반응 #1435729

ord-bc220d7df5d24bfcb6804b98a60cc2ed

반응 방정식

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
수율 96.7%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도Under ice-cooling
  2. 2
    건조dried over sodium sulfate
  3. 3
    농축concentrated

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07211545B2uspto-grants-2007_05