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1-[(4-氯苯基)苯甲基]-哌嗪合成方法的改进
引用本文:金永生,姚斌,吴秋业,赵靖霞. 1-[(4-氯苯基)苯甲基]-哌嗪合成方法的改进[J]. 实用医药杂志(山东), 2005, 22(12): 1108-1109
作者姓名:金永生  姚斌  吴秋业  赵靖霞
作者单位:第二军医大学药学院,上海200433
摘    要:目的探讨西替利嗪的中间体1-犤(4-氯苯基)苯甲基犦-哌嗪的合成方法的改进。方法以氯苯和苯甲酰氯为原料经还原等三步反应得到目标和化合物。结果及结论建立了一种新的合成方法。该法经济实用,收率高达53%,适合工业化生产。

关 键 词:西替利嗪  哌嗪  合成
修稿时间:2005-09-19

Synthesis of 1-[(4-chlorophenyl)phenylmethyl]-piperazine:A improved method
JIN Yongsehng,YAO Bin,WU Qiuye,et al.. Synthesis of 1-[(4-chlorophenyl)phenylmethyl]-piperazine:A improved method[J]. Practical Journal of Medicine & Pharmacy, 2005, 22(12): 1108-1109
Authors:JIN Yongsehng  YAO Bin  WU Qiuye  et al.
Affiliation:JIN Yongsehng,YAO Bin,WU Qiuye,et al.School of Pharmacy,Second Military Medical University,Shanghai 200433,China
Abstract:Objective To study improved synthetic method of 1-[(4-chlorophenyl)phenylmethyl]-piperazine, the intermediate of cetirizine hydrochloride.Methods Chlorobenzene and benzoyl chloride were used as starting reagents,and the title compounds were synthesized then by reduction etc.3 steps reaction.Results and Conclusion A novel synthetic method was completed.This method is economical and practical, higher yield(th recovery rate,53%), and were able to be used in industrializations.
Keywords:Cetirizine Piperazine Synthesis
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