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SQ109合成工艺改进

萧红街 杨艺虹 张珩 钟武

军事医学2013,Vol.37Issue(5):372-375,4.
军事医学2013,Vol.37Issue(5):372-375,4.DOI:10.7644/j.issn.1674-9960.2013.05.00

SQ109合成工艺改进

Improved synthesis of SQ109

萧红街 1杨艺虹 2张珩 1钟武1

作者信息

  • 1. 武汉工程大学化工与制药学院绿色化工过程教育部重点实验室,武汉,430073
  • 2. 军事医学科学院毒物药物研究所,北京,100850
  • 折叠

摘要

Abstract

Objective To improve the synthesis process of N -geranyl-N'-(2-aclamantyl) ethane4 ,2-diamine( SQ109 ) and establish a cost-effective and effecient synthetic route. Methods Geraniol reacted with SOC12 to produce intermediate 2,2 ,1-chloro-3 ,7-dimethyl-2,6-octadiene. The key intermediate 3, N'-(2-geranyl) ethane-1 ,2-diamine, was synthesized via reduction animation starting from intermediate 2. Then intermediate 3 reacted with 2-adamantanone by reduction amina-tion to obtain the target compound. Results and Conclusion The target compound was confirmed by 1H-NMR, LC-MS, and elemental analysis. The overall yeild was 66. 6% (based on geraniol). The advantage of this method lies in the cheap and easily-available raw materials , simple operation and high yield in each step.

关键词

SQ109/抗结核药/磁共振波谱学/合成

Key words

SQ109 / anti-tubercular drugs/ magnetic resonance spectroscopy / synthesis

分类

医药卫生

引用本文复制引用

萧红街,杨艺虹,张珩,钟武..SQ109合成工艺改进[J].军事医学,2013,37(5):372-375,4.

基金项目

国家科技支撑计划资助项目(2011BAI18B01) (2011BAI18B01)

军事医学

OA北大核心CSCDCSTPCD

1674-9960

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