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1,2,3-三氮唑衍生物的合成及其抑制幽门螺杆菌活性研究
引用本文:吴凤艳,陈昌红,彭立望. 1,2,3-三氮唑衍生物的合成及其抑制幽门螺杆菌活性研究[J]. 邵阳学院学报(自然科学版), 2011, 8(3): 58-62
作者姓名:吴凤艳  陈昌红  彭立望
作者单位:邵阳学院生物与化学工程系,湖南邵阳,422000
基金项目:湖南省大学生研究性学习和创新性实验计划项目资助
摘    要:设计并合成了15个未曾见文献报道的1-(2-(4-取代)苯氧乙基)-1H-1,2,3-三氮唑衍生物,并通过NMR、IR、MS确认了它们的结构.对合成条件进行了探讨,得出了叠氮化的最佳合成条件:卤代烃/叠氮化钠摩尔比为1:1.5,反应温度为65℃,幽门螺旋杆菌(HP)体外抑制活性测试结果表明,化合物4c、5d、5k、5l对1 6株HP表现出一定的抑制活性.

关 键 词:1,2,3-三氮唑  合成  幽门螺旋杆菌

Studies on the Synthesis and Anti-Helicobacter Pylori Activity of 1,2,3-Triazole Derivatives
WU Feng-yan,CHEN Chang-hong,PENG Li-wang. Studies on the Synthesis and Anti-Helicobacter Pylori Activity of 1,2,3-Triazole Derivatives[J]. Journal of Shaoyang University(Natural Science Edition), 2011, 8(3): 58-62
Authors:WU Feng-yan  CHEN Chang-hong  PENG Li-wang
Affiliation:WU Feng-yan,CHEN Chang-hong,PENG Li-wang (Department of Biological and Chemical Engineering,Shaoyang University,Shaoyang,Hunan 422000,china)
Abstract:Fifteen unknown 1-(2-(4-subsitituted)phenyloxyethyl)-1,2,3-triazole derivatives winthout recorded report were synthesized,their structures were confirmed by NMR,IR,and MS.Synthetic conditions were discussed,the optimum reaction conditions were obtained as follows: n(RX):n(NaN3)=1:3,reaction temperature 65℃.The preliminary results against Helicobacter pylori(HP) indicated that four compounds 4c,5d,5k and 5l could show a high antibacterial activity against HP.
Keywords:1  2  3-triazole  synthesis  helicobacter pylori
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