IP Library Granted Patent US 8,735,387
Granted Patent B2
US 8,735,387 · App. 13/003,125 · Granted May 27, 2014

Oxazolopyrimidines as Edg-1 receptor agonists

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 8,735,387
App. No.
13/003,125
Granted
May 27, 2014
Kind
B2
Abstract

The present invention relates to oxazolopyrimidine compounds of the formula I in which A, R 1 , R 2 and R 3 are defined as indicated in the claims. The compounds of the formula I modulate the activity of the Edg-1 receptor and in particular are agonists of this receptor, and are useful for the treatment of diseases such as atherosclerosis, heart failure or peripheral arterial occlusive disease, for example. The invention furthermore relates to processes for the preparation of compounds of the formula I, their use, in particular as active ingredients in pharmaceuticals, and pharmaceutical compositions comprising them.

Claims (20)

1. A compound selected from any of the following compounds:

2-(3-fluoro-phenyl)-5-morpholin-4-ylmethyl-7-propoxy-oxazolo[5,4-d]pyrimidine,

3-(5-morpholin-4-ylmethyl-7-propoxy-oxazolo[5,4-d]pyrimidin-2-yl)-phenol,

2-(2-chloro-5-fluoro-phenyl)-5-[1,4]oxazepan-4-ylmethyl-7-propoxy-oxazolo[5,4-d]pyrimidine,

2-(2-chloro-pyridin-4-yl)-5-morpholin-4-ylmethyl-7-propoxy-oxazolo[5,4-d]pyrimidine,

5-cyclohexylmethyl-7-propoxy-2-m-tolyl-oxazolo[5,4-d]pyrimidine,

5-(1-phenyl-ethyl)-7-propoxy-2-m-tolyl-oxazolo[5,4-d]pyrimidine,

3-{4-[5-(4-chloro-benzyl)-7-propoxy-oxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethyl-phenoxy}-propane-1,2-diol,

1-{4-[5-(4-chloro-benzyl)-7-ethoxy-oxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethyl-phenoxy}-3-diethylamino-propan-2-ol,

1-{4-[5-(4-chloro-benzyl)-7-ethoxy-oxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethyl-phenoxy}-3-morpholin-4-yl-propan-2-ol,

1-hydroxy-cyclopropanecarboxylic acid (3-{4-[5-(4-chloro-benzyl)-7-ethoxy-oxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethyl-phenoxy}-2-hydroxy-propyl)-amide,

N-(3-{4-[5-(4-chloro-benzyl)-7-propoxy-oxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethyl-phenoxy}-2-hydroxy-propyl)-acetamide,

4-{4-[5-(4-chloro-benzyl)-7-propoxy-oxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethyl-phenoxy}-butyric acid,

(2-{4-[5-(4-chloro-benzyl)-7-propoxy-oxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethyl-phenoxy}-acetylamino)-acetic acid,

3-(3-{4-[5-(4-chloro-benzyl)-7-propoxy-oxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethyl-phenoxy}-2-hydroxy-propylamino)-propionic acid,

(S)-1-(2-{4-[5-(4-chloro-benzyl)-7-propoxy-oxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethyl-phenoxy}-acetyl)-pyrrolidine-2-carboxylic acid,

1-(5-tert-butyl-4H-[1,2,4]triazole-3-sulfonyl)-3-{4-[5-(4-chloro-benzyl)-7-ethoxy-oxazolo[5,4-d]pyrimidin-2-yl]-2,6-dimethyl-phenoxy}-propan-2-ol, and

4-[5-(4-chloro-benzyl)-7-ethoxy-oxazolo[5,4-d]pyrimidin-2-yl]-2-fluoro-phenol,

including any stereoisomeric forms, any mixture of stereoisomeric forms in any ratio, or a physiologically acceptable salt thereof, or a physiologically acceptable solvate of any of them.

2. A pharmaceutical composition, comprising at least one compound of as claimed in claim 1 , or a physiologically acceptable salt thereof, or a physiologically acceptable solvate of any of them, and a pharmaceutically acceptable carrier.

Assignments (2)
CHANGE OF NAME Recorded Jun 20, 2012
From: SANOFI-AVENTIS
To: SANOFI
Reel/Frame 028413/0927 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2011
From: KADEREIT, DIETER; SCHAEFER, MATTHIAS; CZECHTIZKY, WERNGARD
To: SANOFI-AVENTIS
Reel/Frame 026141/0124 →