IP Library Granted Patent US 7,714,126
Granted Patent B2
US 7,714,126 · App. 11/601,429 · Granted May 11, 2010

Diacylglycerol acyltransferase inhibitors

Assignee: Via Pharmaceuticals, Inc.
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 7,714,126
App. No.
11/601,429
Granted
May 11, 2010
Kind
B2
Abstract

Provided herein are compounds of the formula (I): as well as pharmaceutically acceptable salts thereof, wherein the substituents are as those disclosed in the specification. These compounds, and the pharmaceutical compositions containing them, are useful for the treatment of diseases such as, for example, obesity, type II diabetes mellitus and metabolic syndrome.

Claims (30)

1. A compound of the formula (I):

wherein:

R 1 is phenyl or phenyl substituted with a group selected from the group consisting of alkyl, —O-alkyl, haloalkoxy, methoxy-ethoxy, halogen, or cycloalkyl containing 4 to 7 carbon atoms;

R 2 is C;

R 3 is N;

R 4 is S or O;

R 5 is C;

R 6 is H, alkyl, halogen, haloalkyl, or thioalkyl;

R 7 is

wherein one of R 8 and R 9 is nitrogen and the other is carbon;

R 10 is —NR 11 R 12 , O-alkyl, hydroxy-dimethylethylamino, hydroxyl-methylethylamino, cyclohept-2-ylamino, morpholino, thiomorpholino, oxothiomorpholino, dioxothiomorpholino, alkyl-carbamoyl-alkyl-amino, difluoroazetidine, ethoxyazetidine, or a 4- to 6-membered cyclic ring having from 1 to 3 hetero ring atoms selected from the group consisting of S, N and O substituted with a group selected from the group consisting of amino, —N(CH 3 )C(O)CH 3 , cyclopropanecarbonyl-methyl, —OCH 3 , —OCH 2 C(O)OC(CH 3 ) 3 , OCH 2 C(O)OH, —CH 2 OH, —CH 2 OCH 3 and —OH;

R 11 is H, lower alkyl, alkoxyalkyl, alkyl-aryl, trifluoromethyl, cyclopropylmethoxy-ethyl, —CH 2 CH 2 CN, hydroxyalkyl, cycloalkyl, or a 4- to 6-membered cyclic ring having from 1 to 3 hetero ring atoms selected from the group consisting of S, N and O, unsubstituted or substituted with a group selected from the group consisting of —OCH 3 , —CH 2 OH, —CH 2 OCH 3 , —OCH 2 C(O)OC(CH 3 ) 3 , —OCH 2 C(O)OH and —OH;

R 12 is H or lower alkyl;

or a pharmaceutically acceptable salt thereof.

2. The compound according to claim 1 wherein:

R 1 is unsubstituted phenyl or phenyl substituted with a group selected from the group consisting of alkyl and halogen.

3. The compound according to claim 1 wherein:

R 10 is —NR 11 R 12 ;

R 11 is H, lower alkyl, alkyl ether, alkyl alcohol, acyl or a 5- or 6-membered cyclic ring having from 1 to 3 hetero ring atoms selected from the group consisting of S, N and O, unsubstituted or substituted with a group selected from the group consisting of —OCH 3 , —CH 2 OH, —CH 2 OCH 3 and —OH;

R 12 is H or lower alkyl;

or a pharmaceutically acceptable salt thereof.

4. The compound according to claim 1 , wherein R 6 is —CF 3 .

5. The compound according to claim 1 wherein said compound has the formula:

wherein R 1 , R 6 , and R 10 have definitions as defined previously.

6. The compound according to claim 1 , wherein said compound is 2-phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid [6-(ethyl-methyl-amino)-pyridin-3-yl]-amide.

7. The compound according to claim 1 , wherein said compound is 2-(2-chloro-phenyl)-4-propyl-oxazole-5-carboxylic acid {6-[(2-methoxy-ethyl)-methyl-amino]-pyridin-3-yl}-amide.

8. The compound according to claim 1 , wherein said compound is 2-phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid [6-((S)-2-hydroxy-1-methyl-ethylamino)-pyridin-3-yl]-amide.

9. The compound according to claim 1 , wherein said compound is 2-phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid {6-[(2-methoxy-ethyl)-methyl-amino]-pyridin-3-yl}-amide.

10. The compound according to claim 1 , wherein said compound is 2-(2-chloro-phenyl)-5-trifluoromethyl-oxazole-4-carboxylic acid {6-[(2-methoxy-ethyl)-methyl-amino]-pyridin-3-yl}-amide.

11. The compound according to claim 1 , wherein said compound is 2-phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid (6-thiomorpholin-4-yl-pyridin-3-yl)-amide.

Assignments (5)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE'S ADDRESS PREVISOUSLY RECORDED ON REEL 027216 FRAME 0440.ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT OF ASSIGNORS INTEREST Recorded Jun 12, 2012
From: VIA, LLC
To: MADRIGAL PHARMACEUTICALS, INC.
Reel/Frame 028390/0021 →
COLLATERAL ASSIGNMENT OF PATENTS Recorded Nov 16, 2011
From: MADRIGAL PHARMACEUTICALS, INC.
To: BAY CITY CAPITAL FUND IV, L.P.
Reel/Frame 027241/0166 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 11, 2011
From: VIA PHARMACEUTICALS, INC.
To: VIA, LLC
Reel/Frame 027216/0375 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 11, 2011
From: VIA, LLC
To: MADRIGAL PHARMACEUTICALS, INC.
Reel/Frame 027216/0440 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 17, 2009
From: HOFFMANN-LA ROCHE INC.
To: VIA PHARMACEUTICALS, INC.
Reel/Frame 022552/0847 →
Continuity (3)
Provisional Application 6074057800 · Nov 28, 2005
Provisional Application 6084935200 · Oct 4, 2006
Related Publication 20070123504A1 · May 31, 2007