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引用本文:余茜1,李树军2,黄汉忠2*,王平保2,闫少杰2.盐酸氨溴索的合成[J].中国现代应用药学,2012,29(3):230-232.
1.河南大学药学院,河南 开封 475000;2.天津药物研究院化学制药部,天津 300193.Synthesis for Ambroxol Hydrochloride[J].Chin J Mod Appl Pharm(中国现代应用药学),2012,29(3):230-232.
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盐酸氨溴索的合成
余茜1,李树军2,黄汉忠2*,王平保2,闫少杰2
YU Qian1, LI Shujun2, HUANG Hanzhong2*, WANG Pingbao2, YAN Shaojie2
摘要:
目的 合成盐酸氨溴索并改进合成工艺。方法 以2-氨基苯甲酸甲酯作为起始原料,经溴代、还原、氧化、缩合、成盐等反应制得盐酸氨溴索。结果 所得产物经核磁共振氢谱、质谱、红外等确证其结构,总收率为54.6%。结论 该工艺原料易得,方法简便,总杂<0.1%,适合工业化生产。
关键词:  盐酸氨溴索  祛痰药  合成
DOI:
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基金项目:
Synthesis for Ambroxol Hydrochloride
1.河南大学药学院,河南 开封 475000;2.天津药物研究院化学制药部,天津 3001931,2
1.School of Pharmacy, Henan University, Kaifeng 475000, China;2.Centre for Chemical Pharmaceutical Research, Tianjin Institute of Pharmaceutical Research, Tianjin 300193, China
Abstract:
OBJECTIVE To synthesis ambroxol hydrochloride and optimize the process. METHODS Ambroxol hydrochloride was synthesized from methyl 2-aminobenzoate via bromination, reduction, oxidation, condensation and salification. RESULTS Chemical structure of ambroxol hydrochloride was confirmed by 1H-NMR, MS and IR. The total yield of ambroxol hydrochloride was 54.6%. CONCLUSION The starting materials are easy to get and the method is simple. The total impurities content are <0.1%, and the method is suitable for industry.
Key words:  ambroxol hydrochloride  expectorants  synthesis
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