青霉烷酸二苯甲酯亚砜的合成方法探索  

Study on the Synthesis Method of the Benzhydryl s-Oxopenicillanate

作　　者：李国青[1] 张瑛[1] 吴金波 李立[3] 

机构地区：[1]天津大学化工学院,天津300072 [2]华北制药集团有限责任公司,河北石家庄050015 [3]河北科技大学理学院,河北石家庄050018

出　　处：《河北化工》2006年第11期37-37,63,共2页Hebei Chemical Industry

摘　　要：由6-APA合成了他唑巴坦的重要中间体——青霉烷酸二苯甲酯亚砜。在氧化反应中,使用双氧水作氧化剂,在消去溴的反应中,使用铝粉代替锌粉,合成了目标化合物,三步总收率为60.7%,为该化合物的合成提供了新的路线。Synthesis of the benzhydryl s-oxopenicillanate using 6-aminopenicillanic acid （Ⅰ） as starting material was conducted through in a total yield 60.7%.Ai powder instead the Zn in the process. Thus, Ⅰ was brominated to 6-bromopenicillanic acid, then esterifiation to obtaind Ⅱ in 83%yiel＆ Ⅱ was reacted with H2O2in water to obtain Ⅲ ,the yield is 95%, Ⅲ was reduced by AL powder to get the target compound, which is one important intermediates for tazobactam.

关 键 词：他唑巴坦 6-APA 青霉烷酸二苯甲酯亚砜 氧化 脱溴 

分 类 号：TQ464[化学工程—制药化工]