发明名称 PROCESS FOR PREPARING CEPHALOSPORIN INTERMEDIATES
摘要 <p>7-Substd. -3-cephem intermediate N,N-dimethyl acetamide solvates of formula (I)[DMAC=N,N-dimethylacetamide are prepd. by condensating [(Z)-2-(2-tert-butoxycarbonyl prop-2-oxyimino)-2(2- triphenylmethylaminothiazol-4-yl acetyl halide with (6R, 7R)-7amino- 3-(1-pyridiium-methyl)ceph-3-em-4-carboxylate in the presence of N,N- dimethylacetamide. Thus, (I) is obtained in 65.2% yield by acylating the aminocephem in DMAC. Deblocking of (I) with HCO2H-HCl give 62% ceftazidime.2HCl. (I) crystallises directly from a soln. of the cephem in DMAC, so that other purification steps are avoided.</p>
申请公布号 KR870000612(B1) 申请公布日期 1987.03.25
申请号 KR19830006051 申请日期 1983.12.21
申请人 ELI LILLY AND COMPANY 发明人 CHOU, TA-SEN;HEATH, PERRY CLARK
分类号 C07D501/04;A61K31/545;A61K31/565;C07D;C07D501/00;C07D501/38;C07D501/46;C07D501/56;(IPC1-7):C07D501/46 主分类号 C07D501/04
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