发明名称 PROCEDE POUR LA PREPARATION DES DERIVES DE 2-OXYNDOL-1-CARBOXAMIDE
摘要 Carboxamide derivs. of formula(I) and their salts are prepd. by reacting II with R2-N=C=O or III with R1-C(=O)-OH in an inactive solvent. In (I), X=H, F, Cl, Br, alkyl, alkoxy, alkylthio, CF3, PhCONH or di-(C1-3) alkylsulphamoyl; Y=H, F, Cl, Br, C1-4 alkylthio or CF3; or X+Y=4,5-, 5,6- or 6,7-OCH2O or -OCH2CH2O-; R1=alkyl, cycloalkenyl, opt. substd. Ph, or (CH2)n-QR; Q=divalent radical derived from furan, thiophene, oxazole or benzo(b)thiophene; n=0,1 or 2; R=H or C1-3alkyl; R2=alkyl or alkoxy. (I) are inhibitors of cyclo- oxygenase and lipoxygenase enzymes. They have analgesic and anti- inflammatory activities and are esp. suitable for treating acute pain and for chronic admin. in treatment of arthritis.
申请公布号 RO91141(A) 申请公布日期 1987.06.30
申请号 RO19850118604 申请日期 1985.05.03
申请人 PFIZER INC,US 发明人 KADIN SAUL B.,US
分类号 C07D209/42;A61K31/40;A61K31/403;A61K31/404;A61K31/44;A61K31/4427;A61K31/443;A61K31/4433;A61P25/04;A61P29/00;A61P43/00;C07D209/18;C07D209/34;C07D209/60;C07D209/70;C07D209/94;C07D333/00;C07D401/06;C07D401/12;C07D405/06;C07D405/12;C07D409/06;C07D409/12;C07D491/04;C07D491/048;C07D491/056;C07D495/04 主分类号 C07D209/42
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