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2,6-二吡啶基-1,4-二氢吡啶衍生物的合威
引用本文:王书香,段洁,李志艳.2,6-二吡啶基-1,4-二氢吡啶衍生物的合威[J].广州化工,2010,38(3):53-54.
作者姓名:王书香  段洁  李志艳
作者单位:河北大学化学与环境科学学院,河北,保定,071002
基金项目:河北大学自然科学基金资助课题 
摘    要:以烟酰乙酸乙酯、醛和醋酸铵为原料,合成了一系列2,6-二吡啶基-1,4-二氢吡啶衍生物,收率为40%~88%。探讨了溶剂和底物结构对反应的影响。与在乙醇中回流反应相比,该反应在无溶剂条件下进行时,反应时间短,产物收率高。

关 键 词:2    6-zptt啶基-1    4-二氢吡啶  无溶剂  Hantzsch缩合

Synthesis of 2,6-dipyridinyl-1,4-dihydropyridines
WANG Shu-xiang,DUAN Jie,LI Zhi-yan.Synthesis of 2,6-dipyridinyl-1,4-dihydropyridines[J].GuangZhou Chemical Industry and Technology,2010,38(3):53-54.
Authors:WANG Shu-xiang  DUAN Jie  LI Zhi-yan
Affiliation:WANG Shu -xiang, DUAN Jie, LI Zhi -yah (College of Chemistry and Environmental Science, Hebei University, Hebei Baoding 071002, China)
Abstract:A rang of 2,6 - dipyridinyl - 1,4 - dihydropyridines were prepared with 40% - 88% yields condensation of ethyl nicotinoylaeetate, aldehydes and ammonium acetate, and the effects of solvent and the substrate were investigated. Under solvent -free condition, that carried out in ethanol under refluxing condition. the reaction time was shorter and the yield was through the structure of higher than
Keywords:2  6 - dipyridinyl - 1  4 - dihydropyridines  solvent - free  Hantzsch reaction
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