桂利嗪
烷基化
化学
哌嗪
卤化物
组胺
氟桂利嗪
酒
组合化学
烷基
有机化学
药理学
催化作用
色谱法
钙
医学
作者
Yu Tian,Hongbo Dong,Zheng Shi,Li-jia Cheng,Xiaoheng Guo,Xinjie Lian,Feng Liu
标识
DOI:10.2174/1570178615666180110161450
摘要
Classical methods for the synthesis of diarylmethylpiperazine drugs generally lead to the generation of high levels of waste. In this study, we have developed a simple and efficient route to the anti-histamine drugs Meclizine 1, Buclizine 2, Clocinizine 3, Cinnarizine 4, Flunarizine 5 and Flotrenizine 6. The advantage of this route lies on the replacement of harmful alkyl halides by readily available alcohols to achieve the N-alkylation of the piperazine unit. This procedure was further extended to the synthesis of other diarylmethylpiperazine drugs and derivatives. Keywords: Diarylmethylpiperazine drugs, N-alkylation, synthesis, anti-histamine drugs, derivatives, alcohol.
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