发明名称 PROCESS FOR PREPARING 6- -SUBSTITUTED PENICILLANIC ACIDS
摘要 <p>The title compds. (I; R15=F, Cl, Br, iodo, C1-4 alkoxy, C1-4 alkylthio; R13=H, ester; n=o 1, 2) were prepd. asβ-lactamase inhibitors forβ-lactam antibiotic formulations. Thus, 2.95g Na 6-chloro-6-iodopenicillanic acid was dissolved in 125mL benzene and treated with 1.08mL Et3N. This mixt. was reacted with 0.977mL trimethylcillyl chloride and refluxed with 15mg azobisisobutyronitrile and 2.02mL tri-n-butylene-HCl to give Na 6-β-chloropenicillanic acid.</p>
申请公布号 KR840000589(B1) 申请公布日期 1984.04.24
申请号 KR19800000921 申请日期 1980.03.04
申请人 PFIZER INC. 发明人 MICHAEL STEPHEN KELLOGG;ERNEST SEIICHI HAMANAKA
分类号 A61K31/43;A61K31/545;C07D499/00;C07D499/04;(IPC1-7):07D499/00 主分类号 A61K31/43
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