تفاعل #1435726

ord-19a55d3a7d5d40f3895a55aa03dd0f25

معادلة التفاعل

[Cl-].[NH4+]
ammonium chloride
Fc1cc(F)c(-c2c(Cl)nc3nccn3c2Cl)c(F)c1
5,7-dichloro-6-(2,4,6-trifluorophenyl)imidazo[1,2-a]pyrimidine
CC1CCNCC1
4-methylpiperidine
CC1CCN(c2c(-c3c(F)cc(F)cc3F)c(Cl)nc3nccn23)CC1
5-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)-7-chloroimidazo[1,2-a]pyrimidine
المردود 80.9%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةUnder ice-cooling
  2. 2
    غسيلThe separated organic layer was washed with water
  3. 3
    تجفيفdried over sodium sulfate
  4. 4
    تركيزconcentrated
  5. 5
    غسيلThe residue was washed with t-butyl methyl ether

الإجراء التجريبي

Under ice-cooling, 0.64 g of 5,7-dichloro-6-(2,4,6-trifluorophenyl)imidazo[1,2-a]pyrimidine and 0.79 g of 4-methylpiperidine were mixed. The mixture was allowed to stand at room temperature for one hour, and chloroform and aqueous saturated ammonium chloride solution were added to the reaction mixture. The separated organic layer was washed with water, dried over sodium sulfate and concentrated. The residue was washed with t-butyl methyl ether to give 0.62 g of 5-(4-methylpiperidin-1-yl)-6-(2,4,6-trifluorophenyl)-7-chloroimidazo[1,2-a]pyrimidine

المصدر

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