反応 #1435729
ord-bc220d7df5d24bfcb6804b98a60cc2ed
反応方程式
chloroform
5,7-dichloro-6-(2-chloro-6-fluorophenyl)imidazo[1,2-a]pyrimidine
4-methylpiperidine
→
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温度Under ice-cooling
- 2乾燥dried over sodium sulfate
- 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.