IP Library › Granted Patent US 7,902,181
Granted Patent B2
US 7,902,181 · App. 12/331,719 · Granted Mar 8, 2011

Compounds 010

Assignee: AstraZeneca AB
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Quick Facts
Patent No.
US 7,902,181
App. No.
12/331,719
Granted
Mar 8, 2011
Kind
B2
Abstract

The present invention provides compounds of formula (I) in which n, y, X 1 , X 2 , A, B, R 1 , R 2 , R 3 , R 4 and R 5 are as defined in the specification, a process for their preparation, pharmaceutical compositions containing them and their use in therapy.

Claims (169)

1. A compound of formula (I)

wherein

n independently represents 0, 1, 2, 3 or 4;

X 1 represents a methylene group;

y represents 0, 1 or 2;

each R 1 independently represents halogen, hydroxyl, carboxyl, cyano, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, trifluoromethyl, NR 6 R 7 , C(O)NR 6 R 7 , NR 6a C(O)R 7a , SO 2 NR 6 R 7 , NR 6a SO 2 R 7a or S(O) m R 8 and R 1 is optionally substituted with hydroxy, halogen or

C 1 -C 6 alkoxy;

R 2 represents a hydrogen atom or a C 1 -C 6 alkyl group optionally substituted by at least one substituent selected from halogen, hydroxyl, carboxyl, cyano, trifluoromethyl, C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, NR 9 R 10 , C(O)NR 11 R 12 , NR 13 C(O)R 14 , SO 2 NR 15 R 16 , NR 17 SO 2 R 18 and S(O) p R 19 ;

R 3 represents a hydrogen atom or a C 1 -C 6 alkyl group optionally substituted by at least one substituent selected from halogen, hydroxyl, carboxyl, cyano, trifluoromethyl, C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, NR 20 R 21 , C(O)NR 22 R 23 , NR 24 C(O)R 25 , SO 2 NR 26 R 27 , NR 28 SO 2 R 29 and S(O) q R 30 ,

R 4 represents a hydrogen atom or a C 1 -C 6 alkyl group optionally substituted by at least one substituent selected from halogen, hydroxyl, carboxyl, cyano, trifluoromethyl, C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, NR 31 R 32 , C(O)NR 33 R 34 , NR 35 C(O)R 36 , SO 2 NR 37 R 38 , NR 39 SO 2 R 40 and S(O) r R 41 ,

R 5 represents a hydrogen atom or a C 1 -C 6 alkyl group optionally substituted by at least one substituent selected from halogen, hydroxyl, carboxyl, cyano, trifluoromethyl, C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, NR 42 R 43 , C(O)NR 44 R 45 , NR 46 C(O)R 47 , SO 2 NR 48 R 49 , NR 50 SO 2 R 51 and S(O) t R 52 , or

R 3 and R 4 together with the carbon atoms to which they are attached represent a cyclopropyl ring, or

R 4 and R 5 together with the carbon atom to which they are attached form a saturated or unsaturated, 3- to 6-membered carbocyclic or heterocyclic ring which ring may be optionally substituted with at least one substituent selected from halogen, hydroxyl, carboxyl and C 1 -C 6 alkyl;

A and B each independently represent a 5- to 10-membered aromatic ring system optionally comprising at least one ring heteroatom selected from nitrogen, oxygen and sulphur, the ring system being optionally substituted by at least one substituent selected from halogen, carboxyl, hydroxyl, oxo, nitro, cyano, mercapto, C 3 -C 6 cycloalkyl, C 2 -C 6 alkenyl, trifluoromethyl, C 1 -C 6 alkoxy, C 1 -C 6 alkylcarbonyl, C 1 -C 6 alkylcarbonyloxy, C 1 -C 6 alkoxycarbonyl, —NR 53 R 54 , —C(O)NR 55 R 56 , NR 57 C(O)R 58 , SO 2 NR 59 R 60 , NR 61 SO 2 R 62 , S(O) v R 63 , saturated 4- to 7-membered heterocyclyloxy, benzyloxy,

C 1 -C 6 alkylpiperazinyl and a C 1 -C 6 alkyl group (itself optionally substituted by hydroxyl, C 1 -C 6 alkoxy, NR 64 R 65 , phenyl or morpholinyl);

m, p, q, r, t and v each independently represent 0, 1 or 2;

X 2 represents a bond, an oxygen or sulphur atom, SO, SO 2 , NR 66 , C(O)NR 66 , NR 66 C(O), SO 2 NR 66 , NR 66 SO 2 , C 1 -C 3 alkyl, ethenyl or ethynyl;

R 6 and R 7 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 6 and R 7 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 9 and R 10 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 9 and R 10 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 11 and R 12 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 11 and R 12 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 15 and R 16 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 15 and R 16 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 20 and R 21 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 20 and R 21 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 22 and R 23 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 22 and R 23 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 26 and R 27 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 26 and R 27 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 31 and R 32 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 31 and R 32 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 33 and R 34 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 33 and R 34 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 37 and R 38 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 37 and R 38 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 42 and R 43 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 42 and R 43 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 44 and R 45 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 44 and R 45 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 48 and R 49 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 48 and R 49 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 53 and R 54 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 53 and R 54 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 55 and R 56 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 55 and R 56 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 59 and R 60 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 59 and R 60 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

R 64 and R 65 each independently represent hydrogen, C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, or R 64 and R 65 together with the nitrogen atom to which they are attached form a 4- to 7-membered saturated heterocyclic ring;

each group R 6a , R 7a , R 8 , R 13 , R 14 , R 17 , R 18 , R 19 , R 24 , R 25 , R 28 , R 29 , R 30 , R 35 , R 36 , R 39 , R 40 , R 41 , R 46 , R 47 , R 50 , R 51 , R 52 , R 57 , R 58 , R 61 , R 62 , and R 63 independently represents a hydrogen atom or a C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl group; and

R 66 represents a hydrogen atom or a C 1 -C 6 alkyl group; or

a pharmaceutically acceptable salt thereof.

2. A compound according to claim 1 wherein n is 2.

3. A compound according to claim 1 or claim 2 , wherein X 1 is methylene.

4. A compound according to any one of claims 1 to 3 , wherein R 2 represents a hydrogen atom.

5. A compound according to claim 1 , wherein R 3 , R 4 and R 5 each represent a hydrogen atom.

6. A compound according to claim 1 , wherein A represents phenyl.

7. A compound according to claim 1 , wherein B represents a 5- to 10-membered aromatic ring system optionally comprising one or two ring heteroatoms independently selected from nitrogen, oxygen and sulphur, the ring system being optionally substituted by at least one substituent selected from halogen, carboxyl, hydroxyl, cyano, C 1 -C 6 alkoxy, —NR 53 R 54 , —C(O)NR 55 R 56 , NR 57 C(O)R 58 , SO 2 NR 59 R 60 , S(O) v R 63 , pyrrolidinyloxy, benzyloxy, methylpiperazinyl and C 1 -C 6 alkyl (itself optionally substituted by hydroxyl, C 1 -C 6 alkoxy, NR 64 R 65 , phenyl or morpholinyl).

8. A compound according to claim 7 , wherein the aromatic ring system in B is selected from phenyl, pyrazolyl, pyridinyl, indolyl, oxazolyl, quinolinyl, pyrimidinyl and thienyl.

9. A compound according to claim 1 , wherein X 2 represents a bond.

10. A compound according to claim 1 being:

(S)-N-((S)-2-(3′-Chlorobiphenyl-4-yl)-1-cyanoethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(3′-(piperidin-1-ylmethyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-2-(biphenyl-4-yl)-1-cyanoethyl)pyrrolidine-2-carboxamide,

(S)-N-((S)-2-(4-(1-Benzyl-1H-pyrazol-4-yl)phenyl)-1-cyanoethyl)-piperidine-2-carboxamide,

(S)-N-((S)-2-(4′-Carbamoylbiphenyl-4-yl)-1-cyanoethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(3′-cyanobiphenyl-4-yl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-2-(3′-(Aminomethyl)biphenyl-4-yl)-1-cyanoethyl)piperidine-2-carboxamide,

(S)-N-((S)-2-(3′-Acetamidobiphenyl-4-yl)-1-cyanoethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4′-(morpholinomethyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4-(pyridin-3-yl)phenyl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4′-hydroxy-2′-methylbiphenyl-4-yl)ethyl)piperidine-2-carboxamide,

4′-((S)-2-Cyano-2-((S)-piperidine-2-carboxamido)ethyl)biphenyl-3-carboxylic acid,

(S)-N-((S)-1-Cyano-2-(2′-((R)-pyrrolidin-3-yloxy)biphenyl-4-yl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-2-(4-(1H-Indol-2-yl)phenyl)-1-cyanoethyl)piperidine-2-carboxamide,

(2S)-N-[(1S)-1-cyano-2-(3′-methoxybiphenyl-4-yl)ethyl]piperidine-2-carboxamide,

Piperidine-2-carboxylic acid (2-biphenyl-4-yl-1-cyano-ethyl)-amide,

(2S,4R)-N-((S)-2-(biphenyl-4-yl)-1-cyanoethyl)-4-hydroxypyrrolidine-2-carboxamide,

(S)-N-((S)-1-cyano-2-(3′-cyanobiphenyl-4-yl)ethyl)azetidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-[4-(dimethylsulfamoyl)phenyl]phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-(4-1,2-oxazol-4-ylphenyl)ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(3-methylsulfanylphenyl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(4-hydroxyphenyl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(4-cyanophenyl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(4-methoxyphenyl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(2-methylpyrazol-4-yl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-[3-hydroxypropyl)phenyl]phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-2-(4-Benzo[1,3]dioxol-5-ylphenyl)-1-cyano-ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(3,4-difluorophenyl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(4-fluoro-2-phenylmethoxy-phenyl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(3-fluoro-4-methoxy-phenyl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(3,4-dimethoxyphenyl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(2,4-dimethoxyphenyl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-2-[4-(3-Carbamoylphenyl)phenyl]-1-cyano-ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(2,5-dioxabicyclo[4.4.0]deca-7,9,11-trien-8-yl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-2-[4-[4-(Aminomethyl)phenyl]phenyl]-1-cyano-ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(2-dimethylaminopyrimidin-5-yl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(4-methylthiophen-3-yl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(3-fluoro-4-propoxy-phenyl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(2-methoxypyridin-3-yl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(2-methylpyrazol-3-yl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-[3-(dimethylcarbamoyl)phenyl]phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(4-ethylsulfonyl-2-methyl-phenyl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(3,5-difluoro-2-methoxy-phenyl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-[3-(hydroxymethyl)phenyl]phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(2-methoxypyrimidin-5-yl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-[6-(4-methylpiperazin-1-yl)pyridin-3-yl]phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(2-hydroxyphenyl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-(4-quinolin-8-ylphenyl)ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(2-methylphenyl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(2-phenylmethoxyphenyl)phenyl]ethyl]piperidine-2-carboxamide,

(2S)-N-[(1S)-1-Cyano-2-[4-(2-methylpyridin-3-yl)phenyl]ethyl]piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4-(6-cyanopyridin-3-yl)phenyl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4-(3-(2-hydroxyethyl)-2-oxo-2,3-dihydrobenzo[d]thiazol-5-yl)phenyl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-cyano-2-(4-(3-(2-methoxyethyl)-2-oxo-2,3-dihydrobenzo[d]thiazol-5-yl)phenyl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4′-cyano-3′-fluorobiphenyl-4-yl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4′-cyano-3′-(methylthio)biphenyl-4-yl)ethyl)-piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4′-cyano-3′-(methylsulfonyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4′-cyano-3′-(ethylsulfonyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4′-cyano-3′-(propylsulfonyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide,

(2S)-N-((1S)-2-(4′-Carbamoyl-3′-(methylsulfinyl)biphenyl-4-yl)-1-cyanoethyl)piperidine-2-carboxamide,

(2S)-N-((1S)-1-Cyano-2-(4′-cyano-3′-(2-methyl-1H-imidazol-1-yl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-cyano-2-(3′-cyano-4′-(methylthio)biphenyl-4-yl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(3′-cyano-4′-(methylsulfonyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide,

(S)-tert-Butyl 2-((S)-1-cyano-2-(3′-cyano-4′-(propylsulfonyl)biphenyl-4-yl)ethylcarbamoyl)piperidine-1-carboxylate,

(S)-N-((S)-1-Cyano-2-(4-(3-methyl-2-oxo-2,3-dihydrobenzo[d]thiazol-5-yl)phenyl)ethyl)piperidine-2-carboxamide,

(2S)-N-{(1S)-1-Cyano-2-[4-(1,1-dioxido-2,3-dihydro-1,2-benzisothiazol-5-yl)phenyl]ethyl}piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4-(3-oxo-3,4-dihydro-2H-benzo[b][1,4]thiazin-7-yl)phenyl)ethyl)piperidine-2-carboxamide,

2S)-N-{(1S)-1-Cyano-2-[4-(2-methyl-1,1-dioxido-2,3-dihydro-1,2-benzisothiazol-5-yl)phenyl]ethyl}piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4′-ethylbiphenyl-4-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(4′-(N-methylsulfamoyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-2-(4′-(Azetidin-1-ylsulfonyl)biphenyl-4-yl)-1-cyanoethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(4′-(N-(2-hydroxyethyl)sulfamoyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4′-(methylcarbamoyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(4′-(pyrrolidine-1-carbonyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(4′-(4-methylpiperazine-1-carbonyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(6-(4-cyanophenyl)pyridin-3-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(6-(3-cyanophenyl)pyridin-3-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(6-(2-hydroxyphenyl)pyridin-3-yl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(6-(4-(N,N-dimethylsulfamoyl)phenyl)pyridin-3-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-2-(6-(3-Chloro-5-(dimethylcarbamoyl)phenyl)pyridin-3-yl)-1-cyanoethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(4′-(trifluoromethyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(3′-(piperidine-1-carbonyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(3′-(thiazol-2-ylcarbamoyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(3′-(2-cyanoethylcarbamoyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-2-(3′-(2-amino-2-oxoethyl)biphenyl-4-yl)-1-cyanoethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(3′-(N,N-dimethylsulfamoyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(3′-(pyrrolidin-1-ylsulfonyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(3′-(methylsulfonamidomethyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-2-(3′-(Acetamidomethyl)biphenyl-4-yl)-1-cyanoethyl)-piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(4′-(4-cyanopiperidin-1-ylsulfonyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(4′-(morpholinosulfonyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(4′-(4-methylpiperazin-1-ylsulfonyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(4-(3-methyl-2-oxo-2,3-dihydrobenzo[d]oxazol-5-yl)phenyl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4-(3-(2-methoxyethyl)-2-oxo-2,3-dihydrobenzo[d]-oxazol-5-yl)phenyl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4-(3-methyl-2-oxo-2,3-dihydrobenzo[d]thiazol-6-yl)phenyl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4-(3-(2-hydroxyethyl)-2-oxo-2,3-dihydrobenzo[d]thiazol-6-yl)phenyl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4′-cyanobiphenyl-3-yl)ethyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(4′-(cyanomethyl)-3′-(methylsulfonyl)biphenyl-4-yl)ethyl)-piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(4-(phenylsulfonyl)phenyl)ethyl)piperidine-2-carboxamide,

(S)-N-((1R,2R)-1-Cyano-2-(4′-cyanobiphenyl-4-yl)cyclopropyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((1R,2R)-2-(4′-(Azetidin-1-ylsulfonyl)biphenyl-4-yl)-1-cyanocyclopropyl)piperidine-2-carboxamide trifluoroacetate,

(S)-N-((S)-1-Cyano-2-(4′-(trifluoromethoxy)biphenyl-4-yl)ethyl)piperidine-2-carboxamide,

(S)-N-((S)-1-Cyano-2-(4′-(methylsulfonyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide,

((2S)-N-(1-Cyano-2-(4′-(4-ethylpiperazin-1-ylsulfonyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide ditrifluoroacetate,

(2S)-N-(1-Cyano-2-(4′-(4-methyl-1,4-diazepan-1-ylsulfonyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide ditrifluoroacetate,

(S)-N-((S)-1-Cyano-2-(3′-(morpholinomethyl)biphenyl-4-yl)ethyl)piperidine-2-carboxamide ditrifluoroacetate, or

(S)-N-((S)-1-Cyano-2-(4-(1,2,3,4-tetrahydroisoquinolin-6-yl)phenyl)ethyl)piperidine-2-carboxamide ditrifluoroacetate or a pharmaceutically acceptable salt thereof.

11. A process for the preparation of a compound of formula (I) or a pharmaceutically acceptable salt thereof as defined in claim 1 which comprises reacting a compound of formula (II)

wherein R 3 , R 4 , R 5 , A, X 2 and B are as defined in formula (I), with a compound of formula (III)

wherein PG 1 represents a protecting group and n, X 1 , y, R 1 and R 2 are as defined in formula (I), and optionally thereafter carrying out one or more of the following procedures:

converting a compound of formula (I) into another compound of formula (I)

removing any protecting groups

forming a pharmaceutically acceptable salt.

12. A pharmaceutical composition comprising a compound of formula (I) or a pharmaceutically acceptable salt thereof as claimed in claim 1 in association with a pharmaceutically acceptable adjuvant, diluent or carrier.

13. A combination of a compound of formula (I) or a pharmaceutically acceptable salt thereof as claimed in claim 1 and one or more agents independently selected from:

a non-steroidal glucocorticoid receptor agonist;

a selective β 2 adrenoceptor agonist;

a phosphodiesterase inhibitor;

a protease inhibitor;

a glucocorticoid;

an anticholinergic agent;

a modulator of chemokine receptor function; and

an inhibitor of kinase function.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 5, 2009
From: CAGE, PETER ALAN; LUCKHURST, CHRISTOPHER ANDREW; FURBER, MARK; SANGANEE, HITESH JAYANTILAL; STEIN, LINDA ANNE
To: ASTRAZENECA AB
Reel/Frame 022348/0034 →
Continuity (2)
Provisional Application 61012972 · Dec 12, 2007
Related Publication 20090306042A1 · Dec 10, 2009