发明名称 CEPHALOSPORIN ANALOG
摘要 <p>NEW MATERIAL:Cephalosporin analogs of formula I (X is acyl; R<1> is H, carboxyl- protecting group) and their salts. EXAMPLE:( + or - )cis-7beta-[ ( R )-2-phenyl-2-aminoacetamide ]-4beta-methyl-2-carboxy- 1-azabicyclo[4,2,0]oct-2-en-8-one trifluoroacetate. USE:Antibiotic and its synthetic intermediates. The analogs with R<1> of H has outstanding antibacterial activity against gram-positive and negative bacteria. PREPARATION:For example, the reaction of a compound of formula II' and a carboxylic acid corresponding to acyl group X or its reactive derivative gives the compound of formula I. When necessary, a base is used in the reaction. When R<1> is a carboxyl-protecting group, it is removed and the product is converted into the antibacterial compound with R<1> of H.</p>
申请公布号 JPS5587790(A) 申请公布日期 1980.07.02
申请号 JP19780162007 申请日期 1978.12.26
申请人 KYOWA HAKKO KOGYO KK 发明人 HIRATA TADASHI;OGASA TAKEHIRO;SAITOU HIROMITSU;NAKAMIZO YOSHIHIRO
分类号 C07D463/00;A61K31/435;A61P31/04;C07D471/04 主分类号 C07D463/00
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