反応 #1435734

ord-0d9028f5ce064f77a5c9decc89f5a5ab

反応方程式

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
収率 83.1%

溶媒

反応条件

温度
80°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

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

実験手順

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.

出典

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