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拟肾上腺素药盐酸甲氧明的绿色合成
引用本文:谢宇,胡金刚,贾杰,洪小伟,魏娅. 拟肾上腺素药盐酸甲氧明的绿色合成[J]. 有机化学, 2010, 30(2): 282-284
作者姓名:谢宇  胡金刚  贾杰  洪小伟  魏娅
作者单位:南昌航空大学环境与化学工程学院,南昌,330063
基金项目:国家自然科学基金,江西省自然科学基金,江西省教育厅科技,航空高校基金 
摘    要:以对苯二酚为原料经羟基的甲基化、傅克酰基化、肟化、肟基还原、酮胺氢化5步反应合成了盐酸甲氧明, 中间体和目标产物经核磁共振氢谱、红外光谱及元素分析仪确证了其化学结构, 总收率为37.6%. 与传统盐酸甲氧明工艺相比, 该工艺反应条件温和、简便、经济、产率高及对环境友好.

关 键 词:甲氧明  甲基化  肟化  还原  绿色合成
收稿时间:2009-02-25
修稿时间:2009-08-04

Green Synthesis of the Adrenomimetic Drug Methoxamine Hydrochloride
Xie Yu,Hu Jingang,Jia Jie,Hong Xiaowei,Wei Ya. Green Synthesis of the Adrenomimetic Drug Methoxamine Hydrochloride[J]. Chinese Journal of Organic Chemistry, 2010, 30(2): 282-284
Authors:Xie Yu  Hu Jingang  Jia Jie  Hong Xiaowei  Wei Ya
Affiliation:(School of Environmental and Chemical Engineering, Nanchang Hangkong University, Nanchang 330063)
Abstract:Methoxamine hydrochloride was synthesized from p-dihydroxybenzene by O-methylation, Friedel-Crafts acylation, oximation reaction, oxime reduction and keto-amine hydrogenation reactions. All intermediates and products were characterized by IR, 1H NMR spectra and elemental analysis. The total yield was 37.6%. Compared to the traditional synthetic procedures of methoxamine hydrochloride, the procedures were temperate, convenient, economical, high-yielding and environment-friendly.
Keywords:methoxamine  methylation  oximation  reduction  green synthesis
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