Title of Invention

PIPERIDINE DERIVATIVES USEFUL AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY

Abstract "PIPERIDINE DERIVATIVES USEFUL AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY" The invention provides a compound of formula (I), wherein: T is C(O) or S(O)2; W is C(O) or S(O)2; X is CH2, O or NH; Y is CR5 or N; R1 is optionally substituted aryl or optionally substituted heterocyclyl; R2 is hydrogen or C1-6alkyl; R3 is hydrogen; and R4 is alkyl, optionally substituted aryl, optionally substituted aralkyl or optionally substituted heterocyclyl; that are modulators of chemokine (especially CCR3) activity and are especially useful for treating asthma and/or rhinitis.
Full Text FORM 2
THE PATENTS ACT 1970
[39 OF 1970]
COMPLETE SPECIFICATION
[See Section 10, rule 13]
"PIPERIDINE DERIVATIVES USEFUL AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY"
AstraZeneca AB, a Swedish company of S-151 85 Sodertalje, Sweden,
The following specification particularly describes and ascertain the nature of the invention and the manner in which it is to be performed:-


The present invention concerns piperidine derivatives having pharmaceutical activity, to processes for preparing such derivatives, to pharmaceutical compositions comprising such derivatives and to the use of such derivatives as active therapeutic agents.
Pharmaceutically active piperidine derivatives are disclosed in(W099/38514, WO99/04794 and W'OOO/35877.
Chernokines are chemotactic cytokines that are released by a wide variety of cells to attract macrophages, T cells, eosinophils, basophils and neutrophils to sites of inflammation and also play a role in the maturation of cells of the immune system. Chernokines play an important r61e in immune and inflammatory responses in various diseases and disorders, including asthma and allergic diseases, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis. These small secreted molecules are a growing superfamily of 8-14 kDa proteins characterised by a conserved four cysteine motif. The chemokine superfamily can be divided into two main groups exhibiting characteristic structural motifs, the Cys-X-Cys (C-X-C, or a) and Cys-Cys (C-C, or (3) families. These are distinguished on the basis of a single amino acid insertion between the NH-proximal pair of cysteine residues and sequence similarity.
The C-X-C chernokines include several potent chemoattractants and activators of neutrophils such as interleukin-8 (IL-8) and neutrophil-activating peptide 2 (NAP-2).
The C-C chernokines include potent chemoattractants of monocytes and lymphocytes but not neutrophils such as human monocyte chemotactic proteins 1-3 (MCP-1, MCP-2 and MCP-3), RANTES (Regulated on Activation, Normal T Expressed and Secreted), eotaxin and the macrophage inflammatory proteins lα and 1|3 (MIP-lα and
MIP-1β). .
Studies have demonstrated that the actions of the chernokines are mediated by subfamilies of G protein-coupled receptors, among which are the receptors designated CCR1, CCR2, CCR2A, CCR2B, CCR3, CCR4, CCR5, CCR6, CCR7, CCR8, CCR9, CCR10..CXCR1, CXCR2, CXCR3 and CXCR4. These receptors represent good targets for drug development since agents which modulate these receptors would be useful in the treatment of disorders and 'diseases such as those mentioned above.
Histamine is a basic amine, 2-(4-imidazolyl)-ethylamine, and is formed from histidine by histidine decarboxylase. It is found in most tissues of the body, but is present
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in high concentrations in the lung, skin and in the gastrointestinal tract. At the cellular level inflammatory cells such as mast cells and basophils store large amounts of histamine. It is recognised that the degranulation of mast cells and basophils and the subsequent release of histamine is a fundamental mechanism responsible for the clinical manifestation of an allergic process. Histamine produces its actions by an effect on specific histamine G-protein coupled receptors, which are of three main types, HI, H2 and H3. Histamine HI antagonists comprise the largest class of medications used in the treatment of patients with allergic disorders, especially rhinitis and urticaria. Antagonists of HI are useful in controlling the allergic response by for example blocking the action of histamine on post¬capillary venule smooth muscle, resulting in decreased vascular permeability, exudation and oedema. The antagonists also produce blockade of the actions of histamine on the HI receptors on c-type nociceptive nerve fibres, resulting in decreased itching and sneezing.
Viral infections are known to cause lung inflammation. It has been shown experimentally that the common cold increases mucosal output of eotaxin in the airways. Instillation of eotaxin into the nose can mimic some of the signs and symptoms of a common cold. (See, Greiff L et al Allergy (1999) 54(11) 1204-8 [Experimental common cold increase mucosal output of eotaxin in atopic individuals] and Kawaguchi M et al Int. Arch. Allergy Immunol. (2000) V22 S1 44 [Expression of eotaxin by normal airway epithelial cells after virus A infection].)
The present invention provides a compound of formula (1):

wherein:
TisC(O)orS(O)2;
WisC(O)orS(O)2;
XisCH2,OorNH;
Y is CR5 or N;
R1 is optionally substituted aryl or optionally substituted heterocyclyl;
R2 is hydrogen or C1-6alkyl;
R3 is hydrogen or optionally substituted C1-6 alkyl;
R4 is alkyl, cycloalkyl, optionally substituted aryl, optionally substituted aralkyl or
optionally substituted heterocyclyl;
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R is hydrogen or C1-6 alkyl;
wherein the foregoing aryl and heterocyclyl moieties are optionally substituted by: halogen, cyano, nitro, hydroxy, oxo, S(O)pR25, OC(0)NR6R7, NR8R9, NR10C(O)Rn, NR12C(O)NR13R14, S(0)2NR15R16, NR17S(0)2R18, C(0)NR19R20, C(0)R21, C02R22, NR23CO2R24, C1-6 alkyl, CF3, C1-6 alkoxy(CI.6)alkyl, C1-6 alkoxy, OCF3, C1-6 alkoxy(C1-6)alkoxy (preferably not forming an acetal), C1-6 alkylthio, C2-6 alkenyl, C2-6 alkynyl, C3-10 cycloalkyl (itself optionally substituted by C1-4 alkyl or oxo), methylenedioxy, difluoromethylenedioxy, phenyl, phenyl(C1-4)alkyl, phenoxy, phenylthio, phenyl(C1. 4)alkoxy, heteroaryl, heteroaryl(C1-4)alkyl, heteroaryloxy or heteroaryl(C1-4)alkoxy; wherein any of the immediately foregoing phenyl and heteroaryl moieties are optionally substituted with halogen, hydroxy, nitro, S(O)q(C1-4 alkyl), S(O)2NH2, cyano, C1-4 alkyl, CM alkoxy, C(0)NH2, C(O)NH(CM alkyl), C02H, C02(CM alkyl), NHC(0)(CM alkyl). NHS(O)2(C1-4 alkyl), C(O)(C1-4 alkyl), CF3 or OCF3; p and q are, independently, 0,1 or 2;
R6, R7,R8, R9, R10, R11, R12, R13, R14, R15, R16, R17,R19, R20, R21, R22, and R23 are, independently, hydrogen, C1-6 alkyl (optionally substituted by halogen, hydroxy or C3.10 cycloalkyl), CH2(C2-6 alkenyl), phenyl (itself optionally substituted by halogen, hydroxy, nitro, NH2j NH(CM alkyl), N(C1-4 alkyl)2, S(O)2(C1-4 alkyl), S(0)2NH2, S(O)2NH(C1-4 alkyl), S(O)2N(C1-4 alkyl)2, cyano, C1-4 alkyl, C1-4 alkoxy, C(O)NH2, C(0)NH(C1-4 alkyl), CO2H, CO2(Cw alkyl), NHC(O)(C1-4 alkyl), NHS(O)2(C1-4 alkyl), C(O)(C1-4 alkyl), CF3 or OCF3) or heterocyclyl (itself optionally substituted by halogen, hydroxy, nitro, NH2, NH(C1-4 alkyl), N(C1-4 alkyl)2, S(O)2(C1-4 alkyl), S(O)2NH2, S(O)2NH(C1-4 alkyl), S(O)2N(C1-4 alkyl)2, cyano, C1-4 alkyl, C1-4 alkoxy, C(O)NH2, C(O)NH(C1-4 alkyl), C(O)N(Cw alkyl)2, CO2H, C02(C1-4 alkyl), NHC(0)(C1-4 alkyl), NHS(O)2(C1-4 alkyl), C(O)(C1-4 alkyl), CF3 or OCF3);
alternatively NR6R7, NR8R9, NR13R14, NRI5R16, NR19R20 or N(C1-4 alkyl)2 may, independently, form a 4-7 membered heterocyclic ring, azetidine, pyrrolidine, piperidine, azepine, 1,4-morpholine or 1,4-piperazine, the latter optionally substituted by C1-4alkyl on the distal nitrogen;
R25, R18 and R24 are, independently, C1-6 alkyl (optionally substituted by halogen, hydroxy or C3.10 cycloalkyl), CH2(C2-6 alkenyl), phenyl (itself optionally substituted by halogen, hydroxy, nitro, NH2, NH(C1-4 alkyl), N(C1-4 alkyl)2 (and these alkyl groups may join to form a ring as described for R6 and R7 above), S(O)2(C1-4 alkyl), S(O)2NH2, S(O)2NH(C1-4
4

alkyl), S(O)N(C1-4 alkyl)2 (and these alkyl groups may join to form a ring as described for R6 and R7 above), cyano, C1-4 alkyl, C1-4 alkoxy, C(0)NH2, C(0)NH(C1-4 alkyl), C(0)N(Ci^ alkyl)2 (and these alkyl groups may join to form a ring as described for R6 and R7 above), CO2H, CO2(C1-4 alkyl), NHC(0)(C1-4 alkyl), NHS(O)2(C1-4 alkyl), C(O)(C1-4 alkyl), CF3 or OCF3) or heterocyclyl (itself optionally substituted by halogen, hydroxy,, nitro, NH2, NH(C1-4 alkyl), N(C1-4 alkyl)2 (and these alkyl groups may join to form a ring as described for R6 and R7 above), S(O)2(C1-4 alkyl), S(O)2NH2, S(O)2NH(C1-4 alkyl), S(O)2N(C1-4 alkyl)2 (and these alkyl groups may join to form a ring as described for R6 and R7 above), cyano, C1-4 alkyl, C1-4 alkoxy, C(O)NH2, C(O)NH(C1-4 alkyl), C(0)N(C1-4 alkyl)2 (and these alkyl groups may join to form a ring as described for R6 and R7 above), C02H, CO2(C1-4 alkyl), NHC(0)(C1-4 alkyl), NHS(O)2(C1-4 alkyl), C(0)(C1-4 alkyl), CF3 or OCF3); or an N-oxide thereof; or a pharmaceutically acceptable salt thereof; or a solvate thereof.
Certain compounds of the present invention can exist in different isomeric forms (such as enantiomers, diastereomers, geometric isomers or tautomers). The present invention covers all such isomers and mixtures thereof in all proportions.
Suitable salts include acid addition salts such as a hydrochloride, dihydrochloride, hydrobromide, phosphate, sulfate, acetate, diacetate, fumarate, maleate, tartrate, citrate, oxalate, methanesulfonate or p-toluenesulfonate. Salts also include metal salts, such as alkali metal salts (for example a sodium salt).
The compounds of the invention may exist as solvates (such as hydrates) and the present invention covers all such solvates.
Halogen includes fluorine, chlorine, bromine and iodine.
Alkyl groups and moieties (including those of alkoxy) are straight or branched chain and are, for example, methyl, ethyl, n-propyl, 1-methylethyl or 1,1-dimethylethyl.
Alkenyl is, for example, vinyl or allyl.
Alkynyl is, for example, propargyl.
Cycloalkyl is mono-, bi or tricyclic and is, for example, cyclopropyl, cyclopentyl, cyclohexyl, norbornyl or camphoryl. The cycloalkyl ring is optionally fused to a benzene ring (for example forming a bicyclo[4.2.0]octa-l,3,5-trienyl or indanyl ring system).
Haloalkyl is preferably CF3. Haloalkoxy is preferably OCF3.
Aryl is preferably phenyl or naphthyl.
ArylalkyI is preferably aryl(Ci_4 alkyl) for example benzyl or 2-phenyleth-l-yI.
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Heterocyclyl is an aromatic or non-aromatic 5 or 6 membered ring, optionally fused to one or more other rings, comprising at least one heteroatom selected from the group comprising nitrogen, oxygen and sulfur; or an N-oxide thereof, or an S-oxide or S-dioxide thereof. Heterocyclyl is, for example, furyl, thienyl (also known as thiophenyl), pyrrolyl, 2,5-dihydropyrrolyl, thiazolyl, pyrazolyl, oxazolyl, isoxazolyl, imidazolyl, piperidinyl, morpholinyl, pyridinyl (for example in 6-oxo-l,6-dihydro-pyridinyl), pyrimidinyl, indolyl, 2,3-dihydroindolyl, benzofbjfuryl (also known as benzfuryl), benz[b]thienyl (also known as benzthienyl or benzthiophenyl), 2,3-dihydrobenz[bJthienyl (for example in 1,1-dioxo-2,3-dihydrobenz[b]thienyl), indazolyl, benzimidazolyl, benztriazolyl, benzoxazolyl, benzthiazolyl (for example in lH-benzthiazoi-2-one-yl), 2,3-dihydrobenzthiazolyl (for example in 2,3-dihydrobenzthiazol-2-one-yl), 1,2,3-benzothiadiazolyl, an imidazopyridinyl (such as imidazo[l,2a]pyridinyl), thieno[3,2-b]pyridin-6-yl 1,2,3-benzoxadiazolyI (also known as benzo[l,2,3]thiadiazolyl), 2,1,3-benzothiadiazolyl, benzofurazan (also known as 2,1,3-benzoxadiazolyl), quinoxalinyl, dihydro-1-benzopyryliumyl (for example in a coumarinyl or a chxomonyl), 3,4-dmydro-lH-2,l-benzothiazinyl (for example in 2-dioxo-3,4-dihydro-lH-2,l-benzothia2inyl), apyrazolopyridine (for example lH-pyrazolo[3,4-bjpyridinyl), a purine (for example in 3,7-dihydro-purin~2,6-dione-8-yl), quinolinyl, isoquinolinyl (for example in 2H4soquinolin-l-one-yl), a naphthyridinyl (for example [l,6]naphthyridinyl or [l,8]naphthyridinyl or in lH-[l,8]naphthyridin-4-one-yl), a benzothiazinyl (for example in 4H-benzo[l,4]thiazin-3-one-yl), benzo[d]imidazo[2,l-b]thiazol-2-yl or dibenzo.thiophenyl (also known as dibenzothienyl); or an N-oxide thereof (such as a pyridine N-oxide), or an S-oxide or S-dioxide thereof.
An N-oxide of a compound of formula (I) is, for example, a 1-oxido-[ 1,4']bipiperidinyl-1' -y 1 compound.
In one particular aspect the present invention provides a compound of formula (I) wherein: T is C(O) or S(O)2; W is C(O) or S(0)2; X is CH2, O or NH; Y is CR5 or N; R1 is optionally substituted aryl or optionally substituted heterocyclyl; R2 is hydrogen or C1-6 alkyl; R3 is hydrogen or optionally substituted C1-4 alkyl;R4 is alkyl, optionally substituted aryl, optionally substituted aralkyl or optionally substituted heterocyclyl; R5 is hydrogen or C1-6 alkyl; wherein the foregoing aryl and heterocyclyl moieties are optionally substituted by: halogen, cyano, nitro, hydroxy, oxo, S(O)pR25, OC(O)NR6R7, NR8R9, NR10C(O)RH, NR12C(0)NR13R14, S(O)2NR15R16, NR17S(O)2R18, C(O)NR19R20, C(0)R21, CO2R22, NR23CO2R24, C1-6 alkyl, C1-6 haloalkyl, C1-4 alkoxy(C1-6)alkyl, C1-4 alkoxy, C1-4
6

haloalkoxy, C1-6 alkoxy(C1-6)alkoxy1 C1-6 alkylthio, C1-6 haloalkylthio, C2-6 alkenyl, C2-6 alkynyl, C3-10 cycloalkyl (itself optionally substituted by C1-4 alkyl or oxo), methylenedioxy, difluoromethylenedioxy, phenyl, phenyl(C1-4)alkyl, phenoxy, phenylthio, pheny(C1-4)alkoxy, heteroaryl, heteroaryl(C1-4)alkyl, heteroaryloxy or heteroaryl(C1-4)alkoxy; wherein any of the immediately foregoing phenyl and heteroaryl moieties are optionally substituted with halogen, hydroxy, nitro, S(O)q(C1-4 alkyl), S(O)2NH2, cyano, C1-4 alkyl, C1-4 alkoxy, C(O)NH2, C(O)NH(C1-4 alkyl), CO2H, CO2(C1-4 alkyl), -NHC(0)(C-4 alkyl), NHS(O)2(C1-4 alkyl), C(0)(C1-4 alkyl), CF3 or 0CF3; p and q are, independently, 0, 1 or 2; R6, R7, R8, R9, R10, R11, R12,.R13, R14, R15, R16, R17, R19, R20, R21, R22, and R23 are, independently, hydrogen, C1-6 alkyl (optionally substituted by halogen, hydroxy or C3.10 cycloalkyl), CH2(C2-6 alkenyl), phenyl (itself optionally substituted by halogen, hydroxy, nitro, NH2, NH(C1-4 alkyl), NH(C1-4 alkyl)2, S(O)2(C1-4 alkyl), S(O)2NH2, cyano, C1-4 alkyl, C1-4 alkoxy, C(O)NH2, C(0)NH(C1-4 alkyl), CO2H, CO2(C1-4 alkyl), NHC(0)(CM alkyl), NHS(O)2(C1-4 alkyl), C(0)(C1-4 alkyl), CF3 or OCF3) or heterocyclyl (itself optionally substituted by halogen, hydroxy, nitro, NH2, NH(Q.4 alkyl), N(C1-4 alkyl)2, S(O)2(C1-4 alkyl), S(O)2NH2, S(O)2NH(C1-4 alkyl), S(O)2N(C1-4 alkyl)2, cyano, C1-4 alkyl, C1-4 alkoxy, C(0)NH2, C(O)NH(CM alkyl), C(O)N(C1-4 alkyl)2, CO2H, C02(CM alkyl), NHC(0)(CM alkyl), NHS(0)2(CM alkyl), C(0)(CM alkyl), CF3 or OCF3); alternatively NR6R7, NR8R9, NR13R14, NR15R16, NR^R20, may, independently, form a 4-7 membered heterocyclic ring, azetidine, pyrrolidine, piperidine, azepine, 1,4-morpholine or 1,4-piperazine, the latter optionally substituted by C1-4 alkyl on the distal nitrogen; R25, R18 and R24 are, independently, C1-6 alkyl (optionally substituted by halogen, hydroxy or C3-10 cycloalkyl), CH2(C2-6 alkenyl), phenyl (itself optionally substituted by halogen, hydroxy, nitro, NH2, NH(CM alkyl), N(CM alkyl)2 (and these alkyl groups may join to form a ring as described for R6 and R7 above), S(0)2(CM alkyl), S(0)2NH2) S(O)2NH(C1-4 alkyl), S(O)2N(C1-4 alkyl)2 (and these alkyl groups may join to form a ring as described for R6 and R7 above), cyano, C1-4 alkyl, C1-4 alkoxy, C(0)NH2, C(O)NH(CM alkyl), C(O)N(CM alkyl)2 (and these alkyl groups may join to form'a ring as described for R6 and R7 above), CO2H, CO2(C1-4 alkyl), NHC(0)(C1-4 alkyl), NHS(O)2(C1-4 alkyl), C(O)(C1-4 alkyl), CF3 or OCF3) or heterocyclyl (itself optionally substituted by halogen, hydroxy, nitro, NH2, NH(C1-4 alkyl), N(C1-4 alkyl)2 (and these alkyl groups may join to form a ring as described forR6 and R7 above), S(O)2(C1-4 alkyl), S(O)2NH2, S(O)2NH(C1-4 alkyl), S(O)2N(C1-4 alkyl)2 (and these alkyl groups may join to form a ring as described for
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R6 and R7 above), cyano, C1-4 alkyl, C1-4 alkoxy, C(O)NH2, C(0)NH(C1-4 alkyl), C(O)N(C+ alkyl)2 (and these alkyl groups may join to for1-4 a ring as described for R6 and R7 above), C02H, C02(C1-4 alkyl), NHC(0)(C1-4 alkyl), NHS(0)2(C1-4 alkyl), C(0)(C1-4 alkyl), CF3 or OCF3); or an N-oxide thereof; or a phar1-4aceutically acceptable salt thereof; or a solvate thereof.
In a further aspect X is O.
In another aspect R1 is phenyl substituted with one or 1-4ore of fluorine, chlorine, C1-4 alkyl (especially 1-4ethyl) or C1-4alkoxy (especially 1-4ethoxy).
In a further aspect R1 is phenyl optionally substituted (for exa1-4ple with one, two or three of) by halogen (especially fluoro or chloro), C1-4 alkyl (especially 1-4ethyl) or C1-4 alkoxy. (especially 1-4ethoxy). In a still further aspect R1 is phenyl substituted by one, two or three of: fluoro, chloro, 1-4ethyl or 1-4ethoxy. In another aspect R1 is phenyl optionally substituted by halogen (especially fluoro or chloro), C1-4 alkyl (especially 1-4ethyl); especially optionally substituted (for exa1-4ple independently with one, two or three of, especially two or three of) by fluoro, chloro or 1-4ethyl. In a still further aspect R1 is 3,4-dichlorophenyl, or, additionally 2-chloro-4-fluorophenyl, 2-1-4ethyl-4-chlorophenyl, 2,4-dichloro-3-1-4ethylphenyl or 3,4-dichloro-2-1-4ethylphenyl.
In another aspect one of T and W is C(O) and the other is S(0)2. In a still further aspect T is C(O). In another aspect W is S(0)2.
In yet another aspect of the invention, and when Y is CR5, the co1-4pounds of for1-4ula (I) are preferably trans in ter1-4s of relative stereoche1-4istry, that is, the piperidine ring and the T-N(R3)-W-R4 group are both equatorial on the cyclohexane ring. In a still further aspect of the invention Y is CH or N; especially N. In yet another aspect R" is hydrogen or 1-4ethyl; for exa1-4ple R is hydrogen. In a further aspect R3 is hydrogen or 1-4ethyl; for exa1-4ple hydrogen. In a still further aspect R4 is unsubstituted phenyl, 1-4ono-substituted phenyl, unsubstituted heterocyclyl or 1-4ono-substituted heterocyclyl, the substituents being chosen fro1-4 those described above.
In a further aspect the present 1-4ention provides a co1-4pound of for1-4ula (I) wherein R4 is aryl (for exa1-4ple phenyl or naphthyl; especially phenyl) optionally substituted by one or 1-4ore of C1-6 alkyl (for exa1-4ple 1-4ethyl or ethyl),'C1-4 alkoxy (for exa1-4ple 1-4ethoxy), halogen (for exa1-4ple chloro or fluoro), CF3, CN, CO2(C1-4 alkyl) (for exa1-4ple CO2CH3),
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OH, OCF3) S(0)2(C1-4 alkyl) (for exa1-4ple S(O)2CH3) or NR8R9 (wherein R8 and R9 are, independently, hydrogen or C1-4 alkyl); or heterocyclyl (for exa1-4ple i1-4idazolyl, thienyl, tetrahydrothienyl, thiazolyl, 1,3,4-thiadiazolyl, pyridyl or dihydroisoquinoiinyl) optionally substituted by oxo, halogen (for exa1-4ple chloro or fluoro), C1-4 alkyl (for exa1-4ple 1-4ethyl), NRSR9 (wherein-R8 and R9 are, independently, hydrogen or C1-4 alkyl), piperidinyl or 1-4orpholinyl. 1-4 another aspect R4 is phenyl optionally substituted by one or 1-4ore of C1-6 alkyl (for exa1-4ple 1-4ethyl or ethyl), C1-4 alkoxy (for exa1-4ple 1-4ethoxy), halogen (for exa1-4ple chloro or fluoro), CF3, CN, CO2(C1-4 alkyl) (for exa1-4ple CO2CH3), OH, 0CF3, S(O)2(C+ alkyl) (for exa1-4ple S(O)2CH3) or NR8R9 (wherein R8 and R9 are, independently, hydrogen or C1-4 alkyl).
In a further aspect of the invention R4 is substituted (especially 1-4ono-substituted) phenyl, the substituents being chosen fro1-4 those described above.
In a still further aspect R4 is phenyl or heterocyclyl, either of which is optionally substituted by: halo, hydroxy, nitro, cyano, oxo, a1-4ino, C1-4 alkyl (itself optionally substituted by S(O)2(C1-4 alkyl), S(O)2phenyl), C1-4 alkoxy, S(0)tR26 (wherein k is 0,1 or 2 (preferably 2); and R26 is C1-4 alkyl, C1-4 hydroxyalkyl, C3.7 cycloalkyl(C1-4 alkyl) (such as cyclopropyl1-4ethyl) or phenyl), C1-4 haloalkylthio, C(0)NH2, NHS(0)2(C1-4 alkyl), S(O)2NH2, S(0)2NH(C1-4 alkyl) or S(O)2N(C1-4 alkyl)2.
In yet another aspect R4 is phenyl or heterocyclyl, either of which is optionally substituted by: halo, hydroxy, nitro, cyano, oxo, NR8R9 (wherein R8 and R9 are, independently, hydrogen or C1-6 alkyl), C1-4 alkyl (itself optionally substituted by S(0)2(C1. 4 alkyl), S(O)2phenyl), C1-4 alkoxy, S(O)kR26 (wherein k is 0, I or 2 (preferably 2); and R26 is C1-4 alkyl, C1-4 hydroxyalkyl, C3-7 cycloalkyl(C1-4 alkyl) (such as cyclopropyl1-4ethyl) or phenyl), C1-4 haloalkylthio, C(O)NH2, NHS(0)2(C1-4 alkyl), S(O)2NH2, S(0)2NH(C1-4 alkyl) or S(0)2N(C1-4 alkyl)2.
In one aspect the variable R4 is phenyl optionally substituted by: halo, hydroxy, nitro, cyano, a1-4ino, C1-4 alkyl (itself optionally substituted by S(O)2(C1-4 alkyl), S(0)2phenyl), C1-4 alkoxy, S(O)kR26 (wherein k is 0, 1 or 2 (preferably 2); and R26 is C1-4 alkyl, C1-4 hydroxyalkyl, C3-7 cycloalkyl(C1-4 alkyl) (such as cyclopropylmethyl) or phenyl), C1-4 haloalkylthio, C(O)NH2, NHS(0)2(C1-4 alkyl), S(0)2NH2, S(0)2NH(C1-4 alkyl) or S(O)2N(C1-4 alkyl)2 (and these alkyl groups 1-4ay join to form a ring as described for R6 and R7 above).
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In another aspect tne variable R4 is phenyl optionally substituted by: halo, hydroxy, nitro, cyano, NR8R9 (wherein R8 and R9 are, independently, hydrogen .or C1-6 alkyl), C1-4 alkyl (itself optionally substituted by S(0)2(C1-4 alkyl), S(0)2phenyl), C1-4 alkoxy, S(0)kR26 (wherein k is 0, 1 or 2 (preferably 2); and R26 is C1-4 alkyl, C1-4 hydroxyalkyl, C3. 7 cycloalkyl(C1-4 alkyl) (such as cyclopropylmethyl) or phenyl), C1-4 haloalkylthio, C(0)NH2, NHS(0)2(C1-4 alkyl), S(O)2NH2, S(O)2NH(C1-4 alkyl) or S(O)2N(C1-4 alkyl)2
ft 1
(and these alkyl groups may join to form a ring as described for R and R7 above).
In another aspect the variable R is phenyl optionally substituted by: halo, hydroxy, nitro, cyano, amino, C1-4 alkyl (itself optionally substituted by S(0)2phenyl), C1-4 alkoxy, S(O)kR26 (wherein k is 0,1 or 2; and R26 is C1-4 alkyl or phenyl) or C1-4 haloalkylthio.
In a further aspect the variable R4 is phenyl optionally substituted by: halo, hydroxy, nitro, cyano, NR8R9 (wherein R8 and R9 are, independently, hydrogen or C1-4 alkyl), C1-4 alkyl (itself optionally substituted by S(O)2phenyl), C1-4 alkoxy, S(O)kR25 (wherein k is 0,1 or 2; and R26 is C1-4 alkyl or phenyl) or C1-4 haloalkylthio.
The amine group NR8R9 is, for example, mono-(C1-4) alkylamino (such as NHCH3 or NHCH2CH3) or di-(C1-4) alkylamino (such as N(CH3)2).
In yet another aspect of the invention R4 is phenyl mono-substituted with halogen (for example fluorine or chlorine), C1-4 alkyl (for example methyl or ethyl), C1-4 alkoxy (for example methoxy or ethoxy) or NR8R9 (wherein R8 and R9 are, independently, hydrogen or C1-6 alkyl; and NR8R9 is especially NHCH3, NHCH2CH3 or N(CH3)2).
In a further aspect R4 is phenyl substituted with halogen, alkyl or alkoxy.
In a still further aspect of the invention R4 is phenyl mono-substituted with halogen (especially chlorine) or C1-4 alkyl (especially methyl).
In yet another aspect R5 is hydrogen.
In another aspect the present invention provides a pharmaceutically acceptable salt of a compound of formula (I), for example a metal salt {such as an alkali metal salt (for example the sodium salt)} of a compound of formula (I).
Compounds of formula (la), (lb), (Ic), (Id), (Ie), (If), (Ig) and (lb.) are examples of compounds of formula (I).
In a still further aspect the present invention provides a compound of formula (la):


wherein: X, R1, R2, R3 and R4 are as defined above; or a pharmaceutically acceptable salt thereof.
In a still further aspect the present invention provides a compound of formula (lb):

wherein: X, R1, R2, R3 and R4 are as defined above; or a pharmaceutically acceptable salt thereof.
In a still further aspect the present invention provides a compound of formula (Ic):

wherein: X, R1, R2, R3, R4 and R5 are as defined above; or a pharmaceutically acceptable salt thereof. In another aspect the compounds of formula (Ic) are preferably trans in terms of relative stereochemistry, that is, the piperidine ring and the C(O)N(R3)S(0)2R4 group axe both equatorial on the cyclohexane ring.
In a still further aspect the present invention provides a compound of formula (Id):

wherein: X, Rl, R~, R3 and R4 are as defined above; or a pharmaceutically acceptable salt thereof.
In a still further aspect the present invention provides a compound of formula (Ie):

wherein: X, R , R2, R3 and R4 are as defined above; or a pharmaceutically acceptable salt thereof.
In a still further aspect the present invention provides a compound of formula (If):
-14


(If)

wherein: X, R1, R2, R3, R4 and R5 are as defined above; or a phar1-4aceutically acceptable salt thereof. In another aspect the compounds of for1-4ula (If) are preferably trans in ter1-4s of relative stereoche1-4istry, that is, the piperidine ring and the S(0)2N(R3)C(O)R4 group are both equatorial on the cyclohexane ring.
In a still further aspect the present invention provides a compound of for1-4ula (Ig):




wherein: X, R1, R2, R , R and R5are as defined above: or a pharmaceutically acceptable salt thereof. In another aspect the compounds of formula (Ig) are preferably trans in terms of relative stereochemistry, that is, the piperidine ring and the C(0)N(R2)C(0)R4 group are both equatorial on the cyclohexane ring.
In a still further aspect the present invention provides a compound of formula (Ih):

wherein: X, R1, R2, R3, R4 and R5 are as defined above; or a pharmaceutically acceptable salt thereof. In another aspect the compounds of formula (Ih) are preferably trans in terms of relative stereochemistry, that is the piperidine ring and the S(O)2N(R3)S(0)2R4 group are both equatorial on the cyclohexane ring.
A compound of formula (la) is, for example: N-[[4-(2-Chloro-4-fluorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-4-methyl-benzenesulfonamide;
N-[[4-(2-Chloro^-fluorophenoxy)[l,4-bipiperidmj-l'-yllcarbonylJ^-methyl-benzenesulfonamide;
4-Chloro-N-[[4-(2-chloro-4-fluorophenoxy) [ 1,4-bipiperidin] -1 '-yljcarbonyl]-benzenesulfonamide;
12

2-Chloro-iV-[[4-(2-chloro-4-fluorophenoxy)[l14'-bipiperid1-4]-l'-yI]carbonyl]-
benzenesulfona1-4ide;
N-[[4-(2-ChIoro-4-fluorophenoxy)[ 1,4'-bipiperidin]-1 '-yl]carbonyl]-4-fluoro-
benzenesulfona1-4ide;
N-[[4-(2-CWoro-4-fluorophenoxy)[lJ4'-bipiperidin]-r-yl]carbonyl]-benzenesulfonainide;
N-[[4-(4-Chloro-2-1-4ethylphenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-2-1-4ethyl-
benzenesulfona1-4ide;
4-Chloro-iV-[[4-(4-chloro-2-1-4ethylpb.enoxy)[l,4,-bipiperidin]-r-yl]carbonyI]-
benzenesulfona1-4ide; 2-Chloro-N-[[4-(4-chloro-2-1-4ethylphenoxy)[l,4-bipiperidin]-r~yl]carbonyl]-
benzenesuifona1-4ide;
N-[{4-(4-Choro-2-1-4ethyIphenoxy) [1,4'-bipiperidin]-1 '-yl]carbonyl]-4-fiuoro-
benzenesulfona1-4ide;
N- [[4-(4-Chloro-2-1-4ethylphenoxy)[ 1 ^-bipiperidin] -1-yl]carbonyl]-4-1-4ethyl-
benzenesulfona1-4ide;
N-[[4-4-Chloro-2-1-4ethylpheuoxy)[l,4,-bipiperidin]-1-yl]carbonyl]-benzenesulfona1-4ide;
N-[[4-(2,4-Dichoro-3-1-4ethylphenoxy)[l,4'-bipiperidin]-l'-yl]carbonyl]-2-1-4ethyl-
benzenesulfona1-4ide; N-[[4-(2,4-Dic1-4oro-3-1-4ethylphenoxy)[l,4'-bipiperidin]-l'-yl]carbonyl]-4-1-4ethyl-
benzenesulfona1-4ide;
2-Chloro-iV- [[4-(2,4-dichloro-3-1-4ethylplienoxy) [ 1,4'-bipiperidiii]-1 '-yljcarbonyl]-
benzenesulfona1-4ide;
4-Chloro-Ar-[[4-(2,4-dichloro-3-1-4ethylphenoxy)[l,4,-bipiperidin]-l'-yl]carbonyl]-
benzenesulfona1-4ide; N-[[4-(2,4-Dichloro-3-1-4ethylphenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-4-fluoro-
benzenesulfona1-4ide;
N-[[4-(2,4-DicbIoro-3-1-4ethylphenoxy)[l,4'-bipiperidin]-l'-yi]carbonyl]-
benzenesulfona1-4ide;
N-[[4-(3,4-Dichloro-2-1-4ethylphenoxy)[l,4'-bipiperidin]-1 '-yl]carbonyl]-2-1-4ethyl-
benzenesnlfona1-4ide;
N-[[4-(3,4-Dichloro-2-1-4ethylphenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-4-1-4ethyl-
benzenesulfonamide;
-IS-

2-Chloro-N-[[4-(3,4-dichloro-2-1-4ethylphenoxy)[l,4,-bipiperidin]-1-yl]carbonyl]-
benzenesulfona1-4ide;
4-Chloro-N'-[[4-(3,4-dichloro-2-methylphenoxy)[l34,-bipiperidin]-1-yl]carbonyl]-
benzenesulfona1-4ide;
N-[[4-(3,4-Dichloro-2-methylphenoxy)[l,4'-bipiperid1-4]-l-yl]carbonyl]-4-fluoro-
benzenesulfona1-4ide;
N-[[4-(3,4-Dichloro-2-methylphenoxy)[l,4,-bipiperidin]-l-yl]carbonyl]-
benzenesulfona1-4ide;
N-[[4-(3,4-Dichlorophenoxy)-4'-methyl[lJ4,-bipiperidin]-l-yl]carbonyl]-4-1-4ethyl-
benzenesulfona1-4ide;
N-[[4-(3,4-Dichlorophenoxy)-4,-1-4ethyl[l,4,-bipiperidin]-r-yl3caibonyl]-4-fluoro-
benzenesulfona1-4ide;
N[[4-(3,4-Dich]orophenoxy)-4-methyl[l,4'-bipiperidin]-l-yl]carbonyl]-2-niethyl-
benzenesulfona1-4ide;
4-Chloro-Ar-[[4-(3,4-dichloropb.enoxy)-4'-1-4ethyl[l,4'-bipiperidin]-r-yl]carbonyl]-
benzenesulfona1-4ide;
2-Chloro-N-[[4'(3,4-dichlorophenoxy)-4-methyl[l,4'-bipiperidin]-l-yl]carbonyl]-
benzenesulfona1-4ide;
N-[[4-(3,4-DichIorophenoxy)-4'metliyl[l,4'-bipiperidin]-l-yl]carbonyl]-3-trifIuoromethyl-
benzenesulfonamide;
3-Cyano-N-[[4-3,4-diclilorophenoxy)-4,-methyl[l,4,-bipiperidin]-r-yl]carbonyl]-
benzenesulfona1-4ide;
N-[[4-(3,4-Dichlorophenoxy)[ 1,4'-bipiperidin]-1 '-yljcarbonyl]j-
benzenemethanesulfona1-4ide;
N-[[4-(3,4-Dichlorophenqxy) [ 1,4-bipiperidin]-1 '-yljcarbonylj- 1-4ethanesulfona1-4ide;
N-[[4-(4-Chloro-3-methylphenoxy)[l,4'-bipiperidinj-l-yljcarbonyl]-2-methyl-
benzenesulfonamide;
N-[[4-(4-Chloro-3-1-4ethylphenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-4-methyl-
benzenesulfonamide;
4-Chloro-N-[[4-(4-chloro-3-1-4ethylphenoxy)[l,4,-bipiperidinj-l-yljcarbonyl]-
benzenesulfona1-4ide;
N-[[4-(3,4-Dichlorophenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-N,4-di1-4ethyl-
benzenesulfona1-4ide;
14

N-[[4-[(S^Dichlorophenyl]methyl][1,4'-bipiperidm]-1'-yl]carbony]-4-methy]-
benzenesulfona1-4ide;
4-Chloro-N-[[4-[(3,4-dic1-4orophenyl)1-4ethyl] [1,4'-bipiperidin]-l '-yl]carbonyl]-
benzenesulfona1-4ide;
N-[[4-[(3,4-Dicblorophenyl)amino] [ 1,4'-bipiperidin]-r-yl]carbonyl]-4-methyI-
benzenesulfonamide;
4-Chloro-N-[[4-(3,4-dicblorophenoxy)[l,4'-bipiperidin3-l-yl]carbonyl]-
benzenesulfonamide; . ,
N-[[4-(3,4-Dichlorophenoxy)[ 1,4' -bipiperidin]-l' -yl]carbonyl]-4-1-4ethyl]-
benzenesulfona1-4ide;
N-[[4-(3,4-Dichlorophenoxy)[1,4'-bipiperidin]-l-yl]carbonyl]-2-methyl-
benzenesulfona1-4ide;
3-Bromo-N-[[4-(3J4-dichlorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-.benzenesulfona1-4ide;
4-Bro1-4o-N-[[4-(3,4-dichlorophenoxy)[ 1,4' -bipiperidin]-1' -yl]carbonyl]-
benzenesulfonamide;
3,5-Dichloro-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-
benzenesulfona1-4ide;
3-Cyano-N- [ [4-(3,4-dichlorophenoxy) [1,4' -bipiperidin] -1' -yl]carbonyl] -
benzenesulfona1-4ide;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperid1-4]-l-yl]carbonyl]-2,5-dimethoxy-
benzenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy) [ 1,4' -bipiperidin]-1 '-yl]carbonyl]-3,4-di1-4ethoxy-
benzenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)[ 1,4' -bipiperidin]-1' -yl]carbonyl]-4-(3,3-di1-4ethyl-2-oxo-l -
azetidinyi)-benzenesulfonanude;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidin]-l'-yl]carbonyl]-4-(4,5-dihydro-3-niethyl-5-
oxo- lH-pyrazoI-1 -yl)-benzenesulfona1-4ide;
N-[[4-(3,4-Dichlorophenoxy) [ 1,4'-bipiperidin]-1'-yl]carbonyl]-3-(4,5-dihydro-3-1-4ethyl-5-
oxo-lH-pyrazol-l-yl)-benzenesulfona1-4ide;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperid1-4]-r-yl]carbonyl]-4-hydroxy-
benzenesulfonamide;

N-[[4-(3,4-DicbJorophenoxy)[l,4'-bipiperid1-4]-l'-yI]carbonyl]-3-(trifluoromethyl)-
benzenesulfona1-4ide;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperid1-4]-l-yl]carbonyl]-benzenesulfona1-4ide;
N-[[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]a1-4ino]sulfonyl]-benzoic
acid, 1-4ethyl ester;
2-Bromo-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]- '
benzenesulfonamide;
N-[5-[[[[4-(3,4-DichIorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]amino]sulfonyl]-l,3,4-
thiadiazol-2-yl]-acetamide;
N-[[4-(3,4-Dichlorophenoxy)[ 1,4' -bipiperidin]-1' -yl]carbonyI]-5-(dimethylamino)-1 -
naphthalenesulfona1-4ide;
N-[[4-(3,4-Dichlorophenoxy)[l ,4'-bipiperidin]-1 '-yl]carbonyl]-2-naphthaIenesulfona1-4ide;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2,4-di1-4ethyl-5"
thiazolesulfona1-4ide;
N-[[4-(3,4-Dichlorophenoxy) [ 1,4' -bipiperidin]-1' -yl]carbonyl]-2-( 1 -piperidinyl)-3-
pyridinesulfona1-4ide;
5-Chloro-N-[[4-(3)4-dichlorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-2-
thiophenesulfona1-4ide;
5-Bromo-N-[[4-(3,4-dichlorophenoxy)[l ,4' -bipiperidin]-l-yl]carbonyl]-2-
thiophenesulfona1-4ide;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidin]-l-yI]carbonyl]tetrabydro-3-
thiophenesulfonamide; 1,1 -dioxide 4,5-Dichloro-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidm]-l-yl]carbonyl]-2-
thiophenesulfona1-4ide;
4-Chloro-N-[[4-(3Adichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2,5-dimethyl-
benzenesulfona1-4ide;
4-n-Butyl-N-[[4-(3,4-dichlorophenoxy)[ 1,4' -bipiperidin]-1' -yl]carbonyl]-
benzenesulfonamide;
2,5-Dichloro-N-[[4-(3,4-dichlorophenoxy)[l]4'-bipiperid1-4]-l'-yl]carbonyl]-3-
thiophenesulfona1mide;
4-n-Butoxy-N-[[4-(3,4-dichlorophenoxy)[ 1,4' -bipiperidin]-I-yl]carbonyl]-
benzenesulfonamide;

N-[[4-{3J4-Dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2-(trifluoro1-4ethoxy)-
benzenesulfona1-4ide;
N-[[4-(3,4-Dichlorophenoxy)[ 1,4'-bipiperidin] -1'-yljcarbonyl]-1-methyl-1 H-i1-4idazole-4-
sulfonamide;
5-Amino-N-[[4-(3,4-dic1-4orophenoxy)[l,4'-bipiperidin]-l'-yl]carbonyl]-l,3,4-thiadiazole-
2-sulfonamide;
4-Bromo-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-2-
thiophenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy) [ 1,4' -bipiperidin]-1' -yl]carbonyl]-2-(4-morpholinyl)-3-
pyridinesulfonamide;
6-Bromo-N-[[4-(3,4-dichloroptienoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-3-
pyridinesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-4-(l,l-dimethylethyl)-
benzenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-5-1-4ethyl-2-
pyridinesulfonamide;
N-[[4-(3,4-Dicblorophenoxy)[l,4' -bipiperidin]-1' -yl]carbonyrj-2,5-difhioro-
benzenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)tl,4'-bipiperidin]-r-yl]carbonyl]-4-(trifluoromethoxy)-
benzenesulfonamide; N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-2,475-trifluoro-
benzenesulfonamide;
5-Chloro-N-[[4-(3,4-dichlorophenoxy)[ 1,4'-bipiperidin]-1 '-yl]carbonyl]-2,4-difluoro-
benzenesulfonamide;
4-Chloro-N-[[4-(3,4-dichlorophenoxy)[lJ4'-bipiperidin]-l'-yl]carbonyl]-2,5-difluoro-
benzenesulfonamide;
3-Chloro-N-[[4-(3,4-dichlorophenoxy)[ 1,4' -bipiperidin]-l' -yl]carbonyl]-5-fiuoro-2-
1-4ethyl-benzenesulfonamide;
N-[[4-(2,4-dichloro-3-1-4ethylphenoxy)[ 1,4'-bipiperidin]-1 '-yl]carbonyl]-4-fluoro-
benzenesulfonamide;
2-chloro-N- [[4-(2,4-dichloro-3-1-4ethylphenoxy) [ 1,4'-bipiperidin]-1'-yl]carbonyl]-
benzenesulfonamide;
-)*-

N-[[4-(3,4-dichIoro-2-1-4ethylphenoxy)[l ,4'-bipiperidin]-1 '-yJ]carbonyl]-4-methyl-benzenesulfona1-4ide;
2-chloro-N- [ [4-(3,4-dichloro-2-1-4ethylphenoxy) [ 1,4'-bipiperidin] - l'-yl] carbony 1] -benzenesulfonamide; • N-[[4-(4-chlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-4-methyl-benzenesulfona1-4ide; N-[[4-(2,4-dichloro-3-1-4ethylphenoxy)[l,4'-bipiperidin]-l-yJ]carbonyl]-2-methyl-benzenesulfonamide;
N-[[4-(2,4-dicbloro-3-fluorophenoxy)[l,4,-bipiperidin]-r-yl]carboiiyl]-4-methyl-benzenesulfona1mide;
N-[[4-(4-chloro-2-methylphenoxy)[ 1,4'-bipiperidin]-1 '-yl]carbonyl]-2-methyl-benzenesulfonamide;
2-chloro-N-[[4-(4-chloro-2-methylphenoxy)[l,4,-bipiperidin]-l-yl]carbonyl]-benzenesulfonamide;
4-chloro-N-[[4-(4-chloro-2-1-4ethylphenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-benzenesulfonamide;
N-[[4-(2,4~dichlorophenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyI]-4-methyl-benzenesulfonamide;
N-[[4-(3-chlorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-4-methyl-benzenesulfona1-4ide; 2-chloro-N-[[4^3-chlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-benzenesulfona1-4ide; N-[[4-(3-chlorophenoxy)[l,4,-bipiperidin]-l,-yl]carbonyl]-benzenesulfona1-4ide; 2-chloro-N-[[4-(3-chloro-2-1-4ethylphenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-benzenesulfona1-4ide;
N-[[4-(2-chloro-4-fluorophenoxy)[lJ4,-bipiperidin]-r-yl]carbonyl]-2-methyl-benzenesulfona1-4ide;
2-chloro-N-[[4-(2,4-dichloro-3-fluorophenoxy)[ 1,4'-bipiperidin]-r-yl]carbonyl]-benzenesulfonamide;
4-chloro-N-[[4-(2,4-dichloro-3-fluorophenoxy) [ 1,4'-bipiperidin]-r-ylJcarbonyl]-benzenesulfonamide;
N-[[4-(2,4-dichIoro-3-fluorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-2-methyl-benzenesulfonamide;
2-chloro-N-[[4-(4-chlorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-benzenesulfonamide; 4-chloro-N-[[4-(4-chlorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-benzenesulfona1-4ide; N-[[4-(4-chlorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-2-1-4ethyl-benzenesulfonamide;
18

2-chloro-N-[[4-(2,4-dichlorophenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-
benzenesulfonamide;
4-cbloro-N-[[4-(2,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-
benzenesulfonamide;
N-[[4-(2,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2-methyl-
benzenesulfonamide;
2-cbJoro-N-[[4-(3,4-difluorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-
benzenesulfonamide;
N-[[4-(3,4-difluorophenoxy) [ 1,4-bipiperid1-4]-1 '-yl]carbonyl]-2-methyl-
benzenesulfonamide;
N-[[4-(3,4-difluorophenoxy) [ 1,4'-bipiperid1-4]-1 '-yl]carbonyl]-4-methyl-
benzenesulfona1-4ide;
N-[[4-(3-chloro-2-1-4ethylphetvoxy)[l,4'-bipiperid1-4]-l'-yl]carbouyl1-4-mettiyl-
benzenesulfonamide;
N-[[4-(3-chloro-2-1-4ethylphenoxy)[ 1,4'-bipiperidin]-1 '-yI]carbonyl]-benzenesulfonamide;
3-chioro-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-
benzenesulfonamide;
N-[[4-(3,4-dichlorophenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-4-methoxy-
benzenesulfonamide;
N-[[4-(3,4-dichlorophenoxy)[l,4,-bipiperid1-4J-r-yl]carbonyl]-2,4,5-trifluoro-
benzenesulfonamide;
N-[[4-(3,4-dichiorophenoxy)[ 1,4'-bipiperidin]-1 '-yl]carbonyl]-2,5-difluoro-
benzenesulfonamide;
N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-4(dimethyiamino)-
benzenesulfonamide;
N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carboiiyl]-2-methoxy-
benzenesulfonamide;
4-bro1-4o-N-[[4-(3,4-dichlorophenoxy)[lJ4'-bipiperidin]-l-yl]carbonyl]-
benzenesulfonamide;
3,5-dichloro-N-[[4-(3,4"dichlorophenoxy)[l,4,-bipiperidin]-r-yl]carbonyl]-
benzenesulfonamide;
methyl 2-[[[[4-(3,4-dichlorophenoxy)[l,4,-bipiperidin]-l-yl]carbonyl]amino]sulfonyi]-
benzoate;
19

2-bromo-N-[[4-(3,4-dichlorophenoxy) [ 1,4'-faipiperidin]-1 '-yl]carbonyl]-
benzenesulfonamide;
5-chloro-N-[[4-(3,4-dichlorophenoxy)[l,4,-bipiperidin]-l'-yl]carbonyl]-2-
thiophenesulfonamide;
4J5-dichloro-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2-
thiophenesulfonamide;
4-cbJoro-N-[t4-(3,4-dicblorophenoxy)[l,4,-bipiperidin]-r-yl]carbonyl]-2,5-dimethyl-
benzenesulfonamide;
2,5-dichloro-N-[[4-(3,4-dicnlorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-3-
thiophenesulfonamide;
N-[[4-(3,4-dicblorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2-(trifluoromethoxy)-
benzenesulfonamide;
4-bro1-4o-N-[[4-(3,4-dichlorophenoxy) [ 1,4'-bipiperidin]-i '-yl]carbonyl]-2-
tbiophenesulfonamide;
N-[[4-(3,4-dichJorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyI}-4-(trifluoromethoxy)-
benzenesulfonamide;
5-cbloro-N-[[4-(3,4-dichlorophenoxy)[l,4,-bipiperidin]-r-yl]carbonyl]-2,4-dffluoro-
benzenesulfonamide;
4-chloro-N-[[4-(3,4-dichlorophenoxy)[l,4,-bipiperidra]-l-yl]carbonyl]-2,5-difluoro-
benzenesulfonamide;
3-chloro-N-[[4-(3,4-dichlorophenoxy)[l)4'-bipiperidin]-r-yl]carbonyl]-5-fluoro-2-1-4ethyl-
benzenesulfonamide;
N-[[4-(3,4-dcbiorophenoxy)[l,4'-bipiperidin]-l-yl3carbonyl]--2J6-di1-4ethyl-benzenesulfonamide; or, N-[[4-(3,4-Dichlorophenoxy)[l,4,-bipiperidn]-l-yl]carbonyl]-2-propanesulfonainide.
A compound of for1-4ula (lb) is, for example: 4-(3,4-Dic1-4orophenoxy)-N-(4-methylberizoyl)-[l,4,-bipiperidine]-l'-sulfonamide; 4-(3,4-dichlorophenoxy)-N.-(4-fluorobenzoyl)-[l,4'-bipiperidirie]-l'-sulfonamide; N-{4-chloroben2;oyl)-4-{3,4-dicbJorophenoxy)-[l,4,-bipiperid1-4e]-l'-sulfonamide; 4-(3J4-dichlorophenoxy)-N-(4-methylbenzoyl)-[l)4,-bipiperidine]-l'-sulfona1-4ide; 4-(3,4-dic1-4orophenoxy)-N-[4-(dimethylamino)benzoyl]-[l,4'-bipiperidine]-l-sulfonamide;

4-(3,4-dichlorophenoxy)-N-(4-ethylbenzoyl)-[ 1,4'-bipiperidine]-1 '-sulfonamide;
4-(3)4-dicblorophenoxy)-N-(2-methoxybenzoyl)-[l,4'-bipiperidiiie]-l-sulfona1-4ide;
4-(3,4-dichlorophenoxy)-N--(4-methoxybenzoyl)--[l,4'-bipiperidine]-l-sulfona1-4ide;
N-(2-cblorobenzoyl)-4-(3,4-dichlorophenoxy)-[l)4'-bipiperidine]-l'-sulfona1-4ide;
4-(3,4-dichlorophenoxy)-N-[3-(lethylsulfonyl)benzoyl]-[l,4'-bipiperidine]-r-
sulfona1-4ide;
N-(3-cyanobenzoyl)-4-(3,4-dicblorophenoxy)- [ 1,4'-bipiperidine]-1 '-sulfona1-4ide;
4-(4-c1-4oro-2-methylphenoxy)-N-(4-fluorobenzoyl)-[l,4'-bipiperidine]-l-sulfona1-4ide;
N-(4-chlorobenzoyl)-4-(4-chloro-2-1-4ethylphenoxy)-[ 1,4'-bipiperidine]-1 '-sulfona1-4ide;
4-(4-chloro-2-methylphenoxy)-N-(4-methylbenzoyl)-[ 1,4'-bipiperidine]- r-sulfona1-4ide;
4-(4-chloro-2-methylphenoxy)-N-[4-(dimethylmino)benzoyl]-[ 1,4'-bipiperidine]-1 '-
sulfonamide;
4-(4-chloro-2-methylphenoxy)-N-(4-ethylbenzoyl)-[lJ4'-bipiperidine]-r-sulfona1-4ide;
4-(4-chloro-2-methylphenoxy)-N-(2-methoxybenzoyl)-[l,4'-bipiperidineJ-l '-sulfona1-4ide;
4-(4-chloro-2-methylphenoxy)-N-(4-1-4ethoxybenzoyl)-[l ,4'-bipiperidine]-1 '-sulfona1-4ide;
N-(2-chlorobenzoyl)-4-(4-chloro-2-methylphenoxy)-[l ,4'-bipiperidine]-1 '-sulfona1-4ide;
4-(4-cbloro-2-methylphenoxy)-N-(3-(1-4ethylsulfonyl)benzoyl]-[l,4'-bipiperidine]-r-
sulfonamide;
4-(4-chloro-2-methylphenoxy)-N-(3-cyanobenzoyI)-[l,4'-bipiperidine]-r-sulfona1-4ide;
4-(2,4-dichloro-3-methylphenoxy)-N-(4-fluorobenzoyl)-[l,4'-bipipeiidine]-r-sulfona1-4ide;
N-(4-chlorobenzoyl)-4-(2,4-dicbIoro-3-methylphenoxy)-[ 1,4'-bipiperiduie]-1 '-sulfona1-4ide;
4-(2,4-dichloro-3 -metbylphenoxy)-N-(4-methylbenzoyl)- [ 1,4'-bipiperidinej-1 '-
sulfona1-4ide;
4-(2,4-dichloro-3-methylphenoxy)-N-[4-(dimethylamino)benzoyl]-[ 1,4'-bipiperidine]-1 '-
sulfonamide;
4-(2,4-dichloro-3-1-4ethylphenoxy)-N-(4-ethylbenzoyl)-[ 1,4-bipiperidine]-1 '-sulfonamide;
4-(2,4-dicnloro-3-1-4ethylphenoxy)-N-(2-methoxybenzoyl)-[ 1,4-bipiperid1-4e]-1 '-
sulfonamide;
4-(2,4-dichloro-3-methylphenoxy)-N-(4-methoxybenzoyl)-[l,4,-bipiperidine]-l-
sulfonamide;
N-(2-chlorobenzoyl)-4-(2,4-d[ichloro-3-1-4etbylpbenoxy)-[l,4'-bipiperidine]-r-sulfonanude;
4-(2,4-dicbioro-3-1-4e1-4ylphenoxy)-N-[3-(1-4ethylsulfonyl)benzoyl]-[l,4'-bipiperidine]-r-
sulfonamide;
21

N-(3-cyanobenzoyl)-4-(3,4-dichloropbenoxy)-[l,4'-bipiperidine]-r-sulfonamide;
4-(3,4-dichloro-2-1-4ethy]phenoxy)-N-(4-fluoroben2oyl)-[l,4'-bipiperidine]-r-sulfonarmide;
N-(4-chlorobenzoyl)-4-(3,4-dichloro-2-metliylphenoxy)-[l,4'-bipiperidine]-r-sulfonamide;
4-(3,4-dichloro-2-1-4ethylphenoxy)-N-(4-methylbenzoyl)-[ 1,4-bipiperidine]-1 '-
sulfona1-4ide;
4-(3,4-dicbloro-2-methylphenoxy)-N-[4-(dimethylamino)benzoyl]-[l,4'-bipiperidine]-l-
sulfona1-4ide;
4-(3,4-dichloro-2-methylphenoxy)-N-(4-ethylbenzoyl)-[ 1,4'-bipiperidine]-l '-sulfonamide;
4-(3,4-dichloro-2-methylphenoxy)-N-(2-methoxybenzoyl)-[ 1,4'-bipiperidine]-1 '-
sulfonamide;
4-(3,4-dichloro-2-1-4ethylphenoxy)-N-(4-methoxybenzoyl)-[ 1,4'-bipiperidine]-1 '-
sulfonamide;
N-(2-chlorobenzoyl)-4-(3,4-dichloro-2-methylphenoxy)-[l,4,-bipiperidine]-l-sulfona1-4ide; 4-(3,4-dichloro-2-1-4etliylphenoxy)-N-[3-(niethylsulfonyl)benzoyl]-[l,4,-bipiperidine]-r-sulfonamide;
N-(3-cyanobenzoyl)-4-(3,4-dichloro-2-methylphenoxy)-[ 1,4'-bipiperidine]-1 '-sulfonamide; . N-benzoyl-4-(3,4-dichloro-2-1-4ethylphenoxy)-[l,4'-bipiperidine]-l-sulfonamide; N-benzoyl-4-(2,4-dichlorophenoxy)-[ 1,4-bipiperidine]-1 '-sulfona1-4ide; N-(3-cyanobenzoyl)-4-(3,4-dichloropbenoxy)-[l,4'-bipiperidine]-r-sulfonamide; 4-(3,4-dichlorophenoxy)-N-(4-fluorobenzoyl)-[l ,4-bipiperidine]-1 '-sulfonamide; 4-(3,4-dichlorophenoxy)-N-[3-(1-4ethylsulfonyl)benzoyl]-[l,4'-bipiperidme]-r-sulfona1-4ide;
4-(4-chloro-2-1-4ethylphenoxy)-N-[3-(methylsulfonyl)benzoyl]-[ 1,4'-bipiperidine]-l '-sulfonamide;
N-(2-chlorobenzoyl)-4-(3,4-dicblorophenoxy)-[l,4'-bipiperidine]-r-sulfonamide; N-(4-chlorobenzoyl)-4-(3)4-dicblorophenoxy)-[l,4'-bipiperidine]-r-sulfonamide; N-(4-cblorobenzoyl)-4-(4-cnloro-2-1-4euiylphenoxy)-[l ,4'-bipiperidine]-r-sulfonamide; 4-(3,4-dichlorophenoxy)-N-(2-1-4ethoxybenzoyl)-[ 1 ,4'-bipiperidine]'-l '-sulfonamide; 4-(3,4-dichlorophenoxy)-N-(4-1-4ethoxybenzoyl)-[l,4'-bipiperidine]-l-sulfonamide; 4-(3,4-dicblorophenoxy)-N-(4-1-4ethylbenzoyl)-[l,4,-bipiperidine]-r-sulfonamide; 4-(3,4-dichlorophenoxy)-iV-[(l ,2-dihydro-1 -oxo-4-isoquinolinyl)carbonyl]- [1,4'-bipiperidine]-1 '-sulfona1-4ide; N-(cyclohexylcarbonyl)-4-(3,4~dichlorophenoxy)- [l,4'-bipiperidine]-l'-sulfonamide;
-22

4-(3,4-dichlorophenoxy)-N-(2-1-4ethyl-1 -oxopropyl)- [ 1,4'-bipiperidine]-1 '-sulfona1-4ide; 4-(3,4-dichlorophenoxy)-N-(2-phenylacetyl)-[l ,4'-bipiperidine]-r-sulfonamide; or, N-[[4-(3,4-dichlorophenoxy) [ 1,4'-bipiperidin]-1 '-yI]carboriyl]-2-propanesulfona1-4ide.
A compound of formula (Ic) is, for example: Trans N-[[4-[4-(3,4-Dichlorophenoxy)- l-piperidinyl]cyclohexyl]carbonyl]-4-methyl-benzenesulfonamide;
Trans Ar-[[4-[4-(3,4-Dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-N,4-dimethyl-benzenesulfonamide;
Trans 4-chloro-N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-4-methyl-benzenesulfonamide;
Trans N-[[4-[4-(3)4-dicrdorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2-methyl-benzenesulfonamide;
Trans 3-bro1-4o-N-[[4-[4-(3,4-dichlorophenoxy)-1 -piperidinyl]cyclohexyl]carbonyl]-benzenesulfonamide;
Trans 4-bro1-4o-N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyI]-benzenesulfonamide;
Trans 3,5-dichloro-N-[[4-[4^(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-benzenesulfona1-4ide;
Trans 3-cyano-N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)- l-piperidinyl]cyclohexyl]carbonyl]-2,5-di1-4ethoxy-benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)- l-piperidinyl]cyclohexyl]carbonyl]-3,4-di1-4ethoxy-benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-4-(3,3-dimethyl-2-oxo-1 -azetidinyl)-benzenesuifonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-1 -piperidinyl]cyclohexyl]carbonyl]-4-(4,5-dihydro-3-methyl-5-oxo-lH-pyrazol-l-yl)-benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-1 -piperidinyI]cyclohexyl]c'arbonyl]-3-(4,5-dinydro-3-metbyl-5-oxo-lH-pyrazoI-l-yl)-benzenesulfonamide;
-^3.

Trans N-[[4-[4-(3,4-dichlorophenoxy)-1 -piperidinyl]cyclohexyl]carbonyl]-4-hydroxy-benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-3-(trifluoro1-4ethyl)-benzenesuifonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-
benzenesulfonamide;
Trans 2-[[[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]amino]-
sulfonyl]-benzoic acid, methyl ester;
Trans 2-bro1-4o-N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]caxbonylj-
benzenesulfonamide;
Trans N-[5-[[[[4-[4-(3,4-d'ichlorophenoxy)-l-
piperidinyl]cyclohexyl]carbonyl]ar1-4^o]sulfonyl]-l,3,4-tliiadiazol-2-yl]-acetamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-5-
(dimethylamino)-1 -naphthalenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2-
naphthalenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2,4-dimethyl-5-
thiazolesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2-(l-
piperidinyl)-3-pyridinesulfonamide;
Trans 5-chloro-N-[[4-[4-(3,4-dichlorbphenoxy)-l-piperidmyl]cyclohexyl]carbonyl]-2-
thiophenesulfonamide;
Trans 5-bro1-4o-N-[[4-[4-(3,4-dicrilorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2-
thiophenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]caxbonyl]tetrahydro-3-
thiophenesulfonamide, 1,1 -dioxide;
Trans 4,5-dichloro-N-[[4-[4-(3,4-dichlorophenoxy)- l-piperidinyl]cyclohexyl]carbonyl]-2-
thiophenesulfonamide;
Trans 4-chloro-N-[[4-[4-(3,4Tdichlorophenoxy)-1 -piperidinyl]cyclohexyl]carbonyl]-2,5-
dimethyl-benzenesulfonamide;
Trans 4-n-butyl-N-[[4-[4-(3,4-diclilorophenoxy)-l-piperidmyl]cyclohexyl]carbohyl]-
benzenesulfonamide;
24

Trans 2)5-dichloro-N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-3-tbiophenesuifonamide;
Trans 4-n-butoxy-N-[[4-[4-(3,4-dichlorophenoxy)-l-piperid1-4yl]cyclohexyl]carbonyl]-
benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-1 -piperidinyl]cyclobexyl]carbonyl]-2-
(trifluoromethoxy)-benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)- l-piperid1-4yl]cyclohexyl]carbonyl]- 1-1-4ethyl- 1H-
imidazole-4-sulfonarnide;
Trans 5-a1-4ino-N-[[4-[4-(3,4-dichlorophenoxy)-1 -piperidinyl]cyclohexyl]carbonyl] -1,3,4-
thiadiazole-2-suIfona1-4ide; . Trans 4-bro1-4o-N-[[4-[4-(3,4-dichlorophenoxy)- l-piperidinyl]cyclohexyl]carbonyl]-2-
thiophenesulfonarnide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2-(4-
morpholinyl)-3-pyridinesulfonamide;
Trans 6-bro1-4o-N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexylJcarbonyl]-3-pyridinesulfonamide;
Trans N-[[4-[4-(3?4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-4-(l,l-dimediyIethyl)-benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-5-1-4ethyl-2-pyridinesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclobexyl]carbonyl3-2,5-difluoro-benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl3carbonyl]-4-(trifluoromethoxy)-benzenesulfonamide; ' benzenesulfonamide;
Trans 5-chloro-N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2,4-
difluoro-benzenesulfonamide;
Trans 4-chIoro-N-[[4-[4-(374-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2,5-
difluoro-benzenesulfonamide;
Trans 3-chloro-N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-5-
fluoro-2-methyl-benzenesulfonamide;
-fcT-

Trans N-[[4-[4-(3,4-dichlorophenoxy)-1 -piperid1-4yl]cyclohexyl]carbonyl]-2-methyl-
benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-1 -piperidinyl]cyclohexyl]carbonyl]-2-methoxy-
benzenesulfonamide;
TransN-[[4-[4-(3,4"dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2,6-dimethyl-
benzenesulfonamide; ■
TransN-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-4-methyl-
benzenesulfonamide;
Trans N-[[4-[4-(3J4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-
benzenesulfonamide; or,
Trans N-[[4-[4-(3,4-dichIorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-4-
(dimmethylamino)- benzenesulfonamide.
A compound of formula (Id) is, for example: 4-(3,4-Dichorophenoxy)-N-(2-methylbenzoyl)-[l,4'-bipiperidine]-l-carboxamide; 4-(3,4-Dichlorophenoxy)-N-(4-1-4ethylbenzoyl)"[ 1,4-bipiperidine]-1 '-carboxa1mide; 4-(3I4-Pic1-4orophenoxy)-N-(4-chlorobenzoyl)-[l,4'-bipiperidine]-r-carboxarnide; 4-(3,4-Dichlorophenoxy)-N-benzoyl-[ 1,4'-bipiperidine]-1 '-carboxa1-4ide; 4-(3,4-Dichlorophenoxy)-N-[(4-1-4etbylphenyl)sulfonyl]-[l ,4'-bipiperidine]-1 '-sulfonamide; or,
4-(3,4-dichlorophenoxy)-N-[[4-( 1, l-di1-4ethylethyl)phenyl]sulfonyl]-[ 1,4'-bipiperidine]-1 '-sulfonamide.
A compound of formula (le) is, for example: [4-(3,4-dichlorophenoxy)-N-(phenylsulfonyl)-l,4,-bipiperidine]-l-sulfonamide.
A compound of for1-4ula (If) is, for example: Trans N-benzoy1-4-[4-(3,4-dichlorophenoxy)-l-piperiajnyl]-cyclohexanesulfona1-4ide.
A compound of for1-4ula (Ig) is, for exa1-4ple: Trans ^-[[^^-(S^DicUorophenoxyJ-l-piperidinylJcyclohexyljcarbonyll-benzamide.
A compound of formula (Ih) is, for example: Trans N-[[4-[4-(3,4-Dichlorophenoxy)-l -piperidinyl]cyclohexyl]sulfonyl]-benzenesulfonamide.

WO 03/004487

PCT/SE02/01311

26 Compounds of formula (I) (for example compounds of formula (la), (lb), (Ic), (Id), (Ie), (If), (Ig) or (Ih)) can be prepared by the methods described below.
A compound of formula (Ic), (If), (Ig) or (Ih) where R3 and R5 are both hydrogen may be converted to a compound of formula (Ic), (If), (Ig) or (Ih) where R5 is alkyl and R3 5 is hydrogen by deprotonation to a dianion, for example with 2 equivalents of LDA, . followed by reaction with an alkylating agent, R5Hal (wherein Hal is, for example chlorine).
A compound of formula (Ic), (If), (Ig) or (Ih) where R5 is hydrogen and R3 is not hydrogen may be converted to a compound of formula (Ic), (If), (Ig) or (Ei) where R5 is 10 alkyl and R3 is not hydrogen by deprotonation, for example with 1 equivalent of IDA, followed by reaction with an alkylating agent, R5Hal.
A compound of formula (1), wherein R3 is not hydrogen, can be prepared by alkylating a compound of formula (I), wherein R3 is hydrogen, with a suitable alkylating agent (for example R3-L, wherein L is a leaving group such as triflate, a halide or a diazo 15 group) in the presence of a suitable base (such as sodium hydride) in a suitable solvent. A compound of formula (I), wherein R3 is hydrogen, T is C(O) and Y is N, can be prepared by reacting a compound of formula (11):

with an isocyanate of formula R4WN=C=0 in the presence of a suitable solvent at a 20 suitable temperature (such as room temperature). Isocyanates of formula R4WN=C=0 are
commercially available or can be prepared by optional adaptation of methods described in
the literature.
A compound of formula (I), wherein T is C(O), W is S(0)2 and Y is N, can be
27
prepared by reacting a compound of formula (II) with a compound of formula (XXH). A 25 compound of formula (XXH):


may be prepared from a sulfonamide R4SO2NHR3 and p-nitrophenyl chloroformate in the presence of a base, for example triethylamine and a catalyst, for example DMAP, typically at room temperature.
A compound of formula (II) can be prepared by deprotecting a compound of formula (HI):

for example using trifluoroacetic acid in a suitable solvent (such as dichloromethane) or using a source of hydrogen chloride in a suitable solvent (such as dioxane).
A compound of formula (III), wherein R2 is hydrogen, can be prepared by reacting a compound of formula (IV):

with a compound of formula (V):

in the presence of NaBH(OAc)3 and acetic acid.
A compound of formula (HI), wherein R2 is C1-6 alkyl, can be prepared by reacting a compound of formula (XVII):
with a Grignard reagent of formula R2MgHal (wherein Hal is chlorine, bromine or iodine) in a suitable solvent, such as tetrahydrofuran.
A compound of formula (XVII) can be prepared by reacting a compound of formula (IV) with a compound of formula (V) in the presence of titanium tetrisopropoxide, for example in dichloroethane, followed by the addition of diethylaluminium cyanide to a solution, for example in toluene.
A compound of formula (I), wherein R3 is hydrogen, T is S(O)2, W is C(O) and Y is N, can be prepared by reacting a compound of formula (IX):
-*f


with a compound of formula (II) in the presence of a suitable base (such as triethylamine) in a suitable solvent (such as tetrahydrofuran) at a suitable temperature (such as below ' -60°C). A compound of formula (IX) can be prepared by reacting an acid R4C02H with C1S(O)2N=C=0, for example below 80°C.
Alternatively, a compound of formula (I), wherein R3 is hydrogen, T is S(O)2, W is C(O) and Y is N, can be prepared by reacting a compound of formula (XVIII):

with an acyl halide R4COHal in the presence of a base, for example triethylamine in a suitable solvent, for example dichloromethane, for example at room temperature.
A compound of formula (XVIII) may be prepared by the reaction of a compound of formula (II) with sulfamide, for example in dioxan at reflux.
A further method of preparing a compound of formula (I), wherein R3 is hydrogen, T is S(O)2, W is C(O) and Y is N, is to react a compound of formula (XIX):

with an acyl halide R4COHa] in the presence of a base, for example triethylamine in a suitable solvent, for example dichloromethane, for example at room temperature, followed by deprotection of the carbamate so formed, for example with trifluoroacetic acid in dichloromethane.
A compound of formula (XIX) can be prepared from a compound of formula (IT) and a compound of formula (XX):

in a suitable solvent for example dichloromethane typically at room temperature.
29

A compound of formula (I) wherein T and W are both S(O)2 and Y is N, can be prepared by reacting a compound of formula (X):

with a sulfonamide R S(O)2NHR3 in the presence of a base (such as calcium oxide), in a suitable solvent (such as DMSO) at a temperature preferably in the range 50-110°C. (For example see DE 1618439; DE 1249259; Chemical Abstracts 1967, 67, 116716a). A compound of formula (X) can be prepared by reacting a compound of formula (II) with S(0)2C12 in the presence of a suitable base (such as triethylamine).
Alternatively, a compound of formula (I) wherein T and W are both S(O)2 and Y is N, can be prepared by reacting a compound of formula (XVIII) with a sulfonyl chloride R4SO2C1 in the presence of a base, for example triethylamine, preferably with dimethylaminopyridine as catalyst in a suitable solvent, for example dichloromethane, for example at room temperature.
A'compound of formula (I) wherein T is C(O), W is S(O)2 and Y is CR5, can be prepared by firstly hydrolysing a compound of formula (XI):

wherein the ester is preferably a C1-6 alkyl group, and reacting the product so formed with R4S(O)2NHR3 in the presence of an appropriate coupling agent (such as emyl dimethylaminopropyl carbodiimide (EDCI), with 4-dimethylaminopyridine (DMAP) or 1-hydroxybenzotriazole (HOBT)) in a suitable solvent, for example DMF.
A compound of formula (XI), wherein R2 is hydrogen, can be prepared by reductively animating a compound .of formula (XII):

with a compound of formula (XIII):

30

A compound of formula (XT) where R2 is alkyl can be prepared by amino nitrile formation between compounds of formula (XII) and (XIII) followed by displacement of the nitrile with a grignard reagent.
A compound of formula (I), wherein T and W are both C(O) and Y is CH or N, can-be prepared by heating a compound of formula (XIV):

in the presence of R4C(OR')2N(CH3)2 or R4C(OR')3, wherein R' is methyl or ethyl, or (OR')3 is (OCH2)3CCH3. A compound of formula (XTV) where Y is-CR5 can be prepared . by firstly hydrolysing a compound of formula (XI) and then coupling the product so formed with an amine R3NH2 in the presence of an appropriate coupling agent (such as ethyl dimethylaminopropyl carbodiimide, with 4-dimethylaminopyridine or 1-' hydroxybenzotriazole) in a suitable solvent, for exampleDMF. A compound of formula (XIV) where Y is N and RJ is H may be prepared by reaction of a compound of formula (II) with sodium cyanate in the presence of an acid, for example acetic acid. -A compound of formula (XTV) where Y is N and R3 is alkyl may be prepared by reaction of a compound of formula (II) with a compound of formula (XXI): R3-N=C=0; in an inert solvent, for example dichloromethane, for example at room temperature.
A compound of formula (I), wherein T is S(O)2l W is C(O) and Y is CR5, can be prepared by coupling a compound of formula (XV):

to an acid R4CO2H in the presence of an appropriate coupling agent (such as ethyl dimethylaminopropyl carbodiimide, 4-dimethylaminopyridine or HOBT) in a suitable solvent.
A compound of formula (I), wherein T and W are both S(O)2 and Y is CH, can be prepared by coupling a compound of formula (XV) to a sulfonyl chloride R4S(O)2C1 in the presence of a base and a solvent (such as dichloromethane, N,N-dimethylformamide or tetrahydrofuran).
-2\^

A compound of formula (XV) can be prepared by reductively aminating a compound of formula (XVI):

with a compound of formula (IV) to obtain a compound wherein R2 is hydrogen, or aminonitrile formation followed by a Grignard reaction to obtain a compound wherein R2 is alkyl.
A compound of formula (XVI) can be prepared by reacting

with CH2=CR -S(O)2NHR at an elevated temperature (such as in refluxing toluene) and then hydrolysing the silyl enol ether (such as with acetic acid).
A compound of formula (I) where Y is CR5 and R5 is not hydrogen may be prepared from a compound of formula (I) where Y is CH by reaction of the dianion (R is H) or monoanion (R3 is alkyl) (formed with a suitable base, for example LDA) with an alkylating agent (for example R5-L, wherein L is a leaving group such as triflate or a halide) in a suitable solvent for example THF for example at 0° or below.
Further compounds of formula (I) can be prepared by adaptation of: the routes described above, methods described in the art or the Examples recited below. The intermediates identified above are commercially available or can be prepared by using or adapting methods described in the art.
In another aspect the present invention provides processes for the preparation of compounds of formula (I) (for example a compound of formula (la), (lb), (Ic), (Id), (Ie), (If), (Ig) or (lb.)).
The intermediates of formula (X), (XI), (XTV), (XV), (XVIII) and (XIX) defined herein are novel and these, and processes for their preparation, are provided as further features of the invention.
The compounds of the invention have activity as pharmaceuticals, in particular as modulators of chemokine receptor (especially CCR3) activity, and may be used in the treatment of autoimmune, inflammatory, proliferative or hyperproliferative diseases, or
32

immunologically-mediated diseases (including rejection of transplanted organs or tissues
and Acquired Immunodeficiency Syndrome (AIDS)). In one aspect exa1-4ples of these conditions are:
(1) (the respiratory tract) obstructive diseases of airways including: chronic obstructive pul1-4onary disease (COPD) (such as irreversible COPD); asth1-4a {such as bronchial, allergic, intrinsic, extrinsic or dust asth1-4a, particularly chronic or inveterate asth1-4a (for exa1-4ple late asthma or airways hyper-responsiveness}}; bronchitis (such as eosinophilic bronchitis}; acute, allergic, atrophic rhinitis or chronic rhinitis including rhinitis caseosa, hypertrophic rhinitis, rhinitis purulenta, rhinitis sicca or rhinitis medica1-4entosa; membranous rhinitis including croupous, fibrinous or pseudomembranous rhinitis or scrofoulous rhinitis; seasonal rhinitis including rhinitis nervosa (hay fever) or vaso1-4otor rhinitis; sarcoidosis; fanner's lung and related diseases; nasal polyposis; fibroid lung, idiopathic interstitial pneumonia, antitussive activity, treatment of chronic cough associated with inflammatory conditions of the airways or iatrogenic induced cough;
(2) (bone and joints) arthrides including rheumatic, infectious, autoimmune, seronegative spondyloarthropathies (such as ankylosing spondylitis, psoriatic arthritis or Reiter's disease), Behcet's disease, Sjogren's syndrome or systemic sclerosis;
(3) (skin and eyes) psoriasis, atopic dermatitis, contact dermatitis or other ecz1-4atous dermitides, seborrhoetic dermatitis, Lichen planus, Phemphigus, bullous Phmphigus, Epidermolysis bullosa, urticaria, angioder1-4as, vasculitides erythe1-4as, cutaneous eosinophilias, uveitis, Alopecia areata or vernal conjunctivitis;
(4) (gastrointestinal tract) Coeliac disease, proctitis, eosinophilic gastro-enteritis, mastocytosis, Crohn's disease, ulcerative colitis, irritable bowel disease or food-related allergies which have effects remote from the gut (for example migraine, rhinitis or eczema);
(5) (Allograft rejection) acute and chronic following, for example, transplantation of kidney, heart, liver, lung, bone 1-4arrow, skin or cornea; or chronic graft versus host disease; and/or
(6) (other tissues or diseases) Alzheimer's disease, multiple sclerosis, atherosclerosis, Acquired Immunodeficiency Syndrome (AIDS), Lupus disorders (such as lupus erythematosus or syste1-4ic lupus), erythematosus, Hashi1-4oto's thyroiditis, myasthenia gravis, type I diabetes, nephrotic syndrome, eosinophilia fascitis, hyper IgE syndrome,
32

eosinophilic bronchitis}; acute, allergic, atrophic rhinitis or chronic rhinitis including rhinitis caseosa, hypertrophic rhinitis, rhinitis purulenta, rhinitis sicca or rhinitis medicamentosa; membranous rhinitis including croupous, fibrinous or pseudomembranous rhinitis or scrofoulous rhinitis; seasonal rhinitis including rhinitis nervosa (hay fever) or vasomotor rhinitis; sarcoidosis; fanner's lung and related diseases; nasal polyposis; fibroid lung, idiopathic interstitial pneumonia, antitussive activity, treatment of chronic cough associated with inflammatory conditions of the airways or iatrogenic induced cough;
(2) (bone and joints) arthrides including rheumatic, infectious, autoimmune, seronegative spondyloarthropathies (such as ankylosing spondylitis, psoriatic arthritis or Reiter's disease), Behcet's disease, Sjogren's syndrome or systemic sclerosis;
(3) (skin and eyes) psoriasis, atopic dermatitis, contact dermatitis or other eczmatous dermitides, seborrhoetic dermatitis, Lichen planus, Phemphigus, bullous Phemphigus, Epidermolysis bullosa, urticaria, angiodermas, vasculitides erythemas, cutaneous eosinophilias, uveitis, Alopecia areata or vernal conjunctivitis;
(4) (gastrointestinal tract) Coeliac disease, proctitis, eosinophilic gastro-enteritis, mastocytosis, Crohn's disease, ulcerative colitis, irritable bowel disease or food-related allergies which have effects remote from the gut (for example migraine, rhinitis or eczema);
(5) (Allograft rejection) acute and chronic following, for example, transplantation of kidney, heart, liver, lung, bone marrow, skin or comea; or chronic graft versus host disease; and/or
(6) (other tissues or diseases) Alzheimer's disease, multiple sclerosis, atherosclerosis, Acquired Immunodeficiency Syndrome (AIDS), Lupus disorders (such as lupus erythematosus or systemic lupus), erythematosus, Hashimoto's thyroiditis, myasthenia gravis, type I diabetes, nephrotic syndrome, eosinophilia fascitis, hyper IgE syndrome, leprosy (such as lepromatous leprosy), Peridontal disease, sezary syndrome, idiopathic thrombocytopenia pupura or disorders of the menstrual cycle;
in a warm blooded animal, such as man.
In a further aspect a compound of formula (I) (for example a compound of formula (la), (lb), (Ic), (Id), (le), (If), (Ig) or (Ih)), or a pharmaceutically acceptable salt thereof, is useful in the treatment of asthma {such as bronchial, allergic, intrinsic, extrinsic or dust asthma, particularly chronic or inveterate asthma (for example late asthma or airways
35

leprosy (such as lepromatous leprosy), Peridontal disease, Sezary syndrome, idiopathic thrombocytopenia pupura or disorders of the menstrual cycle. .
The compounds of the invention are also H1 antagonists and may be used in the treatment of allergic disorders.
The compounds of the invention may also be used to control a sign and/or symptom of what is commonly referred to as a cold (for example a sign and/or symptom of a common cold or influenza or other associated respiratory virus infection).
According to a further feature of the invention there is provided a compound of formula (I) (for example a compound of formula (la), (Ib),'(Ic), (Id), (Ie), (If), (Ig) or (Ih) or a pharmaceutically acceptable salt thereof or a solvate thereof, for use in a method of treatment of a warm blooded animal (such as man) by therapy (including prophylaxis).
According to a further feature of the present invention there is provided a method for modulating chemokine receptor activity (especially CCR3 receptor activity), or antagonising Hi, in a warm blooded animal, such as man, in need of such treatment, whk comprises administering to said animal an effective amount of a compound of the formul: (I) (for example a compound of formula (la), (lb), (Ic), (Id), (Ie), (If), (Ig) or (Ih)), or a pharmaceutically acceptable salt thereof or a solvate thereof.
The invention also provides a compound of the formula (I) (for example a compound of formula (la), (lb), (Ic), (Id), (Ie), (If), (Ig) or (Ih)), or a pharmaceutically acceptable salt thereof or a solvate thereof, for use as a medicament.
In another aspect the invention provides the use of a compound of formula (I) (for example a compound of formula (la), (lb), (Ic), (Id), (Ie), (If), (Ig) or (Ih)), or a pharmaceutically acceptable salt thereof or a solvate thereof, in the manufacture of a medicament for use in therapy (for example modulating chemokine receptor activity (especially CCR3 receptor activity), or antagonising HI, in a warm blooded animal, such as man).
The invention further provides the use of a compound of formula (I) (for example compound of formula (la), (lb), (Ic), (Id), (Ie), (If), (Ig) or (Ih)), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for use in the treatment of: (1) (the respiratory tract) obstructive diseases of airways including; chronic obstructive pulmonary disease (COPD) (such as irreversible COPD); asthma {such as bronchial, allergic, intrinsic, extrinsic or dust asthma, particularly chronic or inveterate asthma (for example late asthma or airways hyper-responsiveness)}; bronchitis {such as



33

hyper-responsiveness)}; or rhinitis {including acute, allergic, atrophic or chronic rhinitis, such as rhinitis caseosa, hypertrophic rhinitis, rhinitis purulenta, rhinitis sicca or rhinitis medicamentosa; membranous rhinitis including croupous, fibrinous or pseudomembranous rhinitis or scrofoulous rhinitis; seasonal rhinitis including rhinitis nervosa (hay fever) or vasomotor rhinitis}.
In a still further aspect a compound of formula (I) (for example a compound of formula (la), (lb), (Ic), (Id), (Ie), (If), (Ig) or (lb.)), or a pharmaceutically acceptable salt thereof, is useful in the treatment of asthma.
The present invention also provides the use of a compound of formula (I) (for example a compound of formula (la), (lb), (Ic), (Id), (Ie), (If), (Ig) or (lb)), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for use in the treatment of asthma or rhinitis.
The present invention further provides a method of treating a chemokine mediated disease state (especially a CCR3 mediated disease state, especially asthma) in a warm blooded animal, such as man, which comprises administering to a mammal in need of such treatment an effective amount of a compound of formula (I) (for example a compound of formula (la), (lb), (Ic), (Id), (Ie), (If), (Ig) or (Ih)), or a pharmaceutically acceptable salt thereof or solvate thereof.
In order to use a compound of the invention, or a pharmaceutically acceptable salt thereof or solvate thereof, for the therapeutic treatment of a warm blooded animal, such as man, in particular modulating chemokine receptor (for example CCR3 receptor) activity or antagonising HI, said ingredient is normally formulated in accordance with standard pharmaceutical practice as a pharmaceutical composition.
Therefore in another aspect the present invention provides a pharmaceutical composition which comprises a compound of the formula (I) (for example a compound of formula (la), (lb), (Ic), (Id), (Ie), (If), (Ig) or (Ih)), or a pharmaceutically acceptable salt thereof or a solvate thereof (active ingredient), and a pharmaceutically acceptable adjuvant, diluent or carrier. In a further aspect the present invention provides a process for the preparation of said composition which comprises mixing active ingredient with a pharmaceutically acceptable adjuvant, diluent or carrier. Depending on the mode of administration, the pharmaceutical composition will preferably comprise from 0.05 to 99 %w (per cent by weight), more preferably from 0.05 to 80 %w, still more preferably from
36

0.10 to 70 %w, and even more preferably from 0.10 to 50 %w, of active ingredient, all percentages by weight being based on total composition.
The pharmaceutical compositions of this invention may be administered in standard manner for the disease condition that it is desired to treat, for example by topical (such as to the lung and/or airways or to the skin), oral, rectal or parenteral administration. For these purposes the compounds of this invention may be formulated by means known in the art into the form of, for example, aerosols, dry powder formulations, tablets, capsules, syrups, powders, granules, aqueous or oily solutions or suspensions, (lipid) emulsions, dispersible powders, suppositories, ointments, creams, drops and sterile injectable aqueous or oily solutions or suspensions.
A suitable pharmaceutical composition of this invention is one suitable for oral administration in unit dosage form, for example a tablet or capsule which contains between O.lmg and lg of active ingredient.
In another aspect a pharmaceutical composition of the invention is one suitable for intravenous, subcutaneous or intramuscular injection.
Each patient may receive, for example, an intravenous, subcutaneous or intramuscular dose of 0.01mgkg-1 to lOOmgkg-1 of the compound, preferably in the range of 0. lmgkg-1 to 20mgkg-1 of this invention, the composition being administered 1 to 4 times per day. The intravenous, subcutaneous and intramuscular dose may be given by means of a bolus injection. Alternatively the intravenous dose may be given by continuous infusion over a period of time. Alternatively each patient will receive a daily oral dose which is approximately equivalent to the daily parenteral dose, the composition being - administered 1 to .4 times per day.
The following illustrate representative pharmaceutical dosage forms containing the compound of formula (I) (for example a compound of formula (la), (lb), (Ic), (Id), (le), (If), (lg) or (Ih)), or a pharmaceutically-acceptable salt thereof (hereafter Compound X), for therapeutic or prophylactic use in humans:
37


38


(e)
Buffers, pharmaceutically-acceptable cosolvents such as polyethylene glycol, polypropylene glycol, glycerol or ethanol or complexing agents such as hydroxy-propyl β-cyclodextrin may be used to aid formulation.
The above formulations may be obtained by conventional procedures well known in the pharmaceutical art. The tablets (a)-(c) may be enteric coated by conventional means, for example to provide a coating of cellulose acetate phthalate.
The invention will now be illustrated by the following non-limiting Examples in which, unless stated otherwise:
(i) when given, 1-H KMR data is quoted and is in the form of delta values for major diagnostic protons, given in parts per million (ppm) relative to tetramethylsilane (TMS) as an internal standard, determined at 300MHz or 400MHz using perdeuterio DMSO-D6 (CD3SOCD3), methanol-D4 (CD3OD) or CDCI3 as the solvent unless otherwise stated; (ii) mass spectra (MS) were run with an electron energy of 70 electron volts in the chemical ionisation (CI) mode using a direct exposure probe; where indicated ionisation was effected by electron impact (EI) or fast atom bombardment (FAB) or electrospray (ESI); where values for m/z are given, generally only ions which indicate the parent mass are reported, and unless otherwise stated the mass ion quoted is the positive mass ion -(M+H)+;
39-
(iii) the title and sub-title compounds of the examples and methods were named using the ACD/Index name program version 4.55 from Advanced Chemistry Development, Inc; (iv) unless stated otherwise, reverse phase HPLC was conducted using a Symmetry, NovaPak or Xterra reverse phase silica column; and (v) the following abbreviations are used:



Example 1A
N-[[4-(3,4-dichlorophenoxy)[l,4,-bipiperidin]-1-yl]carbonyl]-4"fluoro-benzenesulfonamide (an example of a compound of formula (la)).
To a solution of 4-(3,4-dichlorophenoxy)-1,4'-bipiperidine (Method C; 0.197g) in dichloromethane (5ml) was added 4-fluorobenzenesulfonyl isocyanate (0.121g) dropwise and the reaction was stirred under nitrogen for 12 hours. The solvent was removed under reduced pressure and the resulting product was purified by RPHPLC (Waters Xterra® column), (gradient, 75:25 0.2% aq ammonia / acetonitrile to 5:95. over 10 mins) to give the title compound (60mg; MS fM+Hf (APCI+) 530/532).
1H NMR (399.98 MHz, CD30D) 5 1.50 -1.61 (m, 2H), 2.01 - 2.24 (m, 6H), 2.64 -2.73 (m, 2H), 3.25 - 3.43 (m, 5H), 4.42 - 4.50 (m, 2H), 4.64 - 4.71 (m, 1H), 6.95 - 6.98 (m, 1H), 7.12-7.16 (m, 2H), 7.21 - 7.22 (m, 1H), 7.41 - 7.44 (m, 1H), 7.90 - 7.95 (m, 2H).
The Examples 1B-1AV are examples of compounds of formula (la) and were prepared using similar methodology to that of Example 1A. Recrystallisation was required after chromatography for several Examples.
Example 2A N-[4-(3,4-Dichlorophenoxy)[ 1,4'~bipiperidin]-l '-yl]carbonyl]-
benzenemethanesulfonamide (an example of a compound of formula (la)).
To a stirred solution of para-nitrophenylchloroformate (0.141g) in dichloromethane
(5ml) was added dimethylaminopyridine (0.086g). After 2 minutes
40-

benzenemethanesulfonamide (0.120g) was added followed by triethylamine (0.078g). After 30 minutes 4-(3,4-dichlorophenoxy)-l,4'-bipiperidine (Method C; 0.230g) was added and-the reaction was left to stir for 2 hours. The solvent was removed under reduced pressure and the resulting product was purified by RPHPLC (Waters Xterra® column), (gradient, 90:10 0.2% aq ammonia / acetonitrile to 5:95 over 6 mins) to give the title compound (202mg).
rHNMR (399.98 MHz, CD3OD) 5 1.30 -1.43 (m, 2H), 1.73 -1.84 (m, 4H), 1.98 -2.06 (m, 2H), 2.44 - 2.55 (m, 3H), 2.59 - 2.66 (m, 2H), 2.82 - 2.89 (m, 2H), 4.36 - 4.42 (m, 3H), 4.41 (s, 2H), 6.88 - 6.91 (m, 1H), 7.09 - 7.10 (m, 1H), 7.24 - 7.31 (m, 3H), 7.36 - 7.39 (m, 3H); plus 1 drop of 30% NaOD in D20. ' ES+526/528
The Examples 2B-2X are examples of compounds of formula (la) and were prepared using similar methodology to that of Example 2A.
Example 3A
N-[[4-(3,4-Dichlorophenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-N,4-dimethyl-benzenesulfonamide (an example of a compound of formula (la) where R3 is not hydrogen).
To a solution of iV-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-4-methyl-benzenesulfonamide (Example IB, 0.3g) in methanol / dichloromethane (1:1, 40ml) was added (trimethylsilyl)diazomethane (2M in hexanes) (5ml) dropwise. The reaction was stirred under nitrogen for 12 hours. The solvent was removed under reduced pressure and the resulting product was purified by RPHPLC (Waters Xterra® column), (gradient, 75:25 0.2% aq ammonia / acetonitrile to 5:95 over 6 mins) to give the title compound (83mg).
:H NMR (399.98 MHz, CD3OD) 5 1.42 - 1.53 (m, 2H), 1.63 - 1.71 (m, 2H), 1.82 -1.96 (m, 4H), 2.31 (s, 3H), 2.39 - 2.47 (m, 2H), 2.48 - 2.57 (m, lH)i 2.72 - 2.79 (m, 2H), 2.93 - 3.01 (m, 2H), 3.69 (s, 3H), 4.20 - 4.26 (m, 2H), 4.27 - 4.34 (m, 1H), 6.77 - 6.81 (m, 1H), 7.00 (d, 1H), 7.21 - 7.29 (m, 3H), 7.65 - 7.68 (m, 2H) ES+ 540/542; m. pt. 15M53°C.
41

Example 4A N-Benzoyl-4-(3,4-dichlorophenoxy)- [ 1,4'-bipiperidine]-1 -sulfonamide (an example of a compound of formula (lb)).
Benzoyl sulfamoyl chloride (DE931225, (1955) Chemical Abstracts 1956, 50, 7861a; 248mg) was dissolved in THF (5ml) and cooled to -78°C. Triethylamine (170(11) was added dropwise over 160s and the solution was stirred for 25 min. 4-(3,4-Dichlorophenoxy)-l,4'-bipiperidine (Method C; 329mg) in THF (5ml) was added dropwise over 35min. Water was added then the mixture was evaporated. The residue was purified by RPHPLC (Waters Xterra® Column, eluant 0.1% aq ammonium acetate : acetonitrile 75-5 : 25-95) to give the title compound (37mg; MS [M+H]+ (APCI+) 512/514).
!H NMR (399.98 MHz, DMSO) 5 1.59 (qd, 2H), 1.74 -1.84 (m, 2H), 1.96 (d, 2H), 2.06 (d, 2H), 2.76 (t, 2H), 2.86 - 3.03 (m, 3H), 3.08 - 3.17 (m, 2H), 3.71 (d, 2E), 4.57 -4.64 (m, 1H), 7.02 (dd, 1H), 7.32 (d, 1H), 7.37 (t, 2H), 7.45 (t, 1H), 7.53 (d,. 1H), 7.92 (d, 2H).
Example 5 A
iV-Benzoyl-4-(2,4-dichloro-3-methylphenoxy)-[l,4'-bipiperidine]-l '-sulfonamide (an example of a compound of formula (lb)).
4-(2,4-Dichloro-3-methyIphenoxy)-l,4'-bipiperidine (see Method C; 240mg) was dissolved in dicbloromethane (10ml). Triethylamine (107 ul) was added followed by benzoyl sulfamoyl chloride (154mg). The solution was stirrred for 12h and then concentrated. The residue was purified by by RPHPLC (Waters Xterra® column), (gradient, 90:10 0.2% aq ammonia / acetonitrile to 5:95 over 6 mins) to give the title compound. (70mg, MS [M+H]+ (APCI+) 526/528; m.pt. 223°C)
!H NMR (399.98 MHz, CD3OD) 5 8.00 - 8.03 (m, 2H), 7.38 - 7.43 (m, 1H), 7.31 -7.36 (m, 2H), 7.25 (d, 1H), 6.95 (d, 1H), 4.45 - 4.52 (m, 1H), 3.80 - 3.87 (m, 2H), 2.84 -2.92 (m, 2H), 2.73 - 2.81 (m, 2H), 2.51 - 2.58 (m, 2H), 2.44 (s, 3H), 2.38 - 2.44 (m, 1H), 1.91 - 2.03 (m, 4H), 1.80 - 1.89 (m, 2H), 1.59 -1.70 (m, 2H); plus 1 drop of 30% NaOD in D20.
The Examples 5B-5E are examples of compounds of formula (la) and were prepared using similar methodology to that of Example 5A.
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.example on trans 4-Chloro-N- [[4-[4-(3,4-dichlorophenoxy)-1 -piperidinyljcyclohexyl]-carbonyl]-benzenesulfonamide (an example of a compound of formula (Ic)).
Sodium 4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]-cyclohexanecarboxylate (Method F, 111mg), EDCI (99mg), HOBT (97mg), DMAP (32mg) and p-chlorobenzenesulfonaniide (98mg) were combined in DMF (3ml) and stirred overnight. The solvent was evaporated and the residue was purified by RPHPLC (Waters Xterra® Column, eiuant 0.1% aqueous ammonium acetate : acetonitrile 75-25 : 25-75) to give the title compound (18mg; MS [M+H]+ (APQ+) 545/547/549).
1H NMR (399.98 MHz, DMSO) 8 1.23 (q, 2H), 1.35 (q, 2H), 1.74 -1.97 (m, 7H), 2.02 - 2.11 (m, 2H), 2.88 - 3.07 (m, 4H), 3.09 - 3.21 (m, 2H), 4.56 - 4.67 (m, 1H), 7.02 (dd, 1H), 7.33-(d, 1H), 7.46 (d, 2H), 7.53 (d, 1H), 7.73 (d, 2H).
Example 7A iV-Benzoyl-4-(3,4-dichlorophenoxy)- [ 1,4'-bipiperidine]-1 '-carboxamide (an example of a compound of formula (Id)).
4-(3J4-Dichlorophenoxy)-[l,4'-bipiperidine]-r-carboxamide (Method H, 200mg) and triethylorthobenzoate (3ml) were heated at 150°C for 16h, then allowed to reach ambient temperature. 2M HC1 (2 ml) was added and the resulting solution was stirred for 4h. The volatiles were evaporated and the residue was purified by chromatography (24:1 dichloromethane : methanol) followed by RPHPLC (Waters Xterra® column), (gradient, 75:25 0.2% aq ammonia / acetonitrile to 5:95 over 6 mins) to give the title compound (rn.pt 65-80°C; MS [M+H]+ (ES+) 476/478).
*H NMR (399.98 MHz, DMSO) 8 1.42 (2H, d), 1.58 (2H, d), 1.76 (2H, d), 1.92 (2H, d), 2.39 (2H, t), 2.72 - 2.78 (2H, m), 2.81 - 2.94 (3H, m), 3.79 - 4.22 (2H, m), 4.42 (1H, t), 6.98 (1H, dd), 7.25 (1H, d), 7.44 - 7.52 (3H, m), 7.56 - 7.68 (1H, m), 7.83 - 7.92 (2H, m).
Example 8A iV-(3,4-Dichlorobenzoyl)-4-(3,4-dichlorophenoxy)-[l,4,-bipiperidine]-r-sulfonamide (an example of a compound of formula (lb)).
4-(3,4-DicMorophenoxy)-[l,4'-bipiperidme]-l-sulfonamide (Method G, 200mg), 3,4 dichlorobenzoylchloride (102mg) and triethylamine (0.07ml) were stirred together in dichloromethane (10ml) at ambient temperature for 24 hours. The solvent was evaporated and the resulting product was purified by RPHPLC (Waters Xterra® column), (gradient,
43

75:25 0.2% aq ammonia / acetonitrile to 5:95 over 6 mins) to give the title compound (22mg; m.pt. 166-167°C; MS APCI580/582/584 (M+H)).
!H NMR (399.98 MHz, DMSO) 5 1.57 -1.79 (m, 4H), 1.89 - 2.17 (m, 5H), 2.60 -2.76 (m, 2H), 3.06 - 3.25 (m, 2H), 3.36 - 3.60 (m, 2H), 3.60 - 3.76 (m, 2H), 4.54 - 4.87 (m, 1H), 6.93 - 7.11 (m, 1H), 6.93 - 7.11 (m, 1H), 7.30-7.40 (m, 1H), 7.49 - 7.66 (m, 2H), 7.85 (d, lH),8.12(s, 1H).
The Examples 8B-8F are examples of compounds of formula (lb) and were prepared using similar methodology to that of Example 8 A. Recrystallisation was required after chromatography for several Examples.
Example 9A 4-(3,4-Dichloropb.enoxy)~N-(4-methylbenzoyl)-[ 1,4'-bipiperidine]-1 '-sulfonamide (an example of a compound of formula (lb)).
1,1 -Dimethylethyl [4-(3,4-dichlorophenoxy)-1,4'-bipiperidin-1 '-yl]sulfonylcarbamate (Method L; 400mg) and triethylamine (0.5ml) in dichloromethane (5ml) at ambient temperature were treated with 4-methylbenzoylchloride (163mg). The mixture was stirred overnight, the solvent was evaporated and the residue was dissolved in . DMSO (1ml) and purified by HPLC (Waters XTerra® column) (acetonitrile/aqueous ammonia gradient) to give the title compound as a white solid (70mg). MS [M+H]+ (APCI +) 526/528 (M+H)
!H NMR 5 (DMSO) 1.51 -1.61 (2H, m), 1.67 -1.81 (2H, m), 1.86 -1.96 (2H, m), 1.98 -2.08 (2H, m), 2.33 (3H, s), 2.71 - 2.92 (5H, m), 2/98 - 3.09 (2H, m), 3.72 (2H, d), 4.52 -4.61 (1H, m), 7.01 (1H, dd), 7.20 (2H, d), 7.30 (1H, d), 7.52 (1H, d), 7.82 (2H, d).
The Examples 9B and 9C are examples of compounds of formula (lb) and were prepared using similar methodology to that of Example 9A.
Example 10A
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-4-methyl- ' benzenesulfonamide, sodium salt (an example of a compound of formula (la)).
To N-[[4-(3,4-dichlorophenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-4-methyl-benzenesulfonamide (0.05g) was added 0.1M sodium hydroxide (0.949ml) and methanol


44

(5ml). The solution was stirred until all of the starting material had dissolved. The solvent
was removed under reduced pressure to give the title compound.
Mpt201°C
MS [M+H]+ (APCI+) 526/528
1H NMR 5 (CD3OD) 1.28 -1.42 (2H, m), 1.70 -1.82 (4H, m), 1.96 - 2.04 (2H, m), 2.35
(3H, s), 2.43 - 2.54 (3H, m), 2.56 - 2.66 (2H, m), 2.80 - 2.87 (2H, m), 4.34 - 4.42 (3H, m),
6.87 - 6.90 (1H, m), 7.09 - 7.10 (1H, m), 7.19 - 7.23 (2H, m), 7.35 - 7.38 (1H, m), 7.75 -
7.79 (2H, m).
The Examples 10B-10D are examples of compounds of formula (la) and were prepared using similar methodology to that of Example 10A.
Example 11A
4-(3,4-Dichlorophenoxy)-Ar-[(l,2-dihydro-l-oxo-4-isoquinolinyl)carbonyl]-[l,4'-bipiperidine]-1 '-sulfonamide (an example of a compound of formula (lb)).
To a solution of 1,1-dimethylethyl [[4-(3,4-dichlorophenoxy)[l,4'-bipiperidra]-l'-yl]sulfonyl]-carbamate (Method L; 0.305g) in dichloromethane was added 1,2-dihydro-l-oxo-4-isoquinolinecarbonyl chloride (0.147g, prepared from the corresponding acid by treatment with tbionyl chloride at reflux) followed by triethylamine (0.097ml) and the reaction was stirred under nitrogen for 12 h. The solvent was removed under reduced pressure with the resulting product dissolved in DMSO and purified by HPLC (Waters XTerra® column), (gradient, 75% aqueous (0.2% ammonia) / acetonitrile decreasing to 5% over 10 min) to give 1,1-dimethylethyl [[4-(3,4 dichlorophenoxy)[l,4'-bipiperidin]-r-yl]suIfonyl][(l,2-dihydro-l-Qxo-4-isoquinolinyl)carbonyl]-carbamate. (MS [M+H]+ (ES+) 679/681). . 1,1-DimethylethyI [[4-(3,4 dichlorophenoxy)[l,4-bipiperidinJ-l -yl]sulfonyl][(l,2-dihydro-l-oxo-4-isoquinolinyl)carbonyl]-carbamate was dissolved in dichloromethane (10ml) followed by the addition of trifluoroacetic acid, (3ml) and allowed to stir under nitrogen for 12 h. The solvent was removed under reduced pressure and the resulting product was dissolved in DMSO and purified by HPLC (Waters XTerra® column), (gradient, 90% aqueous (0.2% ammonia) / acetonitrile decreasing to 5% over 10 min) to give the title compound (0.028g) m.pt. 200°C MS [M+H]+(ES+) 579/581
45

]H NMR (399.98 MHz) 5 (CD3OD plus 1 drop NaOD) 1.58 -1.69 (2H, m), 1.71-1.81 (2H, m), 1.92 - 2.05 (4H, m), 2.37 - 2.46 (1H, m), 2.48 - 2.56 (2H, m), 2.76 - 2.90 (4H, m), 3.84 - 3.90 (2H, m), 4.35 - 4.42 (1H, m), 6.86 - 6.90 (1H, m), 7.08 (1H, d), 7.30 - 7.34 (1H, m), 7.37 (1H, d), 7.49 - 7.54 (1H, mj, 8.27 - 8.31 (1H, m), 8.44 (1H, s), 8.75 (1H, d)
Example 12A iV-(Cyclohexylcarbonyl)-4-(3,4-dichlorophenoxy)- [ 1,4'-bipiperidine]-1 '-sulfonamide (an example of a compound of formula (lb)).
To a solution of 1 J-diniethyietbyIC[4-(3,4-dicnlorophenoxy)fl,4'-bipiperidinJ-r-yl]sulfonyl]-carbamate (Method L; 0.305g) in chloroform was added cyclohexanecarbonyi chloride (0.094ml), triethylamine (0.097ml) and dimethylaminopyridine (0.086g). The reaction mixture was heated in a CEM Discover microwave at 300W for 5 seconds reaching a temperature of 50°C; pressure developed. The.solvent was removed under reduced pressure and the resulting product was dissolved in DMSO and purified by HPLC (Waters XTerra® column), (gradient, 90% aqueous (0.2% ammonia) / acetonitrile decreasing to 5% over 10 min) to give the title compound (0.176g) as a foam. MS [M+Hj+ (ES+) 518/520
1H NMR (399.98 MHz) 5 (CD3OD) 1.10 -1.38 (5H, m), 1.44 -1.62 (3H, m), 1.65 -1.76 (6H, m), 1.82 - 1.89 (2H, m), 1.90 -1.98 (2H, m), 2.07 - 2.16 (1H, m), 2.41 - 2.57 (3H, m), 2.72 - 2.86 (4H, m), 3.74 - 3.80 (2H, m), 4.30 - 4.37 (1H, m), 6.78 - 6.81 (1H, m), 7.02 (lH,d),7.28(lH,d)
Example 13 A 4-(3,4-Dichlorophenoxy)-iV-(2-methyl-1 -oxopropyl)- [ 1,4'-bipiperidine]-V-sulfonamide (an example of a compound of formula (lb)).
To a solution of 4-(3,4-dichlorophenoxy)-[l,4'-bipiperidine]-r-sulfonamide (Method G; 0.408g) in dichloromethane (5ml) was added 2-methyl-propanoyl chloride (0.126ml), triethylamine (0.167ml) and dimethylarninopyridine (0.147g). The reaction was heated in a CEM Discover microwave at 50°C using 50W of power for 10 minutes. The solvent was removed under reduced pressure and the resulting product was dissolved in DMSO and purified by HPLC (Waters XTerra® column), (gradient, 90% aqueous (0.1% aqueous ammonium acetate) / acetonitrile decreasing to 5% over 10 min) to give the title compound (0.152g) as a foam. MS [M+H]+ (ES+) 478/480
46

1H N1-4R (399.98 1-4Hz) 5(CD3OD) 1.30 (6H, d), 1.75-1.91 (2H, 1-4), 1.97-2.11 (2H, 1-4), 2.13 - 2.32 (4H, 1-4), 2.65 (IH, septet), 2.77 - 2.99 (3H, 1-4), 3.02 - 3.12 (2H, 1-4), 3.12 - 3.25 (2H, 1-4), 4.04 - 4.15 (2H, 1-4), 4.62 - 4.72 (IH, 1-4), 7.09 (IH, dd), 7.31 (IH, d), 7.57 (IH, d)
Exa1-4ple 14A 4-(3,4-Dichlorophenoxy)-iV-(2-phenylacetylH 1,4'-bipiperidine]-1 '-sulfona1-4ide (an example of a compound of formula (lb)).
To a solution 4-(3,4-dichlorophenoxy)- [l,4'-bipiperidine]-l'-sulfona1-4ide (method G; O.lOOg) in THF (21-4l) was added potassiu1-4 tert butoxide (0.083g) followed after lh by phenylacetyl chloride (0.097ml). After 12h the solvent was evaporated and the resultant product was dissolved in methanol and loaded onto an Isolute® SCX cartridge which was washed with methanol and eluted with 10% ammonia in methanol. The solvent was evaporated and the residue was dissolved in DMSO and purified by HPLC (Waters XTerra® column), (gradient, 90% aqueous (0.2% ammonia) / acetonitrile decreasing to 75% over 10 min) to give the title compound (0.01 g). 1-4S [1-4+H]+ (ES+) 526/528
!H N1-4R (299.945 1-4Hz) 6 (CD3OD plus 1 drop NaOD) 1.45 - 1.59 (2H, 1-4), 1.70 -1.89 (4H, 1-4), 1.96 - 2.08 (2H, 1-4), 2.23 - 2.35 (IH, 1-4), 2.43 - 2.63 (4H, 1-4), 2.77 - 2.88 (2H, 1-4), 3.45 (2H, s), 3.66 - 3.75 (2H, 1-4), 4.35 - 4.44 (IH, 1-4), 6.88 - 6.94 (IH, 1-4), 7.10 - 7.13 (IH, 1-4), 7.14 - 7.30 (3H, 1-4), 7.33 - 7.42 (3H, 1-4)
Exa1-4ple 15A Ar-[[4-(3,4-Dichlorophenoxy)il,4,-bipiperidin]-r-yl]carbonyl]-2-propanesulfona1-4ide (an exa1-4ple of a compound of for1-4ula (la)).
To a solution 4-(3,4-dichlorophenoxy)-[l,4'-bipiperidine]~r-carboxamide (1-4ethod H; 0.372g) in THF (51-4l) was added potassium tert butoxide (0.337g) followed after lh by 2-propanesulfonyl chloride (0.3371-4l). After a further 2h aqueous a1-41-4oniu1-4 chloride was added and THF was evaporated to leave a precipitate which was collected. The precipitate was purified by HPLC (Waters XTerra® column), (gradient, 95% aqueous (0.2% ammonia) / acetonitrile decreasing to 50% over 10 min) to give the title co1-4pound (0.061g).
1-4S [M+H]+ (ES+) 478/480
!H N1-4R (399.98 1-4Hz) 5 (CD3OD plus 1 drop NaOD) 1.19 (6H, d), 1.23 -1.37 (2H, 1-4), 1.62 -1.70 (2H, 1-4), 1.71 -1.78 (2H, 1-4), 1.88 -1.96 (2H, 1-4), 2.34 - 2.47 (3H, 1-4), 2.48 -
-H&r~

2.60 (2H, m), 2.72 - 2.S0 (2H, m), 3.38 - 3.46 (1H, m), 4.27 - 4.37 (3H, m), 6.79 (1H, dd), 6.99 (lH,d), 7.28 (lH,d)
Example 16A
4-(3,4-Dichlorophenoxy)-Ar-[(4-methylphenyl)sulfonyl]-[l,4'-bipiperidine]-r-sulfonamide sodium salt (an example of a compound of formula (Ie)).
4-(3,4-Dichlorophenoxy)-[l)4'-bipiperidine]-r-sulfonamide (Method L; 582mg), toluenesulfonyl chloride (380mg) and DMAP (ISOmg) were combined and dissolved in dichloromethane (10ml). Triethylamine (0.3mi) was added, followed after 35min by a . second portion of triethylamine (0.3ml). The solution was stirred for 21h and then concentrated. The residue was triturated with methanol and then THF to give a solid (0.65g). A portion of the product (0.34g) was dissolved in warm DMSO (30ml). To this solution was added aqueous sodium hydroxide (1M, 6ml) followed by water (200ml). The solution was allowed to cool overnight and the title compound was collected (175mg). m. pt. 242-243°C MS [M+H]+ (ES+) 562/564
*H NMR (399.98 MHz) 5(DMso) 1.27 (2H, qd), 1.51 -1.60 (2H,m), 1.65 (2H, d), 1.88 -1.94 (2H, m), 2.23 (1H, tt), 2.31 (3H, s), 2.32 - 2.43 (4H, m), 2.68 - 2.75 (2H, m), 3.33 -3.38 (2H, m), 4.37 - 4.43 (1H, m), 6.98 (1H, dd), 7.18 (2H, d), 7.25 (1H, d), 7.48 (1H, d), 7.60 (2H, d)
Example 16B (an example of a compound of formula (Ie)) was prepared using similar methodology to that of Example 16A and recrystallisation was required after chromatography.
48






T





1Q N-[[4-(4-
chlorophenoxy)[l ,4'-
bipiperidin]-l'-
yl]carbonyl]-4-
1-4ethyl-
benzenesulfona1-4ide 492/494 (CD3OD plus 1 drop NaOD) 1.27 - 1.39 (2H, 1-4), 1.70 - 1.84 (4H, 1-4), 1.96 - 2.04 (2H, 1-4), 2.36 (3H, s), 2.40 -2.51 (3H, 1-4), 2.56 - 2.67 (2H, 1-4), 2.79 - 2.87 (2H, 1-4), 4.31 - 4.42 (3H, 1-4), 6.89 (2H, d), 7.20 - 7.24 (4H, 1-4), 7.76 (2H, d) 237-238
1R N-[[4-(2,4-dichloro-3-
1-4ethylphenoxy) [1,4-
bipiperidin]-l'-
yl]carbonyl]-2-
1-4ethyl-
benzenesulfona1-4ide 540/542 (CD3ODplus 1 drop NaOD) 1.27 - 1.41 (2H, 1-4), 1.78 - 1.88 (4H, 1-4), 1.93 - 2.02 (2H, 1-4), 2.44 - 2.55 (3H, 1-4), 2.44 (3H, s), 2.57 - 2.67 (2H, 1-4), 2.66 (3H, s), 2.81 - 2.89 (2H, 1-4), 4.35 - 4.51 (3H, 1-4), 6.95 (1H, d), 7.19 - 7.34 (4H, 1-4), 7.94 -7.97 (1H, 1-4)
IS N-[[4-(2,4-dichloro-3-fluorophenoxy) [ 1,4'-bipiperidin]-!'-yl]carbonyl]-4-
1-4ethyl-benzenesulfona1-4ide (CDCI3) 1.61 (2H, q), 2.07 (4H, t), 2.28 (2H, t), 2.38 (3H, s), 2.70 (2H, t), 2.93 - 3.05 (1H, 1-4), 3.12 (2H, t), 3.18 - 3.28 (2H, 1-4), 4.45 (2H, d), 4.60 - 4.67 (1H, 1-4), 6.79 (1H, dd), 7.24 (2H, d), 7.30 (1H, d), 7.80 (2H, d)





N-[[4-(3-
478/480
chlorophenoxy)[ 1,4'-
bipiperid1-4]-l'-
yl]carboriyl]-
benzenesulfona1-4ide
2-chloro-N-[[4-(3- 526/528
510/512
1-4ethylphenoxy)[l ,4'-bipiperidin]-l'-yl]carbonyl]-benzenesulfona1-4ide
N-[[4-(2-chloro-4-
fluorophenoxy) [1,4-
bipiperid1-4j-1'-
yl]carbonyl]-2-
1-4ethyl-
benzenesulfona1-4ide

(CD3OD plus 1 drop NaOD) 1.26 -1.41 (2H, 1-4), 1.69 -1.85 197-206
(4H, 1-4), 1.95 - 2.04 (2H, 1-4), 2.41 - 2.53 (3H, 1-4), 2.57 -
2.68 (2H, 1-4), 2.79 - 2.88 (2H, 1-4), 4.34 - 4.46 (3H, 1-4), 6.83
- 6.94 (3H, 1-4), 7.22 (1H, dt), 7.39 - 7.46 (3H, 1-4), 7.87-7.89
(2H, 1-4)
(CD3OD plus 1 drop NaOD) 1.32 - 1.43 (2H, 1-4), 1.76 -1.86 223-234
1-4), 2.59 - 2.69 (2H, 1-4), 2.79 - 2.87 (2H, 1-4), 4.35 - 4.48
(3H, 1-4), 6.88 (1H, d), 6.93 (1H, d), 7.08 (1H, t), 7.32 - 7.45
(3H, 1-4), 8.08 (1H, dd)
(D1-4SO) 1.17 -1.46 (2H, 1-4), 1.65 - 2.16 (8H, 1-4), 2.57 (3H, 164-165 s), 2.77 - 3.85 (6H, 1-4), 4.12 - 4.32 (2H, 1-4), 7.12 - 7.34 (5H, 1-4),.7.46 (1H, dd), 7.78 (1H, d)













































The preparations of certain intermediates are now presented.
Method A [ 1,4'1B ipiperidin vl-4-ol
4-Oxo-piperidine-l-carboxylic acid tert-butyl ester (20g) and 4-hydroxypiperidine (6.7g) were stirred together in dichloroethane (200ml) with acetic acid (4ml) at RT for 30 minutes. Sodium triacetoxyborohydride (23g) was then added and the mixture stirred at RT overnight. The mixture was evaporated to dryness and the residue taken into water, extracted with diethyl ether (3x 200ml), the aqueous was basified to pH 9-10 and extracted with dichloromethane (3x 200ml). The dichloromethane extracts were combined, dried (MgS04) and evaporated to leave an oil (19g). The oil was dissolved in methanol (300ml) and treated with concentrated hydrochloric acid (5ml). The mixture was stirred overnight and then evaporated to dryness to leave the title compound as the hydrochloride salt (15g). JH NMR (400MHz, DMSO-D6) 5 1.6-2.4 (m, 9H), 2.8-3.5 (m, 8H), 3.62 (m, 1H), 3.95 (s, 1H), 9.29 and 9.059 (bs, 2H), 10.9 and 11.09 (bs, 1H).
MethodB 4-(3.4-Dichlorophenoxv)piperidine Step a: tert-Butyl 4-(3,4-dichlorophenoxy)-l-piperidinecarboxylate
Diethyl azodicarboxylate (41.0ml) was added to a solution of triphenylphosphine (62.9g) in tetrahydrofuran (800ml) at 0°C. After 15 minutes 3,4-dichlorophenol (39.lg) was added, after a further 15 minutes tert-butyl 4-hydroxy-l-piperidinecarboxylate (48.3g) in tetrahydrofuran (400ml) was added dropwise over 30 min. The solution was stirred at room temperature for 16 hours and concentrated to a small volume. Purification by chromatography (ethyl acetate : wo-hexane 95:5) gave the sub-title compound as an oil (61-3g).
MS: APCI(+ve): 246/248 (M-BOC+2H) Step b: 4-(3,4-Dichlorophenoxy)piperidine
The product from Step a was dissolved in dichloromethane (600ml) and trifluoroacetic acid (300ml) was added. After 24 hours at room temperature the solution was evaporated and the resultant gum triturated under ether to give the sub-title product as a solid (36.6g). The free base was liberated by addition of aqueous NaOH (2M) and extraction with ethyl acetate followed by evaporation of solvent to give the title compound as a gum (25g).

1H NMR: 5(CDC13) 1.77 (1H, br s), 2.05-2.26 (4H, m), 3.20-3.49 (4H, m), 4.61 (1H, s), 6.69-7.52 (3H, m).
Method C 4-(3,4-Dichlorophenoxv)-l-1.4'lbipiperidme Step a: 4-(3,4-Dichlorophenoxy)-[l,4,]bipiperidinyl-l-carboxylic acid tert-butyl ester
4-(3,4-Dichlorophenoxy)piperidine (1.5g) was dissolved in 1,2-dichloroethane (21ml). l-Boc-4-piperidone was added (1.21g) followed by NaBH(OAc)3 (1.8 lg) and acetic acid (0.37g). After 18 hours at room temperature aqueous NaOH (1M) solution and diethyl ether were added. The product was extracted with diethyl ether, the combined organic extracts dried with MgSO4 and concentrated. Purification by chromatography (dichloromethane : methanol 92:8) gave the sub-title product (1.97g; MS: APCI(+ve): 429/431 (M+H)). Step b: 4-(3,4-Dichloro-phenoxy)-[l,4']bipiperidine
The product of Step a was dissolved in dichloromethane (30ml) and trifmoroacetic acid (15ml) was added. After 4 hours at room temperature the solution was evaporated and the resultant gum triturated under ether to give the trifluoroacetate salt of the sub-titled product as a solid (l.l5g). The free base was liberated by addition of aqueous NaOH (2M) and extraction with ethyl acetate followed by evaporation of solvent to give the sub-title compound as a solid (0.68g).
1H NMR: 5(CDC13) 1.38-1.51 (2H, m), 1.74-2.02 (6H, m), 2.38-2.50 (3H, m), 2.56-2.61 (2H, m), 2.79-2.86 (2H, m), 3.14-3.18 (2H ,m), 4.22-4.28 (1H, m), 6.73-7.32 (3H, m).
81
The following inter1-4ediates were prepared in a si1-4ilar 1-4anner to 1-4ethod C:


2 for starting material see WO 00/12478
3 1H NMR (399.978MHz, CDC13): 5 1.44 (2H, qd), 1.74 -1.86 (5H, m), 2.01 - 2.07 (2H, m), 2.38 - 2.42 (1H, m), 2.44 - 2.50 (2H, m), 2.60 (2H, td), 2.82 - 2.87 (2H, m), 3.15 (2H, d), 4.98 (1H, septet), 6.66 (1H, d), 7.50 (1H, dd), S.06 (1H, d).
Method D 4-(-3-Chloro-4-fIuoro-phenoxy)-piperidine
DEAD (0.43ml) was added to a solution of triphenylphosphine (0.72g), 3-chloro-4-fluorophenol (0.403 g) and 4-hydroxy-piperidine-l-carboxylic acid tert-butyl ester (0.5g) in THF at RT. The resulting mixture was stirred overnight, HC1 in dioxan (2ml of 4M) was added and the mixture stirred at RT overnight. The mixture was then evaporated to dryness and triethylamine (5ml) was added. The mixture was evaporated and the residue was dissolved in methanol (10ml), placed onto a SCX cartridge (Varian, lOg, SCX cartridge available from International Sorbent Technology Isolute® Flash SCX-2) and eluted: first with methanol then with 10%NH3 in methanol. The basic fractions were combined and evaporated to give the product as an oil (0.6g).
!H NMR (299.946 MHz, DMSO-D6) 5 1.34 - 1.46 (2H, m), 1.83 -1.91 (2H, m), 2.53 - 2.59 (2H, m), 2.87 - 2.96 (2H, m), 3.22 - 3.39 (1H, m), 4.39 (1H, septet), 6.92 - 6.98 (1H, m), 7.17 - 7.20 (1H, m), 7.30 (1H, t).
The following inter1-4ediates were prepared in si1-4ilar 1-4anner to 1-4ethod D:



1-4ethod E 4-(3.4-DichIorophenoxvV4'-1-4ethvl-l,4'-bipiperidine_dihydrochloride a) l,l-Dimethylethyl4,-cyano-4-(3,4-dichlorophenoxy)-[l,4,-bipiperidine]-lcarboxylate
4-(3,4-Dichlorophenoxypiperidine) (1-4ethod B step b; 5001-4g) was dissolved in dichloroethane (21-4l) with l-Boc-4-piperidone (4461-4g). Titaniu1-4 teraisopropoxide
-fe-

(0.85ml) was added and the mixture was stirred overnight. The solvent was evaporated and toluene (5ml) was added followed by diethylaluminium cyanide (3ml of 1M solution in toluene). The mixture was stirred for 3h, then ethyl acetate was added (5ml) followed by water (0.5ml) and the mixture was stirred for a further 2h. The mixture was filtered through a GF filter paper, and evaporated to give the subtitle compound (912mg; MS [M+H]+ (APCI+) 454/456).
!H NMR (399.98 MHz, CD3OD) 5 1.36 (s, 9H), 1.57 -1.77 (m, 4H), 1.90 -1.99 (m, 2H), 2.04 - 2.12 (m, 2H), 2.44 - 2.52 (m, 2H), 2.77 - 2.87 (m, 2H), 3.02 - 3.13 (m, 2H), 3.82 (dt, 2H), 4.31 - 4.40 (m, 1H), 6.81 (dd, 1H), 7.02 (d, 1H), 7.29 (d, 1H).
b) 1,1-Dimethylethyl 4-(3,4-dichlorophenoxy)- 4'-methyl-[l,4'-bipiperidine]-r-carboxylate
1,1 -Dimethylethyl 4'-cyano-4-(3,4-dichlorophenoxy)-[ 1,4'-bipiperidine]-1 '-carboxylate (lOOmg) was dissolved in THF (6ml). Methyl magnesium bromide (3M in ether, 220jil) was added and the mixture was stirred at RT for 2h. Further methyl magnesium bromide (220uJ) was added and the solution was stirred for a further 60h. Potassium carbonate solution (saturated aqueous) was added and the mixture was extracted with DCM. The organic phase was dried, filtered and evaporated to give the subtitle compound (lOOmg; MS [M+H]+ (APGI+) 443/445).
1H NMR (299.945 MHz, CD30D) 5 1.01 (s, 3H), 1.47 (s, 9H), 1.69 -1.84 (m, 4H), 1.97 - 2.08 (m, 2H), 2.42 - 2.52 (m, 2H), 2.81 - 2.92 (m, 2H), 3.36 - 3.42 (m, 2H), 3.45 -3.57 (m, 2H), 3.62 - 3.89 (m, 2H), 4.32 - 4.41 (m, 1H), 6.89 (dd, 1H), 7.10 (d, 1H), 7.38 (d, 1H).
c) 4-(3,4-dichlorophenoxy)- 4'-methyl-l,4'-bipiperidine dihydrochloride
1,1 -Dimethylethyl 4-(3,4-dichlorophenoxy)- 4'-methyl-[l ,4'-bipiperidine]-r-carboxylate (lOOmg) was dissolved in ethanol (5ml). Hydrogen chloride (2ml of 4M in dioxan) was added and the solution was stirred overnight. Further hydrogen chloride solution (2ml) was added and the mixture was stirred for a further 2h. The solvents were evaporated to give the title compound (95mg; MS [M+H]+ (APCI+) 343/345).
Method F trans Sodium 444-(3.4-dichlorophenoxvyi-piperidinvl1-cvclohexanecarboxvlate a)Ethyl4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]-cyclohexanecarboxylate
4-(3,4-Dichlorophenoxy)piperidine (Method B, 1.44g), ethyl 4-oxocyclohexanecarboxylate (10g) and acetic acid (0.34ml) were combined in THF 10ml

and the solution was cooled in ice. Sodium triacetoxy borohydride (1.45g) was added and the mixture was stirred overnight and allowed to come to ambient temperature. The reaction mixture was poured onto a stirred saturated aq solution of sodium bicarbonate. The mixture was extracted with ethyl acetate thrice, the organic phases were washed with brine, dried, filtered and evaporated. The residue was purified on an SCX cartridge (International Sorbent Technology Isolute® Flash SCX-2), washed with methanol and then product eluted with 0.7M ammonia in methanol. Further purification by chromatography (silica, 9Q-.9-.1 DCM: methanol •. triethylamine.) gave. the. subtitle compound (1.59g; MS [M+H]+ (APCI+) 400/402) as a mixture of cis/trans isomers.
1HMMR (399.98 MHz, CD3OD) 5 1.23 (t), 1.25 (t), 1.28 -1.59 (m), 1.70-1.81 (m), 1.96 - 2.07 (m), 2.17 - 2.27 (m), 2.32 - 2.40 (m), 2.45 - 2.56 (m), 2.58 - 2.61 (m), 2.80 - 2.89 (m), 3.30 (quintet), 4.10 (q), 4.14 (q), 4.34 - 4.40 (m), 6.88 (dd), 6.88 (dd), 7.09 (d), 7.09 (d), 7.37 (d), 7.37 (d).
b) trans Sodium 4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]-cyclohexanecarboxylate
Ethyl 4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]-cyclohexanecarboxylate(0.97g) was added to a solution of sodium ethoxide in ethanol (prepared from sodium (1.28g) and ethanol (100ml)). the solution was heated to reflux overnight. Acetic acid was added and the solvent was evaporated. Ethyl acetate, water and sodium hydroxide were added to the residue and an insoluble white solid formed which was collected by filtration and dried in vacuo to give the sub-titled compound (469mg; MS [M-Na]" (APCI-) 370/372) containing sodium acetate.
lR NMR (399.98MHz, CD3OD) 5 1.27 - 1.38 (m, 2H), 1.46 (q, 2H), 1.72 - 1.81 (m, 2H), 1.95 - 2.09 (m, 7H), 2.40 (t, 1H), 2.55 (td, 2H), 2.84 - 2.91 (m, 2H), 4.39 (septet, 1H), 6.89 (dd, 1H), 7.10 (d, 1H), 7.37 (d, 1H). '
Method G 4-(3.4-Dichlorophenoxv)-ri.4'-bipiDeridinel-r-sulfonamide
4-(3,4-Dichlorophenoxy)-l,4'-bipiperidme (5g, 0.0152 mol)'and sulfamide (1.45g, 0.0152 mol) were stirred together in dioxan (150ml) at reflux for 24 hours. The resulting mixture was cooled to ambient temperature, evaporated to dryness and the residue was . triturated with ether to give the title compound as a tan solid (5g; MS APCI409/411 (M+H)).

1H NMR (399.98 MHz, DMSO) 5 1.38 - 2.03 (m, 6H), 2.25 - 2.45 (m, 6H), 2.66 -2.84 (m, 3H), 3.41 - 3.53 (m, 2H), 4.35 - 4.47 (m, 1H), 6.31 - 6.45 (m, 2H), 6.91 - 7.03 (m, 1H), 7.18-7.31 (m, 1H), 7.43 - 7.55 (m, 1H).
Method H 4-(3,-DichlorophenoxyVri ,4'-bipiperidine1-1 '-carboxamide.
4-(3,4-Dichlorophenoxy)-l,4'-bipiperidine (2.0g) was dissolved in glacial acetic -acid (0.60Sml), the solution was diluted with water (6ml) and added with stirring to a solution of sodium cyanate (0.395g) in warm water (3ml). The reaction was allowed to stand for 30 mins. 2M Sodium hydroxide solution was added until the solution was alkaline. The resulting precipitate was collected and washed with water followed by dichloromethane and then dried to leave the sub-title compound (1.3g; ES+ 372/374).
'H NMR (399.98 MHz, DMSO) 5 1.20 -1.31 (m, 2H), 1.51 -1.61 (m, 2H), 1.62 -1.69 (m, 2H), 1.88 -1.95 (m, 2H), 2.32 - 2.44 (m, 3H), 2.55 - 2.64 (m, 2H), 2.70 - 2.77 (m, 2H), 3.92 - 3.99 (m, 2H), 4.37 - 4.44 (m, 1H), 5.86 (s, 2H), 6.95 - 6.99 (m, 1H), 7.24 - 7.25 (m, 1H), 7.49 (d, 1H).
Method I 2,4-Dichloro-3-fluorophenoI
a) N,N-Diethyl-4-chloro-3-fluorophenyl carbamate
A solution of 4-chloro-3-fiuorophenol (26.9g) and diethylcarbamoyl chloride (25g)
in pyridine (100ml) was heated to 100°C for 12 h and then allowed to cool. Water (100ml)
was added and the product was extracted with diethylether/pentane (1:1) (50mlx2). The
combined organic extracts were washed with HC1 (2M, 70ml), NaOH (2M, 75ml) and
dried (MgSO4), filtered and evaporated to give the subtitle compound as an oil (37.7g)
1H NMR 8 (CDC13) 1.18 -1.26 (6H, m), 3.35 - 3.44 (4H, m), 6.90 (1H, ddd), 6.99 - 7.02
(1H, m), 7.35 (1H, t) ' •
b) N, N-Diethyl-2,4-dichloro-3-fluorophenyl carbamate
To a solution of N,N-diethyl-4-chloro-3-fluorophenyl carbamate (15g) in THF (100ml) and TMEDA (9.7ml) at -90°C was added secBuLi. (1.3M, 49.5ml) whilst maintaining the temperature between -80°C and -90°C. The mixture was stirred at -80°C for 2h. 1,1,1,2,2,2-Hexachloroethane (17.39g) as a solution in THF (50ml) was added. During this period the reaction was allowed to warm to 0°C. Water (50ml) was added and the product was extracted with pentane. The combined organic extracts were dried (MgSO4) and filtered. Evaporation of solvent and purification by HPLC (Waters XTerra®

t
column)(gradient (25% MeCN/NH3(aq) (0.1%) to 95% MeCN//NH3(aq) (0.1%)) gave the
subtitle compound as an oil (9.3g).
'H NMR 8 (CDC13) 1.19 -1.32 (6h, m), 3.36 -3.51 (4H, m), 7.03 (1H, dq), 7.26 - 7.33 (1H,
m).
2,4-Dichloro-3-fluorophenol
N,N-Diethyl-2,4-aichloro-3-fraorophenyl carbamate (8.14g) was dissolved in THF
(17ml). A solution of lithium aluminium hydride (33ml of 1M in THF) was added
dropwise and the resulting solution was stirred overnight. Ethanol was added followed by
hydrochloric acid (2M, 17ml). The resulting suspension was filtered and the solid was
washed with ether. The phases were separated, the aqueous phase was extracted thrice
with ether and the combined organic phases were dried (MgSOzi), filtered and evaporated
to give the title compound (3.4g).
1H NMR 5 (CD3OD) 6.65 (1H, dd), 7.11 (1H, t)
Method J
2,6-Dimethvl-benzenesulfonamide
To a solution of 2,6-dimethyl-benzenethiol (2ml) in water (20ml), chlorine gas was introduced over 15 minutes resulting in precipitation of an orange solid. The reaction was left to stir in a stoppered flask for a further 60 minutes. An excess of ammonia solution (0.88 sg) was added and the mixture was left to stir for 12h. The reaction was evaporated to remove ammonia and then filtered. The solid was washed with water followed by iso-hexane to give the title compound. -MS [M-H]" (ES-) 184 !H NMR 8 (DMSO) 2.59 (6H, s), 7.18 (2H, d), 7.27 (2H, s), 7.30 (1H, t)
Method K trans 4-[4-(3,,4-Dichlorophenoxv)-l-piperidinyIl-cvclohexanecarboxvlic acid a) trans Ethyl 4-[4-(3,4-dichlorophenoxy)-l-piperidinyll-cyclohexanecarboxylate
Ethyl 4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]-cyclohexanecarboxylate (method F, step a, 0.97g) was added to a solution of sodium ethoxide prepared from sodium (1.28g) and ethanol (100ml). The resultant solution was heated under reflux for 18h. Acetic acid (0.1ml) was added and the solvent was evaporated. Ethyl acetate, water and sodium hydroxide were added to the residue and separated. The aqueous phase was extracted twice with ethyl acetate-methanol mixtures and the combined organic phases were washed with brine, dried (MgSO4), filtered and evaporated to give the subtitle compound as an oil.

MS [M+H]+ (APCI+) 400/402
'H NMR of major isomer (ca 3.5:1 ratio) 5 (acetone) 1.20 (3H, t), 1.27 - 1.46 (4H, m), 1.57
- 1.71 (3H, m), 1.84 - 1.90 (2H, m), 1.95 - 2.02 (4H, m), 2.15 - 2.23 (1H, m), 2.27 - 2.41
(2H, m), 2.46 (2H, ddd), 4.06 (2H, q), 4.40 (1H, septet), 6.95 (1H, dd), 7.15 (1H, d), 7.43
(lH,d)
b) trans 4-[4-(3,4-Dichlorophenoxy)-l-piperidinyl]-cyclohexanecarboxylic acid
trans Ethyl 4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]-cyclohexanecarboxylate (0.8g) was dissolved in t-BuOH (180ml) at 38°C. To this was added Candia rugosa lipase powder (3g).This was stirred for 30 minutes then water (20ml) was added over 4 h. The mixture was then stirred for 48h and filtered. The enzyme was washed with 9:1 t-BuOH -water ( 2 x20ml) and the filtrate was evaporated. Ethyl acetate was added to the residue and then decanted. The resultant solid was dissolved in methanoI/DMSO and was purified by HPLC (Waters XTerra® column with at-column dilution of sample) (gradient (5% MeCN/NH3(aq) (0.2%) to 40% MeCN//NH3(aq) (0.2%)) gave the title compound (0.44g) as a white solid, m.pt. 167-168°C MS [M+H]+ (ES+) 372/374
!H NMR 5 (DMSO) 1-19 -1.36 (4H, m), 1.50 -1:59 (2H, m), 1.78 (2H, d), 1.87 -1.96 (4H, m), 2.09 (1H, td), 2.24 - 2.32 (1H, m), 2.38 (2H, td), 2.72 (2H, dt), 4.39 (1H, septet), 6.97 (1H, dd), 7.24 (1H, d), 7.49 (1H, d)
Method L 1,1 -Dimethylethvl [4-(3,4-dichlorophenoxyy 1,4'-bimperidin-1 '-ynsulfonylcarbamate
terf-Butanol (0.48ml) in dichloromethane (2ml) was added to a solution of chlorosulfonylisocyanate (0.43 ml) in dichloromethane (5ml) stirring at 0°C. The resulting solution was then added to a solution of 4-(3,4-dichlorophenoxy)-l,4'-bipiperidine (1.6g) and triethylamine (0.77ml) in dichloromethane (20ml) at 0°C. After stirring at 0°C for 2h, the reaction mixture was washed with 0.1M hydrochloric acid (30ml), dried (MgSO4) and evaporated. The residue was triturated with diethylether (20ml) to. give the title compound as a white solid. (1.9g)
lH NMR 5(DMS0) 1.44 (9H, s), 1.64 -1.77 (2H, m), 1.94 - 2.08 (2H, m), 2.15 - 2.27 (4H, m), 2.86 (2H, t), 3.03 - 3.18 (2H, m), 3.28 - 3.53 (3H, m), 3.76 (2H, d), 4.59 - 4.81 (1H, m), 6.99 - 7.11 (1H, m), 7.33 - 7.39 (1H, m), 7.52 - 7.58 (1H, m)
. U^

EXAMPLE 17 Pharmacological Analysis: Calcium flux [Ca 2+]i assay Human eosinophils
Human eosinophils were isolated from EDTA anticoagulated peripheral blood as previously described (Hansel et al., /. Immunol. Methods, 1991, 145,105-110). The cells were resuspended (5x 106 ml-1) and loaded with 5uM FLUO-3/AM + Pluronic F127 2.2ui/ml (Molecular Probes) in low potassium solution (LKS; NaCl 118mM, MgSO40.8mM, glucose 5.5mM, Na2C03 8.5mM, KC1 5mM, HEPES 20mM, CaCl2 1.8mM, BSA 0.1%, pH 7.4) for
one hour at room temperature. After loading, cells were centrifuged at 200g for 5min and resuspended in LKS at 2.5x106 ml"1. The cells were then transferred to 96 well FLIPr plates (Poly-D-Lysine plates from Becton Dickinson pre-incubated with 5|lM fibronectin for two hours) at 25|il/well. The plate was centrifuged at 200g for 5min and the cells were washed twice with LKS (200(xl; room temperature).
A compound of the Examples was pre-dissolved in DMSO and added to a final concentration of 0.1 %(v/v) DMSO. Assays were initiated by the addition of an A50 concentration of eotaxin and the transient increase in fluo-3 fluorescence (1EX =490nm and km = 520nm) monitored using a FLTPR (Fluorometric Imaging Plate Reader, Molecular Devices, Sunnyvale, U.S.A.).
Compounds of the Examples were found to be antagonists if the increase in fluorescence induced by eotaxin (a selective CCR3 agonist) was inhibited in a concentration dependent manner. The concentration of antagonist required to inhibit the fluorescence by 50% can be used to determine the IC50 for the antagonist at the CCR3 receptor.
Human eosinophil chemotaxis Human eosinophils were isolated from EDTA anticoagulated peripheral blood as previously described (Hansel et al., J. Immunol. Methods, 1991, 145,105-110). The cells were resuspended at 10x106 ml-1 in RPM containing 200 IU/ml penicillin, 200 |ig/ml streptomycin sulfate and supplemented with 10% HTFCS, at room temperature.
Eosinophils (700 µl) were pre-incubated for 15 mins at 37° C with 7 ui of either vehicle or compound (lOOx required final concentration in 10% DMSO). The chemotaxis plate (ChemoTx, 3µm pore, Neuroprobe) was loaded by adding 28pµl of a concentration of eotaxin 0.1 to 100nM (a selective CCR3 agonist over this concentration range) containing a concentration of a compound according to the Examples or solvent to the lower wells of the

chemotaxis plate. The filter was then placed over the wells and 25 µl of eosinophil suspension were added to the top of the filter. The plate was incubated for 1 hr at 37° C in a humidified incubator with a 95% air/5% CCS atmosphere to allow chemotaxis.
The medium, containing cells that had not migrated, was carefully aspirated from above the filter and discarded. The filter was washed once with phosphate buffered saline (PBS) containing 5 mM EDTA to remove any adherent cells. Cells that had migrated through the filter were pelleted by centrifugation (300xg for 5 mins at room temperature) and the filter removed and the supernatant transferred to each well of a 96-well plate (Costar). The pelleted cells were lysed by the addition of 28 ul of PBS containing 0.5% Triton xl00 followed by two cycles of freeze/thawing. The cell lysate was then added to the supernatant. The number of eosinophils migrating was quantified according to the method of Strath et al., J. Immunol. Methods, 1985, .83, 209 by measuring eosinophil peroxidase activity in the supernatant.
Compounds of the Examples were found to be antagonists of eotaxin mediated human eosinophil chemotaxis if the concentration response to eotaxin was shifted to the right of the control curve. Measuring the concentration of eotaxin required to give 50% chemotaxis in the presence or absence of compounds enables the apparent affinity of the compounds at CCR3 to be calculated.
*~*fo -

WE CLAM-4:
1. A piperidine compound of formula (I):


B3

wherein:
T is C(O) or S(O)2;
W is C(O)or S(O)2;
X isCH2,OorNH;
Y isCR5 orN;
R1 is optionally substituted aryl or optionally substituted heterocyclyl;
R is hydrogen or C1-6alkyl;
R3 is hydrogen
R4 is alkyl, optionally substituted aryl, optionally substituted aralkyl or optionally
substituted heterocyclyl;
Rs is hydrogen or C1-6 alkyl;
wherein the foregoing aryl and heterocyclyl moieties are optionally substituted by:
halogen, cyano, nitro, hydroxy, oxo, S(0)pR25, OC(O)NR6R7, NR8R9, NR10C(O)Rn,
NR12C(O)NR13RM, S(O)2NR15R16, NR17S(0)2R18, C(O)NR19R20, C(O)R21, CO2R22,
NR23CO2R24,C1-6 alkyl, CF3, CM alkoxy(C,^)alkyl, C1J6 alkoxy, OCF3, C1_6 alkoxy(C1.
6)alkoxy, C1-4 alkylthio, C2_6 alkenyl, C2-6 alkynyl, C3-10 cycloalkyl (itself optionally
substituted by C1-4 alkyl or oxo), methylenedioxy, difluoromethylenedioxy, phenyl,
phenyl(C1-4)alkyl, phenoxy, phenylthio, phenyl(C1-4)alkoxy, heteroaryl, heteroaryl(Ci.
4)alkyl, heteroaryloxy or heteroaryl(C1-4)alkoxy; wherein any of the immediately
foregoing phenyl and heteroaryl moieties are optionally substituted with halogen,
hydroxy, nitro, S(0)q(C1-4 alkyl), S(0)2NH2, cyano, C1-4 alkyl, C1-4 alkoxy, C(O)NH2,
C(O)NH(C1-4 alkyl), CO2H, CO2(C1-4 alkyl), NHC(0)(C1-4 alkyl), NHS(0)2(C1-4 alkyl),
C(O)(C1-4 alkyl), CF3 or OCF3;
p and q are, independently, 0, 1 or 2;


R6, R7, R8, R9, R10, Rn, R12, R13, R14, R15, R16, R17, R19, R20, R21, R22, and R23 are, independently, hydrogen, C1-6 alkyl (optionally substituted by halogen, hydroxy or C3-10 cycloalkyl), CH2(C2-6 alkenyl), phenyl (itself optionally substituted by halogen, hydroxy, nitro, NH2, NH(C1-4 alkyl), N(C1-4 alkyl)2, S(O)2(C1-4 alkyl), S(0)2NH2, S(O)2NH(C1-4 alkyl), S(0)2N(C1-4 alkyl)2, cyano, C1-4alkyl, C1-4 alkoxy, C(O)NH2, C(0)NH(C1-4 alkyl), C02H, C02(C1-4alkyl), NHC(0)(C1-4 alkyl), NHS(0)2(C1-4 alkyl), C(O)(C1-4 alkyl), CF3 or OCF3) or freterocyc/y/ (itself optionally substituted by halogen, hydroxy, nitro, NH2, NH(C1-4 alkyl), N(C1-4 alkyl)2, S(O)2(C1-4 alkyl), S(0)2NH2, S(0)2NH(C1-4alkyl), S(O)2N(C1-4 alkyl)2, cyano, C1-4 alkyl, C1-4 alkoxy, C(0)NH2, C(0)NH(C1-4 alkyl), C(0)N(C1-4 alkyl)2, C02H, C02(C1-4 alkyl), NHC(0)(C1-4 alkyl), NHS(0)2(1-4 alkyl), C(0)(C1-4 alkyl), CF3orOCF3);
alternatively NR6R7, NR8R9, NRI3R14, NR15R16, NR19R20 or N(Ci_4 alkyl)2 may, independently, form a 4-7 membered heterocyclic ring, azetidine, pyrrolidine, piperidine, azepine, 1,4-morpholine or 1,4-piperazine, the latter optionally substituted by CMalkyl on the distal nitrogen;
R25, R18 and R24 are, independently, C1-4 alkyl (optionally substituted by halogen, hydroxy or C3.10 cycloalkyl), CH2(C2_6 alkenyl), phenyl (itself optionally substituted by halogen, hydroxy, nitro, NH2, NH(C1-4 alkyl), N(C1-4 alkyl)2 (and these alkyl groups may join to form a ring as described for R6 and R7 above), S(0)2(C1-4 alkyl), S(O)2NH2, S(O)2NH(C1-4 alkyl), S(O)2N(C1-4 alkyl)2 (and these alkyl groups may join to form a ring as described for R6 and R7 above), cyano, C1-4 alkyl, C1-4 alkoxy, C(O)NH2, C(O)NH(C1-4 alkyl), C(0)N(Ci^ alkyl)2 (and these alkyl groups may join to form a ring as described for R6 and R7 above), CO2H, CO2(C1-4 alkyl), NHC(O)(C1-4 alkyl), NHS(0)2(C1-4 alkyl), C(0)(CM alkyl), CF3 or OCF3) or heterocyclyl (itself optionally substituted by halogen, hydroxy, nitro, NH2, NH(C1-4 alkyl), N(C1-4 alkyl)2 (and these alkyl groups may join to form a ring as described for R6 and R7 above), S(0)2(C1-4 alkyl), S(O)2NH2, S(O)2NH(C1. 4 alkyl), S(0)2N(C1-4 alkyl)2 (and these alkyl groups may join to form a ring as described for R6 and R7 above), cyano, C1-4 alkyl, C1-4 alkoxy, C(O)NH2, C(0)NH(C1-4 alkyl), C(0)N(C1-4 alkyl)2 (and these alkyl groups may join to form a ring as described for R6 and R7 above), CO2H, C02(C1-4 alkyl), NHC(O)(1-4 alkyl), NHS(0)2(C1-4 alkyl), C(O)(C1-4 alkyl), CF3 or OCF3);
-n-

or an ~N-oxide thereof; or a pharmaceutkally acceptable salt thereof; or a solvate thereof.
2. A compound as claimed in claim 1, wherein X is o.
3. A compound as claimed in claims 1 or 2, wherein R1 is phenyl substituted with one or more of fluorine, chlorine, C1-4 alky I or C1-4 alkoxy.
4. A compound as claimed in claims 1, 2 or 3 wherein one of T and W is C(O) and the other is S(O)2.
5. A compound as claimed in claims 1,2, 3 or 4 wherein T is C(O).
6~. A compound as claimed in claims 1, 2, 3,4 or 5 wherein W is S(O)2.
7. A compound as claimed in claims 1,2, 3, 4, 5 or 6 wherein Y is N.
8. A compound as claimed in claims 1, 2, 3, 4, 5, 6 or 7 wherein R2 is hydrogen or methyl.
9. A compound as claimed in claims 1, 2, 3, 4, 5, 6, 7 or 8 wherein R4 is substituted phenyl, the substituents being chosen from those provided in claim 1.
10. A process for preparing a compound formula (I) as claimed in claim 1 comprising:
^??~
a. when R3 is hydrogen, T is C(O) and Y is N, reacting a compound of formula (II):


with an isocyanate of formula R4WN=C=0 in the presence of a suitable solvent at a suitable temperature;
b. when T is C(O), W is S(O)2 and Y is N, reacting a compound of formula (II)
with a compound of formula (XXII):

c. when R3 is hydrogen, T is S(O)2, W is C(O) and Y is N, reacting a compound of
formula (IX):

with a compound of formula (II) in the presence of a suitable base, in a suitable solvent and at a suitable temperature;
d. when R3 is hydrogen, T is S(O)2, W is C(O) and Y is N, reacting a compound of
formula (XVIII):

with an acyl halide R4COHal in the presence of a base, in a suitable solvent, at room temperature;

e. when R3 is hydrogen, T is S(0)2, W is C(0) and Y is N, reacting a compound of
formula (XIX):

with an acyl halide R4COHal in the presence of a base, in a suitable solvent, for example at room temperature; followed by deprotection of the carbamate so formed;
f. when T and W are both S(O)2 and Y is N, reacting a compound of formula (X):

with a sulfonamide R4S(O)2NHR3 in the presence of a base, in a suitable solvent;
g. when T and W are both S(O)2 and Y is N, reacting a compound of formula
(XVIII) with a sulfonyl chloride R4SO2C1 in the presence of a base, in a suitable solvent;
h. when T is C(O), W is S(O)2 and Y is CR5, can be prepared by firstly hydrolysing a compound of formula (XI):



(XV)

to a sulfonyl chloride R4S(O)2C1 in the presence of a base and a solvent;
I. wherein R3 is not hydrogen, can be prepared by alkylating a compound of formula
(I) wherein R3 is hydrogen, with a suitable alkylating agent in the presence of a suitable
base in a suitable solvent; or,
m. Y is CR5 and R5 is not hydrogen, may be prepared from a compound of formula (I) where Y is CH by reaction of the dianion (R is H) or monoanion (R is alkyl) (formed with a suitable base) with an alkylating agent in a suitable solvent.
II. A compound as claimed in claim 1 which is:
N-[[4-(2-Chloro-4-fluorophenoxy)[l,4'-bipiperidin]-l'-yl]carbonyl]-4-
methyl-benzenesulfonamide;
N-[[4-(2-Chloro-4-fluorophenoxy)[ 1,4' -bipiperidin]-1' yl]carbonyl]-2-methyl-benzenesulfonamide;
4-Chloro-N-[[4-(2-chloro-4-fluorophenoxy)[l,4'-bipiperidin]-r- yl]carbonyl]-benzenesulfonamide;
2-Chloro-N-[[4-(2-chloro-4-fluorophenoxy)[ 1,4' -bipiperidin]-1' - yl]carbonyl] -benzenesulfonamide;
N-[[4-(2-Chloro4-fIuorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-4-fluoro-benzenesulfonamide;
N-[[4-(2-Chloro-4-fluorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl] benzenesulfonanide; N-[[4-(4-Chloro-2-methylphenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2-methyl-benzenesulfonamide;
4-ChJoro-Ar-[[4-(4-chJoro-2-methyJphenoxy)[l ,4 '-bipiperidin]-1 '-yljcarbonyJ]-benzenesulfonamide;

2-Chloro-N-[[4-(4-chloro-2-methylphenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-benzenesulfonamide;
N-[[4-(4-Chloro-2-methylphenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-4-fluoro-benzenesulfonamide;
N-[[4-(4-Chloro-2-methylphenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-4-methyl-benzenesulfonamide;
N-[[4-(4-Chloro-2-methylphenoxy)[l ,4'-bipiperidin]-l'- yl]carbonyl]-benzenesulfonamide;
N-[[4-(2,4-Dichloro-3-methylphenoxy)[l,4'-bipiperidin]-r-yI]carbonyl]-2-methyl-benzenesulfonamide;
7V-[[4-(2,4-Dichloro-3-methylphenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-4-methyl-benzenesulfonamide;
2-Chloro-N[[4-(2,4-dichloro-3-methylphenoxy)[l,4'-bipiperidin]-l- yl]carbonyl]-benzenesulfonamide;
4-Chloro-N-[[4-(2,4-dichloro-3-methylphenoxy)[l,4,-bipiperidin]-l- yl]carbonyl]-benzenesulfonamide;
N-[[4-(2,4-Dichloro-3-methylphenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-4-fluoro-benzenesulfonamide;
-«?,9

wherein the ester is preferably aC1-6 alkyl group, and reacting the product so formed with R4S(0)2NHR3 in the presence of an appropriate coupling agent, in a suitable solvent;
i. when T and W are both C(O) and Y is CR5 or N, can be prepared by heating a
compound of formula (XIV):

in the presence of R4C(OR')2N(CH3)2 or R4C(OR')3, wherein R' is methyl or methyl, or (OR')3 is (OCH2)3CCH3;
j. when T is S(0)2, W is C(O) and Y is CR5, coupling a compound of
formula (XV):

to an acid R4CO2H in the presence of an appropriate coupling agent, in a suitable solvent; k. when T and W are both S(O)2 and Y is CH, coupling a compound of
formula (XV):
■U

N-[[4-(2,4-Dichloro-3-methylphenoxy) [ 1,4'-bipiperidin] -1 '-yl] carbonyl] -
benzenesulfonamide;
N-[[4-(3,4-Dichloro-2-methylphenoxy)[l,4,-bipiperidin]-r-yl]carbonyl]-2-inethyl-
benzenesulfonamide;
N-[[4-(3,4-Dichloro-2-methylphenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-4-methyl-
benzenesulfonamide;
2-Chloro--W'-[[4-(374-dichloro-2-m.etb.ylphenoxy)[l,4,-bipiperidin]-r-yl]carbonyl]-
benzenesulfonamide;
4-Chloro-iV-[[4-(3,4-dichloro-2-methylphenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-
benzenesulfonamide;
N-[[4-(3,4-Dichloro-2-methylphenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-4-fluoro-
benzenesulfonamide;
N- [ [4-(3,4-Dichloro-2-raethylphenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-
benzenesulfonamide;
N-[[4-(3J4"Dicblorophenoxy)-4'-methyl[l,4'-bipiperidin]-r-yl]carbonyl]-4-methyl-
benzenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)^'-methyl[ 1,4'-bipiperidin]- r-yl]carbonyl]-4-fluoro-
benzenesulfonamide;
N-[[4-(314-DicUorophenoxy)^'-methyl[l,4'-bipiperidin]-r-yl]carbonyl]-2-methyl-
benzenesulfonamide;
4-Chloro-iV-[[4-(3,4-dicWorophenoxy)-4'-methyl[l,4'-bipiperidiii]-r-yl]carbonyl]-
benzenesulfonamide;
2-Chloro-iV-[[4-(3,4-dichlorophenoxy)-4'-methyl[ 1,4-bipiperidin]-1 '-yljcarbonyl]-
benzenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)-4'-methyl[ 1,4'-bipiperidin]-r-yl]carbonyl]-3-
trifluoromethyl-benzenesulfonamide;
3-Cyano-A^-[[4-(3J4~ojchlorophenoxy)-4,-methyl[l,4'-bipiperidin]-r-yl]caibonyl]-
benzenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)[l ,4'-bipiperidin]-l '-yl]carbonyl]-
benzenemethanesulfonamide;
N-[[4-(3,4~Dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-
raethanesulfonamide;

N- [[4-(4-Chloro-3-methyIphenoxy) [ 1,4-bipiperidin]-1 '-yl]carbonyl]-2-methyl-
benzenesulfonamide;
N-[[4-(4-ChIoro-3-methylphenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-4-methyl-
benzenesulfonamide;
4-Chloro-iV'-[[4-(4-cWoro-3-methylphenoxy)[l)4'-bipiperidin]-r-yl]carbonyl]-
benzenesulfonamide;
N-[[4-(3)4-Dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbouyl]-iV',4-dimeth.yI-
benzenesulfonamide;
N-[[4-[(3,4-Dicblorophenyl)methyl][l,4'-bipiperidin]-r-yl]carbonyl]-4-methyl-
benzenesulfonamide;
4-Chloro-A'-[[4-[(3,4-dichlorophenyl)metbyl][l,4'-bipiperidin]-r-yl]carbonyI]-
benzenesulfonamide;
^-[[^[(3ADicUorophenyl)aioino][l,4'-bipiperidin]-r-yl]carbonylJ-4-rnethyl-
benzenesulfonamide;
4-Chloro-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-
benzenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-4-methyl-
benzenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2-methyl-
benzenesulfonamide;
3-Bromo-N-[[4-(3,4~dichloropb.enoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-
benzenesulfonamide;
4-Bromo-N- [[4-(3,4-dichlorophenoxy) [ 1,4'-bipiperidm] -1' -yl]carbonyl] -
benzenesulfonamide;
3,5-Dichloro-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-
benzenesulfonamide;
3-Cyano-N-[[4-(3,4-dicbiorophenoxy)[l,4,-bipiperidin]-r-yl]carbonyl]-
benzenesulfonamide;
N-[[4-(3,4-DicMorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2,5-dimetb.oxy-
benzenesulfonamide;
N-[[4-(3,4-Dichloropb.enoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-3,4-dimethoxy-
benzenesulfonamide;

N-[[4-(3)4-Dichlorophenoxy)[l14'-bipiperidin]-l'-yl]carbonyl3-4-(3I3-diniethyI-2-
oxo-1 -azetidinyl)-benzenesuIfonamide;
N-[[4-(3,4-Dicfalorophenoxy)[l,4'-bipiperidin]-l'-yl]carbonyl]-4-(4,5-dihydro-3-methyl-5-oxo-lH-pyrazol-l-yl)-benzenesulfonamide; N-[[4-(3,4-Dichlorophenoxy)[l,4,-bipiperidui]-l'-yl]carbonyl]-3-(4,5-dihydro-3-
methyl-5-oxo- lH-pyrazol-1 -yl)-benzenesulfonamide; N-[[4-(3)4-Dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-4-hydroxy-
benzenesulfonamide; N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidiii]-l'-yl]carbonyl]-3-(trifluoromethyl)-
benzenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)[l ,4' -bipiperidinj-1 '-yl]carbonyl]-
benzenesulfonamide;
4-[[[[4-(3,4-DicbJorophenoxy)[l,4,-bipiperidin]-l'-yl]carbonyl]aniiiio]sulfonyl]-
benzoic acid, methyl ester,
2-Bromo-N-[[4"(3,4-dichlorophenoxy)[l74'-bipiperidin]-r-yl]carbonyl]-
benzenesulfonamide;
N-[5-[[[[4-(3,4-Dichlorophenoxy)[l,4'-bipipcridin]-r-yl]carbonyl]amiBo]sulfonyl]-
1,3,4-thiadiazol-2-yl]-acetamide;
N-[[4-(3,4-DicUoropbenoxy)[l,4'-bipiperidin]4'-yl]caxbonyl]-5-(dimetiylamino)-
1 -naphthalenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2-
naphthalenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidiii]-r-yl]carbonyl]-2,4-diniethyl-5-
thiazolesulfonamide;
N- [[4-(3,4-Dichlorophenoxy) [ 1,4' -bipiperidin] -1' -yl]carbonyl]-2-(l -piperidinyl)-3-
pyridinesulfonamide;
5-Chloro-N-[[4-(3,.4-dichlorophenoxy)[l>4'bipiperidiii]-r-yl]carbonyl]-2-
thiophenesulfonamide;
5-Bromo-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2-tbiophenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidiii]-r-yl]carbonyl]tetrahydro-3-tbiophenesulfonaroide; 1,1-dioxide

4,5-DichJoro-N-[[4-(3.,4-clichlorophenoxy)[l,4'-bipiperidiii]-r-yl]carbonyl]-2-thiophenesulfonamide;
4-Chloro-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-l,-yl]carbonyl]-2,5-dimethyl-benzenesulfonamide;
4-n-Butyl-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-
benzenesulfonamide;
2,5-Dichloro-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-3-
thiopbenesulfonaraide;
4-n-Butoxy-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidiii]-r-yl]carbonyl]-
benzenesulfonamide;
N-[[4-(3,4-Dicblorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2-
Ctxifluoromethoxy)-benzenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidiii]-r-yl]carboQyl]-l-methyHH-
imidazole-4-sulfonamide;
5-Amino-N-[[4-(3,4-dichloropheiioxy)[l,4,-bipiperidin]-r-yl]carbonyl]-l,3,4-
tbiadiazoIe-2-sulfonamide;
4-Bromo-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidm]-r-yl]carbonyl]-2-
thiophenesulfonamide;
N-[[4-(3,4-Dichloroph.enoxy) [ 1,4' -bipiperidin]-1' -yl]carbonyl]-2-(4-morpholmy
3-pyridinesulfonamide;
6-Bromo-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-3-
pyridinesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carboiiyl]-4-(l,l-
dimetbylethyl)-benzenesulfonainide;
N-[[4-(3,4-Dichlorophenoxy)[l ,4' -bipiperidin]-1' -yl]carbonyl]-5-m.ethyl-2-
pyridinesulfonamide;
N-[[4-(3)4-Dichlorophenoxy)[l,4,-bipiperidin]-r-yl]carbonyl]-2,5-difluoro-
benzenesulfonamide;
N-[ [4-(3,4-Dichlorophenoxy) [ 1,4' -bipiperidin]-1' -yl]carbonyl]-4-
(trifluoromethoxy)-benzenesulfonamide;
N-[[4-(3,4-Dichlorophenoxy)[l,4'-bipiperidin]-l-yl]carbonyl]-2,4,5-triQuoro-
benzenesulfonamide;

5-Chloro-N-[[4-(3,4-dichlorophenoxy) [ 1,4' -bipiperidin]-1' -yl]carbonyl]-2,4-
difluoro-benzenesulfonamide;
4-Chioro-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yI]carbonyl]-2,5-
difluoro-benzenesulfonamide;
3-Chloro-N-[[4-(3I4-dicblorophenoxy)[l,4'-bipiperidin]-l'-yl]carbonyl]-5-fluoro-
2-methyl-benzenesu]fonamide;
N-[[4-(2,4^cMoro-3-methylphenoxy)[l,4'-bipiperidiii]-r-yl]carbonyl]-4-fluoro-
benzenesulfonamide;
2-chloro-N-[[4-(2,4-dichloro-3-methylphenoxy)[l,4'-bipiperidin]-l'-yl]carbonyl]-
benzenesulfonamide;
N-[[4-(3,4-dicMoro-2-methylpheiioxy)[l,4,-bipiperidin]-r-yl]carbonyl]-4-met±iyl-
benzenesulfonamide;
2-chloro-N-[[4-(3,4-dichIoro-2-methylphenoxy)[ll4'-bipiperidin]~l'-yl]carbonyl]-
benzenesulfonamide;
N- [[4-(4-chlorophenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-4-mcthyl-
benzenesulfonamide;
N- [ [4-(2,4-dicbJoro-3-methylpheiioxy) [ 1,4'-bipiperidin]-1 '-yl]carbony]]-2-methyl-
benzenesulfonamide;
N-[[4-(2,4-dichloro-3-fluorophenoxy)[l,4'-bipiperidiii]-r-yl]carbonyl]-4-mcthyl-
benzenesulfonamide; N-[[4-(4-chloro-2-methylphenoxy)[l)4,-bipiperidin]-r-yl]carbonyl]-2-roethyl-
benzenesulfonamide;
2-cWoro-N-[[4-(4-chloro-2-niethylphenoxy)[l,4,-bipiperidiii]-r-yl]carbonyl]-
benzenesulfonamide;
4-chloro-N-[[4-(4-chloro-2-methylphenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-
benzenesulfonamide;
N-[[4-(2,4-dichlorophenoxy) [ 1,4'-bipiperidin]-l '-yl]carbonyl]-4-methyl-
benzenesulfonamide;
N-[[4-(3-chlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-4-methyl-
benzenesulfonamide;
2-chloro-N-[[4-(3-chlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-
benzenesulfonamide;
N-[[4-(3-chlorophenoxy) [ 1,4'"bipiperidin]-r-yl]carbonyl]-benzenesulfonainide;

2-chloro-N-[[4-(3-chloro-2-methylphenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-
benzenesulfonamide;
N-[[4-(2-chloro-4-fluoropb.enoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2-methyl-
benzenesulfonamide;
2-chloro-N-[[4-(2,4-dichloro-3-fluorophenoxy)[l,4'-bipiperidin]-r-yl]carboiiyl]-
benzenesulfonamide;
4-chloro-N-[[4-(2>4-dichloro-3-£luorophenoxy)[l,4,-bipiperidiii]-r-yl]carboiiyl]-
benzenesulfonamide;
N-[[4-(2,4-dichloro-3-fluoropheiioxy)[ 1,4'-bipiperidin]-1 '-yl]carbonyl]-2-methyl-
benzenesulfonamide;
2-cbioro-N-[[4-(4-chloropb.enoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-
benzenesulfonamide;
4-chloro-N-[[4-(4-cbJorophenoxy)[l,4'-bipiperidin]-r-yI]carbonyl]-
benzenesulfonamide;
N-[[4-(4-chlorbphenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2-methyl-
benzenesulfonamide;
2-chJoro-N-[[4-(2,4-dicblorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-
benzenesulfonamide;
4-chloro-N-[[4-(2,4-dichlorophenoxy)[l,4'-bipiperidin]-r'yl]carbonyl]-
benzenesulfonamide;
N-[[4-(2,4-dichlorophenoxy)[l34'-bipiperidin]-r-yl]carbonyl]-2-methyl-
benzenesulfonamide;
2-chloro-N-[[4-(3,4-difluorophenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-
benzenesulfonamide;
N-[[4-(3,4-difluorophenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-2-methyl-
benzenesulfonamide;
N-[[4-(3,4-difiuorophenoxy)[l,4,-bipiperidin]-r-yl]carbonyl]^}~inethyl-
benzenesulfonamide;
N-[[4-(3-chloro-2-methylphenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-4-methyl-
benzenesulfonamide;
N-[[4-(3-ehioro-2-methylphenoxy)[l,4'-bipiperidin]-r-yI]carbonyl]-
benzenesulfonamide;

3-chloro-N- [[4-(3,4-dicbloropheQoxy) [ 1,4'-bipiperidin]-1 -yljcarbonyl]-
benzenesulfonarnide;
N-[[4-(3,4-dichlorophenoxy) [ 1 ,4'-bipiperidra]-1 '-yl]carbonyl]-4-methoxy-
benzenesulfonainide;
N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2,4,5-tiifluoro-
benzenesulfonamide;
N-[[4-(3,4-dichlorophenoxy)[l,4,-bipiperidin]-r-yl]carbonyl]-2,5-difluoro-
benzenesulfonamide;
N-[[4-(3,4^cUorophenoxy)[l,4'-bipiperidk]-r-yl]carbonyl]^(dimetfaylamiiio)-
benzenesulfonamide;
N-[[4-(3,4-dichlorophenoxy)[l,4'"bipiperidin]-r-yl]carbonyl]-2-methoxy-
benzenesulfonamide;
4-bromo-N-j;[4-(3,4-dicbJorophenoxy)[lJ4'-bipipeiidiii]-r-yl]carbony]3-
benzenesulfonaroide;
3,5-dichloro-N- [[4-(3,4-dichlorophenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-
benzenesulfonamide;
Methyl 2-[[[[4-(3,4-dicMorophenoxy)[l,4'-bipiperidin]-l'-
yl]carbonyl]arrrino]sulfonyl]-benzoate;
2-bromo-N-[[4-(3,4-dichlorophenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-
benzenesulfonamide; 5-chloro-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidrn]-r-yl]carbonyl]-2-
thiophenesulfonamide;
4,5-dichloro-N-[[;4-(3,4-dichlorophenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-2-
thiophenesulfonanjide;
4-chloro-N-[[4-(3,4-dichlorophenoxy)[l,4'-bipiperidin]-r-yl]carbonyl]-2,5-
dimethyl-benzenesulfonamide;
2,5-dichloro-N-[[4-(3,4-dichlorophenoxy) [1,4'-bipiperidin]-1 '-yl]carbonyl]-3-
thiophenesulfonamide;
N-[[4-(3,4-dichlorophenoxy) [1,4'-bipiperidin]-1 '-yl]carbonyl]-2-
(trifluoromethoxy)-benzenesulfonarnide;
4-bromo-N- [[4-(3,4-dichlorophenoxy) [ 1,4'-bipiperidin] -1 '-yl]carbonyl>2-
thiophenesulfonamide;

4-(4-cMoro-2-methylphenoxy)-N-(4-ethylbenzoylH 1,4'-bipiperidine] -1 '-
sulfonamide;
4-(4-chloro-2-methylphenoxy)-N-(2-methoxybenzoyl)-[l,4'-bipiperiditie]-l'-
sulfonamide;
4-(4-chloro-2-methylphenoxy)-N-(4-methoxybenzoyl)-[ 1,4'-bipiperidine]-1 '-
sulfonamide;
N-(2-chlorobenzoyl)-4-(4-chloro-2-metb.ylphenoxy)-[l,4'-bipiperidine]-l'-
sulfonamide;
4-(4-cMoro-2-methylphenoxy)-N-[3-(methylsulfonyl)benzoyl]-[l,4'-bipiperidine]-
1'-sulfonamide;
4-(4-chloro-2-methylphenoxy)-N-(3-cyanobenzoyl)-[l)4'-bipiperidine]-r-
sulfonamide;
4-(2,4-dichloro-3-methylphenoxy)"N-(4-fluorobenzoyl)-[l,4,-bipiperidine]-r-
sulfonamide;
N-(4-chlorobenzoyl)-4-(2,4-dicfaloro-3-metb.ylphenoxy)-[l,4'-bipiperidine]-r-
sulfonamide;
4-(2,4-dichloro-3-methylphenoxy)-N-(4-methylbenzoyl)-[l,4'-bipiperidine]-r-
sulfonamide;
4-(2,4-dichloro-3-methylphenoxy)-N-[4-(dimethylamino)benzoyl]-[l,4'-
bipiperidine]-l '-sulfonamide;
4-(2,4-dichloro-3-methylphenoxy)-N-(4-ethylbenzoyl)-[l,4'-bipiperidine]-r-
sulfonamide;
4-(2,4-dichloro-3-methylphenoxy)-N-(2-methoxybenzoyl)-[l,4'-bipiperidine]-r-
sulfonamide;
4-(2,4-dichloro-3-metb.ylpb.enoxy)-N-(4-methoxybenzoyl)-[l,4'-bipiperidine]-r-
sulfonamide;
N-(2-chlorobenzoyl)-4-(2,4-dichloro-3-metliylpb.enoxy)-[l,4'-bipiperidine]-r-
sulfonamide;
4-(2,4-dichloro-3-methylphenoxy)-N-[3-(memylsulfonyl)benzoyl]-[l,4'-
bipiperidine]-l '-sulfonamide;
N-(3-cyanobenzoyl)-4-(3,4-dichlorophenoxy)- [ 1,4'-bipiperidioe] -1 '-sulfonamide;
4-(3,4-dichloro-2-methylphenoxy)-N-(4-fluorobenzoyl)-[l,4'-bipiperidine]-r-
sulfonamide;

N-(4-cMorobenzoylH-(3,4-dichloro-2-methylphenoxy)-[l,4'-bipiperidine]-r-sulfonamide;
4-(3,4dichloro-2-methylphenoxy)-NK4-methylbenzoyl)-[1,,4,-bipiperidine]-l,-sulfonamide;
4-(3,4-dichloro-2-methylphenoxy)-N-[4-(dimethylamiiio)beiizoyl]-[l14'-
bipiperidine]-1 '-sulfonamide;
4-(3,4-dicbloro-2-methylphenoxy)-N-(4-ethylbenzoyl)-[l,4'-bipiperidine]-r-
sulfonamide;
4-{3,4-dicbloro-2-methyIpb.enoxy)-N-(2-methoxybenzoyI)-[l ,4'-bipiperidine]-1 '-
sulfonamide;
4-(3,4-dichloro-2-methylphenoxy)-N-(4-methoxybenzoyl)-[lJ4'-bipiperidine]-r-
sulfonamide;
N^2-chIorobenzoyl)-4-(3,4-dichloro-2-meuiylphenoxy)-tl,4'-bipiperidine]-r-
sulfonamide;
4-(3,4-dichloro-2-methylphenoxy)-N-[3-(lIlethylsulfonyl)berizoyl]-[l>4,"
bipiperidine]-1 '-sulfonamide;
N-(3-cyanobenzoyl)-4-(3,4-dicbloro-2-methylphenoxy)-[l,4'bipiperidine]-r-
sulfonamide;
N-benzoyl-4-(3,4-dichloro-2-methylphenoxy)-[ 1,4'-bipiperidine]-1 '-sulfonamide;
N-benzoyl-4-(2,4-dicUorophenoxy)-[l,4'-bipiperidine]-l-sulfonamide;
N-(3-cyanoben2oyl)4-(3,4-d^cMorophenoxy)-[l,4'-bipiperidine]-l'-sulfonamide;
4-(3,4-dichIorophenoxy)-N-(4-fluorobenzoyl)-[l,4'-bipipeiidine]-r-sulfonamide;
4-(3,4-dichlorophenoxy)-N-[3-(methylsulfonyl)benzoyl]-[l,4'-bipiperidine]-r-
sulfonamide;
4-(4-chloro-2-methylphenoxy)-N-[3-(methylsulfonyl)benzoyl]-[l,4'-bipiperidine]-
1'-sulfonamide;
N-(2-chlorobenzoyl)-4-(3,4-dichlorophenoxy)-[ 1,4'-bipiperidine]-1 '-sulfonamide;
N-(4-chlorobenzoyl)-4-(3,4-d^chlorophenoxy)-[l,4'-bipiperidme]-r-sulfonamide;
N-(4-chlorobenzoyl)-4-(4-cbloro-2-methylphenoxy)-[l,4t-bipiperidme]-r-
sulfonamide;
4-(3,4-dicMorophenoxy)-N-(2-memoxybenzoyl)-[l,4'-bipiperidine]-r-sulfonamide;
4-(3,4-dichlorophenoxy)-N-(4-memoxybenzoyl)-[l,4'-bipiperidine]-r-sulfonamide;
4-(3,4-dichlorophenoxy)-N-(4-metb.ylbenzoyl)-[l,4'-bipiperidine]-r-sulfonamide;

4-{3,4-dichlorophenoxy)-iV-[( 1,2-dihydro-1 -oxo-4-isoquinolinyl)carbonyI]- [1,4-bipiperidine]-1 '-sulfonamide;
N-(cyclohexylcarbonyl)-4-(3,4-dichlorophenoxy)-[l,4'-bipiperidine]-r-sulfonamide;
4-(3,4-dichlorophenoxy)-iV-(2-methyl-1 -oxopropyl)- [ 1,4'-bipiperidine]-1 '-
sulfonamide;
4-(3,4-dicMorophenoxy)-//-(2-phenylacetyl)-[l,4'-bipiperidtoe]-r-sulfonamide;
N-[[4-(3,4-dichlorophenoxy) [ 1,4'-bipiperidin]-1 '-yl]carbonyl]-2-
propanesulfonamide;
Trans A'-[[4-[4-(3)4-Dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-4-
methyl-benzenesulfonamide;
Trans ^-[^-^(S^DichlorophenoxyJ-l-piperidinylJcyclohexyllcarbonyl]-//^-
dimethyl-benzenesulfonamide;
Trans 4-chloro-N-[[4-[4-(3,4-dichlorophenoxy)-l-
piperidinyl]cydo'hexyl]carbonyl]-benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-4-
methyl-benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichloropb.enoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2-
methyl-benzenesulfonamide;
Trans 3-bromo-N-[[4-[4-(3,4-dichlorophenoxy)-l-
piperidinyl]cyclohexyl]carbonyl]-benzenesulfonamide;
Trans 4-bromo-N-[[4- [4-(3,4-dichlorophenoxy)-1 -
piperidinyl]cyclohexyl]c.arbonyl]-benzenesulfonamide;
Trans 3,5-dichloro-N-[[4-[4-(3,4-dichlorophenoxy)-1 -
piperidinyl]cyclohexyl]carbonyl]-benzenesulfonamide;
Trans 3-cyano-N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-
benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2,5-
dirnethoxy--benzenesulfonarnide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidrnyl]cyclohexyI]carbonyl]-3,4-
dimethoxy-benzeiiesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-4-(3,3-
dimethyl-2-oxo-1 -azctidinyl)-benzenesulfonamide;

Trans N-[[4-[4-(3,4-dichlorophenoxy)- l-piperidinyl]cyclohexyl]carbonyl]-4-(4,5-dihydro-3-methyl-5-oxo-l H-pyrazol-1 -y])-benzenesulfonarnide;
Trans N-[[4-[4-(3,4-dichloropheiioxy)-l-piperidinyl]cycIohexyl]caTbonyl]-3-(4,5-
dihydro-3-metiiyl-5-oxo-lH-pyTazol-l-yl)-benzenesuIfonamide;
Trans N-[[4~[4-(3,4^ichloropheiioxy)-l-piperidinyl]cyclohexyl]carbonyl]-4-
hydroxy-benzenesulfonamide;
Trans N-[[4-[4"(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-3-
(trifluoromethyl)-benzenesulfonainide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)- l-piperidinyl]cyclobexyl]carbonyl]-
benzenesulfonamide;
Trans 2-[[[[4-[4-(3,4~dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbony]]arnino]-
sulfonyl]-benzoic acid, methyl ester;
Trans 2-bromo-N-[[4-[4-(3,4-dichlorophenoxy)-1 -
piperidkyl]cyclohexyl]carbonyl]-beiizenesulfonamide;
Trans N-[5-[[[[4-[4-(3,4-dichlorophenoxy)-1 -
piperidmyl]cyclohexyl]carbonyl]arrnno]siiIfonyl]-l,3,4-ttdadiazol-2-yl]-acetamide;
Trans N-[[4-[4-(3,4-dicblorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-5-
(dimetbylamino)-1 -naphthalenesulfonamide;
Trans N-[[4-[4-(3,4-dicblorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2-
naphthalenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidrayl]cyclohexyl]carbonyl]-2,4-
dirnethyl-5-thiazolesulfonarnide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-1 -piperidinyl]cyclohexyl]carbonyl]-2-( 1 -
piperidinyl)-3-pyridinesulfonainide;
Trans 5-chloro-N-[[4-[4-(3,4-dichlorophenoxy)-l-
piperidinyl]cyclohexyl]carbonyl]-2-tbiophenesuifonarnide;
Trans 5-bromo-N-[[4-[4-(3,4-dichloroplienoxy)-l-
piperidinyl]cyclohexyI]carbonyl]-2-thioph.enesulfonarnide;
Trans N-[[4-[4-(3,4-dicbloropbenoxy)-l-
piperidinyl]cycIohexyl]carbonyl]tetrabya>o-3-tniophenesuIfonarnide, 1,1 -dioxide;
Trans 4,5-dichloro-N-[[4-[4-(3,4-dicbloiopbenoxy)-l-
pipcridinyl]cyclohexyl]carbonyl]-2-tMophenesulfonamide;

Trans 4-chIoro-N-[[4-[4-(3,4-dichlorophenoxy)-l-
piperidinyl]cyclohexyl]carbonyl]-2,5-^methyI-benzenesulfonamide;
Trans 4-n-butyl-N-[[4-[4-(3,4-dichlorophenoxy)-l-
piperidinyl]cyclohexyl]carbonyl]-benzenesulfonamide;
Trans 2,5-dichloro-N-t[4-[4-{3,4-dichlorophenoxy)-1-
piperidinyl]cyclohexyl]carbonyl]-3-thiopbenesu]fonaniide;
Trans 4-n-butoxy-N-[[4-[4-(3,4-dichlorophenoxy)-1 -
piperidinyl]cycloh.exyl]carbonyl]-benzenesulfonamide;
Trans N-[[4-[4-(3,4-diGhlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2-
(trifluoromethoxy)-benzenesulfonaniide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-l-
methyl-lH-imidazole^-sulfonamide;
Trans 5-amino-N-[[4-[4-(3,4-dichlorophenoxy)-1 -
piperidinyl]cyc]ohexyl]carbonyl]-l,3,4-tbiadiazole-2-sulfonamide;
Trans 4-bromo-N-[[4-[4-(3,4-dichloropHenoxy)-l-
piperidinyl]cyclohexyl]carbonyl]-2-tniophenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2-(4-
morpholinyl)-3-pyridinesulfonamide;
Trans 6-bromo-N-[[4-[4-(3,4-dichlorophenoxy)-l-
piperidinyl]cyclohexyl]carbonyl]-3-pyridinesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-4-(l,l-
dimethylethyl)-benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-5-
methyl-2-pyridinesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2,5-
difluoro-benzenesulfonamide;
Trans N-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-4-
(trifluoromethoxy)-benzenesulfonamide;
Trans N-[[4-[4-(3)4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2,4>5-
trifluoro-benzenesulfonamide;
Trans 5-chloro-N-[[4-[4-(3,4-dichloropbenoxy)-l-
piperidinyl]cyclohexyl]carbonyl]-2,4-difluoro-benzenesulfonamide;

Trans 4-chloro-N-[[;4-[4-(3,4-dicalorophenoxy)-1-
piperidinyl]cyclohexyl]carbonyl]-2,5-difluoro-benzenesulfonaniide;
Trans 3-chloro-N- [[4- [4-(3,4-dichlorophenoxy)-1 -
piperidinyl]cyclohexyl]carbonyl]-5-fluoro-2-methyl-benzenesulfonainide;
Trans iVL[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2-
methyl- benzenesulfonamide;
Trans iV-[[4-[4-(3,4-dicnlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2-
methoxy- benzenesulfonamide;
Trans//-[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-2,6-
dimethyl- benzenesulfonamide;
Trans A^[[4-[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclob.exyl]carbonyl]-4-
methyl- benzenesulfonamide;
Trans 7V-[[4-[4-(3,4-dichlorophenoxy)-1 -piperidinyl]cyclohexyl]carbonyl]-
benzenesulfonamide;
Trans Ar-[[4»[4-(3,4-dichlorophenoxy)-l-piperidinyl]cyclohexyl]carbonyl]-4-
(dimethylamino)- benzenesulfonamide;
4-(3,4-Dichlorophenoxy)-N-(2-memylbenzoyl)-[l,4,-bipiperidne]-r-carboxamide;
4-(3,4-DicbJorophenoxy)-N-(4-methylbenzoyl)-[l,4'-bipiperidine]-r-carboxarnide;
4-(3,4-DicMorophenoxy)-N-(4K;hlorobenzoyl)-[l,4'-bipiperidme]-r-carboxarnide;
4-(3,4-Dichlorophenoxy)-N'-benzoyl- [ 1,4'-bipiperidine]-1 '-carboxamide;
4-(3,4-Dichlorophenoxy)-N-[(4-methylphenyl)suIfonyl]-[l,4'-bipiperidine]-r-
sulfonamide;
4-(3,4-dicbJorophenoxy)-N-[[4-(lJ-dimetliylethyl)phenyl]sulfonyl]-[l,4'-
bipiperidine]-1 '-sulfonamide;
[4-(3,4-dichlorophenoxy)-N-(phenylsulfonyl)-14'-bipiperioUne]-r-sulfonamide;
Trans N-benzoyl-4~]4-(3,4-dichlorophenoxy)-1 -piperidinyl]-
cyclohexanesulfonamide;
Trans N-[[4-[4-(3>4-Dicblorophenoxy)-l-piperidiriyl]cyclohexyl]caxbonyll-
benzamide; or,
Trans Ar-[[4-[4-(3,4-Dichlorophenoxy)-l-piperidinyl]cyclohexyl]sulfonyl]-
benzenesulfonamide.t. _
Dated this December 15, 2003.
(RANJNA MEHTA-DUTT)
OF REMFRY AND SAGAR ATTORNEY FOR THE APPLICANTS

Documents:

1142-mumnp-2003-abstract.pdf

1142-mumnp-2003-cancelled-claims.pdf

1142-mumnp-2003-cancelled-other pct document-01-07-2002.pdf

1142-mumnp-2003-claims.pdf

1142-mumnp-2003-correspondence(ipo).pdf

1142-mumnp-2003-correspondence.pdf

1142-mumnp-2003-description(granted).pdf

1142-mumnp-2003-european patent specification-01-07-2002.pdf

1142-mumnp-2003-form 19.pdf

1142-mumnp-2003-form 1a.pdf

1142-mumnp-2003-form 2(granted).pdf

1142-mumnp-2003-form 2(title page).pdf

1142-mumnp-2003-form 3.pdf

1142-mumnp-2003-form 5.pdf

1142-mumnp-2003-form-pct-ib-304-01-07-2002.pdf

1142-mumnp-2003-form-pct-ipea-409-01-07-2002.pdf

1142-mumnp-2003-form-pct-isa-210-01-07-2002.pdf

1142-mumnp-2003-petition under rule 137-01-07-2002.pdf

1142-mumnp-2003-petition under rule 138-01-07-2002.pdf

1142-mumnp-2003-power of authority.pdf

1142-mumnp-2003-wo-international publication report a1-01-07-2002.pdf


Patent Number 211107
Indian Patent Application Number 1142/MUMNP/2003
PG Journal Number 31/2008
Publication Date 01-Aug-2008
Grant Date 17-Oct-2007
Date of Filing 15-Dec-2003
Name of Patentee ASTRAZENECA AB
Applicant Address S-151 85 SODERTALJE, SWEDEN
Inventors:
# Inventor's Name Inventor's Address
1 RICHARD EVANS C/O ASTRAZENECA R & D CHARNWOOD, BACKEWELL ROAD, LOUGHBOROUGH, LEICESTERSHIRE LE11 5RH, GREAT BRITAIN
2 MATTHEW PERRY C/O ASTRAZENECA R & D CHARNWOOD, BACKEWELL ROAD, LOUGHBOROUGH, LEICESTERSHIRE LE11 5RH, GREAT BRITAIN
3 BRIAN SPRINGTHORPE C/O ASTRAZENECA R & D CHARNWOOD, BACKEWELL ROAD, LOUGHBOROUGH, LEICESTERSHIRE LE11 5RH, GREAT BRITAIN
PCT International Classification Number C07D 401/04
PCT International Application Number PCT/SE02/01311
PCT International Filing date 2002-07-01
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 0123037.4 2001-09-25 U.K.
2 0116179.3 2001-07-02 U.K.