发明名称 PREPARATION OF AZETIDINONE DERIVATIVE
摘要 <p>PURPOSE:To prepare the titled substance useful as a synthetic intermediate of antibiotics, easily, under mild condition, without using sulfenyl halide which is to be handled with care, by reacting a thiazolinoazetidinone derivative with a sulfur-containing compound in a water-containing organic solvent in the presence of an acid. CONSTITUTION:The compound of formula IV can be prepared by reacting the thiazolinoazetidinone derivative of formula I (R<1> is lower alkyl, aryl, phenylmethyl or phenyloxymethyl; R<2> is H, hydrocarbon residue, acyl, silyl, etc.) with the sulfur-containing compound of formula II [R<3> is aryl or heterocyclic group; Y is -SR<3> or group of formula III (R<4> and R<5> are amine residue or imide residue)] in the presence of an acid such as perchloric acid in a water-containing organic solvent. The amount of the compound of formula II is preferably 1-2mol per 1mol of the compound of formula I . The amount of water in the water-containing organic solvent is preferably 10-500 equivalent based on the compound of formula I .</p>
申请公布号 JPS5944356(A) 申请公布日期 1984.03.12
申请号 JP19820155674 申请日期 1982.09.06
申请人 OTSUKA KAGAKU YAKUHIN KK 发明人 TORII SHIGERU;TANAKA HIDEO;NOGAMI JIYUNZOU;SASAOKA MICHIO;SHIROI TAKASHI;SAITOU NORIO
分类号 C07D205/08;C07D205/095;C07D401/12;C07D403/12;C07D417/12;C07D417/14 主分类号 C07D205/08
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