AMIDE DERIVATIVES USEFUL AS INHIBITORS OF THE PRODUCTION OF CYTOKINES
Application 352/MUMNP/2005 published 2006-05-05, filed 2005-04-29
The invention concerns amide derivatives of formula (I) wherein R3 is (1-6C)alkyl or halogeno; Q1 is heteroaryl which is optionally substituted with 1, 2, 3, or 4 substituents such as hydroxy, halogeno, trifluoromethyl, (1-6C)alkyl, (1-6C)alkoxy, hydroxy-(1-6C)alkyl, (1-6C)alkoxy-(1-6C)alkyl, hydroxy-(2-6C)alkoxy, amino-(2-6C)alkylamino, N(1-6C)alkyl-(1-6C)alkylamino-(2-6C)alkylamino, aryl, heteroaryl and heterocyclyl; p is 0-2 and R2 is a substituent such as hydroxy and halogeno; q is 0-4; and Q2 includes optionally substituted aryl, cycloalkyl, heteroaryl and heterocyclyl; or pharmaceutically-acceptable salts or in vivo-cleavable esters thereof; processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of diseases or medical conditions mediated by cytokines. Drawing Sheets. NIL Total Pages: 103 (FIG.-NIL)
Applicant
ASTRAZENECA AB
S-15185 SODERTALJE, SWEDEN
Inventor
1. DEARG SUTHERLAND BROWN 2. GEORGE ROBERT BROWN
International Info
Classification: C07D 213/82, 241/44, 215/48, 261/18, 277/68, 239/74, 333/38, 401/12, 401/14, 413/12, 213/81, A61K 31/44, 31/47, 31/495
Publication Number: WO 00/07991
Priority Information
9816838.8 GREAT BRITAIN 1998-08-04
9824939.4 GREAT BRITAIN 1998-11-13