تفاعل #1435734

ord-0d9028f5ce064f77a5c9decc89f5a5ab

معادلة التفاعل

Fc1cc(F)c(-c2c(Cl)nc3nccn3c2Cl)c(F)c1
5,7-dichloro-6-(2,4,6-trifluorophenyl)imidazo[1,2-a]pyrimidine
CCCNCCC
di-n-propylamine
ClC(Cl)Cl
chloroform
CCCN(CCC)c1c(-c2c(F)cc(F)cc2F)c(Cl)nc2nccn12
5-(di-n-propylamino)-6-(2,4,6-trifluorophenyl)-7-chloroimidazo[1,2-a]pyrimidine
المردود 83.1%

المذيبات

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto cool
  2. 2
    تجفيفThe separated organic layer was dried over sodium sulfate
  3. 3
    تركيزconcentrated

الإجراء التجريبي

A mixture of 0.095 g of 5,7-dichloro-6-(2,4,6-trifluorophenyl)imidazo[1,2-a]pyrimidine and 0.12 g of di-n-propylamine was heated at 80° C. for one hour. The reaction mixture was allowed to cool, and chloroform and water were added thereto. The separated organic layer was dried over sodium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give 0.095 g of 5-(di-n-propylamino)-6-(2,4,6-trifluorophenyl)-7-chloroimidazo[1,2-a]pyrimidine.

المصدر

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