IP Library › Granted Patent US 8,350,037
Granted Patent B2
US 8,350,037 · App. 12/691,842 · Granted Jan 8, 2013

Thieno-pyridine derivatives as MEK inhibitors

Assignee: UCB Pharma, S.A.
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Quick Facts
Patent No.
US 8,350,037
App. No.
12/691,842
Granted
Jan 8, 2013
Kind
B2
Abstract

A series of thieno[2,3-b]pyridine derivatives which are substituted in the 2-position by a substituted anilino moiety, being selective inhibitors of human MEK (MAPKK) enzymes, are accordingly of benefit in medicine, for example in the treatment of inflammatory, autoimmune, cardiovascular, proliferative (including oncological) and nociceptive conditions.

Claims (33)

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

wherein

R 1 is hydrogen, halogen, or C 1-6 alkyl;

R 2 is halogen or C 1-6 alkyl;

R 3 is —SO 2 NR b R c ; and

R b and R c , when taken together with the nitrogen atom to which they are both attached, form a heterocyclic ring selected from optionally substituted azetidinyl, optionally substituted pyrrolidinyl, optionally substituted piperidinyl, optionally substituted morpholinyl, optionally substituted thiomorpholinyl, optionally substituted piperazinyl, optionally substituted homopiperidinyl, optionally substituted homomorpholinyl and optionally substituted homopiperazinyl;

wherein the one or more optional substituents are each independently selected from the group consisting of:

C 1-6 alkyl, hydroxy, hydroxy(C 1-6 )alkyl, C 1-6 alkoxy, C 1-6 alkoxy(C 1-6 )alkyl, amino(C 1-6 )alkyl, (amino)(hydroxy)(C 1-6 )alkyl, halogen, oxo, C 2-6 alkylcarbonyl, carboxy, carboxy(C 1-6 )alkyl, C 2-6 alkoxycarbonyl, C 2-6 alkoxycarbonyl(C 1-6 )alkyl, di(C 1-6 )alkyl-hydrazinylcarbonyl, amino, C 1-6 alkylamino, di(C 1-6 )alkylamino, C 2-6 alkylcarbonylamino, C 2-6 alkoxycarbonylamino, C 2-6 alkoxycarbonylamino (C 1-6 )alkyl, C 2-6 alkoxycarbonyl-(C 1-6 )alkylamino(C 1-6 )alkyl, aminocarbonylamino, aminocarbonyl, C 1-6 alkylamino-carbonyl, di(C 1-6 )alkylaminocarbonyl, aminosulfonyl, C 1-6 alkylsulfonyl and C 1-6 alkylaminocarbonyl(C 1-6 )alkyl.

2. A compound according to claim 1 , wherein R b and R c are taken together with the nitrogen atom to which they are attached to form a cyclic group selected from optionally substituted azetidin-1-yl, optionally substituted pyrrolidin-1-yl and optionally substituted piperidin-1-yl.

3. A compound according to claim 1 wherein the cyclic group formed by R b and R c and the nitrogen atom to which they are attached is optionally substituted with one or more of hydroxy, amino, amino(C 1-6 )alkyl, C 2-6 alkoxycarbonylamino, carboxy(C 1-6 )alkylamino (C 1-6 )alkyl or C 2-6 alkoxycarbonyl(C 1-6 )alkylamino(C 1-6 )alkyl.

4. A compound according to claim 3 wherein the cyclic group formed by R b and R c and the nitrogen atom to which they are attached is substituted with hydroxy, amino, amino(C 1-6 )alkyl, C 2-6 alkoxycarbonylamino, carboxy(C 1-6 )alkylamino(C 1-6 )alkyl or C 2-6 alkoxycarbonyl(C 1-6 )alkylamino(C 1-6 )alkyl.

5. A compound or a pharmaceutically acceptable salt or N-oxide thereof according to claim 1 , having the following formula (II):

wherein:

R 12 is halogen.

6. A compound according to claim 5 , wherein R 12 is bromo or iodo.

7. A compound or a pharmaceutically acceptable salt or N-oxide thereof according to claim 1 , which is selected from the group consisting of:

N-(2-Fluoro-4-iodophenyl)-3-(pyrrolidin-1-ylsulfonyl)thieno[2,3-b]pyridin-2-amine;

3-{[3-(Aminomethyl)azetidin-1-yl]sulfonyl}-N-(2-fluoro-4-iodophenyl)thieno-[2,3-b]pyridin-2-amine;

tert-Butyl [(3R)-1-({2-[(2-fluoro-4-iodophenyl)amino]thieno[2,3-b]pyridin-3-yl}sulfonyl)pyrrolidin-3-yl]carbamate;

3-{[(3R)-3-Aminopyrrolidin-1-yl]sulfonyl}-N-(2-fluoro-4-iodophenyl)thieno[2,3-b]pyridin-2-amine;

tert-Butyl [(3S)-1-({2-[(2-fluoro-4-iodophenyl)amino]thieno[2,3-b]pyridin-3-yl}sulfonyl)pyrrolidin-3-yl]carbamate;

3-{[(3S)-3-Aminopyrrolidin-1-yl]sulfonyl}-N-(2-fluoro-4-iodophenyl)thieno[2,3-b]pyridin-2-amine;

N-(2-Fluoro-4-iodophenyl)-3-(piperazin-1-ylsulfonyl)thieno[2,3-b]pyridin-2-amine hydrochloride;

3-(Aminomethyl)-1-({2-[(2-fluoro-4-iodophenyl)amino]thieno[2,3-b]pyridin-3-yl}sulfonyl)azetidin-3-ol;

Ethyl N-{[1-({2-[(2-fluoro-4-iodophenyl)amino]thieno[2,3-b]pyridin-3-yl}sulfonyl)azetidin-3-yl]methyl}-beta-alaninate;

Ethyl N-{[1-({2-[(2-fluoro-4-iodophenyl)amino]thieno[2,3-b]pyridin-3-yl}sulfonyl)azetidin-3-yl]methyl}glycinate;

1-({2-[(2-Fluoro-4-iodophenyl)amino]thieno[2,3-b]pyridin-3-yl}sulfonyl)-azetidin-3-ol;

(3R)-1-({2-[(2-Fluoro-4-iodophenyl)amino]thieno[2,3-b]pyridin-3-yl}sulfonyl)-pyrrolidin-3-ol;

tert-Butyl-[1-({2-[(2-fluoro-4-iodophenyl)amino]thieno[2,3-b]pyridin-3-yl}sulfonyl)azetidin-3-yl]carbamate;

3-[(3-Aminoazetidin-1-yl)sulfonyl]-N-(2-fluoro-4-iodophenyl)thieno[2,3-b]pyridin-2-amine;

and

3-({1-[2-(2-Fluoro-4-iodophenylamino)thieno[2,3-b]pyridine-3-sulfonyl]azetidin-3-ylmethyl}amino)propionic acid.

8. A pharmaceutical composition comprising a compound or a pharmaceutically acceptable salt or N-oxide thereof according to claim 1 , in combination with a pharmaceutically acceptable carrier.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 30, 2010
From: JOHNSON, JAMES ANDREW; BROOKINGS, DANIEL CHRISTOPHER; HUTCHINGS, MARTIN CLIVE; LANGHAM, BARRY JOHN; NEUSS, JUDI CHARLOTTE
To: UCB PHARMA, S.A.
Reel/Frame 024157/0212 →
Priority Claims (2)
GB 0714384.5 · Jul 23, 2007 · national
WO PCT/GB2008/002430 · Jul 16, 2008 · international
Continuity (1)
Related Publication 20100179124A1 · Jul 15, 2010