The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Mar. 12, 2013

Filed:

Dec. 12, 2008
Applicants:

George Hynd, Essex, GB;

John Gary Montana, Essex, GB;

Harry Finch, Essex, GB;

Rosa Arienzo, Essex, GB;

Barbara Avitabile-woo, Essex, GB;

Mathias Domostoj, Essex, GB;

Inventors:

George Hynd, Essex, GB;

John Gary Montana, Essex, GB;

Harry Finch, Essex, GB;

Rosa Arienzo, Essex, GB;

Barbara Avitabile-Woo, Essex, GB;

Mathias Domostoj, Essex, GB;

Assignee:
Attorney:
Primary Examiner:
Int. Cl.
CPC ...
A61K 31/4439 (2006.01); C07D 409/12 (2006.01); C07D 401/12 (2006.01);
U.S. Cl.
CPC ...
Abstract

Compound of formula (I) are ligands of the CRTH2 receptor, useful inter alia for treatment of inflammatory conditions. Wherein X is —SO— or *—SONR— wherein the bond marked with an asterisk is attached to Ar; Ris hydrogen, fluoro, chloro, CN or CF; Ris hydrogen, fluoro or chloro; Ris hydrogen, CCalkyl or C-Ccycloalkyl; Aris phenyl or a 5- or 6-membered heteroaryl group selected from furanyl, thienyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, pyridinyl, pyridazinyl, pyrimidinyl and pyrazinyl, wherein the phenyl or heteroaryl groups are optionally substituted by one or more substituents independently selected from fluoro, chloro, CN, C-Ccycloalkyl, —O(C-Calkyl) or CCalkyl, the latter two groups being optionally substituted by one or more fluoro atoms; and Aris phenyl or 5- or 6-membered heteroaryl group selected from pyrrolyl, furanyl, thienyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, pyridinyl, pyridazinyl, pyrimidinyl and pyrazinyl, wherein the phenyl or heteroaryl groups are optionally substituted by one or more substituents independently selected from fluoro, chloro, CN, C-C-Ccycloalkyl, —O(C-Calkyl) or CCalkyl, the latter two groups being optionally substituted by one or more fluoro atoms.


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