IP Library Granted Patent US 9,428,498
Granted Patent B2
US 9,428,498 · App. 14/208,056 · Granted Aug 30, 2016

Substituted imidazo[4,5-c]pyridine compounds and compositions thereof

Inventors: Max Espensen (London, GB); Lee Patient (London, GB); David Evans (London, GB); Edward Savory (London, GB); Iain Simpson (London, GB)
Assignee: Proximagen Limited
C07D471/04
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Quick Facts
Patent No.
US 9,428,498
App. No.
14/208,056
Granted
Aug 30, 2016
Kind
B2
Abstract

The present invention relates to compounds which are inhibitors of SSAO activity. The invention also relates to pharmaceutical compositions comprising these compounds and to the use of these compounds in the treatment or prevention of medical conditions wherein inhibition of SSAO activity is beneficial, such as inflammatory diseases, immune disorders and the inhibition of tumor growth.

Claims (40)

1. A compound of formula (I) or a pharmaceutically acceptable salt, or N-oxide thereof:

wherein:

Y is selected from hydrogen, hydroxyl, —NH 2 , —NH—C 1-4 -alkyl, —NH-halo-C 1-4 -alkyl, or —C 1-4 -alkoxy;

Z is selected from hydrogen, halogen, hydroxyl, cyano, C 1-4 -alkyl, halo-C 1-4 -alkyl, C 1-4 -alkoxy, halo-C 1-4 -alkoxy, —CONH 2 , —SO 2 NH 2 , —NH 2 , —NHC 1-4 -alkyl, or —NHhalo-C 1-4 -alkyl;

R 1 is a phenyl ring, or a 5 or 6-membered heteroaryl ring, either ring being optionally substituted with one or more substituents selected from halogen, cyano, C 1-4 -alkyl, halo-C 1-4 -alkyl, cyano-C 1-4 -alkyl, —OR 5 , —NR 6 C(O)OR 5 , —NR 6 C(O)R 5 , —NR 6 C(O)NR 4A R 4B , —C(O)NR 4A R 4B , —C(O)R 5 , —C(O)OR 5 , and —NR 6 S(O) 2 R 5 ; wherein

R 4A , R 4B R 5 and R 6 are each independently selected from hydrogen, C 1-4 -alkyl or halo-C 1-4 -alkyl, or

R 4A and R 4B together with the nitrogen to which they are attached form a 3-7 membered cyclic amino group, optionally substituted by one or more substituents selected from: halogen, hydroxyl, cyano, C 1-4 -alkyl, halo-C 1-4 -alkyl, C 1-4 -alkoxy, halo-C 1-4 -alkoxy, —CONH 2 , —SO 2 NH 2 , —NH 2 , —NHC 1-4 -alkyl, —NHhalo-C 1-4 -alkyl;

X is —N═;

W is a phenyl ring or a 5 or 6-membered heteroaryl ring, either ring being optionally substituted with one or more substituents selected from halogen, cyano, C 1-4 -alkyl, halo-C 1-4 -alkyl, cyano-C 1-4 -alkyl, —OR 5 , —NR 7A R 7B , —NR 6 C(O)OR 5 , —NR 6 C(O)R 5 , —NR 6 C(O)NR 7A R 7B , —C(O)NR 7A R 7B , —C(O)R 5 , —C(O)OR 5 , —SO 2 R 5 , —SO 2 NR 7A R 7B and —NR 6 S(O) 2 R 5 ;

R 7A and R 7B are independently hydrogen, C 1-4 -alkyl or halo-C 1-4 -alkyl,

V is selected from a bond, —O—, —N(R 6 )—, —(C═O)—, —CONR 6 —, —NR 6 C(O)—, or —C 1-4 -alkylene-, wherein the C 1-4 -alkylene group is optionally substituted by halogen, and wherein any one of the carbon atoms of the C 1-4 -alkylene group may be replaced by —O— or —N(R 6 )—;

R 3 is hydrogen or a 3-7 membered heterocyclic ring, or a cycloalkyl ring selected from cyclopropyl, cyclopentyl and cyclohexyl, or a 5 or 6-membered heteroaryl ring, any one of the rings being optionally substituted with one or more substituents selected from halogen, oxo, hydroxyl, cyano, C 1-4 -alkyl, halo-C 1-4 -alkyl, cyano-C 1-4 -alkyl, —OR 5 , NR 4A R 4B , NR 6 C(O)OR 5 , —NR 6 C(O)R 5 , —NR 6 C(O)NR 4A R 4B , —C(O)NR 4A R 4B , —C(O)R 5 , —C(O)OR 5 , —SO 2 R 5 , —SO 2 NR 4A R 4B and —NR 6 S(O) 2 R 5 .

2. The compound according to claim 1 wherein Y is hydrogen.

3. The compound according to claim 1 wherein Z is hydrogen.

4. The compound according to claim 1 wherein R 1 is phenyl or 6-membered heteroaryl, optionally substituted with one or more substituents selected from halogen, C 1-4 -alkyl or halo-C 1-4 -alkyl.

5. The compound according to claim 1 wherein R 1 is phenyl or pyridyl, optionally substituted with one or more substituents selected from F, Cl or CH 3 .

6. The compound according to claim 1 wherein W is a phenyl ring optionally substituted with one or more substituents selected from halogen, cyano, C 1-4 -alkyl, halo-C 1-4 -alkyl, cyano-C 1-4 -alkyl, —OR 5 , —NR 7A R 7B , NR 6 C(O)OR 5 , —NR 6 C(O)R 5 , —NR 6 C(O)NR 7A R 7B , —C(O)NR 7A R 7B , —C(O)R 5 , —C(O)OR 5 , —SO 2 R 5 , —SO 2 NR 7A R 7B and —NR 6 S(O) 2 R 5 .

7. The compound according to claim 1 wherein W is a 6-membered heterocyclic ring selected from pyridine, pyridazine, pyrazine, or pyrimidine optionally substituted with one or more substituents selected from halogen, cyano, C 1-4 -alkyl, halo-C 1-4 -alkyl, cyano-C 1-4 -alkyl, —OR 5 , —NR 7A R 7B , NR 6 C(O)OR 5 , —NR 6 C(O)R 5 , —NR 6 C(O)NR 7A R 7B , —C(O)NR 7A R 7B , —C(O)R 5 , —C(O)OR 5 , —SO 2 R 5 , —SO 2 NR 7A R 7B and —NR 6 S(O) 2 R 5 .

8. The compound according to claim 1 wherein W is a 5-membered ring selected from oxazole, thiazole or imidazole optionally substituted with one or more substituents selected from halogen, cyano, C 1-4 -alkyl, halo-C 1-4 -alkyl, cyano-C 1-4 -alkyl, —OR 5 , —NR 7A R 7B , NR 6 C(O)OR 5 , —NR 6 C(O)R 5 , —NR 6 C(O)NR 7A R 7B , —C(O)NR 7A R 7B , —C(O)R 5 , —C(O)OR 5 , —SO 2 R 5 , —SO 2 NR 7A R 7B and —NR 6 S(O) 2 R 5 .

9. The compound according to claim 1 wherein W is substituted with one or more substituents selected from fluoro, chloro, cyano, CH 3 or CF 3 .

10. The compound according to claim 1 wherein V is —CH 2 —, —(CH 2 ) 2 —, or —N(R 6 )CH 2 —, or —CH 2 —N(R 6 ) —.

11. The compound according to claim 1 wherein R 3 is cyclopropyl, cyclopentyl or cyclohexyl optionally substituted with one or more substituents selected from halogen, oxo, hydroxyl, cyano, C 1-4 -alkyl, halo-C 1-4 -alkyl, cyano-C 1-4 -alkyl, —OR 5 , —NR 4A R 4B , NR 6 C(O)OR 5 , —NR 6 C(O)R 5 , —NR 6 C(O)NR 4A R 4B , —C(O)NR 4A R 4B , —C(O)R 5 , —C(O)OR 5 , —SO 2 R 5 , —SO 2 NR 4A R 4B and —NR 6 S(O) 2 R 5 .

12. The compound according to claim 1 wherein R 3 is formed from —NR 4A R 4B wherein R 4A and R 4B , together with the nitrogen atom to which they are attached join together to form a 4-7 membered heterocyclic ring optionally substituted with one or more substituents selected from halogen, oxo, hydroxyl, cyano, C 1-4 -alkyl, halo-C 1-4 -alkyl, cyano-C 1-4 -alkyl, —OR 5 , —NR 4A R 4B , NR 6 C(O)OR 5 , —NR 6 C(O)R 5 , —NR 6 C(O)NR 4A R 4B , —C(O)NR 4A R 4B , —C(O)R 5 , —C (O)OR 5 , —SO 2 R 5 , —SO 2 NR 4A R 4B and —NR 6 S(O) 2 R 5 .

13. The compound according to claim 1 wherein R 3 is selected from

wherein R 8 is selected from hydrogen, CH 3 , —CONH 2 , —NHCONH 2 , —S(O) 2 CH 3 , and —COCH 3 .

14. The compound according to claim 1 wherein X is —N═, and V is a direct bond.

15. The compound according to claim 1 selected from:

4-({5-[3-(4-Chlorophenyl)-3H-imidazo[4,5-c]pyridin-2-yl]pyridin-2-yl}methyl)morpholine;

4-{5-[3-(4-Fluorophenyl)-3H-imidazo[4,5-c]pyridin-2-yl]pyrimidin-2-yl}piperazin-2-one;

4-{5-[3-(4-Chlorophenyl)-3H-imidazo[4,5-c]pyridin-2-yl]pyrimidin-2-yl}piperazin-2-one;

5-[3-(4-Fluorophenyl)-3H-imidazo[4,5-c]pyridin-2-yl]-N-(oxan-4-yl)pyrimidin-2-amine;

4-{5-[3-(4-Fluorophenyl)-3H-imidazo[4,5-c]pyridin-2-yl]pyrimidin-2-yl}morpholine;

4-{5-[3-(2-Fluoro-4-methylphenyl)-3H-imidazo[4,5-c]pyridin-2-yl] pyrimidin-2-yl}morpholine;

N-(1-{5-[3-(4-Chlorophenyl)-3H-imidazo[4,5-c]pyridin-2-yl]pyridin-2-yl}piperidin-4-yl)acetamide;

1-(4-{5-[3-(4-Fluorophenyl)-3H-imidazo[4,5-c]pyridin-2-yl]pyridin-2-yl}piperazin-1-yl)ethan-1-one;

1-{5-[3-(4-Fluorophenyl)-3H-imidazo[4,5-c]pyridin-2-yl]pyridin-2-yl}-4-methanesulfonylpiperazine;

(1-{5-[3-(4-Chlorophenyl)-3H-imidazo[4,5-c]pyridin-2-yl]pyridin-2-yl}piperidin-4-yl)urea;

4-{5-[3-(4-Fluorophenyl)-3H-imidazo[4,5-c]pyridin-2-yl]pyridin-2-yl}piperazine-1-carboxamide;

and pharmaceutically acceptable salts thereof.

16. A pharmaceutical composition comprising a compound according to claim 1 together with one or more pharmaceutically acceptable carriers and/or excipients.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 14, 2018
From: PROXIMAGEN GROUP LIMITED
To: PROXIMAGEN, LLC
Reel/Frame 047783/0774 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 14, 2018
From: BENEVOLENTAI CAMBRIDGE LIMITED
To: PROXIMAGEN GROUP LIMITED
Reel/Frame 047783/0798 →
CHANGE OF NAME Recorded Dec 14, 2018
From: PROXIMAGEN LIMITED
To: BENEVOLENTAI CAMBRIDGE LIMITED
Reel/Frame 047783/0826 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 2, 2014
From: ESPENSEN, MAX; PATIENT, LEE; EVANS, DAVID; SAVORY, EDWARD; SIMPSON, IAIN
To: PROXIMAGEN LIMITED
Reel/Frame 033008/0275 →
Priority Claims (1)
GB 1304526.5 · Mar 13, 2013 · national
Continuity (1)
Related Publication 20140275040A1 · Sep 18, 2014