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氯雷他定的合成
引用本文:司马利锋,王玥,林艳,李阳,陈立功.氯雷他定的合成[J].化学通报,2012(4):353-356.
作者姓名:司马利锋  王玥  林艳  李阳  陈立功
作者单位:天津大学化工学院
摘    要:以N-甲基-4-哌啶酮和8-氯-10,11-二氢-4-氮杂-5H-二苯并a,d]-5-环庚酮为原料,经McMurry反应得到8-氯-6,11-二氢-11-(1-甲基-4-哌啶烯基)-5H-苯并5,6]庚环1,2-b]吡啶,收率为83.9%,最后与氯甲酸乙酯反应得到氯雷他定,总收率为35.7%。对McMurry反应过程中产生的副产物3、4进行了分离、表征。

关 键 词:氯雷他定  McMurry反应  抗组胺

Synthesis of Loratadine
Sima Lifeng,Wang Yue,Lin Yan,Li Yang,Chen Ligong.Synthesis of Loratadine[J].Chemistry,2012(4):353-356.
Authors:Sima Lifeng  Wang Yue  Lin Yan  Li Yang  Chen Ligong
Institution:(School of Chemical Engineering and Technology,Tianjin University,Tianjin 300072)
Abstract:The McMurry reaction of N-methyl-4-piperidone with 8-Chloro-10,11-dihydro-4-aza-5H-dibenzocyclohepten-5-one afforded 8-Chloro-6,11-dihydro-11-(1-methyl-pipridin-4-ylene)-5H-benzo-cyclohepta pyridine in 83.9% yield,and subsequently was treated with ethyl chlorocarbonate to give Loratadine in a overall yield of 35.7%.The by-products of 3 and 4 generated in McMurry reaction were separated and characterized.
Keywords:Loratadine  McMurry reaction  Antihistamine
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