发明名称 CEPHALOSPORIN ANALOG
摘要 <p>NEW MATERIAL:A compound of formula I: (X is NH2, N3, or phthalimino group; R1 is H, halogen, lower alkoxy group, etc,; R2 is R1, lower alkyl, N3, etc,; R3 is H, alkyl, aryl group, etc.), and its salt. EXAMPLE:(+ or -)Cis,2-tert-butyloxycarbonyl-7-azido-1-azabicyclo[4,2,0]oct-2-ene- 8-one. USE:An intermediate for the synthesis of antibacterials capable of giving powerful antibacterials by introducing various acyl groups into the 7-postion. PROCESS:A compound of formula II: (R21 is H or lower alkyl group) is reacted with a compound of formula III: (R31 is alkyl, aryl group, etc.), and the reaction product is them reacted with an active derivative of the formula X1CH2COOH (X1 is N3 or phthalylimino group) to give a compound of formula IV, which is then reacted with O3, etc., and subjected to the Horner-Wittig reaction to give the objective compound of formula V.</p>
申请公布号 JPS54128591(A) 申请公布日期 1979.10.05
申请号 JP19780034696 申请日期 1978.03.25
申请人 KYOWA HAKKO KOGYO KK 发明人 HIRATA TADASHI;OGASA TAKEHIRO;SAITOU HIROMITSU;NAKAMIZO YOSHIHIRO
分类号 A61K31/435;A61K31/655;A61P31/04;C07D463/00;C07F9/568 主分类号 A61K31/435
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