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五元氮杂环阿魏酸衍生物的合成
引用本文:许勤龙,李家明,王融融,周鹏,邬皓,袁明.五元氮杂环阿魏酸衍生物的合成[J].安徽化工,2011(5):19-23.
作者姓名:许勤龙  李家明  王融融  周鹏  邬皓  袁明
作者单位:安徽中医学院药学院安徽省现代中药重点实验室;
基金项目:国家科技重大专项重大新药创制项目(批准号:2009ZX09103-123); 安徽省高校自然基金重点项目(批准号:KJ2010A206)
摘    要:目的:合成4个五元氮杂环阿魏酸衍生物。方法:以阿魏酸乙酯为起始原料,经Williamson醚化、亲核取代反应和水解反应,合成五元氮杂环阿魏酸衍生物。结果:所合成的目标化合物未见文献报道,目标化合物的结构经IR、1H-NMR、13C-NMR及MS确证。结论:所设计的合成技术简单易行。

关 键 词:阿魏酸  抗血小板聚集  合成

Synthesis of Five-Membered Nitrogen-Containing Heterocycle Ferulic Acid Derivatives
XU Qin-long,LI Jia-ming,WANG Rong-rong,ZHOU Peng,WU Hao,YUAN Ming.Synthesis of Five-Membered Nitrogen-Containing Heterocycle Ferulic Acid Derivatives[J].Anhui Chemical Industry,2011(5):19-23.
Authors:XU Qin-long  LI Jia-ming  WANG Rong-rong  ZHOU Peng  WU Hao  YUAN Ming
Affiliation:XU Qin-long,LI Jia-ming,WANG Rong-rong,ZHOU Peng,WU Hao,YUAN Ming(Department of Pharmacy,Anhui University of Traditional Chinese Medicine,Anhui Key Laboratory of Traditional Chinese Medicine,Hefei 230031,China)
Abstract:Objective:To synthesize four five-membered Nitrogen-containing heterocycle ferulic acid derivatives.Methods:Ferulic acid ethyl ester,imidazole and triazole were used as starting material.The target compounds were synthesized from aryl esters via Willamson etherification,nucleophilic substitution,and hydroxylation.Results: The target compounds have not been reported.The chemical structures were confirmed by IR,1H-NMR,13C-NMR and MS.Conclusion: This synthetic technique is simple and feasible.
Keywords:ferulic acid  platelet aggregation inhibitory  synthesis  
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