反応 #1435729

ord-bc220d7df5d24bfcb6804b98a60cc2ed

反応方程式

ClC(Cl)Cl
chloroform
Fc1cccc(Cl)c1-c1c(Cl)nc2nccn2c1Cl
5,7-dichloro-6-(2-chloro-6-fluorophenyl)imidazo[1,2-a]pyrimidine
CC1CCNCC1
4-methylpiperidine
CC1CCN(c2c(-c3c(F)cccc3Cl)c(Cl)nc3nccn23)CC1
5-(4-methylpiperidin-1-yl)-6-(2-chloro-6-fluorophenyl)-7-chloroimidazo[1,2-a]pyrimidine
収率 96.7%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度Under ice-cooling
  2. 2
    乾燥dried over sodium sulfate
  3. 3
    濃縮concentrated

実験手順

Under ice-cooling, 0.63 g of 5,7-dichloro-6-(2-chloro-6-fluorophenyl)imidazo[1,2-a]pyrimidine and 0.79 g of 4-methylpiperidine were mixed. The reaction mixture was allowed to stand at room temperature for 10 minutes, and chloroform and water were added thereto. The separated organic layer was with water, dried over sodium sulfate and concentrated. The residue was subjected to silica gel chromatography to give 0.73 g of 5-(4-methylpiperidin-1-yl)-6-(2-chloro-6-fluorophenyl)-7-chloroimidazo[1,2-a]pyrimidine.

出典

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