发明名称 Verfahren zur Herstellung neuer Naphthyridinderivate
摘要 <p>(A) Cmpds. (I) and (III):- R' = lower alkyl R2 = H or Me R3 = lower Oalkyl or together = -OCH2O-IA - X = H; IB - X = double bond. (B) Salts (II) of (I). (I) and (II) Analgesics. Dose 100-500 mg. (III) Intermediates for (I) and (II) Racemic cis-1-methyl-3-(3,4-methylenedioxy-phenyl)-4-piperidyl-amine (6.0 g.), 2 N HCl (35 ml.), and 35% HCHO (5 g.) were stirred 30 mins. at 20 deg., heated 30 mins. at 100 deg., evapd., and recryst. from MeOH, giving the racemic-naphthyridine-HCl, m.p. 304 deg.</p>
申请公布号 CH511871(A) 申请公布日期 1971.08.31
申请号 CH19690016742 申请日期 1967.05.31
申请人 SANDOZ AG 发明人 SUEESS,RUDOLF,DR.;LINDENMANN,ADOLF,DR.
分类号 C07D211/02;C07D211/58;C07D211/70;C07D211/72;C07D211/78;(IPC1-7):C07D57/02 主分类号 C07D211/02
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