.19 g) and tributylphosphine (0.25 ml) in dry tetrahydrofuran (6 ml) was added 1-[[(1- piperidinylcarbonyl)azo]carbonyI]-piperidine (0.24 g). The orange solution was heated at 50°C under a nitrogen atmosphere for 2h. Additional 4-hydroxy-l-piperidinecarboxylic acid, U-dimethylethyl ester (0.19 g), tributylphosphine (0.25 ml) and 1-[[(1- piperidinylcarbonyl)azo]carbonyl]-piperidine (0.24 g) were added. Heating was continued and the process described above repeated until reaction was complete as judged by LC/MS. The cooled reaction mixture was diluted with diethyl ether then filtered. The filtrate was concentrated and purified by chromatography on silica gel (3:1 iso-hexane/ethyl acetate) to give the the t-butyloxycarbonyl (BOC)-protected compound as a colourless foam. The foam was dissolved in methanol (10 ml) and 4N hydrochloric acid in dioxane (10 ml) added. The solution was stirred at room temperature under a nitrogen atmosphere until the reaction was complete as judged by LC/MS. Evaporation of solvent followed by trituration with diethyl ether gave the title compound as a colourless solid (0.165 g). MS (APCI +ve) 403 (M+H)+ !HNMR (DMSO-d6) 5 8.80 (2H, bs); 8.21-8.16 (IH, t); 7.37-7.34 (IH, d); 7.16 (IH, m); 7.03-6.99 (IH, m); 4.80-4.68 (IH, m); 3.25-3.18 (2H, m); 3.17-3.01 (2H, m); 2.93-2.90 (2H, d); 2.17-2.02 (2H, m); 1.93 (3H, bs); 1.87-1.73 (2H, m); 1.69-1.57 (6H, AB); 1.51 (6H, s) Prepared as described in Example 38 from 2-chloro-4-hydroxy-N-(tricyclo[3.3.1.l3,7]dec-l-methyJ)-benzamide (0.20 g, Example 37a), (+/-)-3-hydroxy-l-pyrrolidraecarboxylic acid, 1,1-dimethylethyl ester (0.18 g), tributylphosphine (0.25 ml), dry tetrahydrofuran (6 ml) and l-[[(l-piperidinylcarbonyl)azo]carbonyl]- piperidine (0.24 g) to obtain the the t-butyloxycarbonyl (BOC)-protected compound. This compound was treated with 4N hydrochloric acid in dioxane (10 ml) and methanol (10 ml) to yield the title compound as colouless solid (0.165 g). MS (APCI +ve) 389 (M+H)+ hiNMR (DMSO-dfi) 5 8.19-8.15 (IH, t); 7.35-7.32 (IH, d); 6.99 (IH, m); 6.93-6.90 (IH, m); 4.94-4.89 (IH, m); 3.24 (IH, s); 3.08-3.02 (IH, dd); 2.92-2.90 (2H, d); 2.88-2.72 (3H, m); 2.08-1.98 (IH, m); 1.93 (3H. s); 1.76-1.57 (7H, m); 1.51 (6H, s). 3 7 To a solution of 2-chloro4-hydroxy-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)- benzamide (0.20 g, Example 37a), 3-hydroxy-piperidine-l-carboxylic acid, rm-butyl ester (0.189 g) and tributylphosphine (0.23 ml) in dry tetrahydrofuran (6 ml) was added 1-[[(1- piperidinylcarbonyl)azo]carbonyl]-piperidine (0.24 g). The orange solution was heated at 60°C under a nitrogen atmosphere for 2h. Additional 3-hydroxy-piperidine-l-carboxylic acid, tert-butyl ester (0.19 g), tributylphosphine (0.23 ml) and 1-[[(1- piperidinylcarbonyl)azo]carbonyl]- piperidine (0.24 g) were added. Heating was continued and the process described above repeated until reaction was complete as judged by LC/MS. The cooled reaction mixture was diluted with diethyl ether then filtered. The filtrate was concentrated and purified by chromatography on silica gel (25% ethyl acetate : wo-hexane) followed by normal phase HPLC (0-1% ethanol in dichloromethane) to give me t- butyloxycarbonyl (BOC)-protected compound as a colourless foam. The foam was dissolved in methanol (5 ml) and 4N hydrochloric acid in dioxane (0.25 ml) added. The solution was stirred at room temperature under a nitrogen atmosphere until the reaction was complete as judged by LC/MS. Evaporation of solvent followed by trituration with diethyl ether gave the title compound as a colourless solid (0.006 g). MS (APCI +ve) 403/405 (M+H)+ JH NMR (DMS0-d6) 5 8.84 (2H, br s), 8.21 (1H, t); 7.38 (1H, d); 7.18 (1H, s); 7.05 (1H, dd); 4.82 (1H, br s); 3.24 (1H, d); 3.20 (1H, dd); 3.06 (2H, br s); 2.92 (2H, d); 1.94 ■ 1.51(19H,m). 3 7 a) 4-Bromo-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide To a suspension of 4-bromo-2-chlorobenzoic acid (5.00 g) in dichloromethane (25 ml) at 0°C was added oxalyl chloride (3.7 ml) and dimethylformamide (5 drops). The resulting mixture was stirred at room temperature under a nitrogen atmosphere for 1 hour, then concentrated under reduced pressure to yield a solid. The solid was dissolved in dichloromemane (20 ml) and added dropwise to a solution of 1-adamantanemethylamine (3.36g) and N^-diisopropylethylamine (5.55 ml) in dichloromethane (20 ml). The resulting solution was allowed to stir at room temperature under a nitrogen atmosphere for 20h. The reaction mixture was diluted with dichloromethane and washed with water, 10% aqueous potassium carbonate, 10% aqueous potassium hydrogen sulfate and saturated brine. The organic phase was then dried over sodium sulfate, filtered and concentrated under reduced pressure to afford the subtitle compound as a solid (4.28 g). vlS (APCI +ve) 382/384 (M+H)+ H NMR (DMS0-d6) 5 8.39-8.34 (1H, t); 7.78 (1H, m); 7.62-7.59 (1H, m); 7.37-7.34 1H, d), 2.94-2.92 (2H, d); 1.94 (3H, br s); 1.69-1.57 (6H, br AB); 1.52 (6H, s). ' 37 ») 2-Chloro-4-(4-piperazin-l-yI)-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzaniide, lydrocbioride salt 3 7 To a suspension of the 4-bromo-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l -ylmethyl)-enzamide (Example 43a, 0.30 g), piperazine-1-carboxylic acid, 1,1-dimethylethyl ester 0.18 g), cesium carbonate (0.36 g) and (R)-BINAP (0.036 g) in anhydrous toluene (3 ml) /as added palladium (II) acetate (0.009 g) and the mixture heated at 100 °C for 14h in a ressure vessel flushed with nitrogen. The cooled reaction mixture was evaporated under :duced pressure to give an oil which was purified by chromatography on silica gel (2:1 / ro-hexane : ethyl acetate) to give the t-butyloxycarbonyl (BOC)- protected compound as a olourless foam. The foam was dissolved in methanol (15 ml) and 4N hydrochloric acid in ioxane (15 ml) added. The solution was stirred at room temperature under a nitrogen tmosphere until the reaction was complete as judged by LCMS. Evaporation followed by ituration with diethyl ether and methanol yielded the title compound as an off-white jlid/foam (0.161 g). IS (APCI +ve) 388/390 (M+H)+ H NMR (DMSO-d6) 8 8.98 (2H, bs); 8.11-8.07 (1H, t); 7.33-7.31 (1H, d); 7.05 (1H, m); .99-6.95 (ia m); 3.46-3.43 (4H, m); 3.20 (4H, bs); 1.94 (3H, bs); 1.69-1.57 (6H, b AB); .51(6H,bs). xample 42 3 7 -Chloro-4-(3-pyiTolidinylaniino)-N-(tricyclo(3.3.1.1 ' ]dec-l-ylmethyl)-benzamide, ydrochloride salt Prepared according to the method described in Example 41b from 4-bromo-2-chloro-N-(tricyclo[3.3.1.13'7]dec-1 -ylmethyl)-benzamide (0.25 g, Example 41 a), 3-amino-1 -pyrrolidinecarboxylic acid, 1,1 -dimethylemyl ester (0.182 g, Journal of Medicinal Chemistry, 1998,41 (22), 4273-4278), cesium carbonate (0.347 g), (R)-(+)-2,2'-bis(diphenylphosphino)-l,l'-binaphthyl (0.036 g), palladium (H) acetate (0.009 g) and anhydrous toluene (3 ml). The residue was purified by HPLC eluting with a gradient of 0-5% ethanol in dichloromethane. The product was dissolved in methanol and stirred at room temperature for 3h in the presence of 4N hydrochloric acid solution in dioxane (2 ml). The solution was concentrated under reduced pressure and triturated with diethyl, ether to give me title compound as a white powder (0.057 g). MS (APCI +ye) 388 (M+H-HC1)+ H NMR (CD3OD) 5 7.33 (IH, d); 6.71 (IH, d); 6.63 (IH, dd); 4.27-4.21 (IH, m); 3.57-3.40 (3H, m); 3.23 (IH, dd); 3.05 (2H, s); 2.43-2.33 (IH, m); 2.33-2.01 (IH, m); 1.99 (3H, bs); 1.73 (6H,q); 1.62 (6H,d). Example 43 2-Oaoro^-(hexahydro-lH4,4^iazepm-l-yI)-N-(tricycio[3J.l.l3'7]dec-l-ylmethyl)-benzamide, hydrochloride salt Prepared according to the method described in Example 41b from 4-bromo-2-chloro-N-(tricyclo[3.3.1.I3'7]dec-I-yImethyl)-benzamide (0.25 g, Example 41a), hexahydro-lH-1,4-diazepine-l-carboxylic acid, 1,1-dimethylethyl ester (0.182 g), cesium carbonate (0.347 g). (RM+)-2,2'-bis(diphenylphosphino)-l,r-binaphthyI (0.036 g), palladium (H) acetate (0.009 g) and anhydrous toluene (3 ml). The residue was purified by HPLC during with a gradient of 0-5% ethanol in dichloromethane. The product was dissolved in methanol and stirred at room temperature for 3h in presence of 4N hydrochloric acid solution in dioxane (2 ml). The solution was concentrated under reduced pressure and triturated with diethyl ether to give the title compound as a white powder (0.17 g). MS (APCI +ve) 402 (M+H-HC1)+ H NMR (CD3OD) 8 7.41 (1H, d); 6.88 (1H, d); 6.81 (1H, dd); 3.83 (2H, t); 3.63 (2H, t); 3.40 (2H, t); 3.30 (2H, t); 3.06 (2H, s); 2.24-2.16 (2H, m); 1.99 (3H, bs); 1.74 (6H, q); 1.63 (6H,d). According to the procedure described in Example 8, the following compounds were prepared: Example 44 (±>5-[(3-Ammo-l-piperidinyl)methyl]-2-chloro-N-(tricyclo[3.3.1.13'7]dec-l-ylmethyl)-beozamide, hydrocloride salt MS (APCI +ve) MW 416/418 (M+H)+ H NMR (CD3OD) 5 7.70 (IH, bs);7.67 (IH, dd); 7.60 (IH, d); 4.49 (IH, d); 4.45 (IH, d); 3.73-3.58 (2H, m); 3.57-3.45 (IH, m); 3.14-2.95 (4H, m); 2.25-2.04 (2H, m); 1.98 (4H, bs); 1.76 (3H, d); 1.73-1.58 (IH, m); .1.70 (3H, d); 1.63 (6H, bs). MS (APCI +ve) MW 414/416 (M+H)+ !H NMR (CD3OD) 5 7.74 (IH, d); 7.72 (IH, dd); 7.60 (IH d); 4.704.55 (3H, m); 4.45 (IH, d); 4.00 (IH, d); 3.73 (lH,d); 3.60-3.50 (2H, m); 3.07 (2H, s); 2.71 (IH, d); 2.27 (IH, d); 1.98 (3H, bs); 1.77 (3H, d); 1.69 (3H, d); 1.63 (6H, bs). Example 46 2-CbJoro-5-(9-oxa-3,7-diazabicyclo[3.3.1]non.3-ylmethyl)-N-(tricyclo[3.3.1.13'7]dec-l-yhnethyl)- benzamide, hydrochloride salt MS (APCI +ve) MW 442/446 (M+H)+ lH NMR (CD3OD) 5 7.60-7.40 (3H, m); 4.25^.00 (2H, m); 3.70-3.40 (2H, m); 3.46 (4H, m); 3.07 (2H, s); 3.15-2.90 (2H, m); 2.80-2.50 (2H, m); 2.00 (3H, bs); 1.78 (3H, d); 1.71 (3H,d); 1.63 (6H,bs). MS (APCI +ve) MW 442/444 (M+H)+ H NMR (CP3OD) 8 7.91 (IH, s); 7.78 (IH, d); 7.56 (IH, d); 7.46 (IH, bs); 4.44 (2H, bs); 3.65-3.28 (8H, in); 3.08 (2H, bs); 2.48 (2H, bs); 2.05-1.90 (5H, m); 1.77 (3H, d); 1.71 (3H, d); 1.64 (6H, bs). Example 48 trans-2-CMoro-5-{[8-(methyiainino>3-azabicyclo[3.2.1]oct-3-yl]methyI]-N-(tricyclo[3J.l.l3'73dec-l-yImethyl)-benzamide, hydrochloride salt MS (APCI+ve) MW 456/458 (M+H)+ H NMR (CD3OD) 8 7.79 (IH, d); 7.77 (IH, dd); 7.58 (IH, d); 4.71 (2H, bs); 3.80 (2H, d); 3.40 (IH, t); 3.25 (2H, dd); 3.07 (2H, s); 2.86 (3H, s); 2.70 (2H, bs); 2.10-1.90 (7H, m); 1.77 (3H, d); 1.70 (3H, d); 1.63 (6H, bs). Example 49 cis-2-ChIoro-5-[(hexahydropyrrolo[3,4-c]pyrroI-2(lH)-yl)methyl]-N- 37 (tricydo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide, hydrochloride salt MS (APCI +ve) MW 428/430 (M+H)+ !HNMR (DMSO-d6) 5 8.00 (IH, t); 7.65 (IH, s); 7.63 (IH, d); 7,52 (IH, d); 4.34 (2H, bs); 3.60-3.05 (10H, m); 2.97 (2H, d); 1.95 (3H, bs); 1.70 (3H, d); 1.63 (3H, d); 1.57 (6H,s). 3 7 a) [[4-chloro-3-[[(tricyclo[3.3.1.1 ' ]dec-l-ylmethyI)amino]carbonyI]phenyI]- methyl] phosphonic acid, dimethyl ester 3 7 5-BromomethyI-2-chloro-N-(tricycIo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (5.70 g, Example 8b) in lOOml of trimethylphosphite was heated at reflux for 15h. The solvent was removed by azeotropic distillation with toluene under high vacuum to afford the subtitle compound as a yellow solid. MS (APCI +ve) MW 426/428 (M+H)+ H NMR (DMSO-d6) 5 8.34 (1H, t); 7.42 (1H, d); 7.35-7.27 (2H, m); 3.63 (3H, s); 3.58 (3H, s); 3.42 (2H, d); 2.92 (2H, d); 1.94 (3H, bs); 1.67 (3H, d); 1.59 (3H, d); 1.52 (6H, bs). 37 b) 4-[{4-chloro-3-[[(tricycio[3J.1.1 ' ]dec-l-ylmethyI)amino]carbonyI]phenyI] methylene]-l-piperidinecarboxyHc acid, 1,1-dimethyIethyI ester • 3 7 To a solution of the crude [[4-chloro-3-[[(tricyclo[3.3.1.1 ' ]dec~l-yimethyl)aminoJ carbonyl]phenyl] methyl] phosphonic acid, dimethyl ester (2.50 g, Example 50a) in tetrahydrofuran (50 ml) at -78 °C was added a solution of lithium diisopropylamide (7.30 ml, 2M in tetrahydrofuran). The reaction was allowed to warm to room temperature and stirred for 15min. N-t-butoxycarbonylpiperidin-4-one (L52g) in tetrahydrofuran (5 ml) was then added and the mixture stirred for 24h. The reaction was diluted with water and extracted with ethylacetate. The organic layer was washed with brine and dried over magnesium sulfate. The crude material was purified on a silica gel (0 to 5% methanol in dichloromethane) to afford the subtitle compound as a white foam. MS (APCI +ve) MW 443/445 (M+H)+ 'HNMR (DMS0-d6) 5 7.52 (1H, d); 7.34 (1H, d); 7.16 (1H, dd); 6.30 (1H, s); 6.25 (t, 1H); 3.48 (2H, t); 3.40 (2H, t); 3.40 (2H, t); 3.18 (2H, d); 2.42 (t, 2H); 2.32 (t, 2H); 2.05 (3H, bs); 1.73 (3H, d); t .64 (d, 3H), 1.59 (6H, s); 1.47 (9H, bs). c) 2-ChlorO'5-(4-piperidmylidenemethyl)-N-(tricyclo[3.3.1.13'7]dec-l-ylmethyl)-benzamide, hydrochloride salt A solution of 4-[[4-chloro-3-[[(tricyclo[3.3.1.13,7]dec-l-ylmethyl)amino]carbonyl]phenyl] methylene]-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.1 Og, Example 50b) in methanol (3ml) was treated with a 4N solution of hydrochloric acid in dioxane (1 ml) and stirred for 14h at room temperature. The reaction mixture was concentrated under vacuum and the residue recrystallised from iso-propanol/ether to give the title compound as a white solid (0.07lg). MS (APCI +ve) MW 399/401 (M+H)+ !H NMR (DMSO-d6) 5 7.52 (1H, d); 7.34 (1H, d); 7.16 (1H, dd); 6.30 (1H, s); 6.25 (t, 1H); 3.48 (2H, t); 3.40 (2H, t); 3.40 (2H, t); 3.18 (2H, d); 2.42 (t, 2H); 2.32 (t, 2H); 2.05 (3H, bs); 1.73 (3H, d); 1.64 (d, 3H), 1.59 (6H, s); 1.47 (9H, bs). 3 7 To a solution of 2-chloro-5-(4-piperidinylidenemethyl)-N-(tricyclo[3.3.1.1 ]dec-l-ylmethyl)-benzamide, hydrochloride salt (0.10g, Example 50c) in ethanol (10 ml) was added platinum oxide (2mg). The vessel was placed under 3 bars hydrogen pressure for 3h. The catalyst was removed by filtration through a pad of Celite, washed with ethanol and the solution concentrated under vacuum. The crude material was recrystallised from iso-propanol to afford a white solid. The t-butoxycarbonyl protected compound was dissolved in methanol (10ml) and treated with a solution of 4N HCl in dioxane (2 ml). The reaction was stirred for I4h at room temperature, the volatiles removed under vacuum and the residue recrystallised from jso-propanol/ether to afford the hydrochloride salt as a white powder (0.065g). MS (APCI +ve) MW 402/404 (M+H)+ lH NMR (CD3OD) 5 8.38 (1H, 0; 7.38 (1H, d); 7.30-7.20 (2H, m); 3.35 (2H, d); 3.05 (2H, d); 2.92 (2H, td); 2.63 (2H, d); 1.98 (3H, bs); 1.95-1.80 (1H, m); 1.85 (2H, d); 1.77 (3H, d); 1.68 (3H, d); 1.62 (6H, s); 1.40 (2H, q). To a solution of 5-bromo-2-chioro-N-(tricyclo[3.3.1.1 J']dec-l-ylmethyl)-benzamide (0.30g„ Example 23a) in anhydrous tetrahydrofuran (10ml) at-78 °C was added drop wise a solution of n-butyllithium in hexanes (2.5M, 0.72ml). After lOmin. a solution of t-butoxycarbonyi^-piperidone (0-2 Ig) in tetrahydrofuran (2ml) was added. The solution was stirred an additional 20min. then treated with saturated aqueous ammonium chloride solution. The mixture was allowed to warm to room temperature then partitioned between 5thyl acetate and saturated aqueous ammonium chloride solution. The organic extracts were dried over magnesium sulphate and concentrated in vacuo. The residue was chromatographed on silica (ethyl acetate: isohexane/l:4 to 1:2 gradient) to give the t-butoxycarbonyl protected product (0.153g). This was redissolved in methanol (4ml) and treated for 14h with 4N HC1 in dioxan (1ml). The solution was partially concentrated in vacuo and the product precipitated with diethyl ether. The solution was filtered and the white solid washed with diethyl ether to give the title compound (0.09lg) MS (APCI +ve) MW 403 (M+H)+ !HNMR (CD3OD) 5 8.43 (1H, m, br); 7.59 (1H, m); 7.55 (1H, d); 7.49 (1H, d); 3.52-3.30 (4H, m); 3.09 (2H, d); 2.23 (2H, m); 2.04-1.88 (5H, m); 1.95-1.80 (1H, m); 1.84-1.66 (6H,m);1.65(6H,d). Example 53 2-Chloro-5 3 7 Asolutuion of 2-chloro-5-(4-hydroxy-piperidin-4-yI)-N-(tricyclo[3.3.1.1 ' ]dec-l- ylmethyO-benzamide, hydrochloride salt (0.25g7 Example 52) in concentrated hydrochloric acid (10ml) was heated at 100°C for 5h. The solution was allowed to cool slowly. Colourless crystals separated. These were removed by filtration, washed with diethyl ether then acetonitrile and dried to afford the title compound (0.031 g). MS (APCI +ve) MW 385 (M+H)+ ]HNMR CCD3OD) 5 8.44 (1H, m, br); 7.55-7.45 (3H, m); 6.23 (1H, m); 3.S5 (2H, m); 3.47 (2H, t); 3.07 (2H, d); 2.79 (2H, m); 1.98 (3H, m); 1.77 (3H, m); 1.69 (3H, m); 1.63 (6H,s,br). 2-Bromo-5-(4-[{ l,l-dimethyIethyl}oxycarbonyl]-piperazin-l-yl)metfayl -N-(tricyclo[3.3.1.I3,7]dec-l-yiraethyl)-benzamide (Example 65b, 0.89g) was dissolved in dry tetrahydrofuran. Sodium hydride (60% dispersion, 0.07g) was added and the mixture stiired at room temperature for 5min. The mixture was cooled to -70°C under a nitrogen atmosphere and t-butyllithium (1.9ml, 1.7M solution) added. After 5min, ethyl iodide (0.5ml) was added and the mixture stirred at -70°C for 30min. Aqueous ammonium chloride solution was added and the product extracted with diethyl ether, dried (MgSO) and concentrated in vacuo. Chromatography on silica gave the t-butyloxycarbonyl (BOC) protected compound as a foam. This was redissolved in methanol (5ml) and 4N HC1 in dioxane (1ml) added. The mixture was stirred at room temperature for 14h. The solution was partially concentrated under vacuum and the product precipitated with diethyl ether. The resulting solid was filtered and washed with ether to afford the title compound as a white powder (0.040g). lHNMR (DMSO) 5 9.59 (2H, s, far); 8.15 (IK, t); 7.58 (2H, s, br); 7.35 (1H, d); 4.37 (2H; s, br); 3.49 (m); 3.25 (2H, m, br); 2.95 (2H, d); 2.72 (2H, q); 1.94 (3H; s, br); 1.69-1.59 (6H, m); 1.52 (6H, s); 1.165 (3H, t). a) 4-(Toluene-4-sulfonylsulfanyl)-piperidine-l-carboxyIic acid tert-butyl ester 4-Iodo-piperidine-l-carboxylic acid, wrr-butyl ester (1.3g) and potassium toluene-4-thiosulfonate (l.Og) were combined in ethanol (10ml) with cis-dicyclohexane 18-crown-6 (lOmg) and heated under reflux for 12h. After cooling the reaction mixture was partitioned between ethyl acetate and water, the organic layer was separated, washed with water and brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (eluting with ijohexane / ethyl acetate 4:1 to 7:3), to yield the subtitle compound as an oil (0.65g). MS(APCI+ve)3l5 (M-t-H-tBu)+ H NMR (CDC13) 5 7.80-7.85 (2H, m), 7.30-7.40 (2H, m), 3.95-4.10 (1H, m), 3.75-3.85 (1H, m), 3.40-3.50 (1/2H, m), 3.10-3.20 (I/2H, m), 2.95-3.05 (1H. m), 2.-80-2.90 (1H, m), 2.46 (3H, s), 1.90-2.10 (2H, m), 1.50-1.70 (2H, m), 1.43 & 1.45 (9H, pairs). b) 2-Chloro-5-(4-[{l,l-dimethylethyl}oxycarbonyl]piperidiiie-4-ylsuJfanyl)-N- 3 7 (tricyclo[3.3,l.l ' ]dec-l-ylmethyi)-benzamide 3 7 To a solution of 5-bromo-2-chlorp-N-(tricyclo[3.3.1.1 ]dec-l-ylmethyl)-benzamide (0.30$, Example 23a) in anhydrous tetrahydrofuran (10ml) at -78 °C was added dropwise a solution of n-buryllithium in hexanes (2.5M, 0.72ml). After lOmin. a solution of 4-(toluene-4-sulfonylsulfanyl)-piperidine-l-carboxylic acid, terr-butyl ester (0.38g, Example 55a) in tetrahydrofuran (7ml) was added. After a further 1 hour at -78°C the reaction mixture was wanned to ambient temperature and quenched by the addition of water (5ml). The reaction mixture was diluted with ethyl acetate and washed twice with saturated aqueous sodium hydrogen carbonate solution, then with brine and dried over magnesium sulfate. The organic layer was concentrated under reduced pressure to give a residue which was purified by silica gel chromatography (eluting with 0-5% ethanol in dichloromethane) to yield the subtitle compound (0.20g). MS (APCI+ve) 419/21 (M+H-BOQ+ c) 2-Oiloro-5Kpiperidin-4-ylsulfanyl)-N-(tricyclo[3.3.1.13'7]dec-l-ylmethyl)-benzamide, hydrochloride salt 2-Chloro-5-(-(4-[ {1,1 -dimethylediyl} oxycarbonyl]-piperidin-4-ylsulfanyl)-N- 3 7 (tricyclo(3.3.1.I ' ]dec-I-ylmethyl)-benzamide (0.20g, Example 55b) was dissolved in methanol (15 ml) and hydrochloric acid (1.0ml of a 4N solution in dioxane) was added. After stirring at room temperature for 14h, the reaction mixture was basified with saturated sodium hydrogen carbonate solution and extracted twice with dichloromethane. The organic layer was concentrated under reduced pressure to give a residue which was purified by silica gel chromatography (eluting with 0-100% methanol in dichloromethane). The residue was dissolved in dichloromethane (5ml) and hydrochloric acid (IN in diethyl ether, 2ml) added. Evaporation to dryness gave the title compound as the hydrochloride salt (O.OSOg). MS(APa+ve)419/21 (M+H)+ lH NMR (DMS0-d6) 5 8.75 (2H, brd), 8.38 (IH, t), 7.48 (2H, s), 7.37 (IH, s), 3.50-3.60 (IH, m), 3.30 (2H, brd), 2.92-3.05 (4H, m), 2.06 (2H, brd), 1.94 (3H, s), 1.57-1.75 (8H, m, 1.52 (6H,s). Example 56 3 7 2-Chloro-5-(piperidin-4-yIsulfinyI)-N-(tricycio[3.3.1.1 ' ]dec-l-yhnethyl)-benzamide m-Chloroperoxybenzoic acid (166mg) was added to a solution of 2-chIoro-5-(piperidin-4-- 3 7 ylsulfanyl)-N-(tricyclo[3,3.1.1 ' ]dec-1 -ylmethyl)-benzamide (0.35g, Example 55c) in dichloromethane (5ml). After 2h calcium hydroxide (0.20g) was added and 30min. later the salts removed by filtration. The filtrate was concentrated under reduced pressure to give a residue which was purified by silica gel chromatography (eluting with 0-25% ethanol in dichloromethane). The residue was dissolved in methanol (5 ml) and hydrochloric acid (0.5ml of a 4N solution in dioxane) was added. After stirring at room temperature for I4h, the solution was concentrated under reduced pressure and triturated with diethyl ether to yield the title compound as the hydrochloride salt (0.030g). MS (APa +ve) 435/37 (M+H)+ HNMR (DMSO-d6) 8 8.88 (IH, brs), 8.47 (2H, bit), 7.76 (IH, d), 7.67 (IH, dd), 7.61 (IH, d), 3.30-3.40 (2H, m), 3.13 (IH, t), 2.98 (2H, d), 2.80-2.90 (2H, m), 2.15 (IH, d), 1.95 (3H,m), 1.50-1.85 (15H,m). Example 57 m-Chloroperoxybenzoic acid (0.30g) was added to a solution of 2-chloro-5- 3 7 (piperidin-4-ylsulfinyl)-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.30g) in dichloromethane (10ml). After 2h calcium hydroxide (170mg) was added and 30min. later the salts removed by filtration. The filtrate was concentrated under reduced pressure to give a residue which was purified by silica gel chromatography (eluting with 0-2% ethanol in dichloromemane). The residue was dissolved in methanol (5 ml) and hydrochloric acid (0.25ml of a 4N solution in dioxane) was added. After stirring at room temperature for 14h, the solution was concentrated under reduced pressure and triturated with diethyl ether to yield the title compound (0.03g). MS (APCI +ve) 451/53 (M+H)+ lE NMR (DMSO-d6) 5 8.89 (IH, brs), 8.57 (IH, t), 8.50 (1H, brs), 7.87 (2H, ABq), 7.75 (1H, d), 3.71 (IH, td), 3.40 (2H, d), 3.00 (2H, d), 2.80-2.90 (2H, m), 1.95-2.05 (5H, m), 1.50-1.90 (14H,m). Example 58 2-OiIoro-5-{piperidin-4-ylmethyIsuIfanyI)-N-(tricycIo[3.3.1.13'7]dec-l-yImethyI)-benzamide, hydrochloride salt a) 2-ChIoro^5-(4-[{l,l-dimelhyIethyl}oxycarbonyl] piperidin-4-yImethyIsulfanyI)- 37 N-(tricycIo[3J.l.l ' ]dec-l-ylmethyl)-benzamide Trifluoroacetic acid anhydride (2ml) was added to a solution of 2-cbioro-5- 3 7 methylsulphinyl-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (G.53g, Example 58a, WO 99/29661) in dichlororaethane (10ml) and heated under reflux for 1.5h, cooled and concentrated. The resultant residue was dissolved in methanol (30ml), allowed to stand for 1 hour then concentrated. The resultant residue was dissolved in acetone (10ml) and potassium carbonate (0.60g) and 4-iodomethyI-piperidine-l-carboxylic acid tert-butyl ester (0.94g) was added. The reaction mixture was heated under reflux for 3h, cooled and concentrated. The resultant residue was dissolved in ethyl acetate, washed twice with 10% w/w KHSO4 solution, twice with saturated sodium hydrogen carbonate solution, once with brine and dried over magnesium sulfate. The organic layer was concentrated under reduced pressure to give a residue which was purified by silica gel chromatography (eluting with 0- 2% ethanol in dichloromethane), to yield the subtitle compound (0.46g). MS (APQ +ve) 433/35 (M+H-BOQ+ !H NMR (CDCI3) 8 7.61 (1H, d), 7.25-7.31 (2H, m), 6.27 (1H, brt), 4.09 (2H, tad), 3.17 (2H, d), 2.86 (2H, d), 2.66 (2H, t), 2.01 (3H, s), 1.60-1.90 (15H, m), 1.45 (9H/s), 1.18 (2H, dq). b) 2-Chloro-5-(piperidin-4-ylmethyIsulfanyl)-N-(tricyclo[3J.i.l3'7]dec-l-ylmethyl)-benzamide, hydrochloride salt Hydrochloric acid (4N dioxane, 0.5ml) was added to a solution of 2-chloro-5-(4-[{1,1-dimethylethyl }oxycarbonyl] piperidin-4-ylmethylsuifanyl)-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.235g, Example 58a) in methanol (10ml). After 24h the reaction mixture was concentrated, then triturated with ether to give the title compound (0.20g). MS (APCI+ve) 433/35 (M+H)+ H NMR (DMSO-d6) 5 8.76 (1H, brs), 8.48 (1H, brs), 8.35 (1H, t), 7.40 (2H, ABq), 7.28 (1H, d), 3.24 (2H, d), 3.00 (2H, d), 2.92 (2H, d), 2.84 (2H, q), 1.94 (5H, brs), 1.75-1.82 (1H, m), 1.65 (6H, q), 1.52 (6H, s), 1.40 (2H, q). m-Chloroperoxybenzoic acid (0.19g) was added to a solution 2-chloro-5-(4-[{ 1,1- 3 7 dimethylethyl}oxycarbonyl] piperidin-4-ylmethylsulfanyl)-N-(tricyclo[3.3.1.1 ' ]dec-l- ylmethyl)-benzamide (0.165g, Example 58a) in chloroform (10ml). After 5h calcium hydroxide (120mg) was added and 30min. later the salts removed by filtration. The reaction mixture was concentrated, then dissolved in methanol (10 ml) and hydrochloric acid (l.Oml of a 4N solution in dioxane) added. After stirring at room temperature for 14h, concentration under reduced pressure yielded the title compound (0.075g), MS (APCI +ve) 465/67 (M+H)+ H NMR (DMS0-d6) 5 8.70 (1H, brs),.8.55 (1H, t), 8.48 (1H, brs), 7.95 (1H, dd), 7.88 (1H, d), 7.82 (1H, d), 3.47 (2H, d), 3.21 (2H, d), 2.97 (2H, d), 2.89 (2H, d), 2.10-2.25 (1H, m), 1.95 (5H, brs), 1.40-1.80 (14H, m). a) 4-aiIoro-NKtricyclo[3J.l.l3,7]dec-l-ybnethyl>isophthalamic acid n-Butyllithium (3ml, 2M hexanes) was added at -78°C to a solution of 5-bromo-2- 37 chloro-N-(tncyclo[3.3.1.I ' ]dec-l-ylmethyl)benzamide (l.Og, Example 23a) in tetrahydrofuran (20ml). After lOmin. the reaction mixture was decanted onto dry solid carbon dioxide and allowed to warm to ambient temperature. The reaction mixture was acidified with concentrated hydrochloric acid and extracted with ether. The organics were separated, dried over magnesium sulfate and concentrated under reduced pressure to give a residue which was purified by silica gel chromatography (eluting with iso-hexane / emyl acetate 3:1 to 1:1 + 1%ACOH), to yield the subtitle compound as a solid (0.45g). MS(APCI+ve)348/350 (M+H)+ ^NMR (DMS0-d6) 5 13.33 (1H, s), 8.44 (1H, t), 7.94 (1H, dd), 7.87 (1H, d), 7.63 (1H, d), 2.95 (2H, d), 1.95 (3H, s), 1.63 (6H, q), 1.53 (6H, s). 3 7 b) 2-Cbioro-5-(pipera2ine-l-carbonyl)-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)- benzamide, hydrochloride salt Ethyldiisopropylamine (0.3ml) was added at ambient temperature to a solution of 37 4-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmeihyl)-isophthalamic acid (0.15g, Example 60a), 5 piperazine-1-carboxylic acid tert-butyl ester (0.16g) and PyBrOP (0.40g) in N- \| methyipyrroiidinone (10ml). After 5h the reaction mixture was diluted with ethyl acetate and washed twice with water, twice with 10% KHSO4 solution, twice with saturated NaHCC>3 solution and once with brine, then dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel 1 chromatography (eluting with ethanol (0-5%) in dlchlororaethane), then redissolved in methanol (10ml) and treated with hydrochloric acid (4N dioxane, 1ml); After 48h the reaction mixture was concentrated under reduced pressure and recrystallised from iso- hexaxne/propan-2-ol to yield the title compound as a solid (0.1 Og). MS (APCI +ve) 416 / 418 (M+H)+ THNMR (DMSO-d6) 5 9.18 (1H, t), 8.42 (1H, t),7.59 (1H, d),7.47-7.52 (2H, m), 3.50- 3.90 (4H, brs), 3.05-3.25 (4H, brs), 2.94 (2H, d), 1.95 (3H, s), 1.63 (6H, q), 1.52 (6H, s). The following Examples were made in an analogous manner. Example 61 2-aaoro-5-([l,4]d^zepane-l-carbonyl)-N-(tricycIo[3.3.1.13'7]dec-l-yImethyI)-benzamide, hydrochloride salt MS (APCI +ye) 430 / 432 (M+H)+ !H NMR (DMSO-d6) 5 9.10 (2H, brs), 8.06 (IH, brs), 7.53 (IH, d), 7.45-7.48 (2H, m), 3.78 (2H, brs), 3.54 (2H, brs), 3.20-3.25 (4H, m), 2.97 (2H, d), 2.00 (2H, m), 1.95 (3H, s), 1.65 (6H, q), 1.55 (6H, s). MS (APCI +ve) 430 / 432 (M+H)+ !HNMR (DMSO-d6) 5 8.66-8.76 (3H, m), 8.42 (IH, t), 7.89-7.93 (2H, m), 7.60 (IH, d), 4.01-4.09 (IH, m), 3.29 (2H, d), 2.95-3.05 (4H, m), 1.95 (5H, brs), 1.47-1.82 (14H, ra). Example 63 3 7 2-Chloro-5-(hydroxy-4-piperidinyIraethyl)-N-(tricyclo[33.1.1 ' ]dec-l-ylmethyl> benzamide, hydrochloride salt a) 2-Chloro-5-[4-[[{l,l-diniethylethyl}oxycarhonyI]piperidinyI]-hydroxymethyI]- 37 N-(tricyclo[3.3.1.1 ' ] dec-1-ylmethyl) -benzamide 3 7 To a solution of 5-bromo-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-1 -ylmethyl)-benzamide (1.5 g, Example 23a) in anhydrous tetrahydrofuran (50 ml) under a nitrogen atmosphere at -78°C was added dropwise n-butyllithium solution (2.5M in hexanes, 3.4 ml). The mixture was stirred for lOmin. at -78°C, then a solution of 4-formyl-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester (1.09 g, Journal of Medicinal Chemistry, 1999, 42(12), 2180-2190) in anhydrous tetrahydrofuran (10 ml) was added dropwise. The reaction mixture was stirred at -78°C for 30min. then quenched with saturated aqueous ammonium chloride solution (100 ml). The product was extracted twice with ethyl acetate (2x100 ml). The organic extracts were combined, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on silica gel eluting with iso-hexane : ethyl acetate / (2:1) then (1:2), then purified further by HPLC eluting with a gradient of 0-5% ethanol in dichloromethane to give the subtitle compound as a white foam (0.61 g). MS (APCI +ve) 517 (M+H)+ lK NMR (DMSO-d6) 5 8.28 (1H, t); 7.40 (IK, d); 7.33-7.27 (2H, m); 5.33 (IK, d); 4.34 (1H, t); 3.93 (3H, bs); 2.93 (2H, d); 2.61 (2H, bs); 1.94 (3H, bs); 1.63 (6H, q); 1.53 (6H, d); 1.37 (9H, s); 1.34-L23 (2H, m); 1.09 (2H, dt). b) 2-Chloro-5-{hydroxy-4-piperidinylmethyl)-N-(tricyclo[3.3.1.13,7]dec-l-ylmethyO-benzamide, hydrochloride salt A solution of 2-chloro-5-[4-{[{ l,l-dirnethyIethyi}oxycarbonyl]-piperidinyl]- 3 7 hydroxyraethyl]-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.10 g, Example 63a) in methanol (3 ml) was treated with 4N hydrochloric acid solution in dioxane (1 ml). After 14h the solvents were removed under reduced pressure and the residue was triturated with diethyl ether to give the title compound as a white powder (0.062 g). MS (APCI +ve) 417 (M+H-HC1)+ !H NMR (DMSO-d6) 5 8.70 (1H, bs); 8.29 (2H, bt); 7.44 (IH, d); 7.33 (2H, dt), 5.53 (1H, d); 4.40 (IH, t); 3.23 (2H, bs); 2.93 (2H, d); 2.76 (2H, bd); 1.94 (3H, bs); 1.77-1.36 (1H, m); 1.53 (6H, s). Prepared by an analogous route to Example 63 employing 3-formyl-l-piperidinecarboxylic acid, 1,1 -dimethylethyl ester. MS (APCI +ve) MW 417/419 (M+H)+ ^NMR (GD3OD) 5 8.41 (IH, t); 7.46 (1H, d); 7.41 (1H, d); 7.39 (1H, s); 4.65 (0.5H, d); 4.50 (0.5H, d); 3.74 (0.5H, td); 3.66 (IH, q); 3.57 (0.5H, t); 3.44 (0.5H, bd); 3.18 (0.5H, bd); 3.06 (2H, d); 2.86 (2H, qd); 2.10-1.87 (m, 2H); 1.98 (3H, bs); 1.77 (3H, d); 1.68 (3H, bd); 1.63 (6H, s), 1.60-1.50 (m, IH); 1.50-1.36 (m, IH). Example 65 3 7 2-Bromo-5-piperazin-l-ylrnethyl -N-(tricycla[3.3.1.1 '■ ]dec-l-ylmethyl)-benzamide, hydrochloride salt 3 7 a) 2-Bromo-5-bromomethyl -N-(tricyclo[3J3.1.1 -' Jdec-l-ylmethyO-benzamide •> To a solution of 2-bromo-5-bromomethyl-benzoic acid (6.1g) in dichloromethane (100 ml) at 0°C were added dimethylformamide (0.2 ml) followed by oxalylchloride (3 ml). The reaction was stirred at room temperature for 0.5 hour and concentrated under vacuum. The acylchloride was redissolved in dichloromethane (100 ml) and and di- iropropylethylamine (6 ml) followed by adamantanemethylamine (3.5ml) added at 0"C. The mixture was stirred at 0°C for lOmin., then partitioned bejtween diethyl ether and IN aqueous hydrochloric acid. The organic layer was dried over magnesium sulfate and concentrated in vacuo. The crude material was purified by recrystallisation from dichloromethane/ethylacetate/i-hexane to afford the title compound as a white solid (6.5 g) (sample contained some of the corresponding benzyl chloride). . b) 2-Bromo-5-(4-[{l,l-dimethyIethyl}oxycarbonyl]-pip€ra2in-l-yl)inetb.yI-N- 37 (tricydo[3-3.1.1 ' ]dec-l-ylmethyl)-benzamide 37 A mixture of 2-bromo-5-bromomethyl-N-(tricyclof3.3.1.1 ' ]dec-1 -yimethyi)- benzamide (Example 65a, 5.0g), 1-tertbutyloxycarbonylpiperazine (2.3g), potassium carbonate (3.2g), potassium iodide (0.30g) and acetone (75ml) was refluxed in the dark for 14h. The mixture was concentrated in vacuo, partitioned between ethyl acetate and water, then washed with brine. The organic layer was dried over magnesium sulfate and concentrated in vacuo. Recrystallization from ethyl acetate:isohexane gave the subtitle compound as colourless solid (4.7g). MS (APCI +ve) MW 546 (M+H)+ 3 7 c) 2-Bromo-5-piperazin-l-ylmethyI -N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)- benzamide, hydrochloride salt 2-Bromo-5-(4-[ {1,1 -dimethylethyl} oxycarbonyl]-piperazin-1 -yl)methyl -N- 3 7 (tricycio(3.3.I.I ' ]dec-I-yimethyl)-ben2;amide (Example 65b, 0.40g) was dissolved in methanol (15ml), and 4N HCl in dioxane (3ml) added. The mixture was stirred at room temperature for 14h. The solvent was removed under vacuum and the resulting solid was triturated with ether to afford the title compound as a white powder (0.23g). MS (APCI +ve) MW 447(M+H)+ H NMR (DMSO-d6) 5 9.53 (1H, s, br); 8.31 (1H, t); 7.72 (1H, d); 7.60 (1H, m), 4.33 (1H, m); 3.50-3.00 (4H, m); 3.50-3.40 (1H, m); 2.94 (2H, d); 1.94 (3H, bs); 1.71-1.58 (6H,m);1.54(6H,bs). A solution of 5-brorno-2-chloro-Ar-(tricyclo[3.3.1. l3/7]dec- I-ylmethyO-benzamide (3.0 g, Example 23a) in anhydrous tetrahydrofuran (100 ml) was cooled to ~78°C under a nitrogen atmosphere. A solution of methyllithium (1.4M in diethyl ether, 4.9 ml)'was added over 2min. The mixture was stirred at -78GC for lOmin., then a solution tert-butyllithium (1.7M in pentane, 9.3 ml) was added dropwise. The mixture was stirred at -78°C for a further lOmin., then ethylene oxide (1.0 ml) was added. The resulting solution was stirred at -78°C for 30min. then was warmed to 0°C and stirred for another 6h. The reaction mixture was quenched with saturated aqueous ammonium chloride solution (70 ml) and extracted with ethyl acetate (3x100 ml). The combined extracts were dried over anhydrous magnesium sulfate, filtered, and die filtrate concentrated under reduced pressure. The residue was purified by chromatography over silica gel eluting with dichloromethane : ethanol (98:2) to give the subtitle compound as a pale yellow solid (0.89 g>- MS (APCI +ve) 348 (M+Hf 'H NMR (DMSO-ds) 5 8.27 (1H, t), 7.36 (1H, d); 7.28-7.23 (2H, m); 4.65 (1H, t); 3,60 (2H, q); 2.92 (2H, d); 2.73 (2H, t); 1.94 (3H, bs); 1.63 (6H, q); 1.52 (6H, d). b) 2-Chloro-5-(2-oxoethy0-A^-(tricycIo[3.3.1.13'7]dec-l-ylmethyI)-benzamide To a solution of 2-chloro-5-(2-hydroxyethyl)-//-(tricyclo[3.3.1.I3'7]dec-l-ylmethyl)-benzamide (1.07 g, Example 66a) in anhydrous dichloromethane (20 ml) was added Dess-Martin periodinane reagent (1.95 g) and me mixture was stirred at room temperature forlh. Sodium thiosulfate (3.43 g) was dissolved in aqueous sodium bicarbonate solution (28 ml) and added to the reaction mixture. Diethyl ether (50 ml) was then added and the mixture was stirred for lOmin,. The layers were partitioned and the organic layer was washed with water then brine. The organic extracts were then dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to afford the subtitle compound as a white solid (1.06 g). MS (APCI +ve) 346 (M+H)+ 1H NMR (DMSO-d6) S 9.69 (1H, s); 8.32 (1H, t); 7.45 (1H, d); 7.30-7.24 (2H, m); 3.84 (2H, s); 2.92 (2H, d); 1.94 (3H, bs); 1.63 (6H, q); 1.52 (6H, d). c) 2-Chloro-5-[2-(l-piperazinyl)ethyl]-N-(tricyclof3^.U3'7]dec-l-yImethyl)-benzamide hydrochloride salt To a solution of 2-chloro-5-(2-oxoethyi)-A^(tricyclo[3.3.1.13'7]dec-l-ylmethyl)-benzamide (0.101 g, Example 66b) in anhydrous 1,2-dichloroethane (5 ml) was added 1 -piperazinecarboxylic acid, 1,1 -dimethylethyl ester (0,108 g) then sodium triacetoxyborohydride (0.086 g). The reaction mixture was stirred for 14h at room temperature. Water (10 ml) and dichloromethane (10 ml) were added and the layers were partitioned. The organic extract was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by HPLC eluting with a gradient of 0-5% emanol in dichloromethane then by chromatography over silica gel eluting with ethyl acetate. The white powder obtained was dissolved in methanol (5 ml) and a solution of hydrochloric acid in dioxane (4N, 1 ml) was added. The mixture was stirred for 14h at room temperature. Solvents were then removed under reduced pressure and the product obtained was triturated with diethyl ether to afford the title compound as a white powder (0.047 g). MS (APCI+ve) 416 (M+H)+ 1HNMR (CD3OD) δ 8.42 (1H, t); 7.46 (1H, d); 7.41-7.38 (2H, m); 3.63-3.49 (8H, m); 3.48-3.45 (2H, m); 3.19-3.14 (2H, m); 3.06 (2H, s); 1.99 (3H, bs); 1.73 (6H, q); 1.63 (6H,d). Example 67 2-Chloro-5-[2-(2,5-diazabicycio[2.2.11]hept-2-yl)ethyl]-N-(tricyclo[3.3.1.13'7]dec-l-rlmethyl)-benzamide, hydrochloride salt Prepared according to the method described in Example 66c from 2-chloro-5-(2-oxoethyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyI)-benzamide (0.094 g, Example 66b), 2,5-diazabicyclo[2.2.1]heptane-2-carboxylic acid, 1,1-dimethylethyl ester (0.108 g), sodium triacctoxyborohydride (0.081 g) and 1,2-dichloroethane (2 ml). After work-up, the residue was purified by HPLC eluting with a gradient of 0-5% ethanol in dichloromethane. The white powder obtained was dissolved in methanol (2 ml) and a solution of hydrochloric acid in dioxane (4N, 1ml) was added. The mixture was stirred for 14h at room temperature. Solvents were then removed under reduced pressure and the product obtained was triturated with diethyl ether to afford the title compound as a white powder (0.067 g). MS (APCI +ve) 428 (M+H)+ 1H NMR (CD3OD) δ 7.49-7.40 (3H, m); 4.64 (2H, d); 3.92 (2H, d); 3.77-3.48 (4H, m); 3.18 (2H, t); 3.08 (2H, s); 2.61 (1H, bd); 2.28 (1H, bd); 2.00 (3H, bs); 1.75 (6H, q); 1.64 (6H,d). Example 68 5-[2-(4-Amino-1-piperidinyl)ethyl]-2-chloro-N-(tricyclo(3.3.1.l3.7]dec-l-ylmethyl)-benzamide, hydrochloride salt Prepared according to the method described in Example 66c from 2-chloro-5-(2-coethyl)-Ar-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (0.094 g, Example 66b), 4-peridinyl-carbamic acid, lj-dimethylethyl ester (0.109 g), sodium tnacetoxyborohydride .081 g) and 1,2-dichloroethane (2 ml). After work-up, the residue was purified by HPLC ting with a gradient of 0-5% ethanol in dichloromethane. The white powder obtained as dissolved in methanol (2 ml) and a solution of hydrochloric acid in dioxane (4N, 1ml) as added. The mixture was stirred for 14h at room temperature. Solvents were then moved under reduced pressure and the product obtained was triturated with diethyl ether afford the title compound as a white powder (0.065 g). S(APCI+ve)430(M+H)+ 1HNMR (CD3OD) δ 8.43 (1H, t); 7.49-7.38 (3H, m); 3.78 (2H, bd); 3.64-3.42 (2H, m); Ll-3.35 (2H, m); 3.23-3.14 (3H, m); 3.08 (2H, s); 2.33-2.29 (2H, m); 2.13-2.04 (2H, m); O (3H, bs); 1.75 (6H, q); 1.64 (6H, d). ample 69 Chloro-5-[2-{3-piperidinylamino)ethyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-bezamide, dihydrochloride salt Prepared according to the method described in Example 66c from 2-chloro-5-(2-cthyI)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-beiizamide (0.094 g, Example 66b), amino-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.109 g), sodium triacetoxyborohydride (0.081 g) and 1,2-dichloroethane (2 ml). After work-up, the residue was purified by HPLC eluting with a gradient of 0-5% ethanol in dichloromethane. The white powder obtained was dissolved in methanol (2 ml) and a solution of hydrochloric acid in dioxane (4N, 1ml) was added. The mixture was stirred for 14h at room temperature. Solvents were then removed under reduced pressure and the product obtained was triturated with diethyl ether to afford the title compound as a white powder (0.065 g). MS (APCI +ve) 430 (M+H)+ 1H NMR (CD3OD) δ 7.49-7.46 (1H, m); 7.42-7.38 (2H, m); 3.76 (1H, bd); 3.64-3.54 (1H, m); 3.44-3.34 (3H, m); 3.19-2.98 (4H, m); 3.08 (2H, s); 2.34 (1H, bd); 2.18-2.12 (1H, m); 2.00 (3H, bs); 1.89-1.78 (2H, m); 1.74 (6H, q); 1.64 (6H, d). Example 70 5-[2-(3-Amino-l-piperidinyI)ethyI]-2-chloro-N-(tricyclo[3.3.1.l3'7]dec-l-ylmethyl)-benzamide, hydrochloride salt Prepared according to the method described in Example 66c from 2-chloro-5-(2-oxoethyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (0.094 g, Example 66b), 3-piperidinyl-carbamic acid, 1,1-dimethylethyl ester (0.109 g), sodium triacetoxyborohydride (0.081 g) and 1,2-dichloroethane (2 ml). After work-up, the residue was purified by HPLC eluting with a gradient of 0-5% ethanol in dichloromethane then by HPLC eluting with a gradient of 0-2% ethanol in dichloromethane. The white powder obtained was dissolved in methanol (2 ml) and a solution of hydrochloric acid in dioxane (4N, 1ml) was added. The mixture was stirred for 14h at room temperature. Solvents were then removed under reduced pressure and the product obtained was triturated with diethyl ether to afford the tide compound as a white powder (0.032 g). MS (APCI+ve) 430 (M+H)+ 1H NMR (CD3OD) δ 7.49-7.46 (1H, m); 7.42-7.39 (2H, m); 3.80-3.67 (3H, m); 3.46 (2H, t); 3.19 (2H, t); 3.08 (2H, s); 3.09-3.04 (1H, m); 2.14 (1H, bt); 2.00 (3H, bs); 1.74 (6H, q); 1.77-1.68 (2H, m); 1.64 (6H, d). Example 71 2-Chloro-5-[2-(3-pyrroIidinylamino)ethyl]-N-(tricyclo[3.3.l.l3.7]dec-l-ylmethyl)-benzamide, dihydrochloride salt Prepared according to the method described in Example 66c from 2-chloro-5-(2-oxoethyl)-N-(tricyclo(3.3.1.13.7]dec-l-ylmethyl-benzamide (0.094 g, Example 66b), 3-amino-l-pyrrolidinecarboxylic acid, 1,1-dimethylethyl ester (0.101 g), sodium triacetoxyborohydride (0.081 g) and 1,2-dichloroethane (2 ml). After work-up, the residue was purified by HPLC eluting with a gradient of 0-5% ethanol in dichloromethane. The pale orange powder obtained was dissolved in methanol (2 ml) and a solution of hydrochloric acid in dioxane (4N, 1ml) was added. The mixture was stirred for 14h at room temperature. Solvents were then removed under reduced pressure and the product obtained was triturated with diethyl ether to afford the title compound as a pale orange powder [0.033 g). MS (APd +ve) 416 (M+H)+ 1HNMR(CD3OD) δ 7.46-7.39 (3H, m); 4.12 (1H, bs); 3.78-3.71 (1H, m); 3.69-3.57 2H, m); 3.43-3.32 (4H, m); 3.13 (2H, bt); 3.06 (2H, s); 2.62-2.51 (1H, m); 2.38-2.29 1H, m); 1.98 (3H, s); 1.73 (6H, q); 1.63 (6H, s). Example 72 -[2-[(3R)-3-AniinopyrroUdinyl]ethy]]-2-chloro-N-(tricyc]o[3.3.1.13.7]dec-l-ylmethyl)-enzamide, hydrochloride salt Prepared according to the method described in Example 66c from 2-chloro-5-(2-coethyl)-A^-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (0-094 g, Example 66b), /?)-pyrrolidinyl-carbamic acid, 1,1-dimethylethyl ester (0.101 g), sodium acetoxyborobydride (0.081 g) and 1,2-dichloroethane (2 ml). After work-up, the residue as purified by HPLC eluting with a gradient of 0-5% ethanol in dichloromethane. The lite powder obtained was dissolved in methanol (2 ml) and a solution of hydrochloric id in dioxane (4N, 1ml) was added. The mixture was stirred for 14h at room temperature, solvents were then removed under reduced pressure and the product obtained was turated with diethyl ether to afford the title compound as a white powder (0.060 g). S(APCI+ve)416(M+H)+ 1H NMR (CD3OD) δ 7.49-7.41 (3H, m); 4.86 (1H, bs); 4.05-3.80 (2H, m); 3.58 (4H, bs); 3.17 (2H, t); 3.08 (2H, s); 2.66 (1H, bs); 2.28 (1H, bs); 2.00 (3H, s); 1.74 (6H, q); 1.64 (6H, s). Example 73 2-Chloro-5-[2-[2-(hydroxymethyI)-l-piperazinyl]ethyl]-iV-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt Prepared according to the method described in Example 66c from 2-chloro-5-(2-oxoethyI)-iV-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (0.094 g, Example 66b), 3- . (hydroxymethyl)-l-piperazinecarboxylic acid, 1,1-dimethylethyl ester (0.117 g), sodium triacetoxyborohydride (0.081 g) and 1,2-dichloroethane (2 ml). After work-up, the residue was purified by HPLG eluting with a gradient of 0-5% ethanol in dichloromethane then chromatography eluting with ethyl acetate then ethyl acetate : ethanol (95:5). The white powder obtained was dissolved in methanol (2 ml) and a solution of hydrochloric acid in dioxane (4N, 1ml) was added. The mixture was stirred for 14h at room temperature. Solvents were then removed under reduced pressure and the product obtained was triturated with diethyl ether to afford the title compound as a white powder (0.016 g). MS (APCI +ve) 446 (M+H)+ 1H NMR (CD3OD) δ 8.43 (1H, t); 7.48-7.40 (3H, m); 4.14 (1H, bd); 3.93 (1H, bd); 3.81-3.76 (2H, m); 3.74-3.58 (5H, m); 3.57-3.45 (2H, m); 3.28-3.19 (1H, m); 3.17-3.11 (1H, m); 3.07 (2H, s); 1.99 (3H, bs); 1.73 (6H, q); 1.64 (6H, s). Example 74 2-Chloro-5-(hexahydro-1H-l,4-diazepin-l-yl)-N-(2-tricyclo[3.3.1.13.7]dec-l-ylethyl)-benzamide, hydrochloride salt a) 4-[4-Chloro-3-[[(2-tricyclo[3.3.1.13.7]dec-l-ylethyl)amino]carbonyl]phenyl] hexahydro-1H-l,4-diazepine-1-carboxylic acid, 1,1-dimethylethyl ester A solution of 4-(3-carboxy-4-chlorophenyl)hexahydro-lH-l,4-diazepine-l-carboxylic acid, 1,1-dimethylethyl ester (0.075 g, Example 5b) and 1,1'-carbonyidiimidazole (0.034 g) in dimediylformamide (3 ml) was stirred at room temperature of 2.5h. Tricyclo[3.3.1.13.7]decane-l-ethanamine, hydrochloride salt (0.045 g) and N,N-diisopropylethylarnine (0.037 ml) were then added and stirring continued for 14h. The reaction mixture was poured into water and extracted with ethyl acetate three times. The ethyl acetate layers were combined and washed with 2M hydrochloric acid, 10% aqueous sodium hydroxide and brine, then dried over magnesium sulfate and concentrated under reduced pressure. Purification by chromatography on silica gel eluting with 20% ethyl acetate in iso-hexane gave the subtitle compound as a yellow oil (0.053 g). MS (APCI +ve) 460/462 (M-'Bu)' b) 2-Chloro-5-(hexahydro-1H-l,4-dia2epin-l-yI)-N-(2-tricyclo[3.3.1.13.7]dec-l-ylethyl)-benzamide, hydrochloride salt 4-[4-ChIoro-3-[[(2-tricycIo[3.3.1.13.7]dec-l -ylethyl)amino]carbonyl]phenyI]-hexahydro-1H-1,4-diazepine-l-carboxylic acid, 1,1-dimethylethyl ester (0.053g, Example 74a) was dissolved in methanol (5 ml) and hydrochloric acid (0.5 ml from a 4N solution in dioxane) was added. After stirring at room temperature for 14h, the mixture was evaporated to ¾ original volume under reduced pressure. Diethyl ether was gradually added to the solution and the resulting precipitate was collected by filtration, washed with diethyl ether and dried in vacuo to afford the title compound as a cream solid (0.017 g). MS (APCI+ve) 416/418 (M-HC1)+ 1HNMR (DMSO-d6) ¾ 9.07 (2H, bs); 8.18 (1H, t); 7.22 (1H, d); 6.80 (1H, dd); 6.71 (1H, d); 3.70 (2H, m); 3.50 (2H, t); 3.25-3.17 (4H, m); 3.07 (2H, m); 2.09-2.06 (2H, m); 1.93 (3H, bs); 1.68 (3H, d); 1.61 (3H, d); 1.51 (6H, s); 1.34-1.28 (2H, m). Prepared as described in example 74 above using (+/-)-2-chloro-5-[3-[[(1,1-dimethylemoxy)carbonyl]amino]-l-pyrrolidinyl]-ben2oic acid (0.090 g), 1,1'-carbonyldiimidazole (0.043 g), tricyclo[3.3.1.13.7]decane-l-emanamine, hydrochloride salt (0.057 g), N,N-diisopropylethylamine (0.046 ml) and dimethylformamide (3 ml). This compound was treated with 4N hydrochloric acid in dioxane (0.5 ml) and methanol (5 ml) to yield the title compound (0.025 g). . MS (APCI +ve) 402/404 (M-HC1)+ 1HNMR (DMSO-d6) δ 8.24 (3H, bs); 8.18 (1H, t); 7.24 (1H, d); 6.60 (1H, dd); 6.49 (1H, d); 3.93 (1H, m); 3.54-3.37 (2H, m); 3.31-3.17(4H, m); 2.37-2.28 (1H, m); 2.07 (1H, m); 1.93 (3H, bs); 1.68 (3H, d); 1.61 (3H, d); 1.51 (6H, s); 1.34-1.28 (2H, m). Example 76 2-Chloro-S-(4-piperidinylcarbonyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt a) 4-[4-Chloro-3-[[(tricyclo[3.3.1.13.7]dec-1-ylmethyl)amino]carbonyl]benzoyl]-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester To dimethyl sulphoxide (0.155 ml) in anhydrous dichloromethane (11 ml) at -78°C was added oxalyl chloride (0.086 ml) and the mixture was stirred for 5min. at -78°C. A solution of 4-[[4-chloro-3-[[(tricyclo[3.3.1.13.7.]dec-l-ylmethyl)amino]carbonyl]phenyl]-hydroxymethyl]-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.47 g, Example 64) in anhydrous dichloromethane (3 ml) was added dropwise and the mixture was stirred for 15min. at -78°C. Triethylamine (0.633 ml) was then added and the solution was wanned to room temperature. After 45min. at room temperature, the reaction mixture was poured onto water and the layers were separated. The organic extract was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by HPLC eluting a gradient of 0-5% ethanol in dichloromethane to give the subtitle compound as a white foam (0.31 g). MS(APCI+ve) 15(M+H)+ 1H NMR (DMSO-d6) 5 8.46 (1H, t); 8.06-8.01 (1H, m); 7.95-7.92 (1H, m); 7.70-7.65 (1H, m); 3.97 (2H, bd); 3.72-3.61 (1H, m); 2.97 (2H, t); 2.92 (2H, bs); 1.96 (3H, bs); 1.77 (2H, d); 1-65 (6H, q); 1.55 (6H, s); 1.41 (9H, s); 1.48-1.33 (2H, m). b) 2-Chloro-5-(4-piperidinyicarbonyI)-N-(tricyclo[3.3.1.l3.7]dec-l-ylmethyl)-benzamide, hydrochloride salt A solution of 4-[4-chloro-3-[[(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)amino]carbonyl] benzoyl]-1-piperidinecarboxylic acid, 1,1 -dimethylethyl ester (0.07 g, Example 76a) in methanol (3 ml) was treated with 4N hydrochloric acid solution in dioxane (1 ml). After ]4h the solvents were removed under reduced pressure and the residue was triturated with diethyl ether to give the title compound as a white powder (0.025 g). MS (APCI +ve) 415 (M+H-HC1)+ 1H NMR (DMSO-d6) δ 8.90 (1H, bs); 8.64 (1H, bs); 8.46 (1H, t); 8.03 (1H, d); 7.95 (1H, s); 7.69 (1H, d); 3.81 (1H, t); 3.24-3.18 (2H, m); 3.09-2.99 (2H, m); 2.96 (2H, d); 2.01 (2H, dd); 1.95 (3H, s); 1.79 (2H, t); 1.64 (6H, q); 1.45 (6H, s). Example 77 a) 4-[l-[4-Chloro-3-[[(tricydo[3.3.1.1 3.7]dec-1 -yImethyl)ainino]carbonyI] phenyl]-1-hydroxyethyl]- 1-piperidinecarboxylic acid, 1,1-dimethylethyl ester 2-Chloro-5-[1-hydroxy-1-(4-piperidinyl)ethyl]-N-(tricyclo[3.3.1.13.7]dec-1-ylmethyl)-benzamide, hydrochloride salt To methyl magnesiumbromide (3M solution in diethyl ether, 0.225 ml) in anhydrous diethyl ether (7 ml) under a nitrogen atmosphere was added slowly 4-[4-chloro-3-[[(tricyclo[3.3.1 .l3.7]dec-l-ylmethyl)amino]carbonyl] benzoyl]-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.23 g, Example 76a) in anhydrous diethyl ether (7 ml). The reaction mixture was stirred for 14h at room temperature, then poured onto crushed ice. A solution of 10% aqueous potassium hydrogen sulphate was added keeping the pH of the solution >4. The layers were separated, and the aqueous layer was extracted with ethyl acetate (4x25 ml). The organic extracts were combined, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was dissolved in methanol (3 ml) and hydrochloric acid (4N solution in dioxane, 2 ml) and stirred for 14h at room temperature. Solvents were then removed under reduced pressure and the product (0.11 g) was redissolved in dichloromethane (3 ml). Triethylamine (0.066 ml) was added followed by di-tert-butyl-dicarbonate (0.055 g) and the reaction mixture was stirred for 1 hour at room temperature. Water was added and the layers were partitioned. The organic extract was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by HPLC eluting with a gradient of 0-5% ethanol in dichloromethane, then by RPHPLC eluting with a gradient of 75-5% of 0.1% aqueous ammonium acetate in acetonitrile to give the subtitle compound as a white foam (0.06 g). MS (APCI+ve)431 (M+H-BOC)+ b) 2-Chloro-5-[1-hydroxy-l-(4-ptperidinyl)ethyl]-N-(tricyclo[3.3.l.l3.7]dec-l-ylmethyl)-benzamide, hydrochloride salt To a solution of 4-[l-[4-chloro-3-[[(tricyclo[3.3.1.13.7]dec-l-ylmethyI)amino] carbonyl] phenyl]-l-hydroxyethyl]-l-piperidinecarboxylicacid, 1,1-dimethylethyl ester (0.07 g, Example 77a) in methanol (3 ml) was added 4N hydrochloric acid solution in dioxane (1 ml). After 14h the solvents were removed under reduced pressure and the residue was triturated with diethyl ether to give the title compound as a white powder (0.038 g). MS(APCI+ve)431 (M+H-HC1)+ 1H NMR (DMSO-d6) δ 8.78 (1H, bs); 8.28 (1H, t); 7.44-7.40 (3H, m); 5.21 (1H, s); 3.25 (1H, d); 3.16 (1H, d); 2.98-2.89 (2H, m); 2.79-2.67 (2H, m); 1.94 (3H, bs); 1.84-1.75 (2H, m); 1.63 (6H, q); 1.53 (6H, s); 1.42 (3H, s); 1.53-1.31 (3H, m). Prepared as described in Example 12b using 2-chloro-5-hydroxy-iV-(tricyclo[3.3.1.13.7]dec-l-methyl)-benzamide (Example 12a) and 4-(2-hydroxyethyl)-l-piperazinecarboxylic acid, 1,1-dimethylethyl ester. MS (APCI+ve) 432 (M+H)+ 1H NMR (CD3OD) δ 8. 40 (1H, t); 7.41 (1H, d); 7.14-7.06 (2H, m); 4.45 (2H, t); 3.76-3.58 (10H, m); 3.07-3.03 (2H, m); 1.98 (3H, s); 1.77 (3H, d); 1.69 (3H,d);1.62(6H,s). Example 79 2-Chloro-5-[2-(4-piperidinyl)ethoxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt Prepared as described in Example 12b using 2-chloro-5-hydroxy-N-(tricyclo[3.3.1.13.7]dec-l-methyl)-benzamide (Example 12a) and 4-(2-hydroxyethyl)-I-piperidinecarboxylic acid, 1,1-dimethylethyl ester. MS (APCI +ve) 431 (M+H)+ 1H NMR (DMSO-d6) δ 8.75 (1H, brs); 8. 49 (1H, brs); 8. 27 (1H, t); 7.37 (1H, d); 6.99 (1H, dd); 6.91 (1H, d); 4:03 (2H, t); 3.22 (2H, d); 2.92 (2H, d); 2.82 (2H, t); 1.94 (3H, s); 1.82 (2H, d); 1.79-1.70 (1H, m); 1.69-1.64 (5H, m); 1.59 (3H, d); 1.53 (6H, s); 1.43-1.30 (2H,m). Example 80 2-Chloro-S-[2-(4-piperidinyIoxy)ethoxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyI)-benzamide, hydrochloride salt Prepared as described in Example 12b using 2-chloro-5-hydroxy-N-(tricyclo[3.3.1.13.7]dec-l-methyl)-benzamide (Example 12a) and 4-(2-hydroxyethoxy)-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester. MS (APCI +ve) 447 (M+H)+ 1HNMR (CD3OD) δ 8. 39 (1H, brt); 7.38-7.33 (1H, m); 7.06-6.98 (2H, m); 4.22-4.16 (2H, m); 3.88-3.82 (2H, m); 3.80-3.71 (1H, m); 3.36-3.24 (2H, m); 3.16-3.04 (4H, m); 1.99 (3H, s); 2.08-1.86 (4H, m); 1.78 (3H, d); 1.69 (3H, d); 1.62 (6H, s). Prepared as described in Example 12b using 2-chloro-5-hydroxy-iV-(tricyclo[3.3.1.13,7]dec-l-methyl)-benzamide (0.20g, Example 12a) and 4-[2-(2-hydroxyethoxy)ethyl]-l-piperazine carboxylic acid; 1,1-dimethylethyl ester (0.26g). MS (APa +ve) 476 (M+H)+ 1HNMR (CD3OD) δ 7.7(1H, dd); 7.04-7.01 (2H, m); 4.25-4.18 (2H, m); 3.94 (2H, t); 3.91-3.87 (2H, m); 3.80-3.43 (10H, m); 3.06 (2H, s); 1.99 (3H, s); 1.75 (3H, d); 1.67 (3H, d); 1.62 (6H, s). Example 82 2-Chloro-5-[(5,6-dihydro-l(4H)-pyrimidinyl)methyl]-N-(tricycIo[3.3.1.13.7]dec-l- ylmethyl)-benzamide Prepared according to the method described in Example 8 from 5-bromomethyl-2-cfaloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (Example 8b,) and 1,4,5,6-tetrahydro- pyrimidine. MS (APCI+ve) 400/402 (M+H)+ 1H NMR (CDCl3) δ 7.84 (IH, s); 7.60 (1H, d); 7.43 (1H, d); 7.29 (1H, dd); 6.51 (1H, t); 4.39 (2H, s); 3.40-3.10 (3H, m); 3.17 (2H, d); 3.14 (1H, t); 2.01 (3H, s); 1.91 (q, 2H); 1.74 (3H, d); 1.64 (3H, d); 1.59 (6H, bs). Example 83 2-Chloro-5-[[4-[(2-hydroxyethyl)amino]-l-piperidinyl]methyl]-N-(tricyclo[3.3.1.1.3.7]dec-l-ylmethyl)-benzamide, hydrochloride salt a) 2-Chloro-5-[(4-oxo-l-piperidinyl)methyl]-iV-(tricyclo[3.3.l.l3.7]dec-l-ylmethyl)- benzamide Prepared according to the method described in Example 8c from 5-bromomethyl-2-chloro-A^tricyclo[3.3.1.13,7]dec-l-ylmethyl)-benzamide (Example 8b) and 4-piperidinone. MS (APCI +ve) 456/458 (M+H)+ b) 2-Chloro-5-[[4-[(2-hydroxyethyl)amino]-l-piperidinyl]methyl]-N. (tricydo[3.3.l.l3.7]dec-l-ylmethyl)-benzamide, hydrochloride salt To a solution of 2-chloro-5-[(4-oxo-l-pipcridinyl)methyl]-N-(tricyclo[3.3.1.13,7]dec-l-ylmethyl)-benzamide (0.150g, Example 83a) in methanol (3ml) at room temperature were added ethanolamine (0.11ml) and sodium cyanoborohydride (0.068g). The pH was adjusted to 6 by adding a 4N solution of hydrogen chloride in dioxane and the reaction stirred for 48h. The reaction was acidified with concentrated hydrochloric acid until gas evolution ceased. The precipitate was removed by filtration and the filtrate concentrated under vacuum. The residue was partitioned between ethyl acetate and water. The aqueous layer was basified with 5% aqueous sodium hydroxide and extracted with dichloromethane. The organics were washed with brine and dried over magnesium sulfate. The crude material was purified on silica gel (5% 7N ammonia in methanol/95% dichloromethane) to afford a white foam which was dissolved in ether/methanol and treated with a 4N solution of hydrogen chloride in dioxane to give the title compound (0.135 g). MS (APCI +ve) 460/462 (M+H)+ 1H NMR (CD3OD) δ 8.47 (1H, t); 7.67 (1H, d); 7.64 (1H, dd); 7.60 (1H, d); 4.39 (2H, s); 3.81 (2H, t); 3.62 (2H, bd); 3.52 (1H, t); 3.23-3.10 (4H, m); 3.09 (2H, d); 2.39 (2H, d); 2.07 (2H, q); 1.99 (s, 3H); 1.77 (3H, d); 1.70 (3H, d); 1.64 (6H, d). a) 2-Chloro-5-(l-oxa-6-azaspiro[2^]oct-6-ylmethyl)-N-(tricyclo[33.1.13.7]dec-l-ylmethyl)-benzamide To dimethylsulfoxide (2ml) was added sodium hydride (0.033g, 60 % in oil) at room temperature. The mixture was stirred for 5min. at this temperature and a solution of limethylsulfoxonium iodide (0.178g) in dimethylsulfoxide (2ml) was added. After 30min.,2-chloro-5-[(4-oxo-l-piperidinyl)methyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (0.28g, Example 83a) in dimethylsulfoxide (2ml) was added and the reaction itirred at room temperature for 3h before being quenched with ice/water (20ml). The nixture was extracted three times with ethyl acetate, the combined organic layers washed vim brine and dried over magnesium sulfate. The crude material was purified on silica gel, eluting with ethyl acetate to afford the subtitle compound as a white foam (0.25g). MS(APCI+ve) 429/431 (M+H)+ 1HNMR (CDCl3) δ 7.68 (1H, s); 7.40-7.30 (2H, m); 6.27 (1H, t); 3.54 (2H, s); 3.18 2H, d); 2.70-2.50 (6H, m); 2.00 (s, 3H); 1.90-1.75 (2H, m); 1.74 (3H, d); 1.66 (3H, d); 59 (6H, bs); 1.80-1.50 (m, 2H). 2-ChIoro-5-[[4-hydroxy-4-[[(l-methyIethyl)amino]metfayl]-l-iperidinyI]methyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide In a sealed tube 2-chloro-5-(l-oxa-6-azaspiro[2.5]oct-6-ylmethyl)-N-ricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (Example 84a, 0.15g) was dissolved in a mixture of ethanol (4ml) and di-isopropylamine (1ml) and heated at 65°C for 14h. The volatiles were removed under vacuum and the residue purified on silica gel (5% 7N ammonia in methanol/95% dichloromethane) to afford the title compound as a white solid (0.115g). MS (APCI+ve) 488/490 (M+H)+ 1H NMR (CD 3OD) δ 7.45-7.35 (3H, m); 3.55 (2H, s); 3.06 (2H, s); 2.76 (1H, q); 2.70-2.55 (2H, m); 2.54 (2H, s); 2.50-2.35 (2H, m); 1.99 (s, 3H); 1.77 (3H, d); 1.70 (3H, d); 1.63 (10H, bs); 1.07 (m, 2H). Example 85 2-Chloro-5-{(1,2,3,6-tetrahydro-3-pyridinyl)methyl]-N-(tricyclo[3.3.l.l3.7]dec-l-ylmethyl)- benzamide, hydrochloride salt To pyridine (6ml) at 0°C was added portionwise lithium aluminium hydride (0.24g). The mixture was allowed to warm to room temperature and was stirred for 24h. Lithium iodide (0.220g) and pyridine (1ml) were added and the reaction stirred for a further lh. 5-Bromomethyl-2-chloro-N-(tricyclo[3.3.1 .l3.7]dec-l-ylmethyl)-benzamide (0.30g, Example 8b) in dry pyridine (2ml) was added to the solution at room temperature. After 2h, die mixture was quenched at 0°C with a cold 15 % aqueous solution of acetic acid, stirred for an hour and concentrated under vacuum. The residue was taken in 1N sodium hydroxide, extracted with dichloromethane and the organic layers dried over magnesium sulfate. The crude material was purified on silicagel (2 to 10% 7N ammonia in methanol/dichioromethane) then treated with a 4N solution of hydrogen chloride in dioxane and methanol to give the title compound (0.20g). MS (APCI +ve) 399/401 (M+H)+ 1H NMR (CD3OD) δ 8.42 (1H, t); 7.43 (1H, dd); 7.32 (1H, dd); 7.30 (d; 1H); 5.89 (1H, d); 5.80 (1H, d); 3.64 (2H, s); 3.40-3.30 (1H, m); 3.06 (4H,.d); 1.99 (s, 3H); 1.78 (3H, d); 1.68 (3H,d);1.63(6H,d). Example 86 2-Chloro-5-(3-piperidinylmethyl)-iV-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, acetate salt a) 2-Chloro-5-(3-piperidinylmethyl)-N-(tricyclo[33.1.13.7]dec-l-ylmethyl)-benzamide, acetate salt To pyridine (12 ml) at 0 °C was added portionwise lithium aluminium hydride (0.46g). The mixture was allowed to warm to room temperature and was stirred for 24h. Lithium iodide (0.44g) and pyridine (5ml) were added and the reaction stirred for a further 1h. The solution was cooled to -10 °C and 5-bromomethyl-2-chloro-iV-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (Example 8b, 0.5g) in dry pyridine (5ml) added. After 1 hour, the mixture was quenched at -10 degrees with cold water, then 1N sodium hydroxide. The solution was stirred for1h then concentrated under vacuum. The residue was taken in water, extracted with dichloromethane and the organic layers dried over magnesium sulfate. The crude material was purified on silica gel (ethylacetate : i-hexane / 4 : 1) to afford the subtitle compound as a white foam (0.355g). b) 2-Chloro-5-(3-piperidinylmethyl)-iV-(tricycIo[3.3.1.13.7]dec-l-ylmethyl). benzamide, acetate salt 2-Chloro-5-(3-pyridinylmethyl)-N-CtricycIo [3.3.1.13.7]dec-1 -ylmethyl)-benzamide (0.10g, Example 86a) was dissolved in methanol and treated with a 4N solution of hydrogen chloride in dioxane. The hydrochloride salt was isolated and hydrogenated in ethanol over platinium oxide following the procedure described in Example 51 to give the title compound as the acetate salt after purification by reverse phase HPLC (0.1 % aqueous ammonium acetate/acetontrile) (0.053g). MS (APCI +ve) 401/403 (M+H)+ . 1HNMR (CD3OD) δ 7.42 (1H, d); 7.31-7.25 (2H, m); 3.38-3.28 (1H; m); 3.28-3.18 (1H; 2m); 3.07 (2H, s); 2.86 (1H, dt); 2.72-2.61 (1H, m); 2,65 (1H, d); 2.13-2.05 (1H; m); 2.01 (3H, s); 1.94 (3H, s); 1.90-1.85 (1H; m); 1.85-1.60 (2H; m); 1.80 (3H, d); 1.71 (3H, d); 1.64 (6H,d); 1.29 (1H, qd). Example 87 2-bromo-S-[[4-[(2-hydroxyethyI)amino]-l-piperidinyI]methyl]-N-(tricycIo[33.1.13.7] dec-l-ylmethyl- benzamide Prepared according to the procedures described in Example 83a and 83b from 2-bromo-5-bromomethyl-N-(tricyclo[3.3.1. l3.7]dec-l-yimethyl)-benzarnide (Example 65a), 4-piperidane and ethanolamine MS (APCI +ve) MW 505/506 (M+H)+ 1H NMR (CDCl3) δ 7.53 (1H, d); 7.52 (1H, d); 7.26 (1H, dd); 6.05 (1H; t); 3.65 (2H; t); 3.46 (2H, s); 3.17 (2H, d); 2.82 (2H, t); 2.60-2.45 (1H, m); 2.20-1.95 (7H; m); 1.95-1.82 (2H, bd); 1.75 (3H, d); 1.66 (3H, d); 1.61 (6H, d); 1.50-1.35 (2H, qd). Example 88 2-Chloro-5-[(E)-3-piperidinylidenemethyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide a) 2-Chloro-S-[(E)-(5,6-dihydro-3(4H)-pyridinylidene)methyl]-N-(tricyclo[33.1.13.7]dec-l-ylmethyl)-benzamide 2-Chloro-5-formyl-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide (0.152 g, Example 31a) and 2,3,4,5-tetrahydropyridine trimer (Org. Synth., 1977, Voi.56, 118-122, 0.038 g) were dissolved in methanol (3 ml) and heated at reflux for 4h. The mixture was evaporated under reduced pressure then purified by HPLC eluting a gradient of 0-5% ethanol in dichloromethane to give the subtitle compound as a white foam (0.046 g), SIS (APQ +ve) 397 (M+H)+ 1HNMR (CD3OD) δ 7.98 (1H, s); 7.51 (3H, s); 6.83 (1H, s); 3.66-3.62 (2H, m); 3.07 (2H, s); 2.78-2.73 (2H, m); 1.99 (3H, bs); 1.73 (6H, q); 1.774.69 (2H, m); 1.64 (6H, s). 2-Cbioro-5-[(E)-3-piperidinylidenemethyl]-N-(tricycio[3.3.1.l3,7]dec-l-yimethyl)-benzamide Sodium borohydride (0.009 g) in methanol (0.5 ml) was added to a solution of 2-chloro-5-[(E)-(5,6-dihydro-3(4H)-pyridinylidene)methyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (0.046 g, Example 88a,) in methanol (1.5 ml). The reaction mixture was stirred for 4h under an atmosphere of nitrogen at room temperature. Concentrated hydrochloric acid (0.01 ml) was added and the mixture was evaporated under reduced pressure. An aqueous solution of sodium hydroxide (2M, 2 ml) was added to rebasify the residue followed by water (10 ml) and dichloromethane (10 ml). The layers were partitioned and the aqueous layer was extracted further with dichloromethane (2x10 ml). The organic extracts were combined, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give the title compound as a white powder (0.024 g). MS (APCI+ve) 399 (M+H)+ 1H NMR (CD3OD) δ 7.43 (1H, d); 7.29-7.26 (2H, m); 6.38 (1H, s); 3.45 (2H, s); 3.07 (2H, s); 2.96 (2H, t); 2.55 (2H, t); 2.00 (3H, bs); 1.75 (6H, q); 1.81-1.64 (2H, m); 1.64 (6H,s). Pharmacological Analysis Certain compounds such as benzoylbenzoyl adenosine triphosphate (bbATP) are known to be agonists of the P2X7 receptor, effecting the formation of pores in the plasma membrane (Drag Development Research (1996), 37(3). p.126). Consequently, when the receptor is activated using bbATP in the presence of ethidium bromide (a fluorescent DNA probe), an increase in the fluorescence of intracellular DNA-bound ethidium bromide is observed. The increase in fluorescence can be used as a measure of P2X7 receptor activation and therefore to quantify the effect of a compound on the P2X7 receptor. In this manner, each of the title compounds of Examples 1 to 88 was tested for antagonist activity at the P2X7 receptor. Thus, the test was performed in 96-well flat bottomed microtitre plates, the wells being filled with 250 µl of test solution comprising 200 ul of a suspension of THP-1 cells (2.5 x 106 cells/ml) containing 10-4 M ethidium bromide, 25 µl of a high potassium buffer solution containing 10 M bbATP, and 25 µl of the high potassium buffer solution containing 3x10-5 M test compound. The plate was covered with a plastics sheet and incubated at 37 °C for one hour. The plate was then read in a Perkin-Elmer fluorescent plate reader, excitation 520 nm, emission 595 nm, slit widths: Ex 15 nm, Em 20 nm. For the purposes of comparison, bbATP (a P2X7 receptor agonist) and pyridoxal 5-phosphate (a P2X7 receptor antagonist) were used separately in the test as controls. From the readings obtained, a PIC50 figure was calculated for each test compound, this figure being the negative logarithm of the concentration of test compound necessary to reduce the bbATP agonist activity by 50%. Each of the compounds of Examples 1 to 88 demonstrated antagonist activity, having a PIC50 figure > 4.50. WE CLAIM; wherein m represents 1, 2 or 3; each R independently represents a hydrogen or halogen atom; A represents C(O)NH or NHC(O); Ar represents a group X represents a bond, an oxygen atom or a group CO, CH2, OCH2, NR5 , CH2NR5 , CONR5 or S(O)n; n is 0, 1 or 2; one of R2 and R3 represents a halogen, nitro, amino or a C1-C6 alkyl, and the other of R2 and R3 represents a hydrogen atom; either R4 represents a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and optionally an oxygen atom, the heterocyclic ring system being optionally substituted by one or more substituents independently selected from fluorine atoms, hydroxyl, carboxyl, cyano, C1-C6 alkyl, C1-C6 hydroxyalkyl, -NR6R7, -(CH2)rNR6R7 and -CONR6R7, or R represents a 3- to 8-membered saturated carbocyclic ring system substituted by one or more substituents independently selected from -NR6 R7 , -(CH2)rNR6 R7 and -CONR R , the ring system being optionally further substituted by one or more substituents independently selected from fluorine atoms, hydroxyl and C1-C6 alkyl; r is 1,2, 3,4, 5 or 6; R5 represents a hydrogen atom or a C1-C6 alkyl or C3-C8 cycloalkyl group; R6 and R7 each independently represent a hydrogen atom or a C1-C6 alkyl, C2-C6 hydroxyalkyl or C3-C8 cycloalkyl group, or R6 and R7 together with the nitrogen atom to which they are attached form a 3- to 8-membered saturated heterocyclic ring; with the provisos that, (a) when A represents C(O)NH and R4 represents an unsubstituted 3- to 8-membered saturated aliphatic heterocyclic ring system containing one nitrogen atom, then X is other than a bond, and (b) when A represents C(0)NH and X represents a group CH2 or OCH2 then R4 does not represent an unsubstituted imidazolyl, unsubstituted morpholinyl, unsubstituted piperidinyl or unsubstituted pyrrolidinyl group, and (c) when A represents NHC(O) and R4 represents an unsubstituted 3- to 8-membered saturated aliphatic heterocyclic ring system containing one nitrogen atom, then X is other than a bond, and (d) when A represents NHC(O) and X represents OCH2 then R4 does not represent an unsubstituted 1-piperidinyl or unsubstituted 1-pyrrolidinyl group; or a pharmaceutically acceptable salt or solvate thereof. 2. A compound as claimed in claim 1, wherein A represents NHC (O). 3. A compound as claimed in claim 1 or claim 2, wherein Ar represents a group 4. A compound as claimed in claims 1 to 3, wherein X represents a bond, an oxygen atom or a group CO, CH2, OCH2, NH, CH2NH, CONH or S(O)n. 5. A compound as claimed in claims 1 to 4, wherein the heterocyclic ring system in the group R4 is pyrrolidinyl, piperidinyl, piperazinyl or homopiperazinyl. 6. A compound as claimed in claims 1 to 4, wherein the saturated carboxylic ring in the group R4 is cyclopentyl or cyclohexyl. 7. A compound of formula (I), or a pharmaceutically acceptable salt or solvate thereof, as claimed in claim 1 being: 2-Nitro-3-piperazin-l-yl-N-(tricyclo[3.3.1.13.7]dec-l-ylroethyl)-benzamide, 2-Amino-3-piperazin-1 -yl -N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, dihydrochloride salt, 2-Chloro-3-piperazin-l-yl -N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, 2-Chloro-5-piperazin-l-yl -N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, 2-Chloro-5-(hexahydro-1H-1,4-diazepin-1-yl)-N-(tricyclo[3.3.1.13.7]dec-1-ylmethyl)- benzamide, hydrochloride salt, 5-(4-Amino-1-piperidinyl)-2-chloro-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)- benzamide, hydrochloride salt, (+/-)-5-(3-Amino-1 -pyrrolidinyl)-2-chloro-N-(tricyclo[3.3.1. l3.7]dec-1 -ylmethyl)- benzamide, hydrochloride salt, 2-Chloro-5-piperazin-l-ylmethyl-N-(tricycIo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5'[(hexahydro-lH-l,4-diazepin-l-yl)methyl]-N-(tricyclo[3.3.1.13.7]dec-l- ylmethyl)-benzamide, hydrochloride salt, 5-[(4-Amino-l-piperidinyl)methyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, hydrochloride salt, 5-[(3-Amino-l-pyrrolidiny])methyl]-2-ch3oro-N-(tricyclo[3.3.1.1 3.7]dec-l-ylmethy])- benzamide, hydrochloride salt, 2-Chloro-5-(4-piperidinyloxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt, (R)-2-Chloro-5-(2-pyrrolidinylroethoxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, hydrochloride salt, (S)-2-Chloro-5-(2-pyrrolidinylmethoxy)-N-(tricyclo[3.3.1,13.7]dec-l-ylmethyl)- benzamide, hydrochloride salt, 2-Chloro-5-(3-piperidinylmethoxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, hydrochloride salt, cis-5-[(4-Aminocyclohexyl)oxy]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, hydrochloride salt, 2-Methyl-5-(l-piperazinylmethyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-(1-piperazinylmethyl)-N-(2-tricyclo[3,3.1.1 3.7]dec-l-ylethyl)-benzamide, hydrochloride salt, (+/-)-2-Chloro-5-(3-pyrro]idinyloxy>N-(tricyc]o[3.3.1.13.7}dec-1 -ylmethyl)-benzamide, hydrochloride salt, (+/-)-2-Chloro-5-(3-piperidinyloxy)-N-(tricyclo[3.3.1.1 3.7]dec-1 -ylmethyl)- benzamide, hydrochJoride salt, trans-5-[(4-Aminocyclohexyl)oxy]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, cis-(+/-)-5-[(3-Aminocyclopentyl)oxy]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-1 - ylmethyl)-benzamide, (S,S)-2-Chloro-5-(2,5-diazabicyc]o[2.2.1]hept-2-yl)-N-(tricyclo[3.3.1.13.7]dec-l- ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-(2-methyl-l-piperaziny])-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt, {+/-)-2-Chloro-5-(3-pyrrolidinylamino)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethy!)- benzamide, hydrochloride salt, (+/-)-5-(3-Amino-l-piperidinyl)-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, (+/-)-2-Ch]oro-5-(3-piperidinylamino)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, 2-Chloro-5-[hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl]-N-(tricyc]of3.3.1.13.7]dec-1 - ylmethyl)-benzamide, N-[2-methyl-5-(4-piperidinyloxy)phenyI]-tricyclo[3.3.1.13.7]decane-l-acetamide, hydrochloride salt, N-[2-chloro-5-(4-piperidinyloxy)phenyl]-tricyclo[3.3.1.13.7]decane-1 -acetamide, hydrochloride salt, 2-Chloro-5-[(4-piperidinylamino)methyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, dihydrochloride salt, 5-[[[4-(Aminornethyl)cyclohexyl]amino]methyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec- l-ylmethyl)-benzamide, dihydrochloride salt, 5-[[(4-Aminocyclohexyl)arnino]rnethyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l- ylmethyl)-benzamide, dihydrochloride salt, 5-[(1-Azabicyclo[2.2.2]oct-3-ylamino)methyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-1 - ylmethyl)-benzamide, N-[4-(3-Aminopyrrolidin-l-yl)-2-methylphenyl]-2-(tricyclo[3.3.1.13.7]dec-l- yl)acetamide, dihydrochloride salt, N-(2-Methyl-4-piperazin-l-ylphenyl)-2-(tricycloI3.3.1.13.7]dec-l-yl)acetamide, dihydrochloride salt, cis-4-(3-Amino-cyclopentyloxy)-2-chloro-N-(tncyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, hydrochloride salt, 2~Chloro-4-(4-piperidinyloxy)-N-(tricyclo[3.3.1.13,7]dec-1 -ylmethyl)-benzamide, hydrochloride salt, (+/-)-2-Chloro-4-(pyrrolidin-3-yloxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, 2-Chloro-4-(piperidin-3-yloxy)- N-(tricyclo[3.3.1.13.7]dec-l-ylmethy])-benzamide, hydrochloride salt, 2-Chloro-4-(4-piperazin~l-yl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethy])-benzamide, hydrochloride salt, 2-Chloro-4-(3-pyrrolidinylamino)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide hydrochloride salt, 2-Chloro-4-(hexahydro-1H-l,4-diazepin-l-yl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt, (±)-5-[(3-Amino-l-piperidinyl)methyl]-2-ch]oro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-(2,5-diazabicyclo[2.2.1]hept-2-ylmethyl)-N-(tricyclo[3.3.1.13.7]dec-1-ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-(9-oxa-3,7-diazabicyclo[3.3.1]non-3-ylmethyl)-N- (tricyclo[3.3.1.13.7)dec-l-ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-(3,7-diazabicyclo[3.3.1]non-3-ylmethy])-N-(tricyclo[3.3.1.13.7]dec-l- ylmethyl)-benzamide, hydrochloride salt, trans-2-Chloro-5-[[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]methyl]-N- (tricyclo[3.3.1.13.7] Jdec-l-ylmethyl)-benzamide, hydrochloride salt, cis-2-Chloro-5-[(hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)methyl]-N- 3 7 (tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide, hydrochloride sail, 2-Chloro-5-(4-piperidinylrnethyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-(4-hydroxy-piperidin-4-yl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-(l,2,3,6-tetrahydro-pyridin-4-yl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt, 2-Ethyl-5-piperazin-l-ylmethyl-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt, 2-Chloro-5-(piperidin-4-ylsulfanyl)-N-(tricycloI3.3-1.13.7 ]dec-l-ylmethyl)- befrcarrMe, Yiy&TocMoride sa)t, 2-Chloro-5-(piperidin-4-ylsuIfinyl)-N-(tricyclo[3.3.113.7]dec-l-ylmethyi)- benzamide, 2-Chloro-5-(piperidin-4-ylsulfonyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, hydrochloride salt. 2-Chloro-5-(piperazine-l-carbonyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, hydrochloride salt, 2-Chloro-5-([1,4]diazepane-l-carbonyl)-N-(tricyclo(3.3.3. 3.7 ]dec-l-ylmethyl)- benzamide, hydrochloride salt, 4-Chloro-N1-(piperidin-4-yl-)-N2-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- isophthalamide, hydrochloride salt, 2-Bromo-5-piperazin-l-ylmethyl-N-(tricyclo[3.3.1.13.7]dec-l-ylrnethyl)-benzamide, hydrochloride salt, 2-Chloro-5-(hexahydro-lH-l,4-diazepin-l-yl)-N-(2-tricycIo[3.3.1.13.7]dec-l-ylethyl)- benzamide, hydrochloride salt, (+/-)-5-(3-Amirio-l-pyrrolidinyl)-2-chloro-N-(2-tricyclo[3.3.1.13.7]dec-l-ylethyl)- benzamide, hydrochloride salt, 2-Chloro-5-(4-piperidinylcarbonyl)-N-(tricyclo[3.3.1.l 3.7]dec-l-ylmethyl)-benzamide, hydrochloride salt, 2-Ch!oro-54(5,6-dihyclrol(4H)-pyriraidinyI)rnethyl]-N-(tricyclo[3.3.1.13.7]dec-l- ylmethyl )-benzamide, 2-Chloro-5-[[4-[(2-hydroxyethyl)amino]-l-piperidinyl]methyl]-N- (tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide hydrochloride salt, 2-Chloro-5-[[4-hydroxy-4-[[(1-methylethyl)amino]methyl]-1-piperidinyl]methyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, 2-Chloro-5-[(l ,2,3,6-tetrahydro-3-pyridinyl)methyl]-N-(tricyclo[3.3.1.13.7]dec-1- ylmethyl)- benzamide, hydrochloride salt, 2-Chloro-5-(3-piperidinylmethyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)- benzamide, acetate salt, or 2-bromo-5-[[4-[(2-hydroxyethyl)amino]-l-piperidinyl]methyl]-N-(tricyc]o[3.3.1.13.7] dec-l-ylmethyl- benzamide. 8. A process for the preparation of a compound of formula (I) as claimed in claim 1 which comprises: (i) when X represents A CH2 group, R4 represents a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and optionally an oxygen atom, the heterocyclic ring system being optionally substituted by one or more substituents independently selected from fluorine atoms, hydroxyl, carboxyl, cyano, C1-C6 alkyl, C1-C6 hydroxyalkyl, -NR6R7, -(CH2)rNR6R7 and -CONR6R7 and R is linked to X through a nitrogen atom, reacting a compound of general formula wherein one of R and R represents a hydrogen atom and the other of R and R represents a group -CH2L11 in which L represents a leaving group and m, A, R1 , R2 and R3 are as defined in formula (I), with a compound of general formula R4-H (III) in the presence of a base, wherein R4' represents a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and optionally an oxygen atom, the heterocyclic ring system being optionally substituted by one or more substituents independently selected from fluorine atoms, hydroxyl, carboxyl, cyano, C1-C6 alkyl, C1-C6 hydroxyalkyl, -NR6R7, -(CH2)rNR6R7 and -CONR6R7 and wherein R6 and R7 are as defined in formula (I); or (ii) when X represents an oxygen atom or a group OCH2 reacting a compound of general formula wherein one of R12 and R13 represents a hydrogen atom and the other of R12 and R13 represents a hydroxyl group and m, A, R1 , R2 and R3 are as defined in formula (I), with a compound of general formula wherein Y represents a bond or a group CH2 and R4 is as defined in formula (I), in the presence of l,l-(azodicarbonyl)dipiperidine and tributylphosphine; or (iii) when X represents a bond, an oxygen atom or a group OCH2 or NR5 , and A is NHC(O), reacting a compound of general formula wherein one of R and R represents a group -X'-R4 and the other of R14 and R15 represents a hydrogen atom, X' represents a bond, an oxygen atom or a group OCH2 or NR5 , L 2 represents a leaving group and R2 , R 3 , R 4 and R5 are as defined in formula (I), with a compound of general formula wherein m and R1 are as defined in formula (I), optionally in the presence of a coupling agent; or (iv) when X represents a bond, an oxygen atom or a group OCH2 or NR5 and A is C(0)NH, reacting a compound of general formula wherein R2 and R3 are as defined in formula (I) and R14 and R15 are as defined in formula (VI) in (iii) above, with a compound of general formula wherein m and R are as defined in formula (I), in the presence of a base; or (v) when X represents a bond or a group NR5 , reacting a compound of general formula wherein one of R16 and R17 represents a leaving group, L3 , and the other of R16 and R17 represents a hydrogen atom and m, A, R1 , R2 and R3 are as defined in formula (I), with a compound of general formula wherein Z represents a hydrogen atom or a group NHR and R5 and R4 and R5 are as defined in formula (I), optionally in the presence of a palladium catalyst, a phosphine ligand and a base; or (vii) when X represents a group CH2NR , reacting a compound of formula (II) a; defined in (i) above with a compound of formula (XI) as defined in (v) above wherein Z represents a group NHR ; or (x) when X represents a group CH2 and R4 represents an unsubstituted 4-to 6-membered saturated aliphatic heterocyclic ring system containing one nitrogen atom, reacting a compound of formula (II) as defined in (i) above, with a compound of general formula (xi) when X represents a group CO, CONR5 or SO2, and A is NHC(O), reacting a compound of general formula wherein one of R and R represents a group -X"-R4 and the other of R18 and R19 represents a hydrogen atom, X" represents a group CO, CONR5 or SO2, L4 represents a leaving group and R2 , R3 , R 4 and R5 are as defined in formula (I), with a compound of formula (VII) as defined in (iii) above, optionally in the presence of a coupling agent; or (xii) when X represents a group CO, CONR5 or SO2, and A is C(O)NH, reacting a compound of general formula wherein R2 and R3 are as defined in formula (I) and R18 and R19 are as defined in formula (XIII) in (xi) above, with a compound of formula (IX) as defined in (iv) above, in the presence of a base; or (xiii) when X represents a sulfur atom, reacting a compound of formula (X) as defined in (v) above, with an organolithium reagent and then with a compound of general formula 4 wherein Tol represents a tolyl group and R is as defined in formula (I); or (xiv) when X represents a CH2 group, reacting a compound of formula (X) as defined in (v) above, with an organolithium reagent and then with a compound of general formula 4 wherein R is as defined in formula (I), optionally followed by a reduction reaction; or (xv) when X represents a bond, reacting a compound of formula (X) as defined in (v) above, with an organolithium reagent and then with a compound of general formula 4 wherein R is as defined in formula (I), optionally followed by a reduction reaction; (xvi) when X represents a group SO, oxidising a corresponding compound of formula (I) in which X represents a sulphur atom; or wherein one of R20 and R21 represents a group CHO and the other of R20 and R21 represents a hydrogen atom, and m. A, R1 , R2 and R3 are as defined in formula (I), with a compound of general formula (XX), R4 -H, wherein R4 is as defined in formula (I), in the presence of a reducing agent; or (xxi) when X represents a group CH2NR", reacting a compound of formula (XIX) as defined in (xx) above, with a compound of general formula (XXI), R4 - Z, wherein Z' represents a group NHR5 , and R4 and R5 are as defined in formula (I), in the presence of a reducing agent; or (xxiii) when X represents a group CH2 reacting a compound of formula (II) as defined in (i) above with trimethylphosphite, and then with a compound of formula (XVI) as defined in (xiv) above, or with a compound of formula (XVII) as defined in (xv) above or with a compound of general formula (XVIA), R4 CHO in which R4 is as defined in formula (I), in the presence of abase, followed by a reductIon reaction; or (xxviii) when X represents a group CH2 and R4 represents a 3-piperidinyl or 2-piperazinyl group, reacting a compound of formula (II) as defined in (i) above with a reagent formed by combining pyridine or pyrazine with an aluminium hydride reagent, followed by a reduction reaction; or (xxx) when X represents a bond or NR5 and R4 represents a carbon-linked piperidyl wherein one of R26 and R27 represents a pyridyl, pyrazinyl, NR -pyridyl, NR -pyrazinyl, and the other of R26 and R27 represents a hydrogen atom, and m, A, R1, R2 and R3 are as defined in formula (I), with a source of hydrogen and a hydrogenation catalyst; or and optionally after (i), (ii), (iii), (iv), (v), (vii), (x), (xi), (xii), (xiii), (xiv), (xv), (xvi), (xx), (xxi), (xxiii), (xxviii) or (xxx), converting the compound of formula (I) to a further compound of formula (I) and, if desired, forming a pharmaceutically acceptable salt or solvate of the compound of formula (I), wherein each of the above process steps is conducted in an organic solvent of the kind such as herein described and at a temperature of 0 to 200°C. 9. A pharmaceutical composition comprising from 0.1 to 70 %w/w of a compound of formula (I), or a pharmaceutically acceptable salt or solvate thereof, as claimed in any one of claims 1 to 7 in association with a pharmaceutically acceptable adjuvant, diluent or carrier. 10. A process for the preparation of a pharmaceutical composition as claimed in claim 9 which comprises mixing in a manner as herein described, from 0.1 to 70% w/w of the compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof, as defined in any one of claims 1 to 7 with a pharmaceutically acceptable adjuvant, diluent or carrier. Dated this 01st day of October, 2001. [DEEPA KACHROO TIKU] OF REMFRY & SAGAR ATTORNEY FOR THE APPLICANT[S]

Full Text

FORM 2
THE PATENTS ACT 1970
[39 OF 1970]
&
THE PATENTS RULES, 2003
COMPLETE SPECIFICATION
[See Section 10; rule 13]
"AN ADAMANTANE COMPOUND"
ASTRAZENECA AB, a Swedish company of S-151 85 Sodertalje, Sweden
The following specification particularly describes the invention and the manner in which it is to be performed:

ADAMANTANE DERIVATIVES
The present invention relates to adamantane derivatives, a process for their preparation, pharmaceutical compositions containing them, a process for preparing the pharmaceutical compositions, and their use in therapy.
Adamantane derivatives are known in the art, e.g. from WO 95/04720 for use as astrin and cholecystokinin receptor ligands, from Chem. Abs. (1977), Volume 86, No. 13 36: 89560d) for use as analgesics, and from US-A-3 464 998 as antibiotics.
The P2X7 receptor (previously known as P2Z receptor), which is a ligand-gated ion channel, is present on a variety of cell types, largely those known to be involved in the uflammatory/immune process, specifically, macrophages, mast cells and lymphocytes A and B). Activation of the P2X7 receptor by extracellular nucleotides, in particular denosine triphosphate, leads to the release of interleukin-113 (IL-1β) and giant cell formation (macrophages/microglial cells), degranulation (mast cells) and proliferation (T cells), apoptosis and L-selectin shedding (lymphocytes). P2X7 receptors are also located a antigen-presenting cells (APC), keratinocytes, salivary acinar cells (parotid cells), spatocytes and mesangial cells.
It would be desirable to make compounds effective as P2X7 receptor antagonists for be in the treatment of inflammatory, immune or cardiovascular diseases, in the aetiologies which the P2X7 receptor may play a role.
In accordance with the present invention, there is therefore provided a compound of general formula

wherein m represents I, 2 or 3, preferably 1 or 2;
each R independently represents a hydrogen or halogen (e.g. fluorine, chlorine, bromine or
iodine) atom, preferably a hydrogen atom;
A represents C(0)NH or, preferably, NHC(O);
AT represents a group

X represents a bond, an oxygen atom or a group CO, (CH2)1-6. CH=, (CH2)1-6O, O(CH2)1-6 O(CH2)2-6O, O(CH2)2-3O(CH2)1-3, CR'(OH), (CH2)1-3O(CH2)1-3, (CH2)1-3O(CH2)2-3O, NR5. (CH2)1-6NR5, NR5(CH2)1-6, (CH2)1-3NR5(CH2)1-3. O(CH2)2-6NR5, O(CH2)2-3NR5(CH2)1-3, (CH2)1-3NR5(CH2)2-3O, NR5(CH2)2-6O,
NR5(CH2)2-3O(CH2)1-3. CONR5, NR5CO, s(O)n, s(O)nCH2, CH2s(O)n, SO2NR5
or NR5SO2; n is 0,1 or 2;
R'represents a hydrogen atom or a C1-C5 alkyl, preferably methyl, group;

one of R2 and R3 represents a halogen, cyano, nitro, amino, hydroxyl, or a group
selected from (i) C1-C6 alkyl optionally substituted by at least one C3-C6 cycloalkyl,
(ii) C3-C8 cycloalkyl, (iii) C1-C6 alkyloxy optionally substituted by at least one
C3-C6 cycloalkyl, and (iv) C3-C8 cycloalkyloxy, each of these groups being optionally

substituted by one or more fluorine atoms, and the other of R2 and R3 represents a
hydrogen or halogen atom;

either R4 represents a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring
system containing one or two nitrogen atoms and optionally an oxygen atom, the
heterocyclic ring system being optionally substituted by one or more substituents
independently selected from fluorine atoms, hydroxyl, carboxyl, cyano, C1-C6 alkyl.
C1-C6 hydroxyalkyl, -NR6R7, -(CH2)rNR6R7 and -CONR6R7,
or R4 represents a 3- to 8-membered saturated carbocyclic ring system substituted by one

or more substituents independently selected from -NR6 R7 , -(CH2)rNR6 R7 and

-CONR6 R 7 , the ring system being optionally further substituted by one or more substituents independently selected from fluorine atoms, hydroxyl and C1-C6 alkyl;
r is 1, 2, 3,4, 5 or 6;

R5 represents a hydrogen atom or a C1-C6 alkyl or C3-C8 cycloalkyl group;
R6 and R7 each independently represent a hydrogen atom or a C1-C6 alkyl,
C2-C5 hydroxyalkyl or C3-C8 cycloalkyl group, or R and R together with the nitrogen
atom to which they are attached form a 3- to 8-membered saturated heterocyclic ring;
with the provisos that,

(a) when A represents C(O)NH and R4 represents an unsubstituted 3- to 8-membered
saturated aliphatic heterocyclic ring system containing one nitrogen atom, men X is other than a bond, and
(b) when A represents C(O)NH and X represents a group (CH2)1-6 or O(CH2)1-6, then

R4 does not represent an unsubstituted imidazolyl, unsubstituted morpholinyl,
unsubstituted piperidinyl or unsubstituted pyrrolidinyl group, and

(c) when A represents NHC(O) and R4 represents an unsubstituted 3- to 8-membered
saturated aliphatic heterocyclic ring system containing one nitrogen atom, then X is other than a bond, and
(d) when A represents NHC(O) and X represents O(CH2)1-6, NH(CH2)1-6 or SCH2, then
R4 does not represent an unsubstituted 1-piperidinyl or unsubstituted 1-pyrrolidinyl
group, and

(e) when A represents NHC(O) and X represents O(CH2)2-3NH(CH2)2, then R4 does not
represent an imidazolyl group;
or a pharmaceutically acceptable salt or solvate thereof.

In the context of the present specification, unless otherwise indicated, an alkyl substituent or alkyl moiety in a substituent group may be linear or branched. Examples of
alkyl groups/moieties containing up to 6 carbon atoms include methyl, ethyl, propyl,

isopropyl, butyl, isobutyl, tert-butyl, pentyl and hexyl. When one of R2 and R3 represents a
C1-C6 alkyl/C1-C6 alkyloxy optionally substituted by at least one C3-C6 cycloalkyl, it
should be understood that one or both of the alkyl and cycloalkyl moieties may be
optionally substituted by fluorine atoms. In relation to R4 , a 3- to 9-membered saturated or
unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and
optionally an oxygen atom may be a monocyclic or bicyclic ring system. Further in
relation to R4 , a 3- to 8-membered saturated carbocyclic ring system may be a monocyclic

or bicyclic ring system. When R6 or R7 represents a C2-C6 hydroxyalkyl in the substituent NR6R7, -(CH2)rNR6R7 or -CONR6R7, it will be appreciated that the hydroxyl group will not be bonded to the same carbon atom as the nitrogen atom. When R and R together with the nitrogen atom to which they are attached form a 3- to 8-membered saturated heterocyclic ring, the ring obtained is moncyclic.
Preferably X represents a bond, an oxygen atom or a group CO, (CH2)1-6, CH=, O(CH2)1-6, O(CH2)2-6O, O(CH2)2-3O(CH2)1-3. CR'(OH), NR5, (CH2)1-6NR5, CONR5, S(O)n or S(O)nCH2-

One of R2 and R3 represents a halogen (e.g. fluorine, chlorine, bromine or iodine),
cyano, nitro, amino, hydroxyl, or a group selected from (i) C1-C6 alkyl, preferably C1-C4
alkyl, optionally substituted by at least one (e.g. 1, 2 or 3) C3-C6 cycloalkyl (i.e.
cyclopropyl, cydobutyl, cyclopentyl or cyclohexyl), (ii) C3-C8 cycloalkyl (e.g.
cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl), (iii) C1-C6 alkyloxy, preferably C1-C4
alkyloxy, optionally substituted by at least one (e.g. 1, 2 or 3) C3-C6 cycloalkyl (i.e.
cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl), and (iv) C3-C8 cycloalkyloxy (e.g.
cyclopropyloxy, cyclobutyloxy, cyclopentyloxy or cyclohexyloxy), each of these groups
being optionally substituted by one or more (e.g. 1, 2, 3 or 4) fluorine atoms, and die other

of R2 and R3 represents a hydrogen or halogen (e.g. fluorine, chlorine, bromine or iodine)
atom.

Preferably, one of R2 and R3 represents a halogen (especially chlorine or bromine)
atom or a nitro, amino or C1-C6 alkyl (especially methyl or ethyl) group and the other of

R2 and R3 represents a hydrogen atom.

R4 may represent a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and optionally an oxygen atom, the heterocyclic ring system being optionally substituted by one or more (e.g. 1, 2,3 or 4) substituents independently selected from fluorine atoms, hydroxyl, carboxyl, cyano, C1-C6 alkyl, preferably C1-C4 alkyl, C1 -C6 hydroxyalkyl, preferably C1-C4 hydroxyalkyl, -NR6R7, -(CH2)rNR6R7 and -CONR6R7.
The 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system in the group R4 may be a monocyclic ring system such as pyrrolidinyl (e.g. 1-pyrrolidinyl, 2-
pyrrolidinyl or 3-pyrrolidinyl), piperidinyi (e.g. 1-piperidinyl, 2-piperidinyI, 3-piperidinyl
or 4-piperidinyl), 4-piperiden-3-yl, piperazinyl (e.g. 1-piperazinyl), homopiperazinyl,

Alternatively, R4 may represent a 3- to 8-membered saturated carbocyclic ring
system substituted by one or more (e.g. 1, 2 or 3) substituents independently selected from
NR6 R7 , -(CH2)rNR6 R7 and -CONR6R7, the ring system being optionally further
substituted by one or more (e.g. 1, 2, 3 or 4) substituents independently selected from
fluorine atoms, hydroxyl and C1-C6 alkyl, preferably C1-C4 alkyl.
The 3- to 8-membered saturated carbocyclic ring in the group R is preferably a monocyclic ring system such as a cyclopentyl or cyclohexyl ring.

When X represents a bond or a group CO, (CH2)1-6, O(CH2)2-6. O(CH2)2-3O(CH2)2-3, (CH2)1-3O(CH2)2-3. NR5(CH2)2-6, (CH2)1-3NR5(CH2)2-3,
O(CH2)2-3NR5(CH2)2-3, NR5(CH2)2-3O(CH2)2-3, NR5CO, SO2 or NR5SO2,
R4 preferably represents a group:

When X represents an oxygen or sulphur atom or a group CH=, (CH2)1-6O, OCH2, O(CH2)2-6O, O(CH2)2-3OCH2, CROH, (CH2)1-3OCH2, (CH2)1-3O(CH2)2-3O, NR5, (CH2)1-6NR5, O(CH2)2-6NR5, NR5CH2, (CH2)1-3NR5CH2, O(CH2)2-3NR5CH2.
(CH2)1-3NR5(CH2)2-3O, NR5(CH2)2-6O, NR5(CH2)2-3OCH2, CONR5, SO, S(O)nCH2,
CH2S(O)n or SO2NR5 , R4 preferably represents a group:

R represents a hydrogen atom, or a C1-C6, preferably C1-C4, alkyl (e.g. methyl, ethyl, propyl, butyl, pentyl or hexyl) or C3-C8, preferably C3-C6, cycloalkyl (e.g. cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl) group.
R6 and R7 each independently represent a hydrogen atom, or a C1-C6, preferably C1-C4, alkyl (e.g. methyl, ethyl, propyl, butyl, pentyl or hexyl), C2-C6 hydroxyalkyl or C3-C8, preferably C3-C6, cycloalkyl (e.g. cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl) group, or R and R together with the nitrogen atom to which they are attached form a 3- to 8-membered, preferably 3- to 6-membered, saturated heterocyclic ring such as a pyrrolidinyl or piperidinyl ring.
Preferred compounds of the invention include:
2-Nitro-3-piperazin-1 -yl-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide,

2-Amino-3-piperazin-l-yl -N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, dihydrochloride salt,
2-Chloro-3-piperazin-l-yl -N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide,
2-Chloro-5-piperazin-1 -yl -N-(tricyclo[3.3.1.1 3.7]dec-l-ylmethyl)-benzamide,
2-Chloro-5-(hexahydro-1H-1,4-diazepin-1 -yl)-N-(tricyclo[3.3.1.13.7]dec-1 -y imethyl)-
benzamide, hydrochloride salt,
5-(4-Arnino-l-piperidinyl)-2-chloro-N-(tricyclo(3.3.1.13.7]dec-l-ylmethyl)-
benzamidc, hydrochloride salt,
(+/-)-5-(3-Amino-1-pyrrolidinyl)-2-chloro-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-
benzamide, hydrochloride salt,
2-Chloro-5-piperazin-l-ylmethyl-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide, hydrochloride salt,
2-Chloro-5-[(hexahydro-1H-1,4-diazepin-1 -yl)methyl] -N-(tricyclo[3.3.1.13.7]dec-1 -
ylmethyl)-benzamide, hydrochloride salt,
5-[(4-Amino-l-piperidinyl)methyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide, hydrochloride salt,
5-[(3-Amino-l-pyrTolidinyl)methyI]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide, hydrochloride salt,
2-Chloro-5-(4-piperidinyloxy)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide,
hydrochloride salt,
(R)-2-Chloro-5-(2-pyrrolidinylmethoxy)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt,
(S)-2-Chloro-5-{2-pyrrolidinylmethoxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide, hydrochloride salt,
2-Chloro-5-(3-piperidinylmethoxy)-N-(tricyclo[3.3.1.13.7]dec-1-ylmethyl)-
benzamide, hydrochloride salt,
cis-5-[(4-Aminocyclohexyl)oxy]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-
benzamide, hydrochloride salt,
2-Methyl-5-( 1 -piperazinylmethyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide,
hydrochloride salt,

2-Chloro-5-( 1-piperazinylmethyl)-N-(2-tricyclo[3.3.1.13.7]dec-1-ylethyl)-benzamide, hydrochloride salt,
(+/-)-2-Chloro-5-(3-pyrrolidinyloxy)-N-(tricyclo[3.3.1.13.7]dec- l-yimethyl}-benzamide, hydrochloride salt,
(+/-)-2-Chloro-5-(3-piperidinyloxyhN-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt,
trans-5-[(4-Aminocyclohexyl)oxy]-2-chloro-N-(tricyclo[3.3.1.13.7]dec- 1-yimethy!)-benzamide,
cis-(+/-)-5-[(3-Aminocyclopentyl)oxy]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamidc,
(S,S)-2-Chloro-5-(2,5-diazabicyclo[2.2.1 ]hept-2-yl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylrnethyl)-benzamide, hydrochloride salt,
2-Chloro-5-(2-methyl-1 -piperazinyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt,
(4y-)-2-Chloro-5-(3-pyrrolidinylamino)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-bcnzamide, hydrochloride salt,
(+/-)-5-(3-Amino-1 -pipericiinyl)-2-chloro-N-(tricycIo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide,
(+/-)-2-Chloro-5-(3-piperidinylamino)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide,
2-Chloro-5-[hexahydropymjlo[3,4-c]pyrrol-2(lH)-yl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide,
N-[2-methyI-5-(4-piperidinyloxy)phenyl]-tricyclo[3.3.1.13.7]decane-1 -acetamide,
hydrochloride salt,
NT-[2-chloro-5-(4-piperidinyloxy)phenyl]-tricyclo[3.3.1.13.7]decane-l-acetamide,
hydrochloride salt,
2-Chloro-5-[(4-piperidinyl^mino)methyl]-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-
benzamide, dihydrochloride salt,
5-[[[4-(Aminomethyl)cyclohexyl]amino]rnethyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-
l-ylmethyl)-benzamide, dihydrochloride salt,

5-[[(4-Aminocyclohexyl)amino]methyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-
ylmediyl)-benzamide, dihydrochloride salt,
5-[(l-Azabicyclo[2.2.2]oct-3-ylamino)methyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-yimethyl)-benzamide,
N-(4-(3-Aminopyrrolidin-1 -yl)-2-methylphenyl]-2-(tricyclo[3.3.1.1 3.7]dec-1 -
yl)acetamide, dihydrochloride salt,
N-(2-Methyl-4-piperazin-l-ylphenyl)-2-(tricyclo[3.3.1.13.7]dec-l-yl)acetamide,
dihydrochloride salt,
cis-4-(3-Amino-cyclopentyloxy)-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-
benzamide, hydrochloride salt,
2-Chloro-4-(4-piperidinyloxy)-N-(tricyclo[3.3.1.13,7]dec-l-ylraethyl)-benzamide, hydrochloride salt,
(+/-)-2-Chloro-4-(pyrrolidin-3-yloxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide,
2-Chloro-4-(piperidin-3-yloxy)- N-(tricyclo[3.3.1.13.7] dec-1-yimethyO-benzamide,
hydrochloride salt,
2-Chloro-4-(4-piperazin-1 -yI)-N-(tricyclo[3.3.1.13.7]dec-1 -yimethyO-benzamide,
hydrochloride salt,
2-Chloro-4-(3-pyrrolidinyIamino)-N-(tricyclo(3.3.1.13.7]dec-1-yimethyO-benzamide,
hydrochloride salt,
2-Chloro-4-(hexahydro-lH-l,4-diazepin-l-yl)-N-(tricyclo[3.3.1.13.7]dec-l-
ylmethyl)-benzamide, hydrochloride salt,
(±)-5-[(3-Amino-l-piperidinyl)methyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-
ylmethyO-benzamide, hydrochloride salt,
2-Chloro-5-(2,5-diazabicyclo[2.2.1 ]hept-2-ylmethyl)-N-(tricyclo(3.3.1.13.7]dec-1 -
yimethyl)-benzamide, hydrochloride salt,
2-Chloro-5-{9-oxa-3,7-diazabicyclo[3.3.1]non-3-ylmethyl)-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide, hydrochloride salt,
2-Chloro-5-(3,7-diazabicydo[3.3.1 }non-3-yimethyO-N-(tricyclo[3.3.1.13.7]dec-l -yimethyO-benzamide, hydrochloride salt.

trans-2-Chloro-5-[[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]inethyl]-N-
tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt,
cis-2-Chloro-5-[(hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)methyl]-N-
tricyclo[3.3.1.13.7]dec-l -yimethyl)-benzamide, hydrochloride salt,
2-Chloro-5-(4-piperidinyiidenernethyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-
lenzamide, hydrochloride salt,
2-Chloro-5-(4-piperidinylmethyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide,
ydrochloride salt,
2-Chloro-5-(4-hydroxy-piperidin-4-yl)-N-(tricyclo [3.3.1.13.7]dec-1 -ylmethyl)-
benzamide, hydrochloride salt,
2-Chloro-5-(l,2,3,6-tetrahydro-pyridin-4-yl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyi)-benzamide, hydrochloride salt,
2-Ethyl-5-piperazin-1 -ylmethyl -N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide,
hydrochloride salt,
2-Chloro-5-(piperidin-4-ylsulfanyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide, hydrochloride salt,
2-Chloro-5-(piperidin-4-ylsulfmyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-
benzamide,
2-Chloro-5-(piperidin-4-ylsulfonyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide, hydrochloride salt,
2-Chloro-5-(piperidin-4-ylmethylsulfanyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide, hydrochloride salt,
2-Chloro-5-(piperidin-4-ylmethanesulfonyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-
benzamide, hydrochloride salt,
2-Chloro-5-(piperazine-1 -carbonyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-
benzamide, hydrochloride salt,
2-Chloro-5-([ 1,4]diazepane-1 -carbonyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-
snzamide, hydrochloride salt,
4-Chloro-N^piperidin-4-yl-)-N2-(tricyclo[3.3. 1.13.7]dec-1 -ylmethyl)-
ophthalamide, hydrochloride salt,

2-Chloro-5-{hydroxy-4-piperidinylmethyl)-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethy])-benzamide, hydrochloride salt,
(±)-2-Chloro-5-(hydroxy-3-piperidinylmethyl)-N-(tricyc]o[3.3.1.13.7]dec-1 -methyl)-benzamide, hydrochloride salt,
2-Bromo-5-piperazin-1 -ylmethyl-N-(tricyclof3.3.3.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt,
2-Chloro-5-[2-( 1 -piperaziny l)ethyl ]-N-(tricyclo [3.3.1.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt,
2-Chloro-5-[2-(2,5-diazabicycIo[2.2.1 ]hept-2-yl)ethyl]-N-(tricyclo[3.3.1. l3.7]dec-1 -lmethyl)-benzamide, hydrochloride salt,
5-[2-(4-Amino-1 -piperidinyl)ethyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-enzamide, hydrochloride salt,
2-Chloro-5-[2-(3-piperidinylamino)ethyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-enzamide, dihydrochloride salt,
5-[2-(3-Amino-1 -piperidinyl)ethyI]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-enzamide, hydrochloride salt,
2-Chloro-5-[2-{3-pyrrolidinylamino)ethyl]-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-enzamide, dihydrochloride salt,
5-[2-[(3R)-3-Aminopyrrolidinyl]ethyl]-2-chloro-N-(tricyclo[3.3.1.1I3.7]dec-1-[methyl)-benzamide, hydrochloride salt,
2-Chloro-5-[2-[2-(hydroxymethyl)-1 -piperazinyl]ethyl]-N-(tricyclo[3.3.1.13.7]dec-1 -[methyl)-benzamide, hydrochloride salt,
2-Chloro-5-(hexahydro-1H-1,4-diazepin-1 -yl)-N-(2-tricyclo[3.3.1. l3.7]dec-1 -ylethyl)-snzamide, hydrochloride salt,
(+/-)-5-(3-Amino- l-pyrrolidinyl)-2-chloro-N-(2-tricyclo[3.3.1.13.7]dec-1 -ylethyl)-benzamide, hydrochloride salt,
2-Chloro-5-(4-piperidinylcarbonyI)-N-(tricyclo[3.3.1.13.7]dec-1-ylmethyl)-benzamide, hydrochloride salt,
2-Chloro-5-[1 -hydroxy-1 -(4-piperidinyl)ethyl]-N-(tricycio[3.3.1.13.7]dec-1 -ylmethyl)-snzamide, hydrochloride salt,

2-Chloro-5-[2-( 1 -piperazinyl)ethoxy)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt,
2-Chloro-5-[2-(4-piperidinyl)ethoxy)-N-(tricyclo[3.3.1. l3.7]dec-l-yimethyl)-benzamide, hydrochloride salt,
2-Chloro-5-[2-(4-piperidinyloxy)ethoxy)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide, hydrochloride salt,
2-Chloro-5-[2-[2-(l-piperazinyl)ethoxy]ethoxy]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyi)-benzamide, hydrochloride salt,
2-Chloro-5-[(5,6-dihydro-1 (4H)-pyrimidmyl)methy\]-N-(tricyclo[33.l. l3.7]dec-1 -ylmethyl)-benzamide,
2-Chloro-5-[[4-[(2-hydroxyethyl)amino]-l-pipcridinyl]methyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt,
2-Chioro-5-[[4-hydroxy-4-[[( 1 -methylethyl)amino]methyI]-1 -piperidinyljmethyl]-N-(tricyclo[3.3.1. l3.7]dec-1-ylmethyl)-benzamide,
2-Chloro-5-[( 1,2,3,6-tetrahydro-3-pyridinyl)methyl]-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)- benzamide, hydrochloride salt,
2-Chloro-5-(3-piperidinylmethyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)- benzamide, acetate salt,
2-bromo-5-[[4-[(2-hydroxyethyl)amino]-l-piperidinyl]methyl]-A/-(tricyclo[3.3.1.13.7] dec-1-ylmethyl-benzamide, and
2-Chloro-5-[(E)-3-piperidinylidenemethyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide.
The present invention further provides a process for the preparation of a compound
of formula (I) as defined above which comprises:
(i) when X represents a CH2 group, R4 represents a 3- to 9-membered saturated
or unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and
optionally an oxygen atom, the heterocyclic ring system being optionally substituted by one
or more substituents independently selected from fluorine atoms, hydroxyl, carboxyl,

wherein one of R10 and R11 represents a hydrogen atom and the other of R10 and R11
represents a group -CH2L1 in which L represents a leaving group (e.g. a halogen atom)

and m, A, R1 , R2 and R3 are as defined in formula (I), with a compound of general formula
R4'-H (III)

in the presence of a base (e.g. diisopropylethylamine), wherein R4' represents a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and optionally an oxygen atom, the heterocyclic ring system being optionally substituted by one or more substituents independently selected from fluorine atoms, hydroxyl, carboxyl, cyano, C1-C6 alkyl, C1-C6 hydroxyalkyl, -NR6 R7 , -(CH2)rNR R and -CONR R and wherein R and R are as defined in formula (I); or
(ii) when X represents an oxygen atom or a group 0(CH2h-6, 0(CH2h-60. 0(CH2)2-30(CH2)i.3, 0(CH2)2-6NR5 or 0(CH2)2-3NR5(CH2)i.3, reacting a compound of general formula

12 13 12 13
wherein one of R and R represents a hydrogen atom and the other of R and R
12 3
represents a hydroxyl group and m. A, R , R and R are as defined in formula (I), with a
compound of general formula

wherein Y represents a bond or a group (CH2)i-6, 0(0*2)2-6. (01*2)1-30(0*2)2-3, NR5(0*2)2-6 or (OJ2)i-3NR5(CH2)2-3 and R4 is as defined in formula (I), in the presence of 1,1 -(azodicarbonyl)dipiperidine and tributylphosphine (under conditions of the Mitsunohu reaction: Tetrahedron Lett. (1993), 34, 1639); or
(iii) when X represents a bond, an oxygen atom or a group 0(0*2) 1-6. 0(0*2)2-60, 0(CH2)2.30(O*2)i.3, NR5, NR5(CH2),.6, NR5(CH2)2-60 or NR (0*2)2-30(0*2)1.3 and A is NHC(O), reacting a compound of general formula
14 15 4 14 15
wherein one of R and R represents a group -X'-R and the other of R and R
represents a hydrogen atom, X'represents a bond, an oxygen atom or a group 0(O*2)i-6,
0(O*2)2-60, 0(O*2)2-30(O*2)i-3, NR5. NR5(0*2)i-6, NR5(O*2)2-60 or
5 2
NR (0*2)2-30(0*2)1.3, L represents a leaving group (e.g. a hydroxy! or chloride leaving

"> 3 4 5
group) and R~, R , R and R are as defined in formula (I), with a compound of general
formula

wherein m and R are as defined in formula (I), optionally in the presence of a coupling agent (e.g. 1,1 '-carbonyldiimidazole); or
(iv) when X represents a bond, an oxygen atom or a group 0(CH2)i-6,
0(CH2)2.60? 0(CH2)2-30(CH2)i-3, NR5, NR5(CH2),.6l NR5(CH2)2-60 or
5 NR (CH2)2-30(CH2)]-3 and A is C(0)NH, reacting a compound of general formula

2 3 14 15
wherein R and R are as defined in formula (I) and R and R are as defined in formula
(VI) in (iii) above, with a compound of general formula

wherein m and R are.as defined in formula (I), in the presence of a base (e.g. diuopropyiamine); or

(v) when X represents a bond or a group NR , NR (CH2)i.6, NR5(CH2)2-60 or NR (CH2)2-30(CH2) 1.3, reacting a compound of general formula

wherein one of R and R represents a leaving group, L .such as a halogen atom and the other of R and R represents a hydrogen atom and m, A, R , R and R are as defined
in formula (I), with a compound of general formula
R4-Z (XI)
wherein Z represents a hydrogen atom or a group NHR , (CH2)i-6NHR , 0(CH2)2-6NHR5 or a group (CH2)i-30(CH2)2-3NHR5 and R4 and R5 are as defined in formula (I), optionally in the presence of a palladium catalyst (e.g. palladium acetate), a phosphine ligand (e.g. BINAP) and a base (e.g. cesium carbonate); or
(vi) when X represents a group CHiO, reacting a compound of formula (H) as defined in (i) above with a compound of formula (V) as defined in (ii) above wherein Y represents a bond, in the presence of a base (e.g. sodium hydride) or in the presence of a metal salt (e.g. silver trifluoromethanesulfonate); or
(vii) when X represents a group CHbNR , reacting a compound of formula (II) as defined in (i) above with a compound of formula (XI) as defined in (v) above wherein Z represents a group NHR ; or
(viii) when X represents a group CH20(CH2) 1.3 or CH20(CH2)2-30, reacting a compound of formula (H) as defined in (i) above with a compound of formula (V) as defined m (ii) above wherein Y represents a group (CH2)i_3 or 0(CH2)2-3> m the presence

of a base (e.g. sodium hydride) or in the presence of a metal salt (e.g. silver trifluoromethanesulfonate); or
(ix) when X represents a group CH3NR CH2 or CH2NR5 (0*2)2.3 O reacting a compound of formula (II) as defined in (i) above with a compound of formula (XI) as
5 5
defined m (v) above wherein Z represents a group CH2NHR or 0(CH2)2-3NHR ; or
4 (x) when X represents a group CHT and R represents an unsubstituted 4- to
6-membered saturated aliphatic heterocyclic ring system containing one nitrogen atom,
reacting a compound of formula (II) as defined in (i) above, with a compound of general
formula

wherein s and t independently represent 1 or 2; or

18 19 4 18 19
wherein one of R and R represents a group -X"-R and the other of R and R
represents a hydrogen atom, X" represents a group CO, CONR , NR CO, SO2,
5 5 4
NR SO2 or SO2NR , L represents a leaving group (e.g. a hydroxyl or chloride leaving
2 3 4 5
group) and R , R , R and R are as defined in formula (I), with a compound of formula
(VII) as defined in (iii) above, optionally in the presence of a coupling agent (e.g.
1,1 '-carbonyIdiimidazole); or

(xii) when X represents a group CO, CONR5, NR5CO, S02, NR5S02 or 5 SO2NR and A is C(0)NH, reacting a compound of general formula
I
2 3 18 19
wherein R and R are as defined in formula (I) and R and R are as defined in formula
(XHI) in (xi) above, with a compound of formula (DC) as defined in (iv) above, in the
presence of a base (e.g. diisopropylamine); or
(xiii) when X represents a sulfur atom, reacting a compound of formula (X) as defined in (v) above, with an organolithium reagent such as n-butyllithium (e.g. at -70 °C) and then witii a compound of general formula

4 wherein Tol represents a tolyl group (4-memylphenyl) and R is as defined in formula (I);
or
(xiv) when X represents a CHOH or CH2 group, reacting a compound of formula (X) as defined in (v) above, with an organolithium reagent (e.g. methyllithium/t-butyllithium or n-butyllithium at -70 °C) and then with a compound of general formula
wherein R is as defined in formula (I), optionally followed by a reduction reaction, e.g. with methyloxalylchloride and triethylamine followed by tributyltin hydride in the presence of azobiswobutyronitrile; or
(xv) when X represents a bond, reacting a compound of formula (X) as defined in (v) above, with an organolithium reagent such as n-butyllithium (e.g. at -70 °C) and then with a compound of general formula

wherein R is as defined in formula (I), optionally followed by a reduction reaction, e.g. with methyloxalylchloride and triethylamine followed by tributyltin hydride in the presence of azobiswobutyronitrile;
(xvi) when X represents a group SO, oxidising a corresponding compound of formula (I) in which X represents a sulphur atom (e.g. using, as oxidising agent, 3-chloroperoxybenzoic acid or potassium peroxymonosulphate (commercially sold under the trade mark "OXONE")); or
(xvii) when X represents a group SCHb, reacting a compound of formula (X) as defined in (v) above, witJi an organolithium reagent (e.g. memyllithium and/or t-butyllithium at -70 °C) and then with a compound of general formula
4 wherein R is as defined in formula (I); or
- (xviii) when X represents a group SOCHi or SO2CH2, oxidising a corresponding compound of formula (I) in which X represents a group SCH2 (e.g. using, as oxidising agent, 3-chloroperoxybenzoic acid or potassium peroxymonosulphate (commercially sold under the trade mark "OXONE")); or
(xix) when X represents a group CH=, reacting a compound of formula (II) as defined in (i) above with trimethyl phophite and then with a compound of formula (XVII) as defined in (xv) above in the presence of a base (e.g. lithium diisopropylamide); or
(xx) when X represents a group (CH2)i-6. reacting a compound of general formula

20 21
herein one of R and R represents a group CHO or a group (CH^uCHO and the
20 21 12 3
her of R and R represents a hydrogen atom, and m, A, R , R and R are as defined
4 4
formula (I), with a compound of general formula (XX), R -H, wherein R is as defined
fonnula (I), in the presence of a reducing agent (e.g. sodium triacetoxyborohydride, in a
itable solvent such as dichloroethane); or
(xxi) when X represents a group (CH2)i-6NR5, (CH2)i-3NR3(CH2)i.3 or !H2)i-3NR (CH^oO. reacting a compound of formula (XIX) as defined in (xx) above,
4
ith a compound of general formula (XXI), R Z', wherein Z' represents a group HR5, (CH2)i-3NHR5, 0(CH2)2-3NHR5 and R4 and R5 are as defined in formula (I), in e presence of a reducing agent (e.g. sodium triacetoxyborohydride, in a suitable solvent ch as dichloroethane); or
(xxii) when X represents a group (CH2)i.30(CH2)i-3 or (CH^ioOtCH^O, acting a compound of formula (XK) as defined in (xx) above in which one of R20 and :1 represents a group CHO or a group (CH2)i-2CHO and the other of R20 and R21 presents a hydrogen atom, with a reducing agent (such as sodium borohydride), followed reaction with a compound of general formula (XXII), R -E, wherein E represents a aup (CH2)i-3L or 0(CH2)2-3L , L is a leaving group (such as a halogen atom or a
4
Iphonate ester group, e.g. p-toluenesulphonate) and R is as defined in fonnula (I), in the ssence of a base (such as sodium hydride); or

(xxiii) when X represents a group (CHi)i-6, reacting a compound of formula (II) as defined in (i) above with trimethylphosphite and then with a compound of formula (XVI)
as defined in (xiv) above, a compound of formula (XVII) as defined in (xv) above or a
4 4
compound of general formula (XVIA), R (CHJJMCHO in which R is as defined in
formula (I), in the presence of a base (e.g. lithium diisopropylamide), followed by a
reduction reaction (for example, with hydrogen and a platinum oxide catalyst); or
(xxiv) when X represents a group (CH2)2-60, reacting a compound of general formula

wherein one of R22 and R23 represents a group (CH2)2-6L6 and the other of R20 and R21 represents a hydrogen atom, L6 represents a leaving group (e.g. a halogen atom or a sulphonate ester group such as p-toluenesulphonate) and m. A, R\ R2 and R3 are as defined in formula (I), witii a compound of formula (V) as defined in (ii) above in which Y represents a bond; or
(xxv) when X represents a group CR'(OH) in which R' is a CpCe alkyl group, oxidising a corresponding compound of formula (I) in which X represents CH(OH) (e.g. using the oxidant dimethylsulphoxide/oxalyl chloride), followed by reaction with a Ci-C* alkyllithium reagent; or

(xxvi) when X represents a group CH2S, reacting a compound of formula (II) as defined in (i) above with a compound of general formula (XXIV), R4-SH, wherein R4 is as defined in formula (I), in the presence of a base (e.g. sodium hydride); or
(xxvii) when X represents a group CH2SO or CH2S02, oxidising a corresponding compound of formula (I) in which X represents a group CH2S (e.g. using, as oxidising agent, 3-chloroperoxybenzoic acid or potassium peroxymonosulphate (commercially sold under the trade mark "OXONE")); or
(xxviii) when X represents a group CH2 and R4 represents a 3-piperidinyl or 2-piperazinyI group, reacting a compound of formula (II) as defined in (i) above with a reagent formed by combining pyridine or pyrazine with an aluminium hydride reagent (e.g. lithium aluminium hydride), followed by a reduction reaction (e.g. with hydrogen and a platinum catalyst); or
(xxix) when X represents a group CH= and R4 represents a 3-piperidinyl group, reacting a compound of general formula

wherein one of R24 and R25 represents an aldehyde group -CHO, and the other of R24 and
j 25
R represents a hydrogen atom and m, A, R , R and R are as defined in formula (I), with 2,3,4,5-tetrahydropyridine (BuU.Chem.Soc.Jpn. 1983, 56, 3199), followed by a reduction reaction (e.g. with sodium borohydride in a protic solvent such as methanol); or

(xxx) when X represents a bond, NR5 or NR5(CH2),.
vherein one of R26 and R27 represents a pyridyl, pyrazinyl, NR5-pyridyl, NR5-pyrazinyl, >IR5(CH2) t.6-pyridyl or NR5(CH2)t^-pyrazinyl group and the other of R26 and R27 epresents a hydrogen atom, and m, A, R1, R2 and R3 are as defined in formula (I), with a ource of hydrogen and a hydrogenation catalyst (such as platinum oxide); or
» (xxxi) when X represents a group CH20(CH2) 1.3 or CH20(CH2)2.30 and A is
■IHQO), reacting a compound of general formula

/herein one of R28 and R29 represents a group -Xw-R and the other of R28 and R29 epresents a hydrogen atom, X™ represents a group CH20(CH2)i-3 or CH20(CH2)2-30, 7 represents a leaving group (e.g. a hydroxyl or chloride leaving group) and R2, R3 and R4 re as defined in formula (I), with a compound of formula (VII) as defined in (iii) above, prionally in the presence of a coupling agent (e.g. l,l'-carbonyldiimidazoIe); or
(xxxii) when X represents a group CH20(CH2)i-3 or CH20(CH2)2.30 and A is '(O)NH, reacting a compound of general formula

2 3 28 29
wherein R and R are as defined in formula (I) and R and R are as defined in formula
(XXVII) in (xxxi) above, with a compound of formula (JX) as defined in (iv) above, in the
presence of a base (e.g. diisopropylamine);
and optionally after (i), (ii), (iii), (iv), (v), (vi), (vii), (viii), (ix), (x), (xi), (xii), (xiii), (xiv), (xv), (xvi), (xvii), (xviii), (xix), (xx), (xxi), (xxii), (xxiii), (xxiv), (xxv), (xxvi), (xxvii), (xxviii), (xxix), (xxx), (xxxi) or (xxxii) converting the compound of formula (I) to a further compound of formula (I) and, if desired, forming a pharmaceutically acceptable salt or solvate of the compound of formula (I).
The processes of the invention may conveniently be carried out in a solvent, e.g. an organic solvent such as dichloromethane, dichloroethane, tetrahydrofuran, dioxane, xylene or dimethylformamide, at a temperature, e.g. in the range from 0 to 200 °C, preferably in the range from 0 to 150 °C.
Compounds of formula (H) in which A is NHC(O) may be prepared by reacting a compound of general formula
wherein L represents a leaving group (e.g. a hydroxyl or chloride leaving group) and R , R , R and R are as defined in formula (II), with a compound of formula (VI!) as

defined above, optionally in the presence of a coupling agent (e.g. 1,1-carbonyidiimidazole).
Compounds of formula (XXX) in which one of R and R represents a hydrogen atom and the other of R andR represents a group-CH2L and L1 represents a bromine atom can be prepared by reacting a compound of general formula

wherein one of R and R represents a hydrogen atom and the other of R and R
2 3
represents a methyl group and R and R are as defined in formula (I), with
N-bromosuccinimide and catalytic azobisijobutyronitrile or dibenzoylperoxide, optionally followed by chlorination with oxalyl chloride and catalytic dimethylformamide or with thionyl chloride.
Compounds of formula (II) in which A is C(0)NH and L represents, for example, a bromine atom may be prepared by reacting a compound of general formula

2 3 30 31
wherein R and R are as defined in formula (I) and R and R are as defined in formula
(XXXI) above, with a compound of formula (IX) as defined above, in the presence of a
base (e.g. diwopropylethylamine), followed by reaction with N-bromosuccinimide and
catalytic azobiswobutyronitrile or dibenzoylperoxide.

Compounds of formula (tV)in which A is NHC(O) may be prepared in an analogous manner to compounds of formula (II) in which A is NHC(O), using instead of the intermediate compound of formula (XXX), an intermediate compound of general formula
11 2
wherein L represents a leaving group (e.g. a hydroxyl or chloride leaving group) and R ,
R3, R12 and R13 are as defined in formula (IV).
Compounds of formula (IV) in which A is C(0)NH may be prepared by reacting a compound of general formula
wherein R2, R3, R12 and R13 are as defined in formula (IV), with a compound of formula (K) as defined above, optionally in the presence of a base (e.g. ditropropylethylamine).
Compounds of formula (Vl) can be prepared by reacting a compound of general formula
■39 33 34
wherein R represents a hydrogen atom or a C j -Q alkyl group, one of R and R
represents a leaving group, L12, $uch as a halogen atom (e.g. bromine or iodine) or a
33 34
trifraorometiianesutfonate group ^ *&* *&& ^ *■ ^ ^ wpwswfts ^ hT&rcfgti* ttssHi,
and R2 and R3 are as defined in formula (VI), with a compound of general formula

wherein X' and R are as defined in formula (VI), in the presence of a palladium catalyst (e.g. palladium acetate), a phosphine ligand (e.g. BINAP) and a base (e.g. cesium :arbonate) (1996 J. Am. Chem. Soc, 7215-6; 1997 J. Am. Chem. Soc, 3395), followed by a hydrolysis reaction (e.g. with sodium hydroxide) and optionally a chlorination reaction (e.g. with oxalyl chloride and catalytic dimethyl? ormamide or with thlonyl chloride).
Compounds of formula (Vlfl) may conveniently be prepared by reacting a compound Df formula (VI) in which L represents a hydroxy! group with diphenyiphosphoryl azide in Jie presence of a base such as triethylamine.
Compounds of formula (X) in which A is NHC(O) may be prepared in an analogous nanner to compounds of formula (H) in which A is NHC(O), using instead of the ntermediate compound of formula (XXX), an intermediate compound of general formula
n 2
vherein L represents a leaving group (e.g. a hydroxyl or chloride leaving group) and R ,
I3, R16 and R17 are as defined in formula (X).
Compounds of formula (X) in which A is C(0)NH may be prepared in an analogous nanner to compounds of formula (TV) in which A is C(0)NH, using instead of the ntermediate compound of formula (XXXW), an intermediate compound of general ormula

wherein R", R , R and R are as defined in formula (X).
Compounds of formula (XII) can be prepared as described in Syn. Lett. (1998) 379-380.
5 Compounds of formula (XIH) in which X" represents a group CO, CONR , SO2 or
SO2NR can be prepared by reacting a compound of general formula
wherein one of R andR represents a group COL orS02L and the other of R and
R represents a hydrogen atom, L represents a leaving group (e.g. a halogen atom),v"
37 2 3-
R represents a hydrogen atom or a C\~C$ alky I group, and R and R are as defined in
formula (XIII), with a compound of formula (XXXVI) in which X' represents a bond or a
group NR , in the presence of a base such as diwoprbpylethylamine and catalytic
dimethylaminopyridine, followed by a hydrolysis reaction (e.g. sodium hydroxide) and,
optionally, a chlorination reaction (e.g. with oxalyl chloride and catalytic
dimethylformamide or with thionyl chloride).
Compounds of formula (XM) in which X" represents a group represents a group NR3CO or NR5S02can be prepared by reacting a compound of general formula

38 39 5 38 39
wherein one of R and R represents a group NHR and the other of R and R
represents a hydrogen atom, R is as defined for compound (XXXEC), and R2 and R3 are
as defined in formula (XIII), with a compound general formula (XLI), R -J, wherein

4
J represents a group COC1 or S02C1 and R is as defined in formula (I), in the presence of a base such as diwopropylethylamine.
Compounds of formula (XIV) may conveniently be prepared by reacting a compound of formula (XIII) in which L4 represents a hydroxyl group with diphenylphosphoryl azide in the presence of a base such as triethylamine.
Compounds of formula (XIX) in which one of R20 and R21 represents a group (CH2)i.5CHO and the other of R20 and R21 represents a hydrogen atom can be prepared by oxidising a compound of general formula
wherein one of R40 and R41 represents a group (CH2)2-60H and the other of R40 and R41 represents a hydrogen atom, and m, A, R1, R2 and R3 are as defined in formula (I), using as the oxidising agent, for example, Dess Martin Periodinane reagent.
Compounds of formula (XL.TI) in which one of R40 and R41 represents a group (CH2)20H and the other of R40 and R41 represents a hydrogen atom can be prepared from a compound of general formula (X) as defined above, an organolithium reagent such as methyllithium (at -70 °C) followed by n-butyllithium (at -70 °C), and then treatment with ethylene oxide.
Compounds of formula (XIII) in which one of R40 and R41 represents a group (CH^OH and the other of R40 and R41 represents a hydrogen atom can be prepared by

reacting a compound of general formula (X) as defined above with a compound of general formula

in the presence of a palladium catalyst such as tetrakis(triphenylphosphine)palladium(0), followed by reduction with, for example, hydrogen and a platinum oxide catalyst.
Compounds of formula (XIX) in which one of R20 and R21 represents a group CHO and the other of R20 and R21 represents a hydrogen atom (which are equivalent to compounds of formula (XXV)) can be prepared from a compound of general formula (X) as defined above, with an organolithium reagent such as methyllithium (at -70 °C) followed by n-butyllithium (at -70 °C) and then with dimethylformamide.
Compounds of formula (XXTII) in which L represents an iodine atom or p-toluenesulphonyloxy group may be prepared by reacting a compound of formula (XLH) as defined above with iodine/triphenylphosphine/imidazole or with a sulphonyl chloride such as p-toiuenesulphonyl chloride, in the presence of a base such as diisopropylethylamine.
26 27
Compounds of formula (XXVI) in which one of R and R represents a pyridyl or
9fi 97
pyrazinyl group and the other of R and R represents a hydrogen atom can be prepared from a compound of formula (X) as defined above by reaction with a pyridyl or pyrazinyl boronic acid in the presence of a palladium catalyst such as tetrakis(triphenylphosphine)palladium(0).
9rt 97
Compounds of formula (XXVT) in which one of R and R represents a NR5-pyridyl, NR -pyrazinyl, NR (CH2) ^-pyridyl or NR (CH2)i-6-pyrazinyl group and
26 27
the other of R and R represents a hydrogen atom can be prepared from a compound of formula (X) as defined above by reaction with a compound NHR pyridyl,

NHR'pyraziny], NHR"(CH2)i.6-pyridy' or NHR'fCH^i-a-pyrazinyl, in the presence of a palladium catalyst (e.g. palladium acetate), a phosphine ligand (e.g. BINAP) and a base (e.g. cesium carbonate).
Compounds of formulae (HI), (V), (VII), (K), (XI), (XV), (XVI), (XVIA), (XVII),
(xvin), (xx), (xxi), (xxn), (xxiv), (xxvn), (xxvni), (XXXD, (xxxn), (xxxm),
(XXXIV), (XXXV), (XXXVI), (XXXVH), (XXXVUO, (XXXIX), (XL), (XLI), (XLS) and fxl.TTT) are either commercially available, are well known in the literature or may be prepared easily using known techniques.
Compounds of formula (D can be convened into further compounds of formula (I) using standard procedures. For example, compounds of formula (I) in which one of R and
R represents a nitro group can be converted to compounds of formula (I) in which one of
2 3
R and R represents an amino group by reduction using iron powder and ammonium
chloride in ethanol/water under reflux conditions. The latter compounds can in turn be
2 3
converted into compounds of formula (I) in which one of R and R represents a halogen
atom, e.g. chlorine, by diazotization (e.g. with sodium nitrite) and reaction with copper
chloride. Compounds of formula (I) in which R or R represents a hydrogen atom can be
converted to compounds of formula (I) in which R or R represents a C j -Cg alkyl,
C2-C6 hydroxyalkyl, C3-C8 cycloalkyl or a 3- to 8-membered saturated heterocyclic ring
by standard chemical procedures.
It will be appreciated by those skilled in the art that in the processes of the present invention certain functional groups such as hydroxyl or amino groups in the starting reagents or intermediate compounds may need to be protected by protecting groups. Thus, the preparation of the compounds of formula (I) may involve, at an appropriate stage, the removal of one or more protecting groups.
The protection and deprotection of functional groups is described in Protective Groups in Organic Chemistry', edited by J.W.F. McOmie, Plenum Press (1973) and

Protective Groups in Organic Synthesis', 2nd edition, T.W. Greene and P.G.M. Wuts, Wiley-Interscience (1991).
The compounds of formula (I) above may be converted to a pharmaceutically acceptable salt or solvate thereof, preferably an acid addition salt such as a hydrochloride, hydrobromide, phosphate, acetate, fumarate, maleate, tartrate, citrate, oxalate, methanesuiphonate orp-toluenesulphonate, or an alkali metal salt such as a sodium or potassium salt.
Certain compounds of formula (I) are capable of existing in stereoisomeric forms. It will be understood that the invention encompasses all geometric and optical isomers of the compounds of formula (I) and mixtures thereof including racemates. Tautomers and mixtures thereof also form an aspect of the present invention.
The compounds of the present invention are advantageous in that they possess pharmacological activity. They are therefore indicated as pharmaceuticals for use in the treatment of rheumatoid arthritis, osteoarthritis, psoriasis, allergic dermatitis, asthma, chronic obstructive pulmonary disease (COPD), hyperresponsiveness of the airway, septic shock, glomerulonephritis, irritable bowel disease, Crohn's disease, ulcerative colitis, atherosclerosis, growth and metastases of malignant cells, myoblastic leukaemia, diabetes, Alzheimer's disease, meningitis, osteoporosis, burn injury, ischaemic heart disease, stroke and varicose veins.
Accordingly, the present invention provides a compound of formula (I), or a phannaceutically acceptable salt or solvate mereof, as hereinbefore defined for use in therapy.
In anouier aspect, the invention provides the use of a compound of formula (I), or a pharmaceutically acceptable salt or solvate thereof, as hereinbefore defined in the manufacture of a medicament for use in therapy.

In the context of the present specification, the term "therapy" also includes "prophylaxis" unless there are specific indications to the contrary. The terras "therapeutic" and "therapeutically" should be construed accordingly.
The invention further provides a method of effecting immunosuppression (e.g. in the treatment of rheumatoid arthritis, irritable bowel disease, atherosclerosis or psoriasis) which comprises administering a therapeutically effective amount of a compound of formula (I), or a pharmaceutically acceptable salt or solvate thereof, as hereinbefore defined to a patient.
The invention also provides a method of treating an obstructive airways disease (e.g. asthma or COPD) which comprises administering to a paitient a therapeutically effective amount of a compound of formula (I), or a pharmaceutically acceptable salt or solvate thereof, as hereinbefore defined to a patient.
For the above-mentioned therapeutic uses the dosage administered will, of course, /ary with the compound employed, the mode of administration, the treatment desired and he disorder indicated. The daily dosage of the compound of formula (I)/sait/soIvate ^active ingredient) may be in the range from 0.001 mg/kg to 30 mg/kg.
The compounds of formula (I) and pharmaceutically acceptable salts and solvates hereof may be used on their own but will generally be administered in the form of a iharmaceutical composition in which the formula (I) compound/salt/solvate (active ngredient) is in association with a pharmaceutically acceptable adjuvant, diluent or carrier. Depending on the mode of administration, the pharmaceutical composition will preferably :omprise from 0.05 to 99 %w (per cent by weight), more preferably from 0.10 to 70 %w, >f active ingredient, and, from 1 to 99.95 %w, more preferably from 30 to 99.90 %w, of a )hannaceutically acceptable adjuvant, diluent or carrier, all percentages by weight being >ased on total composition.

Thus, the present invention also provides a pharmaceutical composition comprising a compound of formula (I), or a pharmaceuticaily acceptable salt or solvate thereof, as hereinbefore defined in association with a pharmaceuticaily acceptable adjuvant, diluent or carrier.
The invention further provides a process for the preparation of a pharmaceutical composition of the invention which comprises mixing a compound of formula (I), or a pharmaceuticaily acceptable salt or solvate thereof, as hereinbefore defined with a pharmaceuticaily acceptable adjuvant, diluent or carrier.
The pharmaceutical composition of the invention may be administered topically (e.g. to the lung and/or airways or to the skin) in the form of solutions, suspensions, heptafiuoroalkane aerosols and dry powder formulations; or systemically, e.g. by oral administration in the form of tablets, capsules, syrups, powders or granules, or by parenteral administration in the form of solutions or suspensions, or by subcutaneous administration or by rectal administration in the form of suppositories or transdermally.
The present invention will now be further explained by reference to the following illustrative examples.

To a suspension of 3-chloro-2-nitrobenzoic acid (2.68 g) in dichloromethane (10 ml) at 0°C was added oxaiyi chloride (3 ml) and dimethylformamide (1 drop). The resulting mixture was stirred at room temperature under a nitrogen atmosphere for 1 hour, then concentrated under reduced pressure to yield a solid. The solid was dissolved in dichloromethane (10 ml) and cooled to 0°C. A solution of 1-adamantanemediylamine (2.19g) and iV.A'-dii.sopropylethylamine (II ml) in dichloromethane (10 ml) was added portion-wise and the resulting solution allowed to stir at room temperature under a nitrogen atmosphere for 2h. The reaction mixture was poured into water and the organic phase separated and washed wim 2N hydrochloric acid, 10% aqueous sodium hydroxide and saturated brine. The organic phase was then dried over sodium sulfate, filtered and concentrated under reduced pressure and the resulting solid re-crystallized from iso-propanol to afford the subtitle compound as a solid (3.52 g).
MS (APCI +ve) 349 (M+H)+
'H NMR (DMSO-d6) 5 8.74 (1H, t); 7.89 (1H, m); 7.75-7.69 (2H, m); 2.91 (2H, d),
1.93 (3H, bs); 1.64 (6H, dd); 1.47 (6H, d)
b) 3-(4-{ 1,1-dimethylethyl }oxycarbony!]-piperazin-l -yl>2-nitro-Ar-
3 7 (tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide
3 7 A mixture of 3-chloro-2-mtro-/V-(tricyclo [3.3.1.1 ' ]dec-1 -ylmethyl)-benzamide
(2.80 g, Example la) and piperazine-1-carboxylic acid, tert-buty\ ester (7.47 g) in dry
dimethyl sulfoxide (10 ml) was heated at 120°C under a nitrogen atmosphere for 24h. The
cooled reaction mixture was diluted with water and extracted tiirice with ethyl acetate. The
combined extracts were washed with water, dried over sodium sulfate, filtered, and the
filtrate concentrated under reduced pressure to give a solid. Purification by
chromatography over silica gel, during wim M-c-hexane/ethyi acetate (2:1) gave me subtitle
compound as a solid (3.8 g).
MS (APCI +ve) 499 (M+H)+

'H NMR (DMSO-dg) 5 8.55 (1H, t); 7.62-7.59 (2H. m); 7.43 (1H, dd); 3.38 (4H, bt); 2.90-2.84 (6H, m), 1.93 (3H, bs); 1.63 (6H, dd); 1.47 (6H, d); 1.41 (9H, s)
3 7 c) 2-Nitro-3-piperazin-l-yI WV-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide
A solution of 3-(4- {1,1 -dimethyiethyl} oxycarbonylj-piperazin-1 -yl)-2-nitro-/V-
(tricyclo [3.3.1.1 ' ] dec-l-ylmethyl)-benzamide (0.58 g, Example lb) and hydrochloric
acid (6.4 ml, 4N in dioxane) in tetrahydrofuran (20 ml) was stirred at room temperature
under a nitrogen atmosphere for 18h. The reaction mixture was concentrated under
reduced pressure and the residue dissolved in water, made basic with solid sodium
bicarbonate and extracted with dichloromethane three times. The combined organic
extracts were dried over magnesium sulfate, filtered and the filtrate concentrated under
reduce pressure to give a solid. Purification by chromatography over silica gel, eluting
with 10% methanol in dichloromethane afforded the title compound as a solid (0.165 g).
MS (APCI +ve) 399 (M+H)+
*H NMR (DMSO-dfi) 5 8.52 (1H, t); 7.59 (1H, t); 7.51 (1H d); 7.35 (1H, d); 2.88 (2H, d);
2.81 (4H, m); 2.37 (4H, m); 1.93 (3H, bs); 1.67 (3H, d); 1.60 (3H, d); 1.47 (6H, s)
Example 2
3 7 2-Amkio-3-piperazin-l-yI -iV-(tricyclo[3J.l.l ' ]dec-l-ylmethyl>benzamide,
dihydrocfaloride salt
a) 2-Amino-3-(4-{l,l-dimethylethyl}oxycarbonyl]-piperaziii-l-yI)-A/'-
37 (tricyclt{3J.l.l ' ]dec-l-ylmethyl)-benzaraide
A suspension of 3-(4-{ 1,1 -dimethyiethyl}oxycarbonyl]-piperazin-1 -yl)-2-nitro-iV-
(tricyclo [3.3.1.13' ] dec-l-ylmethyl)-benzamide (3.8 g, Example lb), iron powder (2.13 g)

and ammonium chloride (2.04 g) in 2:1 ethanol/water (90 ml) was heated at reflux, under a nitrogen atmosphere, for 2h. The cooled reaction mixture was filtered and the filtrate partitioned between water and ethyl acetate. The organic layer was separated and washed with water twice further, dried over magnesium sulfate, filtered and the filtrate concentrated under reduced pressure to give a residue. Purification of the residue by chromatography over silica gel, eluting with 20% ethyl acetate in trohexane, yielded the subtitle compound as a solid (2.27 g).
MS (APCI+ve) 469 (M+H)+
3 7 b) 2-Amino-3-piperazin-l-yl-A^-(tricyclo[3«3.1.1 ' ]dec-l-ylmethyl)-benzamide,
dihydrochJoride salt
Prepared as described in Example lc) using 2-amino-3-(4-{ 1,1-dimethyl ethyl}
3 7 oxycarbonyl]-piperazin-l-yl)-/v"-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.2 g,
Example 2a) and hydrochloric acid (5 ml, 4N in dioxane). The reaction mixture was
concentrated under reduced pressure to give a solid which when triturated with diethyl
sther gave the title compound as a solid (0.2 g).
MS(APCI+ve) 369(M-2HC1)+
'HNMR (DMSO-d6) 5 9.16 (2H, bs); 8.14 (IH, t); 7.37 (IH, d); 7.07 (IH, d); 6.64 (IH, t); 3.27 (4H, bs); 2.98 (4H, bs); 2.95 (2H, d); 1.93 (3H, bs); 1.67 (3H, d); 1.59 (3H, d); 1.48 ;6H, s).
Example 3
3 7 J-Chloro-3-piperazin-l-yl -AKtricycIo[3.3.1.1 * ]dec-l-yimethyl)-benzamide

a) 2-Chloro-3-(4-{l,l-dimetbylethyl}oxycarbonyl]-piperazin-l-yI)-A^-(tricycio[3.3.1.13,7]dec-l-ylmethyI)-benzamide
To a solution of 2-amino-3-(4-{ l,l-dimethyIethyl}oxycarbonyi]-piperazin-l-yJ)-/V-(tricycio[3.3.1.1 ]dec-l-ylmethyl)-benzamide (lg„ Example 2a) in tetrahydrofuran (23 ml) was added 1M aqueous hydrochloric acid (2.78 ml) and water (10 ml). The solution was cooled to 0°C and sodium nitrite (1.91 g) added portion-wise, whilst maintaining the internal temperature below 5°C. After stirring at 0-5°C for 0.5h, a pre-cooled suspension of copper (I) chloride (10.58 g) and copper (II) chloride in water (20ml) was added portion-wise to the pale yellow suspension. The mixture was stirred at 0°C for 0.5h then at room temperature for 0.5h. The reaction mixture was poured into a mixture of water and dichloromethane and 1/1 : 0.88 ammonia/water was added until the aqueous phase was homogeneous. The layers were separated and the aqueous phase extracted twice further with dichloromethane. The combined organic extracts were washed with l/l : 0.88 ammonia/water until the aqueous layer was colourless, dried over sodium sulfate, filtered and concentrated under reduced pressure to yield an oil. Purification by chromatography on silica gel, eluting with 20-35% ethyl acetate/jjo-hexane gave the subtitle compound as a solid (0.45 g).
MS (APCI +ve) 388 (M-BOC)+
*H NMR (DMSO-de) 8 8.27 (ltf, t); 7.32 (1H, t); 7.19 (1H, d); 7.04 (1H, d); 3.48 (4H, m);
2.93-2.91 (6H, m); 1.94 (3H, bs); 1.64 (3H, d); 1.59 (3H, d); 1.52 (6H, s); 1.43 (?H, s).
37 b) 2-Chloro-3-piperazin-l-yl -iV-(tricyclo[3.3.1.1 ' ]dec-J.-ylmethyI)-benzamide
To a solution of 2-Chloro'3-(4-{ l,l-dimethylethyl}oxycarbonyl]-piperazin-l-yl)-iV-
(tricyclo[3.3.1.1 ]dec-l-ylmethyl)-benzamide (0.45 g, Example 3a) in dichloromethane
(10 ml) was added trifluoroacetic acid (5 ml). After stirring at room temperature under a
nitrogen atmosphere the reaction mixture was concentrated under reduced pressure to give
a gum. The gum was partitioned between water and dichloromethane and made basic with
solid sodium bicarbonate. The layers were separated and the aqueous layer extracted twice
further with dichloromethane. The combined organic extracts were washed twice with

water, saturated brine then dried over magnesium sulfate, filtered and the filtrate concentrated under reduced pressure to give a foam. The foam was purified by normal phase HPLC (0-20% ethanol/dichloromethane) and chromatography over silica gel, eiuting 10% methanol in dichloromethane, to afford the title compound as a foam (0.05 g).
MS (APCI +ve) 388/90 (M+H)+
'H NMR (DMSO-d6) 5 8.24 (1H, t); 7.31 (1H, t); 7.15 (1H, d); 7.00 (1H, d); 2.96-2.87
(10H, m); 1.93 (3H, bs); 1.67 (3H, d); 1.59 (3H, d); 1.52 (6H, s).

37 a) 2-ChIoro-5-nitro-Ar-(tricyclo[33.1.1 ' ]dec-l-ylmethyl)-benzamide
To a solution of 2-chloro-5-nitrobenzoic acid (1.22g) in N, JV-dirnethylformamide
(1.5 ml) was added carbonyldiimidazole (1.0 g). The resulting reaction mixture was stirred
for 2.5h and then 1-adamantanemethylamine (l.Og) was added. After 14h the reaction
mixture was partitioned between ethyl acetate and water and the organic layer was
separated, washed with water and brine and then dried over sodium sulphate (Na2S04).
The organic layer was concentrated under reduced pressure to give a residue which was
purified by silica gel chromatography (eiuting with 3-10% methanol in dichloromediane) to
yield the subtitle compound as a yellow solid (1.7 g).
MS (APCI +ve) 348/350 (M+H)+
*H NMR (CDC13) 5 8.53 (1H, d), 8.2 (1H, dd), 7.6 (1H, d), 6.2 (1H, bs), 3.2 (2H, d),
2.0(3H,bs), 1.8(12H,m)

b) 5-Amino-2-chloro-/V-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyf)-benzaniide
A solution of the nitro compound from Example 4a, (0.50 g) and ammonium chloride (0.5g) were dissolved in 50% aqueous ethanol. Iron powder (0.5g) was added and the mixture stirred at reflux temperature for 3 hr before being cooled and solids removed by filtration. The modier liquors were treated with 10% sodium hydroxide solution and the product extracted into ethyl acetate. The organic solution was washed with brine, dried over sodium sulphate (Na2SC>4) and concentrated to give a residue which was purified by silica gel chromatography to give the title compound as a white solid (0.4g).
MS (APCI+ve) 319/21 (M+H)+
!HNMR (DMSO-de) 8 8.14 (1H, t); 7.03 (1H, dd); 6.56 (2H, m); 5.36 (2H, s); :
2.89 (2H, d); 1.95 (3H, s); 1.7 (12H, m)
37
c) 2-Chloro-5-Piperazin-l-yl -/V-(tricyclo[3.3.3H ' ]dec-l-ylmethyl)-benzamide
3 7 To a solution of 5-aniino-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide
(1.00 g, Example 4b) in xylene (20 ml) was added Z7i.s-(2-chloroethyl)amine hydrochloride
salt (0.620g). The mixture was heated at 150°C for 12h (a dark solution is obtained). The
cold solution was washed with 2M HC1, the aqueous layer washed with ethyl acetate then
basified with sodium bicarbonate and extracted twice with dichloromethane. The organic
layer was dried over magnesium sulfate, filtered and the filtrate concentrated under reduced
pressure to give "a foam. The crude material was purified on silica gel (0-10%
ethanol/dichloromethane), to afford the title compound as a white solid (0.90 g).
MS (APCI+ve) 388/90 (M+H)+
'H NMR (DMSO-de) 5 8.22 (1H, t); 7.22 (1H, d); 6.96 (1H, dd); 6.84 (1H, d); 3.50-3.20 (7H, m); 3.00-2.90 (2H, t); 2.91 (2H, d); 1.94 (3H, bs); 1.67 (3H, d); 1.59 (3H, d); 1.52 (6H, s).

a) 4-[4-Chloro-3-(ethoxycarbonyl)phenyl]hexahydro-l^-l,4-diazepine-l-carboxylic
acid, 1,1-dimethylethyl ester
' A mixture of 5-bromo-2~chloro-benzoic acid, ethyl ester (0.50 g), hexahydro-1//-1,4-diazepine-1-carboxylic acid, 1,1-dimethylethyl ester (0.46 g), cesium carbonate (0.86 g), palladium (21) acetate (8.5 mg) and (R)-BINAP (35 mg) in toluene (3 ml) was heated at 100 °C for 14h in a pressure vessel flushed with nitrogen. The cooled reaction mixture was poured into water and extracted (3 times) with ethyl acetate. The combined organic extracts were washed with saturated sodium chloride solution and men dried over magnesium sulfate. Evaporation under reduced pressure gave an oil which was purified by chromatography over silica gel, eluting with 20% ethyl acetate in iyo-hexane to yield the subtitle compound as an oil (0.21 g).
MS (APCI +ve) 282/284 (M-BOC)+
b) 4-(3-Carboxy-4-chlorophenyl)hexahydro-lff-l,4-dia2epine-l-carboxylic acid, 1,1-
dimethylethyl ester
A suspension of 4-[4-chloro-3-(ethoxycarbonyl)phenyl]hexahydro- IH-1,4-diazepine-1-carboxyiic acid, 1,1-dimethyiethyi ester (Example 5a, 0.2 lg), lithium hydroxide monohydrate (1.05ml of 3M solution in water) in 1:1 ethanol/water (7 ml) was stirred at room temperature for 14h. More lithium hydroxide monohydrate (0.55ml of 3M solution

in water) was added followed by tetrahydrofuran (1 ml). The resulting solution was stirred for 4h at room temperature then poured into water and extracted with diethyl ether. The aqueous phase was separated, acidified with 2M hydrochloric acid and then extracted with dichloromethane three times. The combined dichloromethane layers were dried over magnesium sulfate and evaporated under reduced pressure to yield the subtitle compound as a glass.
MS (APCI +ve) 298/300 (M-'Bu)+
37
c) Hexahydro-4-[4-methyl-3-[[(tricyclo[3.3.1.1 ' ]dec-l-yImethyl)aminojcarbonyl]-
phenyI]l.ff-l,4-diazepine-l-carboxylic acid, 1,1-dimethylethyl ester
A solution of 4-(3-carboxy-4-chlorophenyOhexahydro-1H-1,4-diazepine-1 -carboxylic acid, 1,1-dimethylethyl ester (Example 5b, 0.10 g) and N,N'-carbonyldiimidazole (0.045 g) in dimethylformamide (3 ml) was stirred at room temperature for 2h. 1-Adamantanemethylamine (0.050 ml) was then added and stirring continued for 14h. The reaction mixture was poured into water and extracted with ethyl acetate three times. The ethyl acetate layers were combined and washed with 2M hydrochloric acid, 10% aqueous sodium hydroxide and brine, then dried over magnesium sulfate and concentrated under reduced pressure. Purification by chromatography on silica gel, eluting with 20-30% ethyl acetate in wo-hexane, gave the subtitle product as a gum which crystallised on standing.
MS (APCI +ve) 502/504 (M+H)+
d) 2-Chloro-S-(hexahydro-Lff-l,4-diazepin-l-yl)-iV-(tricyclo[3J.l.l3'7]dec-l-
ylmethyl)- benzamide, hydrochloride salt
3 7 Hexahydro-4-[4-methyl-3-[[(tricyclo[3.3.1.1 ' ]dec-l-ylrnethyl)ammo]carbonyl]-
phenyl]-lfM ,4-diazepine-1-carboxylic acid, 1,1-dimethylethyl ester(from Example 5c)
was dissolved in methanol (5 ml) and hydrochloric acid (0.5ml of a 4N solution in dioxane)
was added. After stirring at room temperature for 14h, the mixture was evaporated to 2/3

original volume under reduced pressure. Diethyl ether was gradually added to the solution and the resulting precipitate collected by filtration, washed with diethyl ether and dried in vacuo to afford the title compound as a solid (0.027 g)
MS (APCI +ve) 402/404 (M+H)+
'HNMR (DMSO-d6) 6 9.11 (2H, bs); 8.18 (lH,t); 7.24 (1H, d); 6.81 (1H, dd); 6.71 (1H, d); 3.71 (2H, t); 3.50 (2H,t); 3.19 (2H, bs); 2.93 (2H, bs); 2.92 (2Hf d); 2.08 (2H, m); 1.94 (3H, bs); 1.67 (3H, d); 1.59 (3H, bs); 1.52 (6H, s)

a) 2-Chloro-5-[4-[[(l,l-dunethylethoxy)carbonyl]amino]-l-piperidinyl]-benzoic acid, ethyl ester
Prepared as described in Example 5a) using 5-bromo-2-chloro-benzoic acid, ethyl ester (0.50 g), 4-piperidinyl-carbamic acid, 1,1 -dimethylethyl ester (0.46 g), cesium carbonate (0.86 g), palladium (H) acetate (8.5 mg) and (R)-BINAP (35 mg) and toluene (3 ml) to afford the subtitle compound as an oil (0.17 g).
MS (APCI +ve) 383/385 (M+H)+

b) 2-Chloro-5-[4-([(l,l-dimethyIethoxy)carbonyI]aniino]-l •piperidinyl]- benzoic acid
Prepared as described in example 5b) using 2-chloro-5-[4-[[(l,l-dimethylethoxy)-carbonyi]aminoJ-1 -piperidinylJ-benzoic acid, ethyl ester (Example 6a, 0.17 g), lithium r hydroxide monohydrate (0.88 ml of a 3M solution in water), 1:1 ethanol/water (7 ml) and tetrahydrofuran (1ml) to give the subtitle compound as a solid (0.14 g).
MS (APCI +ve) 354/356 (M+H)+
c) [l-[4-Chloro-3-[[(tricydo[3J.l.l3'7]dec-l-ylmethyl)aniino]carbonyl]phenyl]-4-
piperidinyl]-carbamic acid, 1,1-dimethylethyi ester
Prepared as described in Example 5c) using 2-chloro-5-[4-[[( 1,1-dimethylethoxy)carbonyl]amino]-l-piperidinyl]- benzoic acid (Example 6b, 0.065 g), N,N'-carbonyldiimidazole (0.030 g), 1-adamantanemethylamine (0.032 ml) and dimethylformamide (3 ml) to give die subtitle compound as a solid.
MS (APCI +ve) 501/503 (M+H)+
d) 5-(4-Aniino-l-piperidinyI)-2-chloro-A^-(tricyclo[3J.l.l3'7]dec-l-ylmethyl)-
benzamide, hydrochloride salt
. Prepared as described in example 5d) above using [l-[4-chloro-3-
3 7 [[(tricyclo[3.3.1.1 ' ]dec-l-ylmemyl)amino]carbonyl]phenyl]-4-piperidinyl]-carbamic acid,
1,1-dimeth.ylethyl ester (Example 6c), hydrochloric acid (0.5ml of a 4N solution in
dioxane) and methanol (10 ml). The mixture was heated at reflux for 15 min. to complete
the reaction. After evaporation to two-thirds of the original volume, a solid crystallised on
standing which was collected by filtration and dried in vacuo to give the title compound as
a solid (0.025 g).
MS (APCI +ve) 402/404 (M-HC1)+

'H NMR (DMSO-d6) 8 8.23 (1H, t); 8.11 (IH,bs); 7.28 (1H, d); 7.03 (1H, dd); 6.94
;iH. s); 3.74 (2H, d); 3.20 (1H, m); 2,91 (2H, d); 2.83 (2H, t); 1.98 (2H, bs); 1.94 (3H, bs);
1.69-1.58 (8H,m); 1.52 (6H,s)
Example 7 -Hr-)-5-(3-Amino-l-pyrrolidinyl)-2-chloro-A'-(tricyclo[3.3.1.13'7]dec-l-ylmethyl)-

i) (+/-)-2-Chloro-5-[3-[[(l,l-dimethylethoxy)carbonyl]aniino]-l-pyrrolidinyl]-lenzoic acid, ethyl ester
Prepared as described in Example 5a) using 5-bromo-2-cbloro-benzoic acid, ethyl stcr (0.50 g), 3-pyrrolidinyI-carbamic acid 1,1-dimediylethyl ester (0.42 g), cesium arbonate (0.86 g), palladium (II) acetate (21 mg) and (R)-BINAP (88 mg) and toluene 3 ml) to afford the subtitle compound as an oil (0.25 g).
AS (APCI +ve) 311/313 (M-BOC)+
0 (+/-)-2-Chloro-5-[3-[[(l,l-dimethylethoxy)carbonyl]amino]-l-pyrrolidinyi]-tenzotc acid
Prepared as described in Example 5b) using (+/-)-2-chloro-5-[3-[[(l,l-[imethylethoxy)carbonyl]aminoj-l-pyrrolidinyl]- benzoic acid, ethyl ester (Example 7a, l.25g), lithium hydroxide monohydrate (1.36ml of a 3M solution in water), 1:1 thanol/water (7 ml) and tetrahydrofuran (1ml) to give the subtide compound as a solid 0.23 g).

MS (APGI +ve) 284/286 (M-BOC)+
c) (+/-)-[l-[4-chloro-3-[[(tricyclo[3J.1.13,7]dec-l-ylmethyi)amino]carbonyI]phenyI]-
3-pyrToUdinyl]-carbamic acid, 1,1-dimethylethyl ester
Prepared as described in Example 5c) using (+/-)-2-chloro-5-[3-[[(l,l-dimethylethoxy)carbonyl]amino]-l-pyrrolidinyl]- benzoic acid (Example 7b, 0.070g), N,N'-carbonyldiimidazole (0.033 g), 1-adamantanemethylamine (0.036 ml) and dimethylformamide (3 ml) to give the subtitle compound as a gum.
MS (APCI +ve) 487/489 (M+H)+
d) (+/-)-5K3-Amino-l-pyrrolidinyl)-2-chloro-A^-(tricyclo[33.1.13'7]dec-l-yImethyI)-
benzamide, hydrochloride salt
Prepared as described in example 5d) above using (+/-)-[ l-[4-chloro-3-
3 7 [[(tricyclo[3.3.1.1' ]dec-1 -ylmethyl)amino]carbonyl]phenyl]-3-pyrroIidinyl]-carbamic
icid, 1,1-dimethylethyl ester (Example 7c), hydrochloric acid (0.5ml of a 4N solution in
lioxane) and methanol (5 ml). Evaporation under reduced pressure gave a solid on
trirtuation wim diemyl ether. Recrystallisation from methanol/diethyl ether gave the title
rompound as a solid (0.030 g).
MS (APCI +ve) 388/390 (M+H)+
lH NMR (DMSO-dg) 5 8.24 (3H, bs); 8.20 (1H, t); 7.25 (1H, d); 6.61 (1H, dd); 6.51
;iH, d); 3.94 (1H, m); 3.55-3.32 (2H, m); 3.29 (2H, m); 2.92 (2H, d); 2.37-2.27 (1H, m); U3-2.05 (1H, m); 1.94 (3H, bs); 1.68(3H, d); 1.59 (3H, d); 1.52 (6H, s)

a) 5-Bromomethyl-2-chloro-ben2oic acid
To a stirred solution of 2-chloro-5-methyl-benzoic acid (25g) in chloroform (500ml) at 50°C was added N-bromosuccinimide (27.40g). The flask was purged with nitrogen and azobistsobutyronitrile (0.10g) added in one portion. The solution was heated at reflux for lh. Further azobiswobutyronitrile (0. lOg) was added and the mixture heated a further 3h. The solution was concentrated in vacuo, redissolved in diethyl ether and filtered to remove insoluble succinimide. The ether solution was washed widi 2N aqueos hydrochloric acid solution followed by brine then dried over magnesium sulphate. The solution was concentrated to a volume of 150ml then diluted with isohexane. After further partial concentration crystallization started. The mixture was allowed to stand in an ice-bam for lh. The resulting crystals were filtered, washed with isohexane and dried in vacuo to give the subtitle compound (17g).
b)5-Bromomethyl-2-chIoro-A^-(tricyclo[3.3.1.13,7]dec-l-yImethyl)-benzaniide
To a stirred solution of 5-bromomethyl-2-chloro-benzoic acid (Example 8a, 12.4g) in dichloromethane (250ml) and dimethylformamide (0.12ml) at 0°C was added oxalyl chloride (8.7ml). The cooling bath ws removed and the solution allowed to warm to room temperature. Once gas evolution had ceased the solution was concentrated in vacuo. The residue was redissolved in dichloromethane (300ml), cooled to 0°C and treated with dzuopropyleraylamine (12.4 ml) and adamantylmethylamine (7.54ml). After 15min. at 0°C the solution was poured into diethyl ether (1L) and washed with IN aqueous hydrochloric

acid followed by brine. The organics were dried over magnesium sulphate and concentrated in vacuo to give the title compound as a white powder (19g)
MS (APCI +ve) 396/398 (M+H)+
'H NMR (DMSO-d6) 5 8.39 (1H, t); 7.50-7.40 (2H, m); 4.74 (2H, s); 2.92 (2H, d);
2.50 (3H, s); 1.94 (3H, bs); 1.67 (3H, d); 1.59 (3H, d); 1.52 (6H, s).
c) 2-Chloro-5-(4-[{l,l- (tricyclo[3J.l.l3'7]dec-l-yImethyl)-ben2amide,
3 7 A mixture of 5-bromomethyl-2-chloro-A^-(tricyclo[3.3.1.1' ]dec-1 -ylmethyl)-
benzamide (Example 8b, 0.130g), 1-terrbutyloxycarbonylpiperazine (0.074g) and
dilsopropylethylamine (6.3 ml) in dimethylformamide (3 ml) was heated at 60°C for 3h.
The mixture was diluted with water (10 ml) and extracted with ethyl acetate
(3 x 10 ml). The organic layer was dried over magnesium sulfate, filtered and the filtrate
concentrated under reduced pressure. The crude material was purified on a silica gel
eluting with dichloromethane/ethanol (0-20% gradient) to afford the title compound as a
white foam (0.112g).
MS (APCI +ve) MW 502/504 (M+H)+
JH NMR (DMSO-dfi) 5 8.28 (1H, t); 7.40 (1H, d); 7.32 (1H, dd); 7.29 (1H, d); 3.74 (2H, s); 3.28 (4H, t); 2.90 (2H, d); 2.31 (4H, t); 1.92 (3H, bs); 1.70-1.50 (6H, m); 1.59 (6H, d); 1.37 (9H, s).
d) 2-Chloro-5-piperazm-l-yImethyl -AKtricycto[33.1.13'7]dec-l-ylmethyl)-
benzamide, hydrochloride salt
2-Chloro-5-(4-[ {1,1 -dimethylethyl} oxycarbonyl]-piperazin-1 -yl)methyl -N-
3 7
(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide, (Example 8c, 0.080g) was dissolved in methanol (3ml), 4N HC1 in dioxane (1ml) was added and the mixture stirred at room temperature for 1.5h. The solvent was removed under vacuum and the resulting solid was triturated with ether to afford the title compound as a white powder (0.062g).

MS (APCI +ve) MW 402/404 (M+H)+
'H NMR (DMSO-dg) 5 8.30 (IH, t); 7.63 (2H, bs); 7.55 (IH, d); 4.33 (IH, bs); 4.05 (4H, m); 3.50-3.00 (4H, m); 3.50-3.40 (IH, m); 2.92 (2H, d); 1.92 (3H, bs); 1.70-1.50 (6H,m); 1.57 (6H, bs).
According to the procedure described in Example 8, the following compounds were prepared.

MS (APCI +ve) MW 416/418 (M+H)+
'H NMR (DMSO-de) 8 11.62 (bs, IH), 9.57 (bs, IH); 9.30 (bs, IH); 8.34 (IH, t); 7.80-7.60 (2H, m); 7.59 (IH, d); 4.50-4.30 (bs, 2H); 3.80-3.00 (m, 8H); 2.94 (2H, d); 2.25-2.10 (m, 2H); 1.94 (3H, bs); 1.66 (3H, d); 1.58 (3H, d); 1.54 (6H, s).
Example 10
5-[(4-Amino-l-pip€ridinyI)methyI]-2-chIoro-iV-(tricyclo[3.3.1.13'7]dec-l-ylmethyI)-benzamide, hydrochloride salt

MS (APCI +ve) MW 416/418 (M+H)+
'H NMR (DMSO-de) 5 8.35 (1H, t); 8.30 (2H, bs); 7.66 (1H, d); 7.65 (1H, s); 7.59 (1H, d); 428 (d, 2H); 3.65-3.18 (m, 4H); 3.10-2.90 (1H, m); 2.95 (2H, d); 2.15-2.05 (2H, m); 2.05-1.90 (1H, m); 1.94 (3H, bs); 1.68 (3H, d); 1.61 (3H, d); 1.54 (6H, s).

MS (APCI +ve) MW 402/404 (M+H)+
lH NMR (DMSO-de) 5 8.56 (1H, bs); 8.42 (2H, bs); 8.35 (1H, t); 7.66 (2H, bs); 7.59 (1H, d); 4.60-4.40 (m, 2H); 4.20-3.00 (m, 5H); 2.94 (2H, d); 2.35-1.95 (m, 2H); 1.95 (3H, bs); 1.68 (3H, d); 1.61 (3H, d); 1.54 (6H, s).

a) 2-Chloro-5-hydroxy-Ar-(tricycIo[3.3.1.13,7]dec-l-ylmethyl)-benzamide
To a solution of 2-chloro-5-hydroxybenzoic acid (3.12g) in ACiV-dimethylformamide (50 ml) was added l.T-carbonyldiimidazole (3.0 g). The resulting reaction mixture was stirred for 2.5h and then 1-adamantanemethylamine (3.0g) was added. Stirring was continued for 14h . The reaction mixture was partitioned between ethyl acetate and water and the organic layer was separated, washed with water and brine and then dried over sodium sulphate (Na2SC>4). The organic layer was concentrated under reduced pressure to give a residue which was purified by silica gel chromatography (eluting with 3-10% methanol in dichloromethane) to yield the subtitle compound as a white solid (0.15 g).
MS (APCI+ve) 319/321 (M+H)+
*H NMR pMSO-de) 5 9.85(lH,s), 8.25 (1H, t), 7.24(1H, d), 6.76-6.82(2H, m),
2.90 (2H,d), 1.93(3H, s), 1.67 (3H, d), 1.57 (3H, d), 1.51 (6H, s)
37
b) 2-Cblbro-5-(4-piperidinyloxy)-iV-(tricyclo[3J.l.l ' ]dec-l-ylmethyl)-benzamide,
hydrochloride salt
3 7 To a solution of 2-chloro-5-hydroxy-iV*-(tricyclo [3.3.1.1 ' ]dec-1 -methyl)-benzamide
(0.20 g, Example 12a), 4-hydroxy-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester
(0,19 g) and tributylphosphine (0.23 ml) in dry tetrahydrofuran (6 ml) ,was added 1-[[(1-
piperidinylcarbonyl)azo]carbonyl]-piperidine (0.24 g). The orange solution was heated at

60°C under a nitrogen atmosphere for 2h. At this point additional 4-hydroxy-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.19 g), tnbutylphosphine (0.23 ml) and l-[[(l-piperidinylcarbonyl)azo]carbonyl]- piperidine (0.24 g) were added.. Heating was continued and the process described above repeated until reaction was complete as judged by LC/MS. The cooled reaction mixture was diluted with diethyl ether then filtered. The Filtrate was concentrated and purified by normal phase HPLC (0-2% methanol/ dichloromethane) followed by chromatography on silica gel (0-2% medianol/ dichloromethane) to give the t-butyloxycarbonyl (BOC)-protected compound as a colourless foam. The foam was dissolved in methanol (5 ml) and 4N hydrochloric acid in dioxane (0.25 ml) added. The solution was stirred at room temperature under a nitrogen atmosphere until the reaction was complete as judged by LC/MS. Evaporation of solvent followed by trituration witfi diethyl ether gave the title compound as a colourless solid (0.15 g).
MS (APa+ve) 417/419 (M+H)+
lH NMR (DMSO-dg) 5 8.65 (2H, bs); 8.30 (IH, t); 7.39 (IH, d); 7.07 (IH, dd); 6.99 (IH, d); 4.72-4.67 (IH, m); 3.21 (2H, bm); 3.07 (2H, bm); 2.92 (2H, d); 2.12-2.07 (2H, m); 1.94 (3H, bs); 1.88-1.80 (2H, m); 1.67 (3H, d); 1.59 (3H, d); 1.52 (6H, s)

Preparcd as described in Example 12b using 2-chloro-5-hydroxy-JV-(tricyclo[3.3.1.13'7]dec-l-methyl)-benzamide (0.20 g, Example 12a), N-tBOC-D-prolinoI

(0.19 g) and tributylphosphine (0.23 ml), dry tetrahydrofuran (6 ml) and 1-[[(1-piperidinylcarbonyl)azo]carbonyi]- piperidine (0.24 g) to obtain the butyloxycarbonyl (BOC)-protected compound, followed by treatment with 4N hydrochloric acid in dioxane (0.4 ml) and methanol (5 ml) to yield the title compound as colourless solid (0.14 g)
MS (APCI+ve) 403/405 (M+H)+
'HNMR (CD3OD) 5-8.45 (1H, bt); 7.46 (1H, d); 7.14-7.10 (2H, m); 4.41 (1H, dd); 4.18 (1H, t); 4.10-4.04 (1H, m); 3.41 (2H, t); 3.10 (2H, m); 2.36-2.28 (1H, m); 2.25-2.08 (2H, d); 2.03 (3H, s); 2.00-1.90 (1H, m); 1.83 (3H, m); 1.74 (3H, d); 1.68 (6H, s)

Prepared as described in Example 12b using 2-chloro-5-hydroxy-iV-(tricyclo[3.3.1.13,7]dec-l-methyl)-benzamide (0.20 g- Example 12a), N-tBOC-L-prolinol (0.19 g) and tributylphosphine (0.23 ml), dry tetrahydrofuran (6 ml) and 1-[[(1-piperidinylcarbonyl)azo]carbonyl]- piperidine (0.24 g) to obtain the t-butyloxycarbonyl (BOC)-protected compound, followed by treatment with 4N hydrochloric acid in dioxane (0 J ml) and methanol (5 ml) to yield the title compound as colourless solid (0.07 g)
MS (APQ+ve) 403/405 (M+H)+
'HNMR (CD3OD) 5 8.45 (1H, bt); 7.46 (1H, d); 7.14-7.10 (2H, m); 4.41 (1H, dd); 4.18 (1H, t); 4.104.04 (1H, m); 3.41 (2H, t); 3.10 (2H, m); 2.36-2.28 (lH,m); 2.25-2.08 (2H, d); 2.03 (3H, s); 2.00-1.90 (1H, m); 1.83 (3H, m); 1.74 (3H, d); 1.68 (6H, s)

Prepared as described in Example 12b using 2-chloro-5-hydroxy-N-Cricyclo[3.3.1.13,7]dec-l-methyI)-benzamide (0.20 g- Example 12a), i-piperidinemethanol (0.20 g) and tributylphosphine (0.23 ml), dry tetrahydrofuran (6 ml) nd l-([(l-piperidinylcarbonyl)azo]carbonyI]- piperidine (0.24 g) to obtain the t-•utyloxycarbonyJ (BOC)-protected compound. This compound was treated with 4N ydrochloric acid in dioxane (0.5 ml) and methanol (5 ml) to yield the title compound as olourless solid (0.09 g),
AS (APCI +ve) 417/19 (M+H)+
H NMR (DMSO-d6) 8 8.34 (2H, bs); 8.29 (1H, t); 7.38 (1H, d); 7.01 (1H, dd); 6.93 1H, d); 3.99-3.95 (1H, m); 3.91-3.87 (1H, m); 3.34 (1H, m); 3.23 (1H, bd); 2.92 (2H, d); L82-2.71 (2H, m); 2.22 (1H, m); 1.94 (3H, s); 1.82 (2H, d); 1.72-1.66 (4H, m); 1.59 3H, d); 1.52 (6H, s); 1.39-1.32 (1H, m)
ilxample 16
3 7 is-5-[(4-Aminocyclohexyl)oxy]-2-chloro-N-(tricyclo[3J.l.l ' ]dec-l-ylmethyl)-
lenzamide, hydrochloride salt

Prepared as described in Example 12b using 2-chloro-5-hydroxy-N-
3 7 (tricyclo[3.3.1.1 ' ]dec-l-methyl)-benzamide (0.20 g, Example 12a), trans-4-amino-
cyclohexanol (0.20 g) and tributylphosphine (0.23 ml), dry tetrahydrofuran (6 ml) and
l-[[(l-piperidinylcarbonyl)azo]carbonyl]- piperidine (0.24 g) to obtain the
t-butyloxycarbonyl (BOC)-protected compound. This compound was treated with 4N
hydrochloric acid in dioxane (0.5 ml) and methanol (5 ml) to yield the title compound as
colourless solid (0.065 g).
MS (APCI +ve) 417/19 BP 417
*H NMR (DMSO-d6) 8 8.30 (IH, t); 7.97 (3H, bs); 7.38 (IH, d); 7.02 (IH, dd); 6.92
(IH, d); 4.62 (IH, bs); 3.11 (IH, bs); 2.92 (2H, d); 1.94 (5H, s); 1.76-1.58 (12H, m); 1.52
(6H,s).
Example 17
37 2-MethyI-5-(l-piperazinylmethyl)-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide,
hydrochloride salt

To a solution of 2-bromo-5-(4-[{ l,l-dimethylethyl}oxycarbonyl]-piperazin-l-1)methyl -N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.20g, Example 65b) and etrakis(triphenylphosphine)palladium(0) (2mg) in dry toluene (6 ml) was added etramethyltin (0.2ml). The solution was heated at 130°C in a sealed tube for 18hrs. The :ooled reaction mixmre was evaporated and the residue was treated with 10% KF solution a acetone and stirred for 45min. The mixmre was concentrated and chromatographed on ilica gel (isohexane men 60% ethyl acetate/ 40% isohexane) to give the -butyloxycarbonyl (BOC)-protected compound as a colourless oil. The oil was dissolved n methanol (2 ml) and 4N hydrochloric acid in dioxane (1 ml) added. The solution was tirred at room temperature under a nitrogen atmosphere until the reaction was complete as ndged by LC/MS. Evaporation of solvent followed by trituration with diethyl etiier gave tie title compound as a colourless solid (0.03 g).
AS (APCI +ve) 382 (M+H)+
HNMR (CD3OD) 57.61 (1H, s); 7.55(1H, d); 7.39 (1H, d); 4.45 (2H, s); 3.67-3.46
8H, bm); 3.08 (2H, s); 2.45 (3H, s); 1.99(3H, s); 1.78 (3H, d); 1.71 (3H, d); 1.62 (6H, s)
Example 18
l-OUoro-5-(l-piperazinylinethyl)-N-(2-tricyclo[3J.l.l3'73dec-l-ylethyl)-benzaiiiide, lydrochloride salt

3 7
a) 5-(bromomethyI)-2-chloro-N-(2-tricyclo[3.3.1.1 ' ]dec-l-ylethyl)-benzamide
To a solution of 2-chloro-5-(bromomethyl)-benzoic acid (1.0 g) in dichloromethane (25ml) at 0°C was added dimethylformamide (0.05ml) followed by oxaiyl chloride (0.52 ml). The reaction was allowed to warm to room temperature and stirred for 30min. The volatiles were removed under vacuum and the residue dried under high vacuum. The acylchloride was dissolved in dichloromethane (20 ml) and added to a solution of 2-adamantanethylamine hydrochloride salt (0.95g) in dichloromethane (20ml) and diisopropylethylamine (2 ml) at 0°C. The reaction was allowed to warm to room temperature and stirred for 2h. The organics were washed with water (20ml) then saturated aqueous ammonium chloride solution and the organic layer dried over magnesium sulfate then filtered. The filtrate was concentrated under reduced pressure to a solid. The crude material was recrystallised from dichloromethane/hexane to afford the subtitle compound as,a white solid (1.3 g).
b) 4-[[4-OdoroO-[[(2-tricyclo[33JJ3'7]dec4-ylethyl)ainino]carbonyl]-
phenyl]methyl]-l-piperazinecarboxylic acid, 1,1-dimethylethyl ester
3 7 Arnixture5-(bromomethyl)-2-chloro-N-(2-tncyclo[3.3.1.1 ' ]dec-l-ylethyl)-
benzamide (Example 18a, 0.35g), l-tertbutyloxycarbonylpiperazine (0.213g), potassium
carbonate (0.20g) and potassium iodide (10 mg) in acetone (5 ml) was heated at 60°C for
2h. The acetone was removed under vacuum, the residue taken into dichlorometane and
the solid removed by filtration. The crude material was purified on a silica gel eluting with
dichloromethane/ethanol (0-10% gradient) to afford the subtitle compound as a white foam
(0.383g).

MS (APCI +ve) MW 516/518 (M+H)+
!H NMR (CDC13) 8 7.63 (1H, bs); 7.34 (2H, bs); 6.09 (1H, bs); 3.60-3.30 (8H, m); 2.50-2.30 (4H, bs); 1.97 (3H, bs); 1.72 (3H, d); 1.68 (3H, d); 1.56 (6H, bs); 1.44 (9H, s); 1.50-1.35 (2H,m)
c) 2-Chloro-5-(l-piperazinyImethyl)-N-(2-tricyclo[3.3.1.13'7]dec-l-ylethyl)-
benzamide, hydrochloride salt
3 7 4-[[4-chloro-3-[[(2-tricyclo[3.3.1.1 ' ]dec-l-ylethyl)amino]carbonyl]phenyl]methyl]-
1-piperazinecarboxylic acid, 1,1-dimetfiylethyl ester, (Example 18b, 0.270g) was dissolved
in methanol (3ml), 4N HC1 in dioxane (2ml) was added and the mixture stirred for 14h at
room temperature. The solvent was removed under vacuum and the resulting solid was
triturated with ether to afford the title compound as a white powder (0.207g).
MS (APCI +ve) MW 416/418 (M+H)+
!H NMR (CD3OD) 5 7.69 (1H, s); 7.66 (1H, d); 7.60 (1H, d); 4.86 (2H, s); 3.70-3.50 (8H, m); 3.50-3.35 (2H, m); 1.98 (3H, bs); 1.78 (3H, d); 1.70 (3H, d); 1.62 (6H, bs); 1.50-1.35 (2H,m).

Prepared as described in Example 12b using 2-chloro-5-hydroxy-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.155 g, Example 12a), tributylphosphine

(0.23 ml), (+/-)-3-hydroxy-l-pyrrolidinecarboxylic acid , 1,1-dimethylethyl ester (0.19 g), l-[[(l-piperidinylcarbonyl)azo]carbonyl]-piperidine (0.24 g) and dry tetrahydrofuran (10 ml) to give the t-butyloxycarbonyl (BOC)-protected compound as a colourless foam. This compound was treated with 4N hydrochloric acid in dioxane (0.5 ml) and methanol (5 ml) to yield the title compound as a colourless solid (0.075 g).
MS (APCI+ve) 389/391 (M+H)+
!H NMR (CD3OD) 5 8.42 (1H, bt); 7.42 (1H, d); 7.09-7.03 (2H, m); 5.23 (1H, bm);
3.59-3.41 (4H, m); 3.07 (2H, d); 2.36-2.30 (2H, m); 1.99 (3H, bs); 1.79 (3H, d); 1.70
(3H,d);1.63(6H,d)

Prepared as described in Example 12b using 2-chloro-5-hydroxy-N-
3 7 (tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.15 g, Example 12a), tributylphosphine
(2 x 0.18 ml), 3-hydroxy-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester (2 x 0.14 g),
l-[[(l-piperidinylcarbonyl)azo]carbonyl]-piperidine (2 x 0.18 g) and dry tetrahydrofuran
(6 ml) to give the t-butyloxycarbonyl (BOC)-protected compound as a colourless foam.
This compound was treated with 4N hydrochloric acid in dioxane (0.25 ml) and memanol
(5 ml) to yield the title compound as a colourless foam (0.042 g).

MS (APCI+ve) 403/405 (M+H)+
*H NMR (CD3OD) 5 8.42 (IH, t); 7.41 (IH, d); 7.14-7.10 (2H, m); 4.82 (IH, bm); 3.51 3.39 (IH, m); 3.38 (2H, m); 3.20-3.17 (IH, m); 3.06 (2H. d); 2.10-2.04 (2H, m); 2.00 (3H, bs); 1.94-1.89 (IH, m); 1.84-1.68 (7H, d); 1.64 (6H, d)
Example 21
37 trans-5-[(4-Aminocyclohexyl)oxy]-2-chIoro-N-(tricycIo[3.3.1.1 ' ]dec«l-ylmethyl)-
benzamide

Prepared as described in Example 12b using 2-chloro-5-hydroxy-N-
3 7 (tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.15 g, Example 12a), tributylphosphine
(3 x 0,18 ml), cis- 0.15 g), l-[[(l-piperidinylcarbonyl)azo]carbonyl]-piperidine (3 x 0.18 g) and dry
tetrahydrofuran (6 ml) to give the t-butyloxycarbonyl (BOQ-protected compound as a
colourless foam. This compound was treated with 4N hydrochloric acid in dioxane (0.5
ml) and methanol (3 ml) to yield the tide compound as a colourless foam (0.080 g).
MS (APCI+ve) 417/419 (M+H)+
^NMR (CD3OD) 8 8.38 (IH, t); 7.34 (IH, d); 6.98 (IH, dd); 6.96 (IH, d); 4.30 (IH, m); 3.17 (IH, m); 3.04 (2H, d); 2.22 (2H, bm); 2.09 (2H, m); 1.98 (3H, bs); 1.77 (3H, d); 1.68 (3H, d); 1.62 (6H, s); 1.55 (4H, m)

Example 22
cis-(+/-)-S-[(3-Aminocyclopentyl)oxy]-2-chloro-N-(tricyclo[3.3.1.13' ]dec-l-ylmethyl)-
benzamide

Prepared as described in Example 12b using 2-chloro-5-hydroxy-N-
3 7 (tricyclo[3.3.1.1 * ]dec-l-ylmethyl)-benzamide (0.20 g, Example 12a), tributylphosphine
(0.24 ml), trans-(+/-H3-hydroxycyclopentyl)-carbarnic acid, 1,1-dimethylemyl ester (0.19 g), l-[[(l-piperidinylcarbonyl)azo]carbonyl]-piperidine (0.24 g) and dry tetrahydrofuran (3 ml) to give the t-butytoxycarbonyl (BOC)-protected compound as a colourless foam. This compound was treated with 4N hydrochloric acid in dioxane (0.5 ml) and methanol (5 ml) to yield the title compound as a colourless foam (0.15 g).
MS (APCI+ve) 403/405 (M+H)+
lH NMR (CD3OD) 5 7.36 (1H, d); 7.02-6.98 (2H, m); 4.94-4.90 (1H, m); 3.75-3.68 [lH, m); 3.04 (2H, s); 2.55 (1H, m); 2.24-2.17 (1H, m); 2.09-2.03 (2H, m); 1.98-1.86 ;5H, m); 1.76 (3H, d); 1.68 (3H, d); 1.62 (6H, d)
Example 23
:S^)-2-Chloro-5-(2^-diazabicyclo[2^.1]hept-2-yl)-N-(tricycIo[33.1.13'7]dec-l-rlmethyO-benzamide, hydrochloride salt

37 a) 5-Bromo-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide
Prepared as in Example la from 5-bromo~2-chlorobenzoic acid (7.17g), oxalyl
chloride (5.3ml), dichloromethane (150ml), dimethylformamide (0.05ml),
diisopropylethylamine (6ml) and adamantylmethylamine (5ml) to give the subtitle
compound as white colourless needles (7.3g).
MS (APCI-ve) 382/384 (M-H)+
b) (S^)^CbJoro-5-(2^-diazabicyclo[2^.1]hept-2-yl)-N-(tricyclo[3J.l.l3'7]dec-l-
ylmethyl)-benzamide, hydrochloride salt
37 A mixture of 5-bromo-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide
(1.70 g, Example 23a), 2,5-diazabicyclo[2.2.1]heptane-2-carboxylic acid, 1,1-dimethylethyl
ester (1.06 g), cesium carbonate (2.20 g), (R)-(+)-2,2'-bis(diphenylphosphino)-l,r-
biriaphthyl ((R>(+)-BINAP, 0.20 g), and palladium (ID acetate (0.050 g) in dry toluene (10
ml) was heated at 100°C under nitrogen for 24h. The cooled reaction mixture was filtered,
washing the residue with ethyl acetate. The filtrate was washed with water and brine, dried
(MgS04) and evaporated under reduced pressure to give an orange oil.
The oil was purified by chromatography on silica gel, eluting with 0.5%
methanol/dichloromethane to yield the r-butyloxycarbonyl (BOC) protected compound as a
colourless foam. The foam was dissolved in methanol (20 ml) and 4N hydrochloric acid in

dioxane (2.5 ml) added. The solution was stirred at room temperature until reaction was complete (LCMS). The solution was then evaporated under reduced pressure and the residue triturated with diethyl ether to afford the title compound as an off-white solid (0.92 g).
MS (APCI+ve) 400/402 (M-HC1)+
2H NMR (CD3OD) 8 8.32 (1H, t); 7.30 (1H, d); 6.77-3.70 (2H, m); 4.69 (1H, s); 4.50 (1H, s); 3.73 (1H, dd); 3.67 (2ft s); 3.06 (2H, d); 2.30 (1H, bd); 2.06 (1H, bd); 1.99 (3H, bs); 1.78 (3H, d); 1.70 (3H, d); 1.64 (6H, s); 1.55 (4H, m) Methanol peak masks other H signal.

Prepared as described in Example 23 above from 5-btomo-2-chioto-N-(tricyclo[3.3.1.13'7]dec-l-ylmethyl)-benzamide (0.30 g, Example 23a), 3-methyl-l-piperazinecarboxylic acid, 1,1 -dimethylethyl ester (0.20 g), cesium carbonate (0.36 g), (R)-(+)-2,2'-bis(diphenylphosphino)-l,l'-bmaphthyl ((R)-(+)-BINAP,0.036 g), palladium (H) acetate (0.009 g) and dry toluene (10 ml) to yield the t-butyloxycarbonyl (BOC)-protected compound. This compound was treated with 4N hydrochloric acid in dioxane (0.5 ml) and methanol (5 ml) to yield the title compound as a solid (0.025 g).

MS (APCI+ve) 402/404 (M-HC1)+
JH NMR (CD3OD) 8 8.40 (1H, t); 7.37 (1H, d); 7.11 (1H, dd); 7.07 (1H, d); 4.00-3.96 (1H, m); 3.43-3.39 (3H, m); 3.28-3.19 (3H, m); 3.06 (2H, d); 1.98 (3H, bs); 1.77 (3H, d); 1.70 (3H, d); 1.63 (6H, s); 1.10 (3H, d).

Prepared as described in Example 23 above from 5-bromo-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.30 g, Example 23a), 3-amino-l-pyrrolidinecarboxylic acid, 1,1-dimethyIethyl ester (0.18 g), cesium carbonate (0.36 g), (R)-BINAP (0.036 g), anhydrous toluene (3 ml) and palladium (II) acetate (0.009 g); the mixture was heated for 14h in a pressure vessel flushed with nitrogen. Additional (R)-BINAP (0.036 g) and palladium (H) acetate (0.009 g) were added and heating continued for a further 24h. The cooled reaction mixture was poured into water and extracted witii ethyl acetate three times. The organic fractions were combined and washed with water then brine, and dried (MgSC>4). Evaporation under reduced pressure gave an oil which was purified by normal phase HPLC (0-5% methanol/dichloromethane) to yield the t-butyloxycarbonyl (BOC)- protected compound as a colourless foam. The foam was dissolved in methanol (5 ml) and 4N hydrochloric acid in dioxane (0.5 ml) added. The solution was stirred at room temperature under a nitrogen atmosphere until the reaction was

complete as judged by LCMS. Evaporation followed by trituration witli diethyl ether and methanol yielded the title compound as an off-white solid/foam (0.040 g).
MS (APCI +ve) 388/390 (M-HCl)-f-
lH NMR (CD3OD) 6 8.20 (1H, bt); 7.12 (IE, d); 6.63-6.60 (2H, m); 4.76-4.08 (1H, m): 3.43-3.38 (2H, m); 3.35-3.28 (1H, m); 3.25 (1H, m); 2.94 (2H, s); 2.31-2.22 (1H, m); 2.01-1.94 (1H, m); 1.89 (3H, bs), 1.67 (3H, d); 1.60 (3H, d); 1.53 (6H, s)
Example 26
(+/-)-5-(3-Amino-l-piperidinyI)-2-chIoro-N-(tricyclor3.3.1.13'7]dec-l-ylmethyI)-
benzamide

Prepared as described in Example 23 above from 5-bromo-2-chloro-N-
3 7 ktricycIo(3.3.1.1 ' ]dec-l-ylmetfiyl)-benzamide (0.20 g, Example 23a), 3-piperidinyl-
carbamic acid, 1,1-dimethylethyl ester (0.12 g), cesium carbonate (0.24 g), (R)-(+)-2,2'-
bis(diphenylphosphino)-l,r-binaphthyl ((R)-(+)-BINAP, 0.024 g), palladium (II) acetate
(0.006 g) and dry toluene (3 ml) to yield the t-butoxycarbonyl (BOC)-protected compound.
The t-butoxycarbonyl (BOC)-protected compound was dissolved in methanol (5 ml) and
hydrochloric acid (0.5 ml of a 4N solution in dioxane). After stirring at room temperature
for 24h the mixture was evaporated and the residue partitioned between ethyl acetate and
saturated sodium bicarbonate. The layers were separated and the aqueous phase acidified
with 2M hydrochloric acid and extracted with ethyl acetate. The organic phase was dried

over magnesium sulfate and then evaporated under reduced pressure to give a gum. Purification by chormatography on silica gel, eluting with 4-10% methanol in dichloromethane/aqueous ammonia afforded the title compound as a solid (0.036 g).
MS (APCI+ve) 402/404 (M+H)+
*H NMR (CD3OD) 5 7.25 (1H, d); 7.00 (1H, dd); 6.96 (1H, d); 3.59 (1H, dd); 3.48-3.45 (1H, m); 3.04 (2H, d); 2.91-2.85 (1H, m); 2.82-2.75 (1H, m); 2.58 (1HT dd); 1.98-1.93 (4H, m); 1.85-1.75 (3H, d); 1.70-1.62 (10H, d); 1.34-1.25 (1H, d).

Prepared as described in Example 23 above from 5-bromo-2-chloro-N-(tricyclo[3.3.1.13,7]dec-l-yImethyl)-benzamide (0.30 g, Example 23a), 3-amino-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.19 g), cesium carbonate (0.36 g), (R)-(+)-2^'-bis(diphenylphosphino)-l,l'-binaphthyl ((R)-(+)-BINAP, 0.036 g), palladium (II) acetate (0.008 g) and dry toluene (3 ml) to yield the t-butyloxycarbonyl (BOC)-protected compound. This compound was treated with methanol (5 ml) and hydrochloric acid (0.5 ml of a 4 M solution in dioxane) followed by an acid/base work-up. Purification by

chromatography on silica gel, eluting with 4-10% methanol in dichloromethane/aqueous ammonia afforded the title compound as a solid (0.008 g).
MS (APCI+ve) 402/404 (M+H)+
]H NMR (CD3OD) 8 7.14 (1H, d); 6.68-6.65 (2H, m); 3.47-3.40 (1H, m); 3.25 (1H, m); 3.05-3.02 (3H, m); 2.72-2.65 (1H, m); 2.52-2.47 (1H, m); 2.08-2.04 (1H, m); 1.97 (3H, bs); 1.89-1.82 (1H, m); 1.77 (3H, d); 1.70-1.62 (10H, d); 1.50-1.40 (1H, m).

Prepared as described in Example 23 above from 5-bromo-2-chloro-N-
3 7 (tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.15 g, Example 23a), hexahydro-
pvrrolo[3,4-c]pyrrole-2(lH)-carboxylic acid, 1,1-dimethylethyl ester (0.17 g), cesium
carbonate (0.33 g), (R)-(+)-2,2'-bis(diphenylphosphino)-l,r-binaphthyl ((R)-(+)-BINAP,
0.018 g), palladium (II) acetate (0.004 g) and dry toluene (2 ml) to yield the t-
butyloxycarbonyl (BOC)-protected compound. This compound was treated with methanol
(5 ml) and hydrochloric acid (0.5 ml of a 4 M solution in dioxane) followed by an acid/base
work-up. Trituration of the residue with dichloromethane afforded the title compound as a
solid (0.020 g).

MS (APCI+ve) 414/4I6(M+H)+
'HNMR(CD3OD) 5 8.17 (IH, t); 7.20 (IH, d); 6.63 (IH, dd); 6.54 (IH, d); 3.36 (2H, m); 3.02 (2H, dd); 2.95-2.90 (4H, m); 2.80 (2H, m); 2.60 (2H, dd)); 1.94 (3H, bs); 1.67 (3H, d); 1.59 (3H,d); 1.52 (6H,d).

Prepared as described in Example 12b using N-(5-hydroxy-2-methylphenyl)-tricyclo[3.3.1.13'7]decane-I-acetamide (0.51 g, Example 12, WO 99/29660), tributylphosphine (0.64 ml), l-[[(l-piperidinylcarbonyl)azo]carbonyl]-piperidine (0.65 g), 4-hydroxy-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.52 g) and dry tetrahydrofuran (10 ml) to give the t-butyloxycarbonyi (BOC) protected compound as a colourless solid. This compound was treated with 4N hydrochloric acid in dioxane (0.5 ml) and methanol (5 ml) to yield the title compound as a colourless solid (0.13 g).
MS (APCI+ve) 383 (M-HCD+
*H NMR (CD3OD) 5 7.19 (IH, d); 7.12 (IH, d); 6.83 (IH, dd); 4.71-4.$6 (IH, m); 3.46-3.40 (2H, m); 3.28-3.22 (2H, m); 2.25 (3H, s); 2.21 (IH, s); 2.21-2.14 (2H, m); 2.11-2.04 (5H,m); 1.84-1.73 (12H,m).

Prepared as described in Example 12b using N-(2-chloro-5-hydroxyphenyI)-tricyclo[3.3.1.13,7]decane-l-acetamide (0.25 g, Example 28, WO 99/29660), tributylphosphine (0.29 ml), l-[[(l-piperidinylcarbonyl)azo]carbonyl]-piperidine (0.30 g), 4-hydroxy-l-piperidinecarboxylic acid, 1,1-dimethylethyi ester (0.24 g) and dry tetrahydroruran (10 ml) to give the t-butyloxycarbonyl (BOC) protected compound as a colourless solid. This compound was treated with 4N hydrochloric acid in dioxane (1 ml) and methanol (20 ml) to yield the title compound as a colourless solid (0.08 g).
MS (APd+ve) 375/377 (M-HC1)+
!HNMR (CD3OD) 8 7.55 (1H, d); 7.41 (1H, d); 6.88 (1H, dd); 4.76-4.70 (1H, m); 3.48-3.39 (2H, m); 3.30-3.22 (2H, m); 2.25 (2H, s); 2.22-2.16 (2H, m); 2.14-2.03 (2H, m); 1.84-1.72 (12am).

3 7
a) 2-Chloro-5-formyl-N-(tricyclo[33.1.1 ' ] dec-l-ylmethyl)-benzamide
3 7 A solution of 5-bromo-2-chloro-N-(tricyclo[3.3.1.1' ]dec-l -ylmethyl)-benzamide (3.25 g,
Example 23a) in anhydrous tetrahydrofuran (150 ml) was cooled to -78°C under a nitrogen
atmosphere. A solution of methyllithium (1.4M in diethyl ether, 6.1 ml) was added over
2min. The mixture was stirred at -78°C for lOmin, then a solution tert-butyllithium (1.7M
in pentane, 10.0 ml) was added dropwise. The mixture was stirred at -78°C for a further
lOmin, then dimethylformamide (1.0 ml) was added. The resulting solution was stirred at
-78°C for 30min., quenched with saturated aqueous ammonium chloride solution (100 ml)
and extracted with ethyl acetate. The combined extracts were dried over anhydrous
magnesium sulfate, filtered, and the filtrate concentrated under reduced pressure to give the
subtitle compound as a solid (2.76 g).
MS (APCI +vc) 332 (M+H)+
!HNMR (DMSO-d6) 8 10.04 (1H, s); 8,49 (1H, t); 7.96-7.91 (2H, m); 7.74 (1H, d); 2.96
(2H, d), 1.95 (3H, s); 1.64 (6H, AB); 1.53 (6H, d).
b) 4-[4-CWoro-3-[(tricycIo[3J.l.l3'7]dec-l-ylmethyI)amino]carbonyl]
phenyI]methyl]ainrao]-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester
2-Chloro-5-formyl-N-(tricyclo [3.3.1.13'7] dec-l-ylmethyl)-benzamide (0.270 g, Example 31a) and 3-amino-l-pyrrolidinecarboxylic acid, 1,1-dimethylethyl ester (0.325 g, Journal of Medicinal Chemistry, 1998,41(22), 4273-4278) were dissolved in 1,2-dichloroethane (30 ml), under a nitrogen atmosphere. Sodium triacetoxyborohydride (0.24 g) was added and the mixture was stirred for 14h at room temperature. Water and

dichloromethane were added and the layers were partitioned. The organic extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by HPLC eluting with a gradient of 0-10% of ethanol in dichloromethane, then by chromatography over silica gel eluting with ethyl acetate : iso-hexane (1:1) then ethyl acetate : ethanol (98:2) to give the subtitle compound as a colourless oil (0.158 g).
MS (APCI +ve) 516 (M+H)+
c) 2-Chloro-5-[(4-piperidinylamino)methyl]-N-(tricyclo[3J.l.l3'7]dec-l-ylmethyl)-
benzamide, dihydrochioride salt
3 7 Prepared from 4-[[[4-chloro-3-[[(tricyclo[3.3.1.1 ' ]dec-l-ylmethyI)amino]carbonyl]
phenyl]methyl]amino]-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.158 g,
Example 31b) methanol (3 ml) and 4N hydrochloric acid solution in dioxane (2 ml).
Solvents were removed under reduced pressure and the residue was triturated with ethyl
acetate, iso-hexane and diethyl ether to give the title compound as a white solid (0.126 g).
MS (APCI +ve) 416 (M+H-2HC1H
!HNMR (CD3OD) 5 8.47 (1H, t); 7.62-7.56 (3H, m), 4.33 (2H, s); 3.58-3.55 (3H, m); 3.12
(2H, t); 3.07 (2H, d); 2,44 (2H, d); 2.03-1.92 (5H, m); 1.73 (6H, q); 1.63 (6H, d).

a) [[4-[[[4-Chloro-3-[[(tricyclo[3J.l.l3'7]dec-l-ylmethyl)amino]carhonyl]
phenyJ]methyl]amino]cyclohexyl]methyI]-carbamic acid, 1,1-dimelhyiethyi ester
Prepared according to the method described in Example 3 lb from 2-chloro-5-formyi-N-(tricyclo [3.3.1.13,7] dec-l-ylmethyl)-benzamide (0.30 g, Example 31a), [(4-aminocyclohexyl)methyI]-carbamic acid, 1,1-dimethylethyI ester (0.207 g, WO 97/32882), sodium triacetoxyborohydride (0.135 g) and 1,2-dichloroemane (10 ml). The residue was purified by chromatography over silica gel eluting with ethyl acetate : iso-hexane (1:1) then ethyl acetate : ethanol (9:1) to give the subtitle compound as a colourless oil (0.26 g).
MS (APCI +ve) 544 (M+H)+
b) 5-[[[4-(Aminomethyl)cyclohexyl]aniino3methyI]-2-chloro-N-
37 (tricyclo[33.1.1 ' ]dec-l-ylmethyl)-benzamide, dihydrochloride salt
Prepared from [[4-[[[4-chloro-3-[[(tricyclo[3.3.1.13'7]dec-1 -
ylmethyl)amino]carbonyl] phenyl]methyl]amino]cyclohexyl]methyl]-carbamic acid, 1,1-
dimethylethyl ester (0.26 g, Example 32a) methanol (5 ml) and 4N hydrochloric acid
solution in dioxane (2 ml). Solvents were removed under reduced pressure and the residue
was triturated widi diethyl ether to give the title compound as a white powder (0.191 g).
MS (APCI +ve) 444 (M+H-2HC1)+
*H NMR (CD3OD) 8 7.60-7.58 (3H, m), 4.29 (2H, s); 3.28-3.12 (1H, m); 3.09 (2H, s); 2.84 (2H, d); 2.31 (2H, bd); 2.00 (5H, bs); 1.75 (6H, q); 1.65 (6H, d); 1.71-1.65 (1H, m); 1.63-1.44 (2H, m); 1.31-1.12 (2H, m).
Example 33
3 7 5-[[(4-Aminocyclohexy0amino]niethyl]-2-chloro-N-(tricydo[3.3.1.1 ' ]dec-l-
ylmethyl)-benzamide, dihydrochloride salt

a) [4-[[[4-chloro-3-[[(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)amino]carbonyi]phenyl]-
methyI]amino]cycIohexyI]-carbamic acid, 1,1-dimethylethyI ester
Prepared according to the method described in Example 3 lb from 2-chloro-5-formyl-N-(tncyclo [3.3.l.l3'7] dec-l-ylmethyl)-benzamide (0.30 g, Example 31a), (4-aminocyclohexyl)-carbamic acid, 1,1-dimethylethyl ester (0.194 g, Journal of Organic Chemistry, 1996, 61(25), 8811-8818), sodium triacetoxyborohydride (0.135 g) and 1,2-dichloroethane (10 ml). The residue was purified by chromatography over silica gel eluting with ethyl acetate: iso-hexane (1:1) then ethyl acetate : ethanol (95:5) to give the subtitle compound as a colourless oil (0.24 g).
MS (APCI+ve) 530 (M+H)+
37
b) 5-[[(4-Aminocyclohexyl)amino]methyl]-2-chloro-N-(tricyclo[3-3.1.1 ' ]dec-l-
ylmethyl)-benzamide, dihydrochloride salt
Prepared from [4-{[[4-chloro-3-[[(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)amino]carbonyl]phenyl] methyl]amino]cyclohexyl]-carbamic acid, 1,1-dimethylethyl ester (0.26 g, Example 33a), methanol (5 ml) and 4N hydrochloric acid solution in dioxane (1 ml). Solvents were removed under reduced pressure and the residue was triturated with diethyl ether to give the title compound as a white powder (0.190 g).
MS {APCI +ve) 430 (M+H-2HC1)+
*HNMR (CD3OD) 5 7.61-7.59 (3H, m), 4.30 (2H, s); 3.28-3.11 (2H, m); 3.08 (2H, s);
2.40-2J32 (2H, m); 2.21-2.17 (2H, m); 2.00 (3H, s); 1.74 (6H, q); 1.64 (6H, d); 1.63-1.48
(4am).

Example 34
5-[(l-Azabicyclo[2.2.2]oct-3-yIamino)methyI]-2-chloro-N-(tricycIof3.3.1.13'7]dec-l-ylmethyO-benzamide

Prepared according to the method described in Example 31b from 2-chloro-5-formyl-V-(tricyclo [3.3.1.l3,7]dec-l-ylmethyl)-benzamide (0.30 g, Example 3 la), l-azabicyclo[2.2.2]octan-3-amine dihydrochloride salt (0.18 g), sodium riacetoxyborohydride (0.135 g) and 1,2-dichloroethane (10 ml). The residue was purified >y chromatography over silica gel eluting with ethyl acetate : iso-hexane (1:1) followed by sthyl acetate: ethanol (95:5). Repurification by chromatography over silica gel eluting vith dichloromethane : methanol (95:5) then (9:1) gave the title compound as a white gum 0.013 g).
rfS (APCI +ve) 442 (M+H)+
H NMR (CDC13) 5 7.68 (1H, d); 7.39 (1H, d); 7.31 (1H, dd); 6.41 (1H, t); 3.75 (2H, s); 5.42-3.31 (2H, ra); 3.25-3.09 (6H, m); 2.94 (1H, d); 2.38-2.23 (2H, m); 2.22-2.14 (1H, m); L01 (3H, s); 1.92-1.83 (2H, m); 1.69 (6H, q); 1.59 (6H, d).
Example 35
H4^3-AjninopyiToUdin-l-yl)-2-methylphenyl]-2-(tricyclo[3^.1.13,7]dec-l-rl)acetamide, dihydrochloride salt

a) [l-(3-Methyl-4-nitrophenyl)-pyrroIidin-3-yl]-carbamic acid tert-butyl ester
4-Fluoro-2-methyl-l-nitrobenzene (1 g), pyrrolidin-3-ylcarbamic acid tert-butyl ester (1.2 g), potassium carbonate (1.79 g) and dimethyl sulfoxide (10 ml) were heated together at 80°C under nitrogen for 15h. The mixture was then cooled, diluted with ethyl acetate (200 ml), washed with 2N aqueous hydrochloric acid (200 ml), dried (MgSC>4) then concentrated. Purification of the residue by silica gel chromatography (eluting with 20% ethyl acetate in isohexane) gave the subtitle compound (1.744 g).
XH NMR (DMSO-d6) 5 8.03 - 8.00 (1H, d), 7.28 -7.21 (1H, br d), 6.51 - 6.47 (2H, m), 4.20 - 4.12 (1H, br m), 3.61 - 3.16 (4H, m), 2.56 (3H, s), 2.20 - 2.08 (1H, m), 1.98 -1.85 (lH,m), 1.39(9H,s).
b) [l-(4-Amino-3-methylphenyl)-pyrTolidin-3-yI]-carbamic acid tert-butyl ester
[l-(3-Methyl-4-nitrophenyl)-pyrroIidin-3-yl]-carbamic acid tert-butyl ester (1.744 g, Example 35a), iron powder (1.52 g), ammonium chloride (1.45 g), ethanol (50 ml) and water (50 ml) were refluxed together under nitrogen for 2h. The mixture was cooled and the iron was filtered off. Water (200 ml) was added to the residue and the product extracted into ethyl acetate (3 x 200 ml), dried (MgSC>4), and concentrated to give the subtitle compound (1.56 g).
*H NMR (CDC13) 6.65 (1H, br s), 6.38 (2H, br m), 4.80 (1H, m), 4.33 (2H, br m), 3.60 2.80 (5H, m), 2.31 - 2.17 (4ft m), 1.92 - 1.82 (1H, m), 1.45 (9H, br s).-

c) {l-[4-(2-(tricycIo[3.3.1.1 '7]dec-l-yI)acetyiamino)-3-methylphenyI]-pyrroIidin-3-
yl}-carbamic acid tert-butyl ester
To a solution of adamantan-1-yl-acetic acid (0.46g) in dichloromethane (10ml) at 0°C was added dimethylformamide (0.1ml) followed by oxalyl chloride (2.50 ml). The reaction was allowed to warm to room temperature and stirred for 30min.. The volatiles were removed under vacuum and the residue dried under high vacuum. The residue was dissolved in dichloromethane (10ml) and added to a solution of [l-(4-amino-3-methylphenyl)-pyrrolidin-3-yl]-carbamic acid tert-butyl ester (0.70g, Example 35b) in dichloromethane (10ml) and triethylamine (0.8 ml) at 0°C. The reaction was allowed to warm to room temperature and stirred for 3h. The solution was washed with 2N aqueous hydrochloric acid (20ml), then brine (20 ml) and the organic layer dried over magnesium sulfate then filtered. The filtrate was concentrated under reduced pressure. The crude material was purified by silica gel chromatography (eluting with 1% methanol in dichloromethane) to yield the subtitle compound(l. lg).
MS (APCI +ve) MW 468 (M+H)+
*H NMR (DMSO-d6) 5 8.86 (IH, s); 7.01 - 6.98 (IH, d); 7.18 - 7.14 (IH, br d); 6.33 - 6.27 (3H, m); 4.15 - 4.04 (IH, m); 3.42 - 3.15 (3H, m); 3.00 - 2.97 (IH, m); 2.12 (3H, s); 2.00 (2H, s); 1.99 - 1.80 (5H, m); 1.70 -1.61 (12H, m); 1.39 (9H, s).
d) N44-(3-AniinopyrroUdiii-l-yl)-2-methylphenyl]-2.(tricyclot3^.1.13i7]dec-l-
yOacetamide, dihydrochloride salt
37 {l-[4-(2-(tricycIo[3.3 • I • 1 ' Jdec-1 -yI)acetyIamino)-3-methylphenyI]-pyrroIidin-3-
yl}-carbamic acid tert-butyl ester (0.20 g, Example 35c) was dissolved in methanol (5 ml)
and hydrochloric acid (0.5ml of a 4N solution in dioxane) was added. After stirring at
room temperature for 14h, me mixture was evaporated to 2/3 original volume under
reduced pressure. Diethyl ether was gradually added to me solution and the resulting
precipitate collected by filtration, washed with diethyl ether and dried in vacuo to afford the
title compound as a solid (0.15 g)

MS (APCI +ve) 368 (M+H)+
!HNMR (DMS0-d6) 5 8.92 (1H, s); 8.21 (2H,br s); 7.07 - 7.04 (1H, d); 6.41 - 6.35 (2H, m); 3.91 (1H, br m); 3.50 - 3.39 (2H, m); 3.29 - 3.20 (2H, m); 2.37 - 2.27 (2H, m); 2.14 (3H, s); 2.02 (2H, s); 1.94 (3H, s); 1.70 - 1.58 (12H, m).

a) 4-(3-MethyI-4-nitrophenyI)piperazine-l-carboxyIic acid tert-butyl ester
4-FIuoro-2-methyl-l -nitrobenzene (2 g), piperazine-1-carboxyiic acid tert-butyl ester (4.8 g), potassium carbonate (3.57 g) and dimethyl sulfoxide (20 ml) were heated together at 80 °C under nitrogen for 15h. The mixture was then cooled, diluted with ethyl acetate (200 ml), washed with 2N aqueous hydrochloric acid (200 ml), dried (MgSO,*), and concentrated to give the subtitle compound (4.10g).
MS (APCI+ve) 321 (M)+
*H NMR (DMSO-d6) 5 8.02 - 7.98 (1H, d), 6.89 - 6.86 (2H, m), 3.45 (8H, s), 2.55 (3H, s),
1.42 (9H,s).
b) 4-(4-Amino-3-methylphenyl)piperazine-l-carboxylic acid tert-butyl ester
4-(3-Memyl-4-nitrophenyl)piperazine-l-carboxylic acid tert-butyl ester (2 g, Example 36a), iron powder (1.74 g), ammonium chloride (1.67 g), ethanol (50 ml) and water (50 ml) were refluxed together under nitrogen for 2h. The mixture was cooled and the iron was filtered off. Water (200 mi) was added to the residue and the product

xtracted into ethyl acetate (3 x 200 ml), dried (MgSO,*), and concentrated to give the abtide compound (1.22 g).
H NMR (DMSO-d6) 5 6.62 - 6.52 (3H, m), 4.38 (2H, s), 3.41 (4H, br s), 2.83 (4H, br s), .02 (3H, s), 1.41 (9H,s).
37 I 4-[4- irboxylic acid tert-butyl ester
To a solution of adamantan-1-yl-acetic acid (0.40g) in dichloromethane (10ml) at 'C was added dimethylformamide (0.1ml) followed by oxalyl chloride (2.00 ml). The action was allowed to warm to room temperature and stirred for 30min.. The volatiles ere removed under vacuum and the residue dried under high vacuum. The residue was ssolved in dichloromethane (10ml) and added to a solution of 4-(4-amino-3-ethylphenyl)piperazine-l-caroxylic acid tert-butyl ester (0.60g, Example 36b) in chloromethane (10ml) and triethylamine (0.7 ml) at 0°C. The reaction was allowed to arm to room temperature and stirred for 3h. The solution was washed witii 2N aqueous fdrochloric acid (20ml), then brine (20 ml) and the organic layer dried over magnesium tlfate'then filtered. The filtrate was concentrated under reduced pressure. The crude aterial was was purified by silica gel chromatography (eluting with 1% methanol in chloromethane) to yield the subtitle compound(0.42g).
S (APC1 +ve) MW 468 (M+H)+
INMR (DMSO-d6) 8 8.96 (1H, s); 7.14 - 7.11 (1H, d); 6.79 - 6.72 (2H, m); 3.47 - 3.40
H, m); 3.20 - 3.00 (4H, m); 2.14 (3H, s); 2.03 (2H, s); 1.94 (3H, br s); 1.70 -1.56
2H,m);1.42(9H,s).
i N-(2-MethyM-piperazin-l-ylphenyl)-2-(tricyclo[3.3.1.1 * ]dec-l-yl)acetamide,
hydrochloride salt
3 7 4-[4-(2-(tricycIo[3.3.1.1' Jdec-1 -yi)acety{amino)-3-methyIphenyiJ-piperazine-1 -
rboxylic acid tert-butyl ester (0.05 g, Example 36c) was dissolved in methanol (2 ml) and

hydrochloric acid (0.5ml of a 4N solution in dioxane) was added. After stirring at room temperature for 14h, the mixture was evaporated to 2/3 original volume under reduced pressure. Diethyl ether was gradually added to the solution and the resulting precipitate collected by filtration, washed with diethyl ether and dried in vacuo to afford the title compound as a solid (0.043 g)
MS (APCI +ve) 368 (M+H)+
lKNMR (DMSO-d6) 5 9.01 (3H, brs); 7.18 - 7.15 (IH, d); 6.84 - 6.82 (IH, d); 6.79 - 6.76 (IH, dd); 3.31 - 3.29 (4H, m); 3.28 - 3.16 (4H, m); 2.16 (3H, s); 2.04 (2H, s); 1.94 (3H, br s); 1.69-1.58 (12H,m).

3 7 a) 2-Chloro-4-hydroxy-N-(tricyclo[33.1.1 ' ]dec-l-ylmethyl)-benzamide
To a solution of 2-chloro-4-hydroxybenzoic acid (3.30 g) in dimetiiylformamide (20
ml) was added l,r-carbonyldiimidazole (3.30 g). The reaction mixture was stirred for
2.5h and men I-adamantanemediylamine (3.4 ml) was added. After 14h the reaction
mixture was partitioned between ethyl acetate and 2N aqueous hydrochloric acid and the
organic layer was separated, washed with water then brine and dried (MgSO,*). The
organic layer was concentrated under reduced pressure to give a residue which was purified
by silica gel chromatography (eluting with 10 - 70% ethyl acetate in dichloromethane) to

yield a wnite solid wnicn was inmraied witn emyi acetate to yieia tne suotitie compound as a white solid (3.6 g).
MS (APCI +ve) 320/322 (M+H)+
*H NMR (DMSO-d6) 5 10.12 (1H, s), 8.10 - 8.06 (1H, t), 7.27 - 7.24 (1H, d), 6.81 (1H, d), 6.77 - 6.73 (1H, dd), 2.91 - 2.88 (2H,d), 1.93 (3H, br s), 1.69 -1.56 (6H, br q), 1.50 (6H, br s).
3 7 b) cis-4-(3-Amino-cyclopentyloxy)-2-chloro-N-(tricycIo[3.3.1.1 ' ]dec-l-ylmethyl)-
benzamide, hydrochloride salt
3 7 To a solution of 2-chloro-4-hydroxy-N-(tricyclo[3.3.1.1 ' ]dec-1 -ylmethyl)-
benzamide (0.20 g, Example 37a), rro7W-(3-hydroxycyclopentyl)-carbamic acid, tert-butyl
ester (0.19 g) and tributylphospbirie (0.23 ml) in dry tetrahydrofuran (6 ml) was added
l-[[(l-piperidinylcarbonyl)azo]carbonyl]-piperidine (0.24 g). The orange solution was
heated at 60°C under a nitrogen atmosphere for 2h. Additional trans-
(3-hydroxycyclopentyl)-carbamic acid, terf-butyl ester (0.19 g), tnbutylphosphine (0.23 ml)
and l-[[(l-piperidinylcarbonyl)azo]carbonyl]- piperidine (0.24 g) were added. Heating was
continued and the process described above repeated until reaction was judged complete as
judged by LC/MS. The cooled reaction mixture was diluted with diethyl ether then
filtered. The filtrate was concentrated and purified by chromatography on silica gel (25 -
33% ethyl acetate/ hexane) to give the t-butyloxycarbonyl (BOC)-protected compound as a
colourless foam. The foam was dissolved in methanol (5 ml) and 4N hydrochloric acid in
dioxane (0.25 ml) added. The solution was stirred at room temperature under a nitrogen
atmosphere until the reaction was complete as judged by LC/MS. Evaporation of solvent
followed by trituration with diethyl ether gave the title compound as a colourless solid
(0.24 g).
MS (APCI+ve) 403/405 (M+H)+

H NMR (DMS0-d6) 5 8.18 (1H, t); 7.96 (2H, br s); 7.37 - 7.34 (IH, d); 7.05 (1H, m); 6.97 - 6.94 (IH, m); 4.87 (IH, br m); 3.72 - 3.40 (2H, m); 2.93 - 2.90 (2H, d); 2.04 -1.51 (19H, m); 1.22 (2H, m).

3 7 To a solution of 2-chloro-4-hydroxy-N-(tricyclo[3.3.1.1 ' ]dec-l-methyl)-benzamide
(0.20 gf Example 37a), 4-hydroxy-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester
(0.19 g) and tributylphosphine (0.25 ml) in dry tetrahydrofuran (6 ml) was added 1-[[(1-
piperidinylcarbonyl)azo]carbonyI]-piperidine (0.24 g). The orange solution was heated at
50°C under a nitrogen atmosphere for 2h. Additional 4-hydroxy-l-piperidinecarboxylic
acid, U-dimethylethyl ester (0.19 g), tributylphosphine (0.25 ml) and 1-[[(1-
piperidinylcarbonyl)azo]carbonyl]-piperidine (0.24 g) were added. Heating was continued
and the process described above repeated until reaction was complete as judged by LC/MS.
The cooled reaction mixture was diluted with diethyl ether then filtered. The filtrate was
concentrated and purified by chromatography on silica gel (3:1 iso-hexane/ethyl acetate) to
give the the t-butyloxycarbonyl (BOC)-protected compound as a colourless foam. The
foam was dissolved in methanol (10 ml) and 4N hydrochloric acid in dioxane (10 ml)
added. The solution was stirred at room temperature under a nitrogen atmosphere until the
reaction was complete as judged by LC/MS. Evaporation of solvent followed by trituration
with diethyl ether gave the title compound as a colourless solid (0.165 g).

MS (APCI +ve) 403 (M+H)+
!HNMR (DMSO-d6) 5 8.80 (2H, bs); 8.21-8.16 (IH, t); 7.37-7.34 (IH, d); 7.16 (IH, m); 7.03-6.99 (IH, m); 4.80-4.68 (IH, m); 3.25-3.18 (2H, m); 3.17-3.01 (2H, m); 2.93-2.90 (2H, d); 2.17-2.02 (2H, m); 1.93 (3H, bs); 1.87-1.73 (2H, m); 1.69-1.57 (6H, AB); 1.51 (6H, s)

Prepared as described in Example 38 from 2-chloro-4-hydroxy-N-(tricyclo[3.3.1.l3,7]dec-l-methyJ)-benzamide (0.20 g, Example 37a), (+/-)-3-hydroxy-l-pyrrolidraecarboxylic acid, 1,1-dimethylethyl ester (0.18 g), tributylphosphine (0.25 ml), dry tetrahydrofuran (6 ml) and l-[[(l-piperidinylcarbonyl)azo]carbonyl]- piperidine (0.24 g) to obtain the the t-butyloxycarbonyl (BOC)-protected compound. This compound was treated with 4N hydrochloric acid in dioxane (10 ml) and methanol (10 ml) to yield the title compound as colouless solid (0.165 g).
MS (APCI +ve) 389 (M+H)+
hiNMR (DMSO-dfi) 5 8.19-8.15 (IH, t); 7.35-7.32 (IH, d); 6.99 (IH, m); 6.93-6.90 (IH, m); 4.94-4.89 (IH, m); 3.24 (IH, s); 3.08-3.02 (IH, dd); 2.92-2.90 (2H, d); 2.88-2.72 (3H, m); 2.08-1.98 (IH, m); 1.93 (3H. s); 1.76-1.57 (7H, m); 1.51 (6H, s).

3 7 To a solution of 2-chloro*4-hydroxy-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-
benzamide (0.20 g, Example 37a), 3-hydroxy-piperidine-l-carboxylic acid, rm-butyl ester
(0.189 g) and tributylphosphine (0.23 ml) in dry tetrahydrofuran (6 ml) was added 1-[[(1-
piperidinylcarbonyl)azo]carbonyl]-piperidine (0.24 g). The orange solution was heated at
60°C under a nitrogen atmosphere for 2h. Additional 3-hydroxy-piperidine-l-carboxylic
acid, tert-butyl ester (0.19 g), tributylphosphine (0.23 ml) and 1-[[(1-
piperidinylcarbonyl)azo]carbonyl]- piperidine (0.24 g) were added. Heating was continued
and the process described above repeated until reaction was complete as judged by LC/MS.
The cooled reaction mixture was diluted with diethyl ether then filtered. The filtrate was
concentrated and purified by chromatography on silica gel (25% ethyl acetate : wo-hexane)
followed by normal phase HPLC (0-1% ethanol in dichloromethane) to give me t-
butyloxycarbonyl (BOC)-protected compound as a colourless foam. The foam was
dissolved in methanol (5 ml) and 4N hydrochloric acid in dioxane (0.25 ml) added. The
solution was stirred at room temperature under a nitrogen atmosphere until the reaction was
complete as judged by LC/MS. Evaporation of solvent followed by trituration with diethyl
ether gave the title compound as a colourless solid (0.006 g).
MS (APCI +ve) 403/405 (M+H)+

JH NMR (DMS0-d6) 5 8.84 (2H, br s), 8.21 (1H, t); 7.38 (1H, d); 7.18 (1H, s); 7.05 (1H, dd); 4.82 (1H, br s); 3.24 (1H, d); 3.20 (1H, dd); 3.06 (2H, br s); 2.92 (2H, d); 1.94 ■ 1.51(19H,m).

3 7 a) 4-Bromo-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide
To a suspension of 4-bromo-2-chlorobenzoic acid (5.00 g) in dichloromethane
(25 ml) at 0°C was added oxalyl chloride (3.7 ml) and dimethylformamide (5 drops).
The resulting mixture was stirred at room temperature under a nitrogen atmosphere for 1
hour, then concentrated under reduced pressure to yield a solid. The solid was dissolved in
dichloromemane (20 ml) and added dropwise to a solution of 1-adamantanemethylamine
(3.36g) and N^-diisopropylethylamine (5.55 ml) in dichloromethane (20 ml). The
resulting solution was allowed to stir at room temperature under a nitrogen atmosphere for
20h. The reaction mixture was diluted with dichloromethane and washed with water, 10%
aqueous potassium carbonate, 10% aqueous potassium hydrogen sulfate and saturated
brine. The organic phase was then dried over sodium sulfate, filtered and concentrated
under reduced pressure to afford the subtitle compound as a solid (4.28 g).

vlS (APCI +ve) 382/384 (M+H)+
H NMR (DMS0-d6) 5 8.39-8.34 (1H, t); 7.78 (1H, m); 7.62-7.59 (1H, m); 7.37-7.34
1H, d), 2.94-2.92 (2H, d); 1.94 (3H, br s); 1.69-1.57 (6H, br AB); 1.52 (6H, s).
' 37
») 2-Chloro-4-(4-piperazin-l-yI)-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzaniide,
lydrocbioride salt
3 7
To a suspension of the 4-bromo-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l -ylmethyl)-enzamide (Example 43a, 0.30 g), piperazine-1-carboxylic acid, 1,1-dimethylethyl ester 0.18 g), cesium carbonate (0.36 g) and (R)-BINAP (0.036 g) in anhydrous toluene (3 ml) /as added palladium (II) acetate (0.009 g) and the mixture heated at 100 °C for 14h in a ressure vessel flushed with nitrogen. The cooled reaction mixture was evaporated under :duced pressure to give an oil which was purified by chromatography on silica gel (2:1 / ro-hexane : ethyl acetate) to give the t-butyloxycarbonyl (BOC)- protected compound as a olourless foam. The foam was dissolved in methanol (15 ml) and 4N hydrochloric acid in ioxane (15 ml) added. The solution was stirred at room temperature under a nitrogen tmosphere until the reaction was complete as judged by LCMS. Evaporation followed by ituration with diethyl ether and methanol yielded the title compound as an off-white jlid/foam (0.161 g).
IS (APCI +ve) 388/390 (M+H)+
H NMR (DMSO-d6) 8 8.98 (2H, bs); 8.11-8.07 (1H, t); 7.33-7.31 (1H, d); 7.05 (1H, m);
.99-6.95 (ia m); 3.46-3.43 (4H, m); 3.20 (4H, bs); 1.94 (3H, bs); 1.69-1.57 (6H, b AB);
.51(6H,bs).
xample 42
3 7 -Chloro-4-(3-pyiTolidinylaniino)-N-(tricyclo(3.3.1.1 ' ]dec-l-ylmethyl)-benzamide,
ydrochloride salt

Prepared according to the method described in Example 41b from 4-bromo-2-chloro-N-(tricyclo[3.3.1.13'7]dec-1 -ylmethyl)-benzamide (0.25 g, Example 41 a), 3-amino-1 -pyrrolidinecarboxylic acid, 1,1 -dimethylemyl ester (0.182 g, Journal of Medicinal Chemistry, 1998,41 (22), 4273-4278), cesium carbonate (0.347 g), (R)-(+)-2,2'-bis(diphenylphosphino)-l,l'-binaphthyl (0.036 g), palladium (H) acetate (0.009 g) and anhydrous toluene (3 ml). The residue was purified by HPLC eluting with a gradient of 0-5% ethanol in dichloromethane. The product was dissolved in methanol and stirred at room temperature for 3h in the presence of 4N hydrochloric acid solution in dioxane (2 ml). The solution was concentrated under reduced pressure and triturated with diethyl, ether to give me title compound as a white powder (0.057 g).
MS (APCI +ye) 388 (M+H-HC1)+
*H NMR (CD3OD) 5 7.33 (IH, d); 6.71 (IH, d); 6.63 (IH, dd); 4.27-4.21 (IH, m); 3.57-3.40 (3H, m); 3.23 (IH, dd); 3.05 (2H, s); 2.43-2.33 (IH, m); 2.33-2.01 (IH, m); 1.99 (3H, bs); 1.73 (6H,q); 1.62 (6H,d).
Example 43
2-Oaoro^-(hexahydro-lH4,4^iazepm-l-yI)-N-(tricycio[3J.l.l3'7]dec-l-ylmethyl)-benzamide, hydrochloride salt

Prepared according to the method described in Example 41b from 4-bromo-2-chloro-N-(tricyclo[3.3.1.I3'7]dec-I-yImethyl)-benzamide (0.25 g, Example 41a), hexahydro-lH-1,4-diazepine-l-carboxylic acid, 1,1-dimethylethyl ester (0.182 g), cesium carbonate (0.347 g). (RM+)-2,2'-bis(diphenylphosphino)-l,r-binaphthyI (0.036 g), palladium (H) acetate (0.009 g) and anhydrous toluene (3 ml). The residue was purified by HPLC during with a gradient of 0-5% ethanol in dichloromethane. The product was dissolved in methanol and stirred at room temperature for 3h in presence of 4N hydrochloric acid solution in dioxane (2 ml). The solution was concentrated under reduced pressure and triturated with diethyl ether to give the title compound as a white powder (0.17 g).
MS (APCI +ve) 402 (M+H-HC1)+
*H NMR (CD3OD) 8 7.41 (1H, d); 6.88 (1H, d); 6.81 (1H, dd); 3.83 (2H, t); 3.63 (2H, t);
3.40 (2H, t); 3.30 (2H, t); 3.06 (2H, s); 2.24-2.16 (2H, m); 1.99 (3H, bs); 1.74 (6H, q); 1.63
(6H,d).
According to the procedure described in Example 8, the following compounds were prepared:
Example 44
(±>5-[(3-Ammo-l-piperidinyl)methyl]-2-chloro-N-(tricyclo[3.3.1.13'7]dec-l-ylmethyl)-beozamide, hydrocloride salt

MS (APCI +ve) MW 416/418 (M+H)+
*H NMR (CD3OD) 5 7.70 (IH, bs);7.67 (IH, dd); 7.60 (IH, d); 4.49 (IH, d); 4.45 (IH, d);
3.73-3.58 (2H, m); 3.57-3.45 (IH, m); 3.14-2.95 (4H, m); 2.25-2.04 (2H, m); 1.98
(4H, bs); 1.76 (3H, d); 1.73-1.58 (IH, m); .1.70 (3H, d); 1.63 (6H, bs).

MS (APCI +ve) MW 414/416 (M+H)+
!H NMR (CD3OD) 5 7.74 (IH, d); 7.72 (IH, dd); 7.60 (IH d); 4.704.55 (3H, m); 4.45 (IH, d); 4.00 (IH, d); 3.73 (lH,d); 3.60-3.50 (2H, m); 3.07 (2H, s); 2.71 (IH, d); 2.27 (IH, d); 1.98 (3H, bs); 1.77 (3H, d); 1.69 (3H, d); 1.63 (6H, bs).
Example 46
2-CbJoro-5-(9-oxa-3,7-diazabicyclo[3.3.1]non.3-ylmethyl)-N-(tricyclo[3.3.1.13'7]dec-l-yhnethyl)- benzamide, hydrochloride salt

MS (APCI +ve) MW 442/446 (M+H)+
lH NMR (CD3OD) 5 7.60-7.40 (3H, m); 4.25^.00 (2H, m); 3.70-3.40 (2H, m); 3.46 (4H, m); 3.07 (2H, s); 3.15-2.90 (2H, m); 2.80-2.50 (2H, m); 2.00 (3H, bs); 1.78 (3H, d); 1.71 (3H,d); 1.63 (6H,bs).

MS (APCI +ve) MW 442/444 (M+H)+
*H NMR (CP3OD) 8 7.91 (IH, s); 7.78 (IH, d); 7.56 (IH, d); 7.46 (IH, bs); 4.44 (2H, bs); 3.65-3.28 (8H, in); 3.08 (2H, bs); 2.48 (2H, bs); 2.05-1.90 (5H, m); 1.77 (3H, d); 1.71 (3H, d); 1.64 (6H, bs).
Example 48
trans-2-CMoro-5-{[8-(methyiainino>3-azabicyclo[3.2.1]oct-3-yl]methyI]-N-(tricyclo[3J.l.l3'73dec-l-yImethyl)-benzamide, hydrochloride salt

MS (APCI+ve) MW 456/458 (M+H)+
*H NMR (CD3OD) 8 7.79 (IH, d); 7.77 (IH, dd); 7.58 (IH, d); 4.71 (2H, bs); 3.80 (2H, d); 3.40 (IH, t); 3.25 (2H, dd); 3.07 (2H, s); 2.86 (3H, s); 2.70 (2H, bs); 2.10-1.90 (7H, m); 1.77 (3H, d); 1.70 (3H, d); 1.63 (6H, bs).
Example 49
cis-2-ChIoro-5-[(hexahydropyrrolo[3,4-c]pyrroI-2(lH)-yl)methyl]-N-
37 (tricydo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide, hydrochloride salt

MS (APCI +ve) MW 428/430 (M+H)+
!HNMR (DMSO-d6) 5 8.00 (IH, t); 7.65 (IH, s); 7.63 (IH, d); 7,52 (IH, d); 4.34 (2H, bs); 3.60-3.05 (10H, m); 2.97 (2H, d); 1.95 (3H, bs); 1.70 (3H, d); 1.63 (3H, d); 1.57 (6H,s).

3 7 a) [[4-chloro-3-[[(tricyclo[3.3.1.1 ' ]dec-l-ylmethyI)amino]carbonyI]phenyI]-
methyl] phosphonic acid, dimethyl ester
3 7 5-BromomethyI-2-chloro-N-(tricycIo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (5.70 g,
Example 8b) in lOOml of trimethylphosphite was heated at reflux for 15h. The solvent was
removed by azeotropic distillation with toluene under high vacuum to afford the subtitle
compound as a yellow solid.
MS (APCI +ve) MW 426/428 (M+H)+
*H NMR (DMSO-d6) 5 8.34 (1H, t); 7.42 (1H, d); 7.35-7.27 (2H, m); 3.63 (3H, s); 3.58
(3H, s); 3.42 (2H, d); 2.92 (2H, d); 1.94 (3H, bs); 1.67 (3H, d); 1.59 (3H, d); 1.52 (6H, bs).
37 b) 4-[{4-chloro-3-[[(tricycio[3J.1.1 ' ]dec-l-ylmethyI)amino]carbonyI]phenyI]
methylene]-l-piperidinecarboxyHc acid, 1,1-dimethyIethyI ester
• 3 7
To a solution of the crude [[4-chloro-3-[[(tricyclo[3.3.1.1 ' ]dec~l-yimethyl)aminoJ
carbonyl]phenyl] methyl] phosphonic acid, dimethyl ester (2.50 g, Example 50a) in
tetrahydrofuran (50 ml) at -78 °C was added a solution of lithium diisopropylamide (7.30
ml, 2M in tetrahydrofuran). The reaction was allowed to warm to room temperature and
stirred for 15min. N-t-butoxycarbonylpiperidin-4-one (L52g) in tetrahydrofuran (5 ml)
was then added and the mixture stirred for 24h. The reaction was diluted with water and
extracted with ethylacetate. The organic layer was washed with brine and dried over
magnesium sulfate. The crude material was purified on a silica gel (0 to 5% methanol in
dichloromethane) to afford the subtitle compound as a white foam.
MS (APCI +ve) MW 443/445 (M+H)+

'HNMR (DMS0-d6) 5 7.52 (1H, d); 7.34 (1H, d); 7.16 (1H, dd); 6.30 (1H, s); 6.25 (t, 1H); 3.48 (2H, t); 3.40 (2H, t); 3.40 (2H, t); 3.18 (2H, d); 2.42 (t, 2H); 2.32 (t, 2H); 2.05 (3H, bs); 1.73 (3H, d); t .64 (d, 3H), 1.59 (6H, s); 1.47 (9H, bs).
c) 2-ChlorO'5-(4-piperidmylidenemethyl)-N-(tricyclo[3.3.1.13'7]dec-l-ylmethyl)-benzamide, hydrochloride salt
A solution of 4-[[4-chloro-3-[[(tricyclo[3.3.1.13,7]dec-l-ylmethyl)amino]carbonyl]phenyl] methylene]-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.1 Og, Example 50b) in methanol (3ml) was treated with a 4N solution of hydrochloric acid in dioxane (1 ml) and stirred for 14h at room temperature. The reaction mixture was concentrated under vacuum and the residue recrystallised from iso-propanol/ether to give the title compound as a white solid (0.07lg).
MS (APCI +ve) MW 399/401 (M+H)+
!H NMR (DMSO-d6) 5 7.52 (1H, d); 7.34 (1H, d); 7.16 (1H, dd); 6.30 (1H, s); 6.25 (t, 1H); 3.48 (2H, t); 3.40 (2H, t); 3.40 (2H, t); 3.18 (2H, d); 2.42 (t, 2H); 2.32 (t, 2H); 2.05 (3H, bs); 1.73 (3H, d); 1.64 (d, 3H), 1.59 (6H, s); 1.47 (9H, bs).

3 7
To a solution of 2-chloro-5-(4-piperidinylidenemethyl)-N-(tricyclo[3.3.1.1 ]dec-l-ylmethyl)-benzamide, hydrochloride salt (0.10g, Example 50c) in ethanol (10 ml) was added platinum oxide (2mg). The vessel was placed under 3 bars hydrogen pressure for

3h. The catalyst was removed by filtration through a pad of Celite, washed with ethanol and the solution concentrated under vacuum. The crude material was recrystallised from iso-propanol to afford a white solid. The t-butoxycarbonyl protected compound was dissolved in methanol (10ml) and treated with a solution of 4N HCl in dioxane (2 ml). The reaction was stirred for I4h at room temperature, the volatiles removed under vacuum and the residue recrystallised from jso-propanol/ether to afford the hydrochloride salt as a white powder (0.065g).
MS (APCI +ve) MW 402/404 (M+H)+
lH NMR (CD3OD) 5 8.38 (1H, 0; 7.38 (1H, d); 7.30-7.20 (2H, m); 3.35 (2H, d); 3.05 (2H, d); 2.92 (2H, td); 2.63 (2H, d); 1.98 (3H, bs); 1.95-1.80 (1H, m); 1.85 (2H, d); 1.77 (3H, d); 1.68 (3H, d); 1.62 (6H, s); 1.40 (2H, q).

To a solution of 5-bromo-2-chioro-N-(tricyclo[3.3.1.1 J']dec-l-ylmethyl)-benzamide (0.30g„ Example 23a) in anhydrous tetrahydrofuran (10ml) at-78 °C was added drop wise a solution of n-butyllithium in hexanes (2.5M, 0.72ml). After lOmin. a solution of t-butoxycarbonyi^-piperidone (0-2 Ig) in tetrahydrofuran (2ml) was added. The solution was stirred an additional 20min. then treated with saturated aqueous ammonium chloride solution. The mixture was allowed to warm to room temperature then partitioned between 5thyl acetate and saturated aqueous ammonium chloride solution. The organic extracts were dried over magnesium sulphate and concentrated in vacuo. The residue was

chromatographed on silica (ethyl acetate: isohexane/l:4 to 1:2 gradient) to give the t-butoxycarbonyl protected product (0.153g). This was redissolved in methanol (4ml) and treated for 14h with 4N HC1 in dioxan (1ml). The solution was partially concentrated in vacuo and the product precipitated with diethyl ether. The solution was filtered and the white solid washed with diethyl ether to give the title compound (0.09lg)
MS (APCI +ve) MW 403 (M+H)+
!HNMR (CD3OD) 5 8.43 (1H, m, br); 7.59 (1H, m); 7.55 (1H, d); 7.49 (1H, d); 3.52-3.30
(4H, m); 3.09 (2H, d); 2.23 (2H, m); 2.04-1.88 (5H, m); 1.95-1.80 (1H, m); 1.84-1.66
(6H,m);1.65(6H,d).
Example 53
2-Chloro-5
3 7 Asolutuion of 2-chloro-5-(4-hydroxy-piperidin-4-yI)-N-(tricyclo[3.3.1.1 ' ]dec-l-
ylmethyO-benzamide, hydrochloride salt (0.25g7 Example 52) in concentrated hydrochloric
acid (10ml) was heated at 100°C for 5h. The solution was allowed to cool slowly.
Colourless crystals separated. These were removed by filtration, washed with diethyl ether
then acetonitrile and dried to afford the title compound (0.031 g).
MS (APCI +ve) MW 385 (M+H)+

]HNMR CCD3OD) 5 8.44 (1H, m, br); 7.55-7.45 (3H, m); 6.23 (1H, m); 3.S5 (2H, m); 3.47 (2H, t); 3.07 (2H, d); 2.79 (2H, m); 1.98 (3H, m); 1.77 (3H, m); 1.69 (3H, m); 1.63 (6H,s,br).

2-Bromo-5-(4-[{ l,l-dimethyIethyl}oxycarbonyl]-piperazin-l-yl)metfayl -N-(tricyclo[3.3.1.I3,7]dec-l-yiraethyl)-benzamide (Example 65b, 0.89g) was dissolved in dry tetrahydrofuran. Sodium hydride (60% dispersion, 0.07g) was added and the mixture stiired at room temperature for 5min. The mixture was cooled to -70°C under a nitrogen atmosphere and t-butyllithium (1.9ml, 1.7M solution) added. After 5min, ethyl iodide (0.5ml) was added and the mixture stirred at -70°C for 30min. Aqueous ammonium chloride solution was added and the product extracted with diethyl ether, dried (MgSO*) and concentrated in vacuo. Chromatography on silica gave the t-butyloxycarbonyl (BOC) protected compound as a foam. This was redissolved in methanol (5ml) and 4N HC1 in dioxane (1ml) added. The mixture was stirred at room temperature for 14h. The solution was partially concentrated under vacuum and the product precipitated with diethyl ether. The resulting solid was filtered and washed with ether to afford the title compound as a white powder (0.040g).

lHNMR (DMSO) 5 9.59 (2H, s, far); 8.15 (IK, t); 7.58 (2H, s, br); 7.35 (1H, d); 4.37 (2H; s, br); 3.49 (m); 3.25 (2H, m, br); 2.95 (2H, d); 2.72 (2H, q); 1.94 (3H; s, br); 1.69-1.59 (6H, m); 1.52 (6H, s); 1.165 (3H, t).

a) 4-(Toluene-4-sulfonylsulfanyl)-piperidine-l-carboxyIic acid tert-butyl ester
4-Iodo-piperidine-l-carboxylic acid, wrr-butyl ester (1.3g) and potassium toluene-4-thiosulfonate (l.Og) were combined in ethanol (10ml) with cis-dicyclohexane 18-crown-6 (lOmg) and heated under reflux for 12h. After cooling the reaction mixture was partitioned between ethyl acetate and water, the organic layer was separated, washed with water and brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (eluting with ijohexane / ethyl acetate 4:1 to 7:3), to yield the subtitle compound as an oil (0.65g).
MS(APCI+ve)3l5 (M-t-H-tBu)+
*H NMR (CDC13) 5 7.80-7.85 (2H, m), 7.30-7.40 (2H, m), 3.95-4.10 (1H, m), 3.75-3.85 (1H, m), 3.40-3.50 (1/2H, m), 3.10-3.20 (I/2H, m), 2.95-3.05 (1H. m), 2.-80-2.90 (1H, m), 2.46 (3H, s), 1.90-2.10 (2H, m), 1.50-1.70 (2H, m), 1.43 & 1.45 (9H, pairs).

b) 2-Chloro-5-(4-[{l,l-dimethylethyl}oxycarbonyl]piperidiiie-4-ylsuJfanyl)-N-
3 7 (tricyclo[3.3,l.l ' ]dec-l-ylmethyi)-benzamide
3 7 To a solution of 5-bromo-2-chlorp-N-(tricyclo[3.3.1.1 * ]dec-l-ylmethyl)-benzamide
(0.30$, Example 23a) in anhydrous tetrahydrofuran (10ml) at -78 °C was added dropwise a
solution of n-buryllithium in hexanes (2.5M, 0.72ml). After lOmin. a solution of
4-(toluene-4-sulfonylsulfanyl)-piperidine-l-carboxylic acid, terr-butyl ester (0.38g,
Example 55a) in tetrahydrofuran (7ml) was added. After a further 1 hour at -78°C the
reaction mixture was wanned to ambient temperature and quenched by the addition of
water (5ml). The reaction mixture was diluted with ethyl acetate and washed twice with
saturated aqueous sodium hydrogen carbonate solution, then with brine and dried over
magnesium sulfate. The organic layer was concentrated under reduced pressure to give a
residue which was purified by silica gel chromatography (eluting with 0-5% ethanol in
dichloromethane) to yield the subtitle compound (0.20g).
MS (APCI+ve) 419/21 (M+H-BOQ+
c) 2-Oiloro-5Kpiperidin-4-ylsulfanyl)-N-(tricyclo[3.3.1.13'7]dec-l-ylmethyl)-benzamide, hydrochloride salt
2-Chloro-5-(-(4-[ {1,1 -dimethylediyl} oxycarbonyl]-piperidin-4-ylsulfanyl)-N-
3 7 (tricyclo(3.3.1.I ' ]dec-I-ylmethyl)-benzamide (0.20g, Example 55b) was dissolved in
methanol (15 ml) and hydrochloric acid (1.0ml of a 4N solution in dioxane) was added.
After stirring at room temperature for 14h, the reaction mixture was basified with saturated
sodium hydrogen carbonate solution and extracted twice with dichloromethane. The
organic layer was concentrated under reduced pressure to give a residue which was purified
by silica gel chromatography (eluting with 0-100% methanol in dichloromethane). The
residue was dissolved in dichloromethane (5ml) and hydrochloric acid (IN in diethyl ether,
2ml) added. Evaporation to dryness gave the title compound as the hydrochloride salt
(O.OSOg).
MS(APa+ve)419/21 (M+H)+

lH NMR (DMS0-d6) 5 8.75 (2H, brd), 8.38 (IH, t), 7.48 (2H, s), 7.37 (IH, s), 3.50-3.60 (IH, m), 3.30 (2H, brd), 2.92-3.05 (4H, m), 2.06 (2H, brd), 1.94 (3H, s), 1.57-1.75 (8H, m, 1.52 (6H,s).
Example 56
3 7 2-Chloro-5-(piperidin-4-yIsulfinyI)-N-(tricycio[3.3.1.1 ' ]dec-l-yhnethyl)-benzamide

m-Chloroperoxybenzoic acid (166mg) was added to a solution of 2-chIoro-5-(piperidin-4--
3 7 ylsulfanyl)-N-(tricyclo[3,3.1.1 ' ]dec-1 -ylmethyl)-benzamide (0.35g, Example 55c) in
dichloromethane (5ml). After 2h calcium hydroxide (0.20g) was added and 30min. later
the salts removed by filtration. The filtrate was concentrated under reduced pressure to
give a residue which was purified by silica gel chromatography (eluting with 0-25%
ethanol in dichloromethane). The residue was dissolved in methanol (5 ml) and
hydrochloric acid (0.5ml of a 4N solution in dioxane) was added. After stirring at room
temperature for I4h, the solution was concentrated under reduced pressure and triturated
with diethyl ether to yield the title compound as the hydrochloride salt (0.030g).
MS (APa +ve) 435/37 (M+H)+
*HNMR (DMSO-d6) 8 8.88 (IH, brs), 8.47 (2H, bit), 7.76 (IH, d), 7.67 (IH, dd), 7.61 (IH, d), 3.30-3.40 (2H, m), 3.13 (IH, t), 2.98 (2H, d), 2.80-2.90 (2H, m), 2.15 (IH, d), 1.95 (3H,m), 1.50-1.85 (15H,m).
Example 57

m-Chloroperoxybenzoic acid (0.30g) was added to a solution of 2-chloro-5-
3 7 (piperidin-4-ylsulfinyl)-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.30g) in
dichloromethane (10ml). After 2h calcium hydroxide (170mg) was added and 30min. later
the salts removed by filtration. The filtrate was concentrated under reduced pressure to
give a residue which was purified by silica gel chromatography (eluting with 0-2% ethanol
in dichloromemane). The residue was dissolved in methanol (5 ml) and hydrochloric acid
(0.25ml of a 4N solution in dioxane) was added. After stirring at room temperature for
14h, the solution was concentrated under reduced pressure and triturated with diethyl ether
to yield the title compound (0.03g).
MS (APCI +ve) 451/53 (M+H)+
lE NMR (DMSO-d6) 5 8.89 (IH, brs), 8.57 (IH, t), 8.50 (1H, brs), 7.87 (2H, ABq), 7.75 (1H, d), 3.71 (IH, td), 3.40 (2H, d), 3.00 (2H, d), 2.80-2.90 (2H, m), 1.95-2.05 (5H, m), 1.50-1.90 (14H,m).
Example 58
2-OiIoro-5-{piperidin-4-ylmethyIsuIfanyI)-N-(tricycIo[3.3.1.13'7]dec-l-yImethyI)-benzamide, hydrochloride salt

a) 2-ChIoro^5-(4-[{l,l-dimelhyIethyl}oxycarbonyl] piperidin-4-yImethyIsulfanyI)-
37 N-(tricycIo[3J.l.l ' ]dec-l-ylmethyl)-benzamide
Trifluoroacetic acid anhydride (2ml) was added to a solution of 2-cbioro-5-
3 7 methylsulphinyl-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (G.53g, Example 58a,
WO 99/29661) in dichlororaethane (10ml) and heated under reflux for 1.5h, cooled and
concentrated. The resultant residue was dissolved in methanol (30ml), allowed to stand for
1 hour then concentrated. The resultant residue was dissolved in acetone (10ml) and
potassium carbonate (0.60g) and 4-iodomethyI-piperidine-l-carboxylic acid tert-butyl ester
(0.94g) was added. The reaction mixture was heated under reflux for 3h, cooled and
concentrated. The resultant residue was dissolved in ethyl acetate, washed twice with 10%
w/w KHSO4 solution, twice with saturated sodium hydrogen carbonate solution, once with
brine and dried over magnesium sulfate. The organic layer was concentrated under reduced
pressure to give a residue which was purified by silica gel chromatography (eluting with 0-
2% ethanol in dichloromethane), to yield the subtitle compound (0.46g).
MS (APQ +ve) 433/35 (M+H-BOQ+
!H NMR (CDCI3) 8 7.61 (1H, d), 7.25-7.31 (2H, m), 6.27 (1H, brt), 4.09 (2H, tad), 3.17 (2H, d), 2.86 (2H, d), 2.66 (2H, t), 2.01 (3H, s), 1.60-1.90 (15H, m), 1.45 (9H/s), 1.18 (2H, dq).
b) 2-Chloro-5-(piperidin-4-ylmethyIsulfanyl)-N-(tricyclo[3J.i.l3'7]dec-l-ylmethyl)-benzamide, hydrochloride salt

Hydrochloric acid (4N dioxane, 0.5ml) was added to a solution of 2-chloro-5-(4-[{1,1-dimethylethyl }oxycarbonyl] piperidin-4-ylmethylsuifanyl)-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.235g, Example 58a) in methanol (10ml). After 24h the reaction mixture was concentrated, then triturated with ether to give the title compound (0.20g).
MS (APCI+ve) 433/35 (M+H)+
*H NMR (DMSO-d6) 5 8.76 (1H, brs), 8.48 (1H, brs), 8.35 (1H, t), 7.40 (2H, ABq), 7.28 (1H, d), 3.24 (2H, d), 3.00 (2H, d), 2.92 (2H, d), 2.84 (2H, q), 1.94 (5H, brs), 1.75-1.82 (1H, m), 1.65 (6H, q), 1.52 (6H, s), 1.40 (2H, q).

m-Chloroperoxybenzoic acid (0.19g) was added to a solution 2-chloro-5-(4-[{ 1,1-
3 7 dimethylethyl}oxycarbonyl] piperidin-4-ylmethylsulfanyl)-N-(tricyclo[3.3.1.1 ' ]dec-l-
ylmethyl)-benzamide (0.165g, Example 58a) in chloroform (10ml). After 5h calcium
hydroxide (120mg) was added and 30min. later the salts removed by filtration. The
reaction mixture was concentrated, then dissolved in methanol (10 ml) and hydrochloric
acid (l.Oml of a 4N solution in dioxane) added. After stirring at room temperature for 14h,
concentration under reduced pressure yielded the title compound (0.075g),

MS (APCI +ve) 465/67 (M+H)+
*H NMR (DMS0-d6) 5 8.70 (1H, brs),.8.55 (1H, t), 8.48 (1H, brs), 7.95 (1H, dd), 7.88 (1H, d), 7.82 (1H, d), 3.47 (2H, d), 3.21 (2H, d), 2.97 (2H, d), 2.89 (2H, d), 2.10-2.25 (1H, m), 1.95 (5H, brs), 1.40-1.80 (14H, m).

a) 4-aiIoro-NKtricyclo[3J.l.l3,7]dec-l-ybnethyl>isophthalamic acid
n-Butyllithium (3ml, 2M hexanes) was added at -78°C to a solution of 5-bromo-2-
37 chloro-N-(tncyclo[3.3.1.I ' ]dec-l-ylmethyl)benzamide (l.Og, Example 23a) in
tetrahydrofuran (20ml). After lOmin. the reaction mixture was decanted onto dry solid
carbon dioxide and allowed to warm to ambient temperature. The reaction mixture was
acidified with concentrated hydrochloric acid and extracted with ether. The organics were
separated, dried over magnesium sulfate and concentrated under reduced pressure to give a
residue which was purified by silica gel chromatography (eluting with iso-hexane / emyl
acetate 3:1 to 1:1 + 1%ACOH), to yield the subtitle compound as a solid (0.45g).
MS(APCI+ve)348/350 (M+H)+
^NMR (DMS0-d6) 5 13.33 (1H, s), 8.44 (1H, t), 7.94 (1H, dd), 7.87 (1H, d), 7.63
(1H, d), 2.95 (2H, d), 1.95 (3H, s), 1.63 (6H, q), 1.53 (6H, s).

3 7 b) 2-Cbioro-5-(pipera2ine-l-carbonyl)-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-
benzamide, hydrochloride salt
Ethyldiisopropylamine (0.3ml) was added at ambient temperature to a solution of 37 4-chloro-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmeihyl)-isophthalamic acid (0.15g, Example 60a),
5 piperazine-1-carboxylic acid tert-butyl ester (0.16g) and PyBrOP (0.40g) in N-
| methyipyrroiidinone (10ml). After 5h the reaction mixture was diluted with ethyl acetate
and washed twice with water, twice with 10% KHSO4 solution, twice with saturated
NaHCC>3 solution and once with brine, then dried over magnesium sulfate and
concentrated under reduced pressure. The residue was purified by silica gel
1 chromatography (eluting with ethanol (0-5%) in dlchlororaethane), then redissolved in
methanol (10ml) and treated with hydrochloric acid (4N dioxane, 1ml); After 48h the
reaction mixture was concentrated under reduced pressure and recrystallised from iso-
hexaxne/propan-2-ol to yield the title compound as a solid (0.1 Og).
MS (APCI +ve) 416 / 418 (M+H)+
THNMR (DMSO-d6) 5 9.18 (1H, t), 8.42 (1H, t),7.59 (1H, d),7.47-7.52 (2H, m), 3.50-
3.90 (4H, brs), 3.05-3.25 (4H, brs), 2.94 (2H, d), 1.95 (3H, s), 1.63 (6H, q), 1.52 (6H, s).
The following Examples were made in an analogous manner.
Example 61
2-aaoro-5-([l,4]d^zepane-l-carbonyl)-N-(tricycIo[3.3.1.13'7]dec-l-yImethyI)-benzamide, hydrochloride salt

MS (APCI +ye) 430 / 432 (M+H)+
!H NMR (DMSO-d6) 5 9.10 (2H, brs), 8.06 (IH, brs), 7.53 (IH, d), 7.45-7.48 (2H, m), 3.78 (2H, brs), 3.54 (2H, brs), 3.20-3.25 (4H, m), 2.97 (2H, d), 2.00 (2H, m), 1.95 (3H, s), 1.65 (6H, q), 1.55 (6H, s).

MS (APCI +ve) 430 / 432 (M+H)+
!HNMR (DMSO-d6) 5 8.66-8.76 (3H, m), 8.42 (IH, t), 7.89-7.93 (2H, m), 7.60 (IH, d),
4.01-4.09 (IH, m), 3.29 (2H, d), 2.95-3.05 (4H, m), 1.95 (5H, brs), 1.47-1.82 (14H, ra).
Example 63

3 7 2-Chloro-5-(hydroxy-4-piperidinyIraethyl)-N-(tricyclo[33.1.1 ' ]dec-l-ylmethyl>
benzamide, hydrochloride salt

a) 2-Chloro-5-[4-[[{l,l-diniethylethyl}oxycarhonyI]piperidinyI]-hydroxymethyI]-
37 N-(tricyclo[3.3.1.1 ' ] dec-1-ylmethyl) -benzamide
3 7 To a solution of 5-bromo-2-chloro-N-(tricyclo[3.3.1.1 ' ]dec-1 -ylmethyl)-benzamide
(1.5 g, Example 23a) in anhydrous tetrahydrofuran (50 ml) under a nitrogen atmosphere at
-78°C was added dropwise n-butyllithium solution (2.5M in hexanes, 3.4 ml). The mixture
was stirred for lOmin. at -78°C, then a solution of 4-formyl-l-piperidinecarboxylic acid,
1,1-dimethylethyl ester (1.09 g, Journal of Medicinal Chemistry, 1999, 42(12), 2180-2190)
in anhydrous tetrahydrofuran (10 ml) was added dropwise. The reaction mixture was
stirred at -78°C for 30min. then quenched with saturated aqueous ammonium chloride
solution (100 ml). The product was extracted twice with ethyl acetate (2x100 ml). The
organic extracts were combined, dried over anhydrous magnesium sulfate, filtered and
concentrated under reduced pressure. The residue was purified by chromatography on
silica gel eluting with iso-hexane : ethyl acetate / (2:1) then (1:2), then purified further by
HPLC eluting with a gradient of 0-5% ethanol in dichloromethane to give the subtitle
compound as a white foam (0.61 g).
MS (APCI +ve) 517 (M+H)+
lK NMR (DMSO-d6) 5 8.28 (1H, t); 7.40 (IK, d); 7.33-7.27 (2H, m); 5.33 (IK, d); 4.34 (1H, t); 3.93 (3H, bs); 2.93 (2H, d); 2.61 (2H, bs); 1.94 (3H, bs); 1.63 (6H, q); 1.53 (6H, d); 1.37 (9H, s); 1.34-L23 (2H, m); 1.09 (2H, dt).

b) 2-Chloro-5-{hydroxy-4-piperidinylmethyl)-N-(tricyclo[3.3.1.13,7]dec-l-ylmethyO-benzamide, hydrochloride salt
A solution of 2-chloro-5-[4-{[{ l,l-dirnethyIethyi}oxycarbonyl]-piperidinyl]-
3 7 hydroxyraethyl]-N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide (0.10 g, Example 63a)
in methanol (3 ml) was treated with 4N hydrochloric acid solution in dioxane (1 ml). After
14h the solvents were removed under reduced pressure and the residue was triturated with
diethyl ether to give the title compound as a white powder (0.062 g).
MS (APCI +ve) 417 (M+H-HC1)+
!H NMR (DMSO-d6) 5 8.70 (1H, bs); 8.29 (2H, bt); 7.44 (IH, d); 7.33 (2H, dt), 5.53 (1H, d); 4.40 (IH, t); 3.23 (2H, bs); 2.93 (2H, d); 2.76 (2H, bd); 1.94 (3H, bs); 1.77-1.36 (1H, m); 1.53 (6H, s).

Prepared by an analogous route to Example 63 employing 3-formyl-l-piperidinecarboxylic acid, 1,1 -dimethylethyl ester.
MS (APCI +ve) MW 417/419 (M+H)+
^NMR (GD3OD) 5 8.41 (IH, t); 7.46 (1H, d); 7.41 (1H, d); 7.39 (1H, s); 4.65 (0.5H, d); 4.50 (0.5H, d); 3.74 (0.5H, td); 3.66 (IH, q); 3.57 (0.5H, t); 3.44 (0.5H, bd); 3.18 (0.5H, bd); 3.06 (2H, d); 2.86 (2H, qd); 2.10-1.87 (m, 2H); 1.98 (3H, bs); 1.77 (3H, d); 1.68 (3H, bd); 1.63 (6H, s), 1.60-1.50 (m, IH); 1.50-1.36 (m, IH).

Example 65
3 7 2-Bromo-5-piperazin-l-ylrnethyl -N-(tricycla[3.3.1.1 '■ ]dec-l-ylmethyl)-benzamide,
hydrochloride salt

3 7 a) 2-Bromo-5-bromomethyl -N-(tricyclo[3J3.1.1 -' Jdec-l-ylmethyO-benzamide
•>
To a solution of 2-bromo-5-bromomethyl-benzoic acid (6.1g) in dichloromethane
(100 ml) at 0°C were added dimethylformamide (0.2 ml) followed by oxalylchloride
(3 ml). The reaction was stirred at room temperature for 0.5 hour and concentrated under
vacuum. The acylchloride was redissolved in dichloromethane (100 ml) and and di-
iropropylethylamine (6 ml) followed by adamantanemethylamine (3.5ml) added at 0"C.
The mixture was stirred at 0°C for lOmin., then partitioned bejtween diethyl ether and IN
aqueous hydrochloric acid. The organic layer was dried over magnesium sulfate and
concentrated in vacuo. The crude material was purified by recrystallisation from
dichloromethane/ethylacetate/i-hexane to afford the title compound as a white solid (6.5 g)
(sample contained some of the corresponding benzyl chloride). .
b) 2-Bromo-5-(4-[{l,l-dimethyIethyl}oxycarbonyl]-pip€ra2in-l-yl)inetb.yI-N-
37 (tricydo[3-3.1.1 ' ]dec-l-ylmethyl)-benzamide
37 A mixture of 2-bromo-5-bromomethyl-N-(tricyclof3.3.1.1 ' ]dec-1 -yimethyi)-
benzamide (Example 65a, 5.0g), 1-tertbutyloxycarbonylpiperazine (2.3g), potassium
carbonate (3.2g), potassium iodide (0.30g) and acetone (75ml) was refluxed in the dark for
14h. The mixture was concentrated in vacuo, partitioned between ethyl acetate and water,
then washed with brine. The organic layer was dried over magnesium sulfate and

concentrated in vacuo. Recrystallization from ethyl acetate:isohexane gave the subtitle compound as colourless solid (4.7g).
MS (APCI +ve) MW 546 (M+H)+
3 7 c) 2-Bromo-5-piperazin-l-ylmethyI -N-(tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-
benzamide, hydrochloride salt
2-Bromo-5-(4-[ {1,1 -dimethylethyl} oxycarbonyl]-piperazin-1 -yl)methyl -N-
3 7 (tricycio(3.3.I.I ' ]dec-I-yimethyl)-ben2;amide (Example 65b, 0.40g) was dissolved in
methanol (15ml), and 4N HCl in dioxane (3ml) added. The mixture was stirred at room
temperature for 14h. The solvent was removed under vacuum and the resulting solid was
triturated with ether to afford the title compound as a white powder (0.23g).
MS (APCI +ve) MW 447(M+H)+
*H NMR (DMSO-d6) 5 9.53 (1H, s, br); 8.31 (1H, t); 7.72 (1H, d); 7.60 (1H, m), 4.33
(1H, m); 3.50-3.00 (4H, m); 3.50-3.40 (1H, m); 2.94 (2H, d); 1.94 (3H, bs); 1.71-1.58
(6H,m);1.54(6H,bs).

A solution of 5-brorno-2-chloro-Ar-(tricyclo[3.3.1. l3/7]dec- I-ylmethyO-benzamide (3.0 g, Example 23a) in anhydrous tetrahydrofuran (100 ml) was cooled to ~78°C under a nitrogen atmosphere. A solution of methyllithium (1.4M in diethyl ether, 4.9 ml)'was added over 2min. The mixture was stirred at -78GC for lOmin., then a solution tert-butyllithium (1.7M in pentane, 9.3 ml) was added dropwise. The mixture was stirred at -78°C for a further lOmin., then ethylene oxide (1.0 ml) was added. The resulting solution was stirred at -78°C for 30min. then was warmed to 0°C and stirred for another 6h. The reaction mixture was quenched with saturated aqueous ammonium chloride solution (70 ml) and extracted with ethyl acetate (3x100 ml). The combined extracts were dried over anhydrous magnesium sulfate, filtered, and die filtrate concentrated under reduced pressure. The residue was purified by chromatography over silica gel eluting with dichloromethane : ethanol (98:2) to give the subtitle compound as a pale yellow solid (0.89 g>-
MS (APCI +ve) 348 (M+Hf
'H NMR (DMSO-ds) 5 8.27 (1H, t), 7.36 (1H, d); 7.28-7.23 (2H, m); 4.65 (1H, t); 3,60
(2H, q); 2.92 (2H, d); 2.73 (2H, t); 1.94 (3H, bs); 1.63 (6H, q); 1.52 (6H, d).
b) 2-Chloro-5-(2-oxoethy0-A^-(tricycIo[3.3.1.13'7]dec-l-ylmethyI)-benzamide
To a solution of 2-chloro-5-(2-hydroxyethyl)-//-(tricyclo[3.3.1.I3'7]dec-l-ylmethyl)-benzamide (1.07 g, Example 66a) in anhydrous dichloromethane (20 ml) was added Dess-Martin periodinane reagent (1.95 g) and me mixture was stirred at room temperature forlh. Sodium thiosulfate (3.43 g) was dissolved in aqueous sodium bicarbonate solution (28 ml) and added to the reaction mixture. Diethyl ether (50 ml) was then added and the mixture was stirred for lOmin,. The layers were partitioned and the organic layer was washed with water then brine. The organic extracts were then dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to afford the subtitle compound as a white solid (1.06 g).
MS (APCI +ve) 346 (M+H)+

1H NMR (DMSO-d6) S 9.69 (1H, s); 8.32 (1H, t); 7.45 (1H, d); 7.30-7.24 (2H, m); 3.84 (2H, s); 2.92 (2H, d); 1.94 (3H, bs); 1.63 (6H, q); 1.52 (6H, d).
c) 2-Chloro-5-[2-(l-piperazinyl)ethyl]-N-(tricyclof3^.U3'7]dec-l-yImethyl)-benzamide hydrochloride salt
To a solution of 2-chloro-5-(2-oxoethyi)-A^(tricyclo[3.3.1.13'7]dec-l-ylmethyl)-benzamide (0.101 g, Example 66b) in anhydrous 1,2-dichloroethane (5 ml) was added 1 -piperazinecarboxylic acid, 1,1 -dimethylethyl ester (0,108 g) then sodium triacetoxyborohydride (0.086 g). The reaction mixture was stirred for 14h at room temperature. Water (10 ml) and dichloromethane (10 ml) were added and the layers were partitioned. The organic extract was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by HPLC eluting with a gradient of 0-5% emanol in dichloromethane then by chromatography over silica gel eluting with ethyl acetate. The white powder obtained was dissolved in methanol (5 ml) and a solution of hydrochloric acid in dioxane (4N, 1 ml) was added. The mixture was stirred for 14h at room temperature. Solvents were then removed under reduced pressure and the product obtained was triturated with diethyl ether to afford the title compound as a white powder (0.047 g).
MS (APCI+ve) 416 (M+H)+
1HNMR (CD3OD) δ 8.42 (1H, t); 7.46 (1H, d); 7.41-7.38 (2H, m); 3.63-3.49 (8H, m);
3.48-3.45 (2H, m); 3.19-3.14 (2H, m); 3.06 (2H, s); 1.99 (3H, bs); 1.73 (6H, q); 1.63
(6H,d).
Example 67
2-Chloro-5-[2-(2,5-diazabicycio[2.2.11]hept-2-yl)ethyl]-N-(tricyclo[3.3.1.13'7]dec-l-rlmethyl)-benzamide, hydrochloride salt

Prepared according to the method described in Example 66c from 2-chloro-5-(2-oxoethyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyI)-benzamide (0.094 g, Example 66b), 2,5-diazabicyclo[2.2.1]heptane-2-carboxylic acid, 1,1-dimethylethyl ester (0.108 g), sodium triacctoxyborohydride (0.081 g) and 1,2-dichloroethane (2 ml). After work-up, the residue was purified by HPLC eluting with a gradient of 0-5% ethanol in dichloromethane. The white powder obtained was dissolved in methanol (2 ml) and a solution of hydrochloric acid in dioxane (4N, 1ml) was added. The mixture was stirred for 14h at room temperature. Solvents were then removed under reduced pressure and the product obtained was triturated with diethyl ether to afford the title compound as a white powder (0.067 g).
MS (APCI +ve) 428 (M+H)+
1H NMR (CD3OD) δ 7.49-7.40 (3H, m); 4.64 (2H, d); 3.92 (2H, d); 3.77-3.48 (4H, m);
3.18 (2H, t); 3.08 (2H, s); 2.61 (1H, bd); 2.28 (1H, bd); 2.00 (3H, bs); 1.75 (6H, q); 1.64
(6H,d).
Example 68
5-[2-(4-Amino-1-piperidinyl)ethyl]-2-chloro-N-(tricyclo(3.3.1.l3.7]dec-l-ylmethyl)-benzamide, hydrochloride salt

Prepared according to the method described in Example 66c from 2-chloro-5-(2-coethyl)-Ar-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (0.094 g, Example 66b), 4-peridinyl-carbamic acid, lj-dimethylethyl ester (0.109 g), sodium tnacetoxyborohydride .081 g) and 1,2-dichloroethane (2 ml). After work-up, the residue was purified by HPLC ting with a gradient of 0-5% ethanol in dichloromethane. The white powder obtained as dissolved in methanol (2 ml) and a solution of hydrochloric acid in dioxane (4N, 1ml) as added. The mixture was stirred for 14h at room temperature. Solvents were then moved under reduced pressure and the product obtained was triturated with diethyl ether afford the title compound as a white powder (0.065 g).
S(APCI+ve)430(M+H)+
1HNMR (CD3OD) δ 8.43 (1H, t); 7.49-7.38 (3H, m); 3.78 (2H, bd); 3.64-3.42 (2H, m); Ll-3.35 (2H, m); 3.23-3.14 (3H, m); 3.08 (2H, s); 2.33-2.29 (2H, m); 2.13-2.04 (2H, m); O (3H, bs); 1.75 (6H, q); 1.64 (6H, d).
ample 69
Chloro-5-[2-{3-piperidinylamino)ethyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-bezamide, dihydrochloride salt

Prepared according to the method described in Example 66c from 2-chloro-5-(2-cthyI)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-beiizamide (0.094 g, Example 66b), amino-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.109 g), sodium

triacetoxyborohydride (0.081 g) and 1,2-dichloroethane (2 ml). After work-up, the residue was purified by HPLC eluting with a gradient of 0-5% ethanol in dichloromethane. The white powder obtained was dissolved in methanol (2 ml) and a solution of hydrochloric acid in dioxane (4N, 1ml) was added. The mixture was stirred for 14h at room temperature. Solvents were then removed under reduced pressure and the product obtained was triturated with diethyl ether to afford the title compound as a white powder (0.065 g).
MS (APCI +ve) 430 (M+H)+
1H NMR (CD3OD) δ 7.49-7.46 (1H, m); 7.42-7.38 (2H, m); 3.76 (1H, bd); 3.64-3.54 (1H, m); 3.44-3.34 (3H, m); 3.19-2.98 (4H, m); 3.08 (2H, s); 2.34 (1H, bd); 2.18-2.12 (1H, m); 2.00 (3H, bs); 1.89-1.78 (2H, m); 1.74 (6H, q); 1.64 (6H, d).
Example 70
5-[2-(3-Amino-l-piperidinyI)ethyI]-2-chloro-N-(tricyclo[3.3.1.l3'7]dec-l-ylmethyl)-benzamide, hydrochloride salt

Prepared according to the method described in Example 66c from 2-chloro-5-(2-oxoethyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (0.094 g, Example 66b), 3-piperidinyl-carbamic acid, 1,1-dimethylethyl ester (0.109 g), sodium triacetoxyborohydride (0.081 g) and 1,2-dichloroethane (2 ml). After work-up, the residue was purified by HPLC eluting with a gradient of 0-5% ethanol in dichloromethane then by HPLC eluting with a gradient of 0-2% ethanol in dichloromethane. The white powder obtained was dissolved in methanol (2 ml) and a solution of hydrochloric acid in dioxane (4N, 1ml) was added. The

mixture was stirred for 14h at room temperature. Solvents were then removed under reduced pressure and the product obtained was triturated with diethyl ether to afford the tide compound as a white powder (0.032 g).
MS (APCI+ve) 430 (M+H)+
1H NMR (CD3OD) δ 7.49-7.46 (1H, m); 7.42-7.39 (2H, m); 3.80-3.67 (3H, m); 3.46 (2H, t); 3.19 (2H, t); 3.08 (2H, s); 3.09-3.04 (1H, m); 2.14 (1H, bt); 2.00 (3H, bs); 1.74 (6H, q); 1.77-1.68 (2H, m); 1.64 (6H, d).
Example 71
2-Chloro-5-[2-(3-pyrroIidinylamino)ethyl]-N-(tricyclo[3.3.l.l3.7]dec-l-ylmethyl)-benzamide, dihydrochloride salt

Prepared according to the method described in Example 66c from 2-chloro-5-(2-oxoethyl)-N-(tricyclo(3.3.1.13.7]dec-l-ylmethyl-benzamide (0.094 g, Example 66b), 3-amino-l-pyrrolidinecarboxylic acid, 1,1-dimethylethyl ester (0.101 g), sodium triacetoxyborohydride (0.081 g) and 1,2-dichloroethane (2 ml). After work-up, the residue was purified by HPLC eluting with a gradient of 0-5% ethanol in dichloromethane. The pale orange powder obtained was dissolved in methanol (2 ml) and a solution of hydrochloric acid in dioxane (4N, 1ml) was added. The mixture was stirred for 14h at room temperature. Solvents were then removed under reduced pressure and the product obtained

was triturated with diethyl ether to afford the title compound as a pale orange powder [0.033 g).
MS (APd +ve) 416 (M+H)+
1HNMR(CD3OD) δ 7.46-7.39 (3H, m); 4.12 (1H, bs); 3.78-3.71 (1H, m); 3.69-3.57 2H, m); 3.43-3.32 (4H, m); 3.13 (2H, bt); 3.06 (2H, s); 2.62-2.51 (1H, m); 2.38-2.29 1H, m); 1.98 (3H, s); 1.73 (6H, q); 1.63 (6H, s).
Example 72
-[2-[(3R)-3-AniinopyrroUdinyl]ethy]]-2-chloro-N-(tricyc]o[3.3.1.13.7]dec-l-ylmethyl)-enzamide, hydrochloride salt

Prepared according to the method described in Example 66c from 2-chloro-5-(2-coethyl)-A^-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (0-094 g, Example 66b), /?)-pyrrolidinyl-carbamic acid, 1,1-dimethylethyl ester (0.101 g), sodium acetoxyborobydride (0.081 g) and 1,2-dichloroethane (2 ml). After work-up, the residue as purified by HPLC eluting with a gradient of 0-5% ethanol in dichloromethane. The lite powder obtained was dissolved in methanol (2 ml) and a solution of hydrochloric id in dioxane (4N, 1ml) was added. The mixture was stirred for 14h at room temperature, solvents were then removed under reduced pressure and the product obtained was turated with diethyl ether to afford the title compound as a white powder (0.060 g).
S(APCI+ve)416(M+H)+

1H NMR (CD3OD) δ 7.49-7.41 (3H, m); 4.86 (1H, bs); 4.05-3.80 (2H, m); 3.58 (4H, bs); 3.17 (2H, t); 3.08 (2H, s); 2.66 (1H, bs); 2.28 (1H, bs); 2.00 (3H, s); 1.74 (6H, q); 1.64 (6H, s).
Example 73
2-Chloro-5-[2-[2-(hydroxymethyI)-l-piperazinyl]ethyl]-iV-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt

Prepared according to the method described in Example 66c from 2-chloro-5-(2-oxoethyI)-iV-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (0.094 g, Example 66b), 3- . (hydroxymethyl)-l-piperazinecarboxylic acid, 1,1-dimethylethyl ester (0.117 g), sodium triacetoxyborohydride (0.081 g) and 1,2-dichloroethane (2 ml). After work-up, the residue was purified by HPLG eluting with a gradient of 0-5% ethanol in dichloromethane then chromatography eluting with ethyl acetate then ethyl acetate : ethanol (95:5). The white powder obtained was dissolved in methanol (2 ml) and a solution of hydrochloric acid in dioxane (4N, 1ml) was added. The mixture was stirred for 14h at room temperature. Solvents were then removed under reduced pressure and the product obtained was triturated with diethyl ether to afford the title compound as a white powder (0.016 g).
MS (APCI +ve) 446 (M+H)+
1H NMR (CD3OD) δ 8.43 (1H, t); 7.48-7.40 (3H, m); 4.14 (1H, bd); 3.93 (1H, bd); 3.81-3.76 (2H, m); 3.74-3.58 (5H, m); 3.57-3.45 (2H, m); 3.28-3.19 (1H, m); 3.17-3.11 (1H, m); 3.07 (2H, s); 1.99 (3H, bs); 1.73 (6H, q); 1.64 (6H, s).

Example 74
2-Chloro-5-(hexahydro-1H-l,4-diazepin-l-yl)-N-(2-tricyclo[3.3.1.13.7]dec-l-ylethyl)-benzamide, hydrochloride salt

a) 4-[4-Chloro-3-[[(2-tricyclo[3.3.1.13.7]dec-l-ylethyl)amino]carbonyl]phenyl] hexahydro-1H-l,4-diazepine-1-carboxylic acid, 1,1-dimethylethyl ester
A solution of 4-(3-carboxy-4-chlorophenyl)hexahydro-lH-l,4-diazepine-l-carboxylic acid, 1,1-dimethylethyl ester (0.075 g, Example 5b) and 1,1'-carbonyidiimidazole (0.034 g) in dimediylformamide (3 ml) was stirred at room temperature of 2.5h. Tricyclo[3.3.1.13.7]decane-l-ethanamine, hydrochloride salt (0.045 g) and N,N-diisopropylethylarnine (0.037 ml) were then added and stirring continued for 14h. The reaction mixture was poured into water and extracted with ethyl acetate three times. The ethyl acetate layers were combined and washed with 2M hydrochloric acid, 10% aqueous sodium hydroxide and brine, then dried over magnesium sulfate and concentrated under reduced pressure. Purification by chromatography on silica gel eluting with 20% ethyl acetate in iso-hexane gave the subtitle compound as a yellow oil (0.053 g).
MS (APCI +ve) 460/462 (M-'Bu)'
b) 2-Chloro-5-(hexahydro-1H-l,4-dia2epin-l-yI)-N-(2-tricyclo[3.3.1.13.7]dec-l-ylethyl)-benzamide, hydrochloride salt

4-[4-ChIoro-3-[[(2-tricycIo[3.3.1.13.7]dec-l -ylethyl)amino]carbonyl]phenyI]-hexahydro-1H-1,4-diazepine-l-carboxylic acid, 1,1-dimethylethyl ester (0.053g, Example 74a) was dissolved in methanol (5 ml) and hydrochloric acid (0.5 ml from a 4N solution in dioxane) was added. After stirring at room temperature for 14h, the mixture was evaporated to ¾ original volume under reduced pressure. Diethyl ether was gradually added to the solution and the resulting precipitate was collected by filtration, washed with diethyl ether and dried in vacuo to afford the title compound as a cream solid (0.017 g).
MS (APCI+ve) 416/418 (M-HC1)+
1HNMR (DMSO-d6) ¾ 9.07 (2H, bs); 8.18 (1H, t); 7.22 (1H, d); 6.80 (1H, dd); 6.71 (1H, d); 3.70 (2H, m); 3.50 (2H, t); 3.25-3.17 (4H, m); 3.07 (2H, m); 2.09-2.06 (2H, m); 1.93 (3H, bs); 1.68 (3H, d); 1.61 (3H, d); 1.51 (6H, s); 1.34-1.28 (2H, m).

Prepared as described in example 74 above using (+/-)-2-chloro-5-[3-[[(1,1-dimethylemoxy)carbonyl]amino]-l-pyrrolidinyl]-ben2oic acid (0.090 g), 1,1'-carbonyldiimidazole (0.043 g), tricyclo[3.3.1.13.7]decane-l-emanamine, hydrochloride salt (0.057 g), N,N-diisopropylethylamine (0.046 ml) and dimethylformamide (3 ml). This compound was treated with 4N hydrochloric acid in dioxane (0.5 ml) and methanol (5 ml) to yield the title compound (0.025 g).

. MS (APCI +ve) 402/404 (M-HC1)+
1HNMR (DMSO-d6) δ 8.24 (3H, bs); 8.18 (1H, t); 7.24 (1H, d); 6.60 (1H, dd); 6.49 (1H, d); 3.93 (1H, m); 3.54-3.37 (2H, m); 3.31-3.17(4H, m); 2.37-2.28 (1H, m); 2.07 (1H, m); 1.93 (3H, bs); 1.68 (3H, d); 1.61 (3H, d); 1.51 (6H, s); 1.34-1.28 (2H, m).
Example 76
2-Chloro-S-(4-piperidinylcarbonyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt

a) 4-[4-Chloro-3-[[(tricyclo[3.3.1.13.7]dec-1-ylmethyl)amino]carbonyl]benzoyl]-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester
To dimethyl sulphoxide (0.155 ml) in anhydrous dichloromethane (11 ml) at -78°C was added oxalyl chloride (0.086 ml) and the mixture was stirred for 5min. at -78°C. A solution of 4-[[4-chloro-3-[[(tricyclo[3.3.1.13.7.]dec-l-ylmethyl)amino]carbonyl]phenyl]-hydroxymethyl]-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.47 g, Example 64) in anhydrous dichloromethane (3 ml) was added dropwise and the mixture was stirred for 15min. at -78°C. Triethylamine (0.633 ml) was then added and the solution was wanned to room temperature. After 45min. at room temperature, the reaction mixture was poured onto water and the layers were separated. The organic extract was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by HPLC eluting a gradient of 0-5% ethanol in dichloromethane to give the subtitle compound as a white foam (0.31 g).

MS(APCI+ve) 15(M+H)+
1H NMR (DMSO-d6) 5 8.46 (1H, t); 8.06-8.01 (1H, m); 7.95-7.92 (1H, m); 7.70-7.65 (1H, m); 3.97 (2H, bd); 3.72-3.61 (1H, m); 2.97 (2H, t); 2.92 (2H, bs); 1.96 (3H, bs); 1.77 (2H, d); 1-65 (6H, q); 1.55 (6H, s); 1.41 (9H, s); 1.48-1.33 (2H, m).
b) 2-Chloro-5-(4-piperidinyicarbonyI)-N-(tricyclo[3.3.1.l3.7]dec-l-ylmethyl)-benzamide, hydrochloride salt
A solution of 4-[4-chloro-3-[[(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)amino]carbonyl] benzoyl]-1-piperidinecarboxylic acid, 1,1 -dimethylethyl ester (0.07 g, Example 76a) in methanol (3 ml) was treated with 4N hydrochloric acid solution in dioxane (1 ml). After ]4h the solvents were removed under reduced pressure and the residue was triturated with diethyl ether to give the title compound as a white powder (0.025 g).
MS (APCI +ve) 415 (M+H-HC1)+
1H NMR (DMSO-d6) δ 8.90 (1H, bs); 8.64 (1H, bs); 8.46 (1H, t); 8.03 (1H, d); 7.95
(1H, s); 7.69 (1H, d); 3.81 (1H, t); 3.24-3.18 (2H, m); 3.09-2.99 (2H, m); 2.96 (2H, d); 2.01
(2H, dd); 1.95 (3H, s); 1.79 (2H, t); 1.64 (6H, q); 1.45 (6H, s).
Example 77

a) 4-[l-[4-Chloro-3-[[(tricydo[3.3.1.1 3.7]dec-1 -yImethyl)ainino]carbonyI] phenyl]-1-hydroxyethyl]- 1-piperidinecarboxylic acid, 1,1-dimethylethyl ester
2-Chloro-5-[1-hydroxy-1-(4-piperidinyl)ethyl]-N-(tricyclo[3.3.1.13.7]dec-1-ylmethyl)-benzamide, hydrochloride salt

To methyl magnesiumbromide (3M solution in diethyl ether, 0.225 ml) in anhydrous diethyl ether (7 ml) under a nitrogen atmosphere was added slowly 4-[4-chloro-3-[[(tricyclo[3.3.1 .l3.7]dec-l-ylmethyl)amino]carbonyl] benzoyl]-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (0.23 g, Example 76a) in anhydrous diethyl ether (7 ml). The reaction mixture was stirred for 14h at room temperature, then poured onto crushed ice. A solution of 10% aqueous potassium hydrogen sulphate was added keeping the pH of the solution >4. The layers were separated, and the aqueous layer was extracted with ethyl acetate (4x25 ml). The organic extracts were combined, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was dissolved in methanol (3 ml) and hydrochloric acid (4N solution in dioxane, 2 ml) and stirred for 14h at room temperature. Solvents were then removed under reduced pressure and the product (0.11 g) was redissolved in dichloromethane (3 ml). Triethylamine (0.066 ml) was added followed by di-tert-butyl-dicarbonate (0.055 g) and the reaction mixture was stirred for 1 hour at room temperature. Water was added and the layers were partitioned. The organic extract was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by HPLC eluting with a gradient of 0-5% ethanol in dichloromethane, then by RPHPLC eluting with a gradient of 75-5% of 0.1% aqueous ammonium acetate in acetonitrile to give the subtitle compound as a white foam (0.06 g).
MS (APCI+ve)431 (M+H-BOC)+
b) 2-Chloro-5-[1-hydroxy-l-(4-ptperidinyl)ethyl]-N-(tricyclo[3.3.l.l3.7]dec-l-ylmethyl)-benzamide, hydrochloride salt
To a solution of 4-[l-[4-chloro-3-[[(tricyclo[3.3.1.13.7]dec-l-ylmethyI)amino] carbonyl] phenyl]-l-hydroxyethyl]-l-piperidinecarboxylicacid, 1,1-dimethylethyl ester (0.07 g, Example 77a) in methanol (3 ml) was added 4N hydrochloric acid solution in dioxane (1 ml). After 14h the solvents were removed under reduced pressure and the residue was triturated with diethyl ether to give the title compound as a white powder (0.038 g).

MS(APCI+ve)431 (M+H-HC1)+
1H NMR (DMSO-d6) δ 8.78 (1H, bs); 8.28 (1H, t); 7.44-7.40 (3H, m); 5.21 (1H, s); 3.25 (1H, d); 3.16 (1H, d); 2.98-2.89 (2H, m); 2.79-2.67 (2H, m); 1.94 (3H, bs); 1.84-1.75 (2H, m); 1.63 (6H, q); 1.53 (6H, s); 1.42 (3H, s); 1.53-1.31 (3H, m).

Prepared as described in Example 12b using 2-chloro-5-hydroxy-iV-(tricyclo[3.3.1.13.7]dec-l-methyl)-benzamide (Example 12a) and 4-(2-hydroxyethyl)-l-piperazinecarboxylic acid, 1,1-dimethylethyl ester.
MS (APCI+ve) 432 (M+H)+
1H NMR (CD3OD) δ 8. 40 (1H, t); 7.41 (1H, d); 7.14-7.06 (2H, m); 4.45 (2H, t);
3.76-3.58 (10H, m); 3.07-3.03 (2H, m); 1.98 (3H, s); 1.77 (3H, d); 1.69
(3H,d);1.62(6H,s).

Example 79
2-Chloro-5-[2-(4-piperidinyl)ethoxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt

Prepared as described in Example 12b using 2-chloro-5-hydroxy-N-(tricyclo[3.3.1.13.7]dec-l-methyl)-benzamide (Example 12a) and 4-(2-hydroxyethyl)-I-piperidinecarboxylic acid, 1,1-dimethylethyl ester.
MS (APCI +ve) 431 (M+H)+
1H NMR (DMSO-d6) δ 8.75 (1H, brs); 8. 49 (1H, brs); 8. 27 (1H, t); 7.37 (1H, d); 6.99
(1H, dd); 6.91 (1H, d); 4:03 (2H, t); 3.22 (2H, d); 2.92 (2H, d); 2.82 (2H, t); 1.94 (3H, s);
1.82 (2H, d); 1.79-1.70 (1H, m); 1.69-1.64 (5H, m); 1.59 (3H, d); 1.53 (6H, s); 1.43-1.30
(2H,m).
Example 80
2-Chloro-S-[2-(4-piperidinyIoxy)ethoxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyI)-benzamide, hydrochloride salt

Prepared as described in Example 12b using 2-chloro-5-hydroxy-N-(tricyclo[3.3.1.13.7]dec-l-methyl)-benzamide (Example 12a) and 4-(2-hydroxyethoxy)-l-piperidinecarboxylic acid, 1,1-dimethylethyl ester.
MS (APCI +ve) 447 (M+H)+
1HNMR (CD3OD) δ 8. 39 (1H, brt); 7.38-7.33 (1H, m); 7.06-6.98 (2H, m); 4.22-4.16 (2H, m); 3.88-3.82 (2H, m); 3.80-3.71 (1H, m); 3.36-3.24 (2H, m); 3.16-3.04 (4H, m); 1.99 (3H, s); 2.08-1.86 (4H, m); 1.78 (3H, d); 1.69 (3H, d); 1.62 (6H, s).

Prepared as described in Example 12b using 2-chloro-5-hydroxy-iV-(tricyclo[3.3.1.13,7]dec-l-methyl)-benzamide (0.20g, Example 12a) and 4-[2-(2-hydroxyethoxy)ethyl]-l-piperazine carboxylic acid; 1,1-dimethylethyl ester (0.26g).
MS (APa +ve) 476 (M+H)+
1HNMR (CD3OD) δ 7.7(1H, dd); 7.04-7.01 (2H, m); 4.25-4.18 (2H, m); 3.94 (2H, t); 3.91-3.87 (2H, m); 3.80-3.43 (10H, m); 3.06 (2H, s); 1.99 (3H, s); 1.75 (3H, d); 1.67 (3H, d); 1.62 (6H, s).

Example 82
2-Chloro-5-[(5,6-dihydro-l(4H)-pyrimidinyl)methyl]-N-(tricycIo[3.3.1.13.7]dec-l-
ylmethyl)-benzamide

Prepared according to the method described in Example 8 from 5-bromomethyl-2-cfaloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (Example 8b,) and 1,4,5,6-tetrahydro- pyrimidine.
MS (APCI+ve) 400/402 (M+H)+
1H NMR (CDCl3) δ 7.84 (IH, s); 7.60 (1H, d); 7.43 (1H, d); 7.29 (1H, dd); 6.51 (1H, t); 4.39 (2H, s); 3.40-3.10 (3H, m); 3.17 (2H, d); 3.14 (1H, t); 2.01 (3H, s); 1.91 (q, 2H); 1.74 (3H, d); 1.64 (3H, d); 1.59 (6H, bs).
Example 83
2-Chloro-5-[[4-[(2-hydroxyethyl)amino]-l-piperidinyl]methyl]-N-(tricyclo[3.3.1.1.3.7]dec-l-ylmethyl)-benzamide, hydrochloride salt

a) 2-Chloro-5-[(4-oxo-l-piperidinyl)methyl]-iV-(tricyclo[3.3.l.l3.7]dec-l-ylmethyl)-
benzamide
Prepared according to the method described in Example 8c from 5-bromomethyl-2-chloro-A^tricyclo[3.3.1.13,7]dec-l-ylmethyl)-benzamide (Example 8b) and 4-piperidinone.
MS (APCI +ve) 456/458 (M+H)+
b) 2-Chloro-5-[[4-[(2-hydroxyethyl)amino]-l-piperidinyl]methyl]-N.
(tricydo[3.3.l.l3.7]dec-l-ylmethyl)-benzamide, hydrochloride salt
To a solution of 2-chloro-5-[(4-oxo-l-pipcridinyl)methyl]-N-(tricyclo[3.3.1.13,7]dec-l-ylmethyl)-benzamide (0.150g, Example 83a) in methanol (3ml) at room temperature were added ethanolamine (0.11ml) and sodium cyanoborohydride (0.068g). The pH was adjusted to 6 by adding a 4N solution of hydrogen chloride in dioxane and the reaction stirred for 48h. The reaction was acidified with concentrated hydrochloric acid until gas evolution ceased. The precipitate was removed by filtration and the filtrate concentrated under vacuum. The residue was partitioned between ethyl acetate and water. The aqueous layer was basified with 5% aqueous sodium hydroxide and extracted with dichloromethane. The organics were washed with brine and dried over magnesium sulfate. The crude material was purified on silica gel (5% 7N ammonia in methanol/95% dichloromethane) to afford a white foam which was dissolved in ether/methanol and treated with a 4N solution of hydrogen chloride in dioxane to give the title compound (0.135 g).
MS (APCI +ve) 460/462 (M+H)+
1H NMR (CD3OD) δ 8.47 (1H, t); 7.67 (1H, d); 7.64 (1H, dd); 7.60 (1H, d); 4.39 (2H, s); 3.81 (2H, t); 3.62 (2H, bd); 3.52 (1H, t); 3.23-3.10 (4H, m); 3.09 (2H, d); 2.39 (2H, d); 2.07 (2H, q); 1.99 (s, 3H); 1.77 (3H, d); 1.70 (3H, d); 1.64 (6H, d).

a) 2-Chloro-5-(l-oxa-6-azaspiro[2^]oct-6-ylmethyl)-N-(tricyclo[33.1.13.7]dec-l-ylmethyl)-benzamide
To dimethylsulfoxide (2ml) was added sodium hydride (0.033g, 60 % in oil) at room temperature. The mixture was stirred for 5min. at this temperature and a solution of limethylsulfoxonium iodide (0.178g) in dimethylsulfoxide (2ml) was added. After 30min.,2-chloro-5-[(4-oxo-l-piperidinyl)methyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (0.28g, Example 83a) in dimethylsulfoxide (2ml) was added and the reaction itirred at room temperature for 3h before being quenched with ice/water (20ml). The nixture was extracted three times with ethyl acetate, the combined organic layers washed vim brine and dried over magnesium sulfate. The crude material was purified on silica gel, eluting with ethyl acetate to afford the subtitle compound as a white foam (0.25g).
MS(APCI+ve) 429/431 (M+H)+
1HNMR (CDCl3) δ 7.68 (1H, s); 7.40-7.30 (2H, m); 6.27 (1H, t); 3.54 (2H, s); 3.18 2H, d); 2.70-2.50 (6H, m); 2.00 (s, 3H); 1.90-1.75 (2H, m); 1.74 (3H, d); 1.66 (3H, d); 59 (6H, bs); 1.80-1.50 (m, 2H).
2-ChIoro-5-[[4-hydroxy-4-[[(l-methyIethyl)amino]metfayl]-l-iperidinyI]methyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide
In a sealed tube 2-chloro-5-(l-oxa-6-azaspiro[2.5]oct-6-ylmethyl)-N-ricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (Example 84a, 0.15g) was dissolved in a

mixture of ethanol (4ml) and di-isopropylamine (1ml) and heated at 65°C for 14h. The volatiles were removed under vacuum and the residue purified on silica gel (5% 7N ammonia in methanol/95% dichloromethane) to afford the title compound as a white solid (0.115g).
MS (APCI+ve) 488/490 (M+H)+
1H NMR (CD 3OD) δ 7.45-7.35 (3H, m); 3.55 (2H, s); 3.06 (2H, s); 2.76 (1H, q); 2.70-2.55 (2H, m); 2.54 (2H, s); 2.50-2.35 (2H, m); 1.99 (s, 3H); 1.77 (3H, d); 1.70 (3H, d); 1.63 (10H, bs); 1.07 (m, 2H).
Example 85
2-Chloro-5-{(1,2,3,6-tetrahydro-3-pyridinyl)methyl]-N-(tricyclo[3.3.l.l3.7]dec-l-ylmethyl)- benzamide, hydrochloride salt

To pyridine (6ml) at 0°C was added portionwise lithium aluminium hydride (0.24g). The mixture was allowed to warm to room temperature and was stirred for 24h. Lithium iodide (0.220g) and pyridine (1ml) were added and the reaction stirred for a further lh. 5-Bromomethyl-2-chloro-N-(tricyclo[3.3.1 .l3.7]dec-l-ylmethyl)-benzamide (0.30g, Example 8b) in dry pyridine (2ml) was added to the solution at room temperature. After 2h, die mixture was quenched at 0°C with a cold 15 % aqueous solution of acetic acid, stirred for an hour and concentrated under vacuum. The residue was taken in 1N sodium hydroxide, extracted with dichloromethane and the organic layers dried over magnesium sulfate. The crude material was purified on silicagel (2 to 10% 7N ammonia in

methanol/dichioromethane) then treated with a 4N solution of hydrogen chloride in dioxane and methanol to give the title compound (0.20g).
MS (APCI +ve) 399/401 (M+H)+
1H NMR (CD3OD) δ 8.42 (1H, t); 7.43 (1H, dd); 7.32 (1H, dd); 7.30 (d; 1H); 5.89 (1H, d);
5.80 (1H, d); 3.64 (2H, s); 3.40-3.30 (1H, m); 3.06 (4H,.d); 1.99 (s, 3H); 1.78 (3H, d); 1.68
(3H,d);1.63(6H,d).
Example 86
2-Chloro-5-(3-piperidinylmethyl)-iV-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)- benzamide, acetate salt

a) 2-Chloro-5-(3-piperidinylmethyl)-N-(tricyclo[33.1.13.7]dec-l-ylmethyl)-benzamide, acetate salt
To pyridine (12 ml) at 0 °C was added portionwise lithium aluminium hydride (0.46g). The mixture was allowed to warm to room temperature and was stirred for 24h. Lithium iodide (0.44g) and pyridine (5ml) were added and the reaction stirred for a further 1h. The solution was cooled to -10 °C and 5-bromomethyl-2-chloro-iV-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (Example 8b, 0.5g) in dry pyridine (5ml) added. After 1 hour, the mixture was quenched at -10 degrees with cold water, then 1N sodium hydroxide. The solution was stirred for1h then concentrated under vacuum. The residue was taken in water, extracted with dichloromethane and the organic layers dried over magnesium sulfate. The crude material was purified on silica gel (ethylacetate : i-hexane / 4 : 1) to afford the subtitle compound as a white foam (0.355g).

b) 2-Chloro-5-(3-piperidinylmethyl)-iV-(tricycIo[3.3.1.13.7]dec-l-ylmethyl). benzamide, acetate salt
2-Chloro-5-(3-pyridinylmethyl)-N-CtricycIo [3.3.1.13.7]dec-1 -ylmethyl)-benzamide (0.10g, Example 86a) was dissolved in methanol and treated with a 4N solution of hydrogen chloride in dioxane. The hydrochloride salt was isolated and hydrogenated in ethanol over platinium oxide following the procedure described in Example 51 to give the title compound as the acetate salt after purification by reverse phase HPLC (0.1 % aqueous ammonium acetate/acetontrile) (0.053g).
MS (APCI +ve) 401/403 (M+H)+ .
1HNMR (CD3OD) δ 7.42 (1H, d); 7.31-7.25 (2H, m); 3.38-3.28 (1H; m); 3.28-3.18 (1H; 2m); 3.07 (2H, s); 2.86 (1H, dt); 2.72-2.61 (1H, m); 2,65 (1H, d); 2.13-2.05 (1H; m); 2.01 (3H, s); 1.94 (3H, s); 1.90-1.85 (1H; m); 1.85-1.60 (2H; m); 1.80 (3H, d); 1.71 (3H, d); 1.64 (6H,d); 1.29 (1H, qd).
Example 87
2-bromo-S-[[4-[(2-hydroxyethyI)amino]-l-piperidinyI]methyl]-N-(tricycIo[33.1.13.7] dec-l-ylmethyl- benzamide

Prepared according to the procedures described in Example 83a and 83b from 2-bromo-5-bromomethyl-N-(tricyclo[3.3.1. l3.7]dec-l-yimethyl)-benzarnide (Example 65a), 4-piperidane and ethanolamine

MS (APCI +ve) MW 505/506 (M+H)+
1H NMR (CDCl3) δ 7.53 (1H, d); 7.52 (1H, d); 7.26 (1H, dd); 6.05 (1H; t); 3.65 (2H; t); 3.46 (2H, s); 3.17 (2H, d); 2.82 (2H, t); 2.60-2.45 (1H, m); 2.20-1.95 (7H; m); 1.95-1.82 (2H, bd); 1.75 (3H, d); 1.66 (3H, d); 1.61 (6H, d); 1.50-1.35 (2H, qd).
Example 88 2-Chloro-5-[(E)-3-piperidinylidenemethyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide

a) 2-Chloro-S-[(E)-(5,6-dihydro-3(4H)-pyridinylidene)methyl]-N-(tricyclo[33.1.13.7]dec-l-ylmethyl)-benzamide
2-Chloro-5-formyl-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide (0.152 g, Example 31a) and 2,3,4,5-tetrahydropyridine trimer (Org. Synth., 1977, Voi.56, 118-122, 0.038 g) were dissolved in methanol (3 ml) and heated at reflux for 4h. The mixture was evaporated under reduced pressure then purified by HPLC eluting a gradient of 0-5% ethanol in dichloromethane to give the subtitle compound as a white foam (0.046 g),
SIS (APQ +ve) 397 (M+H)+
1HNMR (CD3OD) δ 7.98 (1H, s); 7.51 (3H, s); 6.83 (1H, s); 3.66-3.62 (2H, m); 3.07
(2H, s); 2.78-2.73 (2H, m); 1.99 (3H, bs); 1.73 (6H, q); 1.774.69 (2H, m); 1.64 (6H, s).
2-Cbioro-5-[(E)-3-piperidinylidenemethyl]-N-(tricycio[3.3.1.l3,7]dec-l-yimethyl)-benzamide

Sodium borohydride (0.009 g) in methanol (0.5 ml) was added to a solution of 2-chloro-5-[(E)-(5,6-dihydro-3(4H)-pyridinylidene)methyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide (0.046 g, Example 88a,) in methanol (1.5 ml). The reaction mixture was stirred for 4h under an atmosphere of nitrogen at room temperature. Concentrated hydrochloric acid (0.01 ml) was added and the mixture was evaporated under reduced pressure. An aqueous solution of sodium hydroxide (2M, 2 ml) was added to rebasify the residue followed by water (10 ml) and dichloromethane (10 ml). The layers were partitioned and the aqueous layer was extracted further with dichloromethane (2x10 ml). The organic extracts were combined, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give the title compound as a white powder (0.024
g).
MS (APCI+ve) 399 (M+H)+
1H NMR (CD3OD) δ 7.43 (1H, d); 7.29-7.26 (2H, m); 6.38 (1H, s); 3.45 (2H, s); 3.07
(2H, s); 2.96 (2H, t); 2.55 (2H, t); 2.00 (3H, bs); 1.75 (6H, q); 1.81-1.64 (2H, m); 1.64
(6H,s).
Pharmacological Analysis
Certain compounds such as benzoylbenzoyl adenosine triphosphate (bbATP) are known to be agonists of the P2X7 receptor, effecting the formation of pores in the plasma membrane (Drag Development Research (1996), 37(3). p.126). Consequently, when the receptor is activated using bbATP in the presence of ethidium bromide (a fluorescent DNA probe), an increase in the fluorescence of intracellular DNA-bound ethidium bromide is observed. The increase in fluorescence can be used as a measure of P2X7 receptor activation and therefore to quantify the effect of a compound on the P2X7 receptor.
In this manner, each of the title compounds of Examples 1 to 88 was tested for antagonist activity at the P2X7 receptor. Thus, the test was performed in 96-well flat
bottomed microtitre plates, the wells being filled with 250 µl of test solution comprising

200 ul of a suspension of THP-1 cells (2.5 x 106 cells/ml) containing 10-4 M ethidium

bromide, 25 µl of a high potassium buffer solution containing 10 M bbATP, and 25 µl of the high potassium buffer solution containing 3x10-5 M test compound. The plate was covered with a plastics sheet and incubated at 37 °C for one hour. The plate was then read in a Perkin-Elmer fluorescent plate reader, excitation 520 nm, emission 595 nm, slit
widths: Ex 15 nm, Em 20 nm. For the purposes of comparison, bbATP (a P2X7 receptor agonist) and pyridoxal 5-phosphate (a P2X7 receptor antagonist) were used separately in the test as controls. From the readings obtained, a PIC50 figure was calculated for each test compound, this figure being the negative logarithm of the concentration of test compound necessary to reduce the bbATP agonist activity by 50%. Each of the compounds of
Examples 1 to 88 demonstrated antagonist activity, having a PIC50 figure > 4.50.

WE CLAIM;

wherein m represents 1, 2 or 3;
each R independently represents a hydrogen or halogen atom;
A represents C(O)NH or NHC(O); Ar represents a group

X represents a bond, an oxygen atom or a group CO, CH2, OCH2, NR5 , CH2NR5 , CONR5
or S(O)n;
n is 0, 1 or 2;
one of R2 and R3 represents a halogen, nitro, amino or a C1-C6 alkyl, and the other of R2
and R3 represents a hydrogen atom;
either R4 represents a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring
system containing one or two nitrogen atoms and optionally an oxygen atom, the
heterocyclic ring system being optionally substituted by one or more substituents
independently selected from fluorine atoms, hydroxyl, carboxyl, cyano, C1-C6 alkyl,
C1-C6 hydroxyalkyl, -NR6R7, -(CH2)rNR6R7 and -CONR6R7,

or R represents a 3- to 8-membered saturated carbocyclic ring system substituted by one or more substituents independently selected from -NR6 R7 , -(CH2)rNR6 R7 and -CONR R , the ring system being optionally further substituted by one or more substituents independently selected from fluorine atoms, hydroxyl and C1-C6 alkyl;
r is 1,2, 3,4, 5 or 6;
R5 represents a hydrogen atom or a C1-C6 alkyl or C3-C8 cycloalkyl group;
R6 and R7 each independently represent a hydrogen atom or a C1-C6 alkyl,
C2-C6 hydroxyalkyl or C3-C8 cycloalkyl group, or R6 and R7 together with the nitrogen
atom to which they are attached form a 3- to 8-membered saturated heterocyclic ring;
with the provisos that,

(a) when A represents C(O)NH and R4 represents an unsubstituted 3- to 8-membered
saturated aliphatic heterocyclic ring system containing one nitrogen atom, then X is other
than a bond, and

(b) when A represents C(0)NH and X represents a group CH2 or OCH2 then R4 does not
represent an unsubstituted imidazolyl, unsubstituted morpholinyl, unsubstituted
piperidinyl or unsubstituted pyrrolidinyl group, and

(c) when A represents NHC(O) and R4 represents an unsubstituted 3- to 8-membered
saturated aliphatic heterocyclic ring system containing one nitrogen atom, then X is other
than a bond, and

(d) when A represents NHC(O) and X represents OCH2 then R4 does not represent an
unsubstituted 1-piperidinyl or unsubstituted 1-pyrrolidinyl group; or a pharmaceutically acceptable salt or solvate thereof.
2. A compound as claimed in claim 1, wherein A represents NHC (O).

3. A compound as claimed in claim 1 or claim 2, wherein Ar
represents a group

4. A compound as claimed in claims 1 to 3, wherein X represents a bond, an oxygen atom or a group CO, CH2, OCH2, NH, CH2NH, CONH or S(O)n.
5. A compound as claimed in claims 1 to 4, wherein the heterocyclic ring system in the group R4 is pyrrolidinyl, piperidinyl, piperazinyl or homopiperazinyl.
6. A compound as claimed in claims 1 to 4, wherein the saturated carboxylic ring in the group R4 is cyclopentyl or cyclohexyl.
7. A compound of formula (I), or a pharmaceutically acceptable salt or solvate thereof, as claimed in claim 1 being:
2-Nitro-3-piperazin-l-yl-N-(tricyclo[3.3.1.13.7]dec-l-ylroethyl)-benzamide,
2-Amino-3-piperazin-1 -yl -N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide,
dihydrochloride salt,
2-Chloro-3-piperazin-l-yl -N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide,
2-Chloro-5-piperazin-l-yl -N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide,
2-Chloro-5-(hexahydro-1H-1,4-diazepin-1-yl)-N-(tricyclo[3.3.1.13.7]dec-1-ylmethyl)-
benzamide, hydrochloride salt,
5-(4-Amino-1-piperidinyl)-2-chloro-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-
benzamide, hydrochloride salt,
(+/-)-5-(3-Amino-1 -pyrrolidinyl)-2-chloro-N-(tricyclo[3.3.1. l3.7]dec-1 -ylmethyl)-
benzamide, hydrochloride salt,

2-Chloro-5-piperazin-l-ylmethyl-N-(tricycIo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt,

2-Chloro-5'[(hexahydro-lH-l,4-diazepin-l-yl)methyl]-N-(tricyclo[3.3.1.13.7]dec-l-
ylmethyl)-benzamide, hydrochloride salt,
5-[(4-Amino-l-piperidinyl)methyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide, hydrochloride salt,
5-[(3-Amino-l-pyrrolidiny])methyl]-2-ch3oro-N-(tricyclo[3.3.1.1 3.7]dec-l-ylmethy])-
benzamide, hydrochloride salt,
2-Chloro-5-(4-piperidinyloxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide,
hydrochloride salt,
(R)-2-Chloro-5-(2-pyrrolidinylroethoxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide, hydrochloride salt,
(S)-2-Chloro-5-(2-pyrrolidinylmethoxy)-N-(tricyclo[3.3.1,13.7]dec-l-ylmethyl)-
benzamide, hydrochloride salt,
2-Chloro-5-(3-piperidinylmethoxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide, hydrochloride salt,
cis-5-[(4-Aminocyclohexyl)oxy]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide, hydrochloride salt,
2-Methyl-5-(l-piperazinylmethyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide,
hydrochloride salt,
2-Chloro-5-(1-piperazinylmethyl)-N-(2-tricyclo[3,3.1.1 3.7]dec-l-ylethyl)-benzamide,
hydrochloride salt,
(+/-)-2-Chloro-5-(3-pyrro]idinyloxy>N-(tricyc]o[3.3.1.13.7}dec-1 -ylmethyl)-benzamide, hydrochloride salt,
(+/-)-2-Chloro-5-(3-piperidinyloxy)-N-(tricyclo[3.3.1.1 3.7]dec-1 -ylmethyl)-
benzamide, hydrochJoride salt,
trans-5-[(4-Aminocyclohexyl)oxy]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide,
cis-(+/-)-5-[(3-Aminocyclopentyl)oxy]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-1 -
ylmethyl)-benzamide,
(S,S)-2-Chloro-5-(2,5-diazabicyc]o[2.2.1]hept-2-yl)-N-(tricyclo[3.3.1.13.7]dec-l-
ylmethyl)-benzamide, hydrochloride salt,

2-Chloro-5-(2-methyl-l-piperaziny])-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt,
{+/-)-2-Chloro-5-(3-pyrrolidinylamino)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethy!)-
benzamide, hydrochloride salt,
(+/-)-5-(3-Amino-l-piperidinyl)-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide,
(+/-)-2-Ch]oro-5-(3-piperidinylamino)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide,
2-Chloro-5-[hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl]-N-(tricyc]of3.3.1.13.7]dec-1 -
ylmethyl)-benzamide,
N-[2-methyl-5-(4-piperidinyloxy)phenyI]-tricyclo[3.3.1.13.7]decane-l-acetamide,
hydrochloride salt,
N-[2-chloro-5-(4-piperidinyloxy)phenyl]-tricyclo[3.3.1.13.7]decane-1 -acetamide,
hydrochloride salt,
2-Chloro-5-[(4-piperidinylamino)methyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide, dihydrochloride salt,
5-[[[4-(Aminornethyl)cyclohexyl]amino]methyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-
l-ylmethyl)-benzamide, dihydrochloride salt,
5-[[(4-Aminocyclohexyl)arnino]rnethyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-l-
ylmethyl)-benzamide, dihydrochloride salt,
5-[(1-Azabicyclo[2.2.2]oct-3-ylamino)methyl]-2-chloro-N-(tricyclo[3.3.1.13.7]dec-1 -
ylmethyl)-benzamide,
N-[4-(3-Aminopyrrolidin-l-yl)-2-methylphenyl]-2-(tricyclo[3.3.1.13.7]dec-l-
yl)acetamide, dihydrochloride salt,
N-(2-Methyl-4-piperazin-l-ylphenyl)-2-(tricycloI3.3.1.13.7]dec-l-yl)acetamide,
dihydrochloride salt,
cis-4-(3-Amino-cyclopentyloxy)-2-chloro-N-(tncyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide, hydrochloride salt,
2~Chloro-4-(4-piperidinyloxy)-N-(tricyclo[3.3.1.13,7]dec-1 -ylmethyl)-benzamide,
hydrochloride salt,

(+/-)-2-Chloro-4-(pyrrolidin-3-yloxy)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide,
2-Chloro-4-(piperidin-3-yloxy)- N-(tricyclo[3.3.1.13.7]dec-l-ylmethy])-benzamide,
hydrochloride salt,
2-Chloro-4-(4-piperazin~l-yl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethy])-benzamide,
hydrochloride salt,
2-Chloro-4-(3-pyrrolidinylamino)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide
hydrochloride salt,
2-Chloro-4-(hexahydro-1H-l,4-diazepin-l-yl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt,
(±)-5-[(3-Amino-l-piperidinyl)methyl]-2-ch]oro-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt,
2-Chloro-5-(2,5-diazabicyclo[2.2.1]hept-2-ylmethyl)-N-(tricyclo[3.3.1.13.7]dec-1-ylmethyl)-benzamide, hydrochloride salt,
2-Chloro-5-(9-oxa-3,7-diazabicyclo[3.3.1]non-3-ylmethyl)-N-
(tricyclo[3.3.1.13.7)dec-l-ylmethyl)-benzamide, hydrochloride salt,
2-Chloro-5-(3,7-diazabicyclo[3.3.1]non-3-ylmethy])-N-(tricyclo[3.3.1.13.7]dec-l-
ylmethyl)-benzamide, hydrochloride salt,
trans-2-Chloro-5-[[8-(methylamino)-3-azabicyclo[3.2.1]oct-3-yl]methyl]-N-
(tricyclo[3.3.1.13.7] Jdec-l-ylmethyl)-benzamide, hydrochloride salt,
cis-2-Chloro-5-[(hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl)methyl]-N-
3 7 (tricyclo[3.3.1.1 ' ]dec-l-ylmethyl)-benzamide, hydrochloride sail,
2-Chloro-5-(4-piperidinylrnethyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)-benzamide,
hydrochloride salt,
2-Chloro-5-(4-hydroxy-piperidin-4-yl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt,
2-Chloro-5-(l,2,3,6-tetrahydro-pyridin-4-yl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt,
2-Ethyl-5-piperazin-l-ylmethyl-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide, hydrochloride salt,

2-Chloro-5-(piperidin-4-ylsulfanyl)-N-(tricycloI3.3-1.13.7 ]dec-l-ylmethyl)-
befrcarrMe, Yiy&TocMoride sa)t,
2-Chloro-5-(piperidin-4-ylsuIfinyl)-N-(tricyclo[3.3.113.7]dec-l-ylmethyi)-
benzamide,
2-Chloro-5-(piperidin-4-ylsulfonyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide, hydrochloride salt.
2-Chloro-5-(piperazine-l-carbonyl)-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
benzamide, hydrochloride salt,
2-Chloro-5-([1,4]diazepane-l-carbonyl)-N-(tricyclo(3.3.3. 3.7 ]dec-l-ylmethyl)-
benzamide, hydrochloride salt,
4-Chloro-N1-(piperidin-4-yl-)-N2-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-
isophthalamide, hydrochloride salt,
2-Bromo-5-piperazin-l-ylmethyl-N-(tricyclo[3.3.1.13.7]dec-l-ylrnethyl)-benzamide,
hydrochloride salt,
2-Chloro-5-(hexahydro-lH-l,4-diazepin-l-yl)-N-(2-tricycIo[3.3.1.13.7]dec-l-ylethyl)-
benzamide, hydrochloride salt,
(+/-)-5-(3-Amirio-l-pyrrolidinyl)-2-chloro-N-(2-tricyclo[3.3.1.13.7]dec-l-ylethyl)-
benzamide, hydrochloride salt,
2-Chloro-5-(4-piperidinylcarbonyl)-N-(tricyclo[3.3.1.l 3.7]dec-l-ylmethyl)-benzamide, hydrochloride salt,
2-Ch!oro-54(5,6-dihyclrol(4H)-pyriraidinyI)rnethyl]-N-(tricyclo[3.3.1.13.7]dec-l-
ylmethyl )-benzamide,
2-Chloro-5-[[4-[(2-hydroxyethyl)amino]-l-piperidinyl]methyl]-N-
(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide hydrochloride salt,
2-Chloro-5-[[4-hydroxy-4-[[(1-methylethyl)amino]methyl]-1-piperidinyl]methyl]-N-(tricyclo[3.3.1.13.7]dec-l-ylmethyl)-benzamide,
2-Chloro-5-[(l ,2,3,6-tetrahydro-3-pyridinyl)methyl]-N-(tricyclo[3.3.1.13.7]dec-1-
ylmethyl)- benzamide, hydrochloride salt,
2-Chloro-5-(3-piperidinylmethyl)-N-(tricyclo[3.3.1.13.7]dec-1 -ylmethyl)- benzamide, acetate salt, or

2-bromo-5-[[4-[(2-hydroxyethyl)amino]-l-piperidinyl]methyl]-N-(tricyc]o[3.3.1.13.7] dec-l-ylmethyl- benzamide.
8. A process for the preparation of a compound of formula (I) as claimed in claim 1 which comprises:

(i) when X represents A CH2 group, R4 represents a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and optionally an oxygen atom, the heterocyclic ring system being optionally substituted by one or more substituents independently selected from fluorine atoms, hydroxyl, carboxyl, cyano, C1-C6 alkyl, C1-C6 hydroxyalkyl, -NR6R7, -(CH2)rNR6R7 and -CONR6R7 and R is linked to X through a nitrogen atom, reacting a compound of general formula

wherein one of R and R represents a hydrogen atom and the other of R and R

represents a group -CH2L11 in which L represents a leaving group and m, A, R1 , R2 and
R3 are as defined in formula (I), with a compound of general formula
R4-H (III)
in the presence of a base, wherein R4' represents a 3- to 9-membered saturated or unsaturated aliphatic heterocyclic ring system containing one or two nitrogen atoms and optionally an oxygen atom, the heterocyclic ring system being optionally substituted by one or more substituents independently selected from fluorine atoms, hydroxyl, carboxyl, cyano, C1-C6 alkyl, C1-C6 hydroxyalkyl, -NR6R7, -(CH2)rNR6R7 and -CONR6R7 and wherein R6 and R7 are as defined in formula (I); or

(ii) when X represents an oxygen atom or a group OCH2 reacting a compound of general formula

wherein one of R12 and R13 represents a hydrogen atom and the other of R12 and R13

represents a hydroxyl group and m, A, R1 , R2 and R3 are as defined in formula (I), with a
compound of general formula

wherein Y represents a bond or a group CH2 and R4 is as defined in formula (I), in the presence of l,l-(azodicarbonyl)dipiperidine and tributylphosphine; or
(iii) when X represents a bond, an oxygen atom or a group OCH2 or NR5 , and A is NHC(O), reacting a compound of general formula

wherein one of R and R represents a group -X'-R4 and the other of R14 and R15
represents a hydrogen atom, X' represents a bond, an oxygen atom or a group OCH2 or

NR5 , L 2 represents a leaving group and R2 , R 3 , R 4 and R5 are as defined in formula (I),
with a compound of general formula

wherein m and R1 are as defined in formula (I), optionally in the presence of a coupling agent; or
(iv) when X represents a bond, an oxygen atom or a group OCH2 or NR5 and A is C(0)NH, reacting a compound of general formula

wherein R2 and R3 are as defined in formula (I) and R14 and R15 are as defined in formula
(VI) in (iii) above, with a compound of general formula

wherein m and R are as defined in formula (I), in the presence of a base; or
(v) when X represents a bond or a group NR5 , reacting a compound of general formula

wherein one of R16 and R17 represents a leaving group, L3 , and the other of R16 and R17

represents a hydrogen atom and m, A, R1 , R2 and R3 are as defined in formula (I), with a
compound of general formula

wherein Z represents a hydrogen atom or a group NHR and R5 and R4 and R5 are as defined in
formula (I), optionally in the presence of a palladium catalyst, a phosphine ligand and a
base; or
(vii) when X represents a group CH2NR , reacting a compound of formula (II) a; defined in (i) above with a compound of formula (XI) as defined in (v) above wherein Z represents a group NHR ; or
(x) when X represents a group CH2 and R4 represents an unsubstituted 4-to
6-membered saturated aliphatic heterocyclic ring system containing one nitrogen atom,
reacting a compound of formula (II) as defined in (i) above, with a compound of general
formula

(xi) when X represents a group CO, CONR5 or SO2, and A is NHC(O), reacting
a compound of general formula
wherein one of R and R represents a group -X"-R4 and the other of R18 and R19

represents a hydrogen atom, X" represents a group CO, CONR5 or SO2, L4 represents a

leaving group and R2 , R3 , R 4 and R5 are as defined in formula (I), with a compound of
formula (VII) as defined in (iii) above, optionally in the presence of a coupling agent; or
(xii) when X represents a group CO, CONR5 or SO2, and A is C(O)NH, reacting a compound of general formula

wherein R2 and R3 are as defined in formula (I) and R18 and R19 are as defined in formula
(XIII) in (xi) above, with a compound of formula (IX) as defined in (iv) above, in the
presence of a base; or
(xiii) when X represents a sulfur atom, reacting a compound of formula (X) as defined in (v) above, with an organolithium reagent and then with a compound of general formula

4 wherein Tol represents a tolyl group and R is as defined in formula (I); or

(xiv) when X represents a CH2 group, reacting a compound of formula (X) as defined in (v) above, with an organolithium reagent and then with a compound of general formula
4 wherein R is as defined in formula (I), optionally followed by a reduction reaction; or
(xv) when X represents a bond, reacting a compound of formula (X) as defined in (v) above, with an organolithium reagent and then with a compound of general formula
4 wherein R is as defined in formula (I), optionally followed by a reduction reaction;
(xvi) when X represents a group SO, oxidising a corresponding compound of formula (I) in which X represents a sulphur atom; or

wherein one of R20 and R21 represents a group CHO and the other of R20 and R21

represents a hydrogen atom, and m. A, R1 , R2 and R3 are as defined in formula (I), with a

compound of general formula (XX), R4 -H, wherein R4 is as defined in formula (I), in the presence of a reducing agent; or
(xxi) when X represents a group CH2NR", reacting a compound of formula (XIX) as
defined in (xx) above, with a compound of general formula (XXI), R4 - Z, wherein Z'

represents a group NHR5 , and R4 and R5 are as defined in formula (I), in the presence of
a reducing agent; or
(xxiii) when X represents a group CH2 reacting a compound of formula (II) as defined in (i) above with trimethylphosphite, and then with a compound of formula (XVI) as
defined in (xiv) above, or with a compound of formula (XVII) as defined in (xv) above or

with a compound of general formula (XVIA), R4 CHO in which R4 is as defined in
formula (I), in the presence of abase, followed by a reductIon reaction; or
(xxviii) when X represents a group CH2 and R4 represents a 3-piperidinyl or 2-piperazinyl group, reacting a compound of formula (II) as defined in (i) above with a reagent formed by combining pyridine or pyrazine with an aluminium hydride reagent, followed by a reduction reaction; or
(xxx) when X represents a bond or NR5 and R4 represents a carbon-linked piperidyl

wherein one of R26 and R27 represents a pyridyl, pyrazinyl, NR -pyridyl, NR -pyrazinyl, and the other of R26 and R27 represents a hydrogen atom, and m, A, R1, R2 and R3 are as defined in formula (I), with a source of hydrogen and a hydrogenation catalyst; or
and optionally after (i), (ii), (iii), (iv), (v), (vii), (x), (xi), (xii), (xiii), (xiv), (xv), (xvi), (xx), (xxi), (xxiii), (xxviii) or (xxx), converting the compound of formula (I) to a

further compound of formula (I) and, if desired, forming a pharmaceutically acceptable salt or solvate of the compound of formula
(I),
wherein each of the above process steps is conducted in an organic
solvent of the kind such as herein described and at a temperature of 0
to 200°C.
9. A pharmaceutical composition comprising from 0.1 to 70 %w/w of a compound of formula (I), or a pharmaceutically acceptable salt or solvate thereof, as claimed in any one of claims 1 to 7 in association with a pharmaceutically acceptable adjuvant, diluent or carrier.
10. A process for the preparation of a pharmaceutical composition as claimed in claim 9 which comprises mixing in a manner as herein described, from 0.1 to 70% w/w of the compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof, as defined in any one of claims 1 to 7 with a pharmaceutically acceptable adjuvant, diluent or carrier.
Dated this 01st day of October, 2001.
[DEEPA KACHROO TIKU]
OF REMFRY & SAGAR
ATTORNEY FOR THE APPLICANT[S]

Documents:

in-pct-2001-01201-mum-cancelled pages(19-06-2007).pdf

in-pct-2001-01201-mum-claims(granted)-(19-06-2007).doc

in-pct-2001-01201-mum-claims(granted)-(19-06-2007).pdf

in-pct-2001-01201-mum-correspondence(19-06-2007).pdf

in-pct-2001-01201-mum-correspondence(ipo)-(18-05-2007).pdf

in-pct-2001-01201-mum-form 1(01-10-2001).pdf

in-pct-2001-01201-mum-form 1(28-12-2006).pdf

in-pct-2001-01201-mum-form 19(31-05-2004).pdf

in-pct-2001-01201-mum-form 2(granted)-(19-06-2007).doc

in-pct-2001-01201-mum-form 2(granted)-(19-06-2007).pdf

in-pct-2001-01201-mum-form 3(01-10-2001).pdf

in-pct-2001-01201-mum-form 3(28-12-2006).pdf

in-pct-2001-01201-mum-form 5(01-10-2001).pdf

in-pct-2001-01201-mum-form-pct-ipea-409(01-10-2001).pdf

in-pct-2001-01201-mum-petition under rule 137(28-12-2006).pdf

in-pct-2001-01201-mum-petition under rule 138(28-12-2006).pdf

in-pct-2001-01201-mum-power of authrity(01-10-2001).pdf

in-pct-2001-01201-mum-power of authrity(28-12-2006).pdf

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Patent Number

208867

Indian Patent Application Number

IN/PCT/2001/01201/MUM

PG Journal Number

35/2007

Publication Date

31-Aug-2007

Grant Date

14-Aug-2007

Date of Filing

01-Oct-2001

Name of Patentee

ASTRAZENECA AB

Applicant Address

S-151 85 SODERTALJE, SWEDEN.

Inventors:

#	Inventor's Name	Inventor's Address
1	LILIAN ALCARAZ MARK FURBER	C/O ASTRAZENECA R & D CHARNWOOD, BAKEWELL ROAD, LOUGHBOROUGH, LEICS. LE11 5RH, ENGLAND.
2	MICHAEL MORTIMORE	C/O VERTEX PHARMACEUTICALS, 8 MILTON PARK, ABINGDON, OXFORDSHIRE OX14 4RY, ENGLAND.

PCT International Classification Number

A61K 31/395

PCT International Application Number

PCT/SE00/00663

PCT International Filing date

2000-04-06

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	9901270.0	1999-04-09	U.K.
2	0002330.9	2000-02-01	U.K.