Phospharylated imidazo[1,2-a]pyridines

被引:7
|
作者
Tolmachev, AA
Yurchenko, AA
Kozlov, ES
Merkulov, AS
Semenova, MG
Pinchuk, AM
机构
[1] Institute of Organic Chemistry, Ukrainian Academy of Sciences, Kiev
关键词
D O I
10.1002/hc.520060507
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The reaction of phosphorus(III) halides with imidazo[1,2-a]pyridines in the presence of bases leads to the formation of 3-phosphorylated imidazo[1,2-a]pyridines. The reaction proceeds in high yield and requires no catalysts. In the compounds obtained, in contrast to phosphorylated indolizines, the phosphorus-heterocycle bond is stable and nor cleaved by dry hydrogen chloride, alcohols, or water. Imidazo[1, 2-a]pyridines with the phosphinic and phosphinous groups can be alkylated both at the phosphorus and at the nitrogen atom of the heterocycle, the alkylation direction being dependent on the strength of the alkylation reagent used. (C) 1995 John Wiley & Sons, Inc.
引用
收藏
页码:419 / 432
页数:14
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