IP Library Granted Patent US 10,590,125
Granted Patent B2
US 10,590,125 · App. 15/215,026 · Granted Mar 17, 2020

Compounds

Inventors: Max Espensen (Cambridge, GB); Lee Patient (Linton, GB); David Evans (Royston, GB); Edward Savory (Cambourne, GB); Iain Simpson (Cambridge, GB)
Assignee: PROXIMAGEN, LLC
C07D471/04A61K31/40C07C53/18
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Quick Facts
Patent No.
US 10,590,125
App. No.
15/215,026
Granted
Mar 17, 2020
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 (29)

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, and —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, and —NHhalo-C 1-4 -alkyl;

R 1 is a phenyl 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 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 , and —NR 6 S(O) 2 R 5 ;

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

W is a pyridyl 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 R 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)—, and —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 )—; and

R 3 is a cyclobutyl 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 .

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

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

4. A compound according to claim 1 wherein R 1 is optionally substituted with one or more substituents selected from halogen, C 1-4 -alkyl, and halo-C 1-4 -alkyl.

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

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

7. A 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 )—.

8. A compound according to claim 1 wherein V is a direct bond.

9. A pharmaceutical composition comprising:

a pharmaceutically acceptable carrier and/or excipient; and

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, and —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, and —NHhalo-C 1-4 -alkyl;

R 1 is a phenyl 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 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 , and —NR 6 S(O) 2 R 5 ,

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

W is a pyridyl 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 R 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)—, and —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 )—; and

R 3 is a cyclobutyl 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 R 4A R 4B and —NR 6 S(O) 2 R 5 .

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 Jul 20, 2016
From: ESPENSEN, MAX; PATIENT, LEE; EVANS, DAVID; SAVORY, EDWARD; SIMPSON, IAIN
To: PROXIMAGEN LIMITED
Reel/Frame 039200/0610 →
Priority Claims (1)
GB 1304526.5 · Mar 13, 2013 · national
Continuity (2)
Continuation 14208056 · Mar 13, 2014
Related Publication 20160326172A1 · Nov 10, 2016