Reaction #1435729

ord-bc220d7df5d24bfcb6804b98a60cc2ed

Reaction equation

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
Yield 96.7%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    TemperatureUnder ice-cooling
  2. 2
    Dryingdried over sodium sulfate
  3. 3
    Concentrationconcentrated

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07211545B2uspto-grants-2007_05