反应 #1435734

ord-0d9028f5ce064f77a5c9decc89f5a5ab

反应方程式

Fc1cc(F)c(-c2c(Cl)nc3nccn3c2Cl)c(F)c1
5,7-dichloro-6-(2,4,6-trifluorophenyl)imidazo[1,2-a]pyrimidine
CCCNCCC
di-n-propylamine
ClC(Cl)Cl
chloroform
CCCN(CCC)c1c(-c2c(F)cc(F)cc2F)c(Cl)nc2nccn12
5-(di-n-propylamino)-6-(2,4,6-trifluorophenyl)-7-chloroimidazo[1,2-a]pyrimidine
收率 83.1%

溶剂

反应条件

温度
80°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度to cool
  2. 2
    干燥The separated organic layer was dried over sodium sulfate
  3. 3
    浓缩concentrated

实验过程

A mixture of 0.095 g of 5,7-dichloro-6-(2,4,6-trifluorophenyl)imidazo[1,2-a]pyrimidine and 0.12 g of di-n-propylamine was heated at 80° C. for one hour. The reaction mixture was allowed to cool, and chloroform and water were added thereto. The separated organic layer was dried over sodium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give 0.095 g of 5-(di-n-propylamino)-6-(2,4,6-trifluorophenyl)-7-chloroimidazo[1,2-a]pyrimidine.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07211545B2uspto-grants-2007_05