반응 #1435726

ord-19a55d3a7d5d40f3895a55aa03dd0f25

반응 방정식

[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
수율 80.9%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도Under ice-cooling
  2. 2
    세척The separated organic layer was washed with water
  3. 3
    건조dried over sodium sulfate
  4. 4
    농축concentrated
  5. 5
    세척The residue was washed with t-butyl methyl ether

실험 절차

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

출처

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