IP Library Granted Patent US 9,598,420
Granted Patent B2
US 9,598,420 · App. 14/753,326 · Granted Mar 21, 2017

Benzodiazepine bromodomain inhibitor

Inventors: James Bailey (Stevenage, GB); Romain Luc Marie Gosmini (Les Ulis, FR); Olivier Mirguet (Les Ulis, FR); Jason Witherington (Stevenage, GB)
Assignee: GlaxoSmithKline LLC
C07D487/04
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,598,420
App. No.
14/753,326
Granted
Mar 21, 2017
Kind
B2
Abstract

Benzodiazepine compounds of formula (I) and salts thereof, pharmaceutical compositions containing such compounds and their use in therapy.

Claims (25)

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

where

R 1 is C 1-3 alkyl;

R 2 is —NR 2a R 2a′ ;

wherein R 2a is hydrogen, and R 2a′ is heterocyclylC 1-4 alkyl,

wherein the heterocyclyl is optionally substituted once by amino, hydroxyl, or methyl;

each R 3 is independently selected from hydrogen, hydroxyl, halo, C 1-6 alkyl, halo C 1-6 alkyl, C 1-6 alkoxy, halo C 1-6 alkoxy, nitro, cyano, CF 3 , —OCF 3 , —COOR 5 , and —C 1-4 alkylOH;

R 4 is hydroxyl, halo, C 1-6 alkyl, haloC 1-6 alkyl, C 1-6 alkoxy, haloC 1-6 alkoxy, nitro, cyano, CF 3 , —OCF 3 , —COOR 5 ; or —OS(O) 2 C 1-4 alkyl;

R 5 is C 1-3 alkyl; and

n is an integer 1 to 5.

2. The compound or salt according to claim 1 , wherein R 2a′ is selected from heterocyclyl-CH 2 —, heterocyclyl-CH 2 CH 2 —, heterocyclyl-CH 2 CH 2 CH 2 — and heterocyclyl-CH 2 CH 2 CH 2 CH 2 —, wherein the heterocyclyl is optionally substituted once by amino, hydroxyl or methyl.

3. The compound or salt according to claim 2 , wherein heterocyclyl is selected from tetrahydrofuranyl, pyrrolidinyl, piperidinyl, tetrahydropyranyl, piperazinyl, morpholino and thiomorpholinodioxide, wherein each group is optionally substituted once by amino, hydroxyl or methyl.

4. The compound or salt according to claim 3 , wherein heterocyclyl is selected from:

5. The compound or salt according to claim 1 , wherein n is 1.

6. The compound or salt according to claim 5 , wherein R 3 is 3-fluoro, 4- chloro, 4-fluoro, 4-methoxy or 4-CF 3 .

7. The compound or salt according to claim 6 , wherein R 3 is 4-chloro.

8. The compound or salt according to claim 1 , wherein R 4 is MeO.

9. The compound or salt according to claim 8 , wherein R 4 is 8-MeO.

10. The compound or salt according to claim 1 which is the S-enantiomer.

11. A compound which is:

2-[(4S)-6-(4-chlorophenyl)-1-methyl-8-(methyloxy)-4H- [1,2,4]triazolo [4,3-a][1,4]benzodiazepin-4-yl]-N-[2-(4-morpholinyl)ethyl]acetamide;

2-[(4S)-6-(4-chloropheny )-1-methyl-8-(methyloxy)-4H- [1,2,4]triazolo [4,3-a][1,4]benzodiazepin-4-yl]-N-[3-(4-morpholinyl)propyl]acetamide; or

2-[(4S)-6-(4-chlorophenyl)- 1 -methyl-8-(methyloxy)-4H- [1,2,4]triazolo [4,3-a][1,4]benzodiazepin-4-yl]-N-[2-(1,1-dioxido-4-thiomorpholinyl)ethyl]acetamide;

or a salt thereof.

12. A pharmaceutical composition which comprises the compound or salt according to claim 1 and one or more pharmaceutically acceptable carriers, diluents or excipients.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 9, 2015
From: BAILEY, JAMES; GOSMINI, ROMAIN LUC MARIE; MIRGUET, OLIVIER; WITHERINGTON, JASON
To: GLAXOSMITHKLINE LLC
Reel/Frame 036516/0542 →
Priority Claims (4)
GB 0919433.3 · Nov 5, 2009 · national
GB 1010509.6 · Jun 22, 2010 · national
WO PCT/EP2010/061518 · Aug 6, 2010 · international
GB 1014231.3 · Aug 25, 2010 · national
Continuity (2)
Continuation 13504971
Related Publication 20150299210A1 · Oct 22, 2015