تفاعل #1435729

ord-bc220d7df5d24bfcb6804b98a60cc2ed

معادلة التفاعل

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
المردود 96.7%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةUnder ice-cooling
  2. 2
    تجفيفdried over sodium sulfate
  3. 3
    تركيزconcentrated

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07211545B2uspto-grants-2007_05