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强效降眼内压药—安普乐定的合成方法探讨
引用本文:白少岩,杨尚军,唐文照.强效降眼内压药—安普乐定的合成方法探讨[J].齐鲁药事,2004,23(5):46-47.
作者姓名:白少岩  杨尚军  唐文照
作者单位:山东省医学科学院药物研究所,济南,250062
摘    要:目的 探讨安普乐定的合成方法。方法 采用对硝基苯胺为原料,经还原、加保护基、甲酰化、氯化、环合、脱保护基六步反应法可进行化学合成。结果及结论 该合成方法所需试剂安全易得,合成条件平和,适于工业化生产。

关 键 词:安普乐定  合成
文章编号:1672-7738(2004)05-0046-02

Research on the synthesis of potent decreasing IOP drug Apraclonidine
Bai Shao-yan,Yang Shang-jun,Tang Wen-zhao.Research on the synthesis of potent decreasing IOP drug Apraclonidine[J].qilu pharmaceutical affairs,2004,23(5):46-47.
Authors:Bai Shao-yan  Yang Shang-jun  Tang Wen-zhao
Abstract:Objective To research the synthesis method of Apraclonidine. Methods Apraclonidine was synthesized from P-Nitraniline by reaction with reduction, adding protection group, formylation, chlorination, cyclization, off-protecting group. Results andconclusion The raw materials were safe and cheap. The reaction conditions were mild. Therefore the industrialization of productioncould be achieved by this method.
Keywords:Apraclonidine  synthesis
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