Reaction #1435729
ord-bc220d7df5d24bfcb6804b98a60cc2ed
Reaction equation
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
Yield 96.7%
Reactants
Reagents
None
Conditions
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1TemperatureUnder ice-cooling
- 2Dryingdried over sodium sulfate
- 3Concentrationconcentrated
Procedure
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.