Реакция #1435729

ord-bc220d7df5d24bfcb6804b98a60cc2ed

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураUnder ice-cooling
  2. 2
    Сушкаdried over sodium sulfate
  3. 3
    Концентрированиеconcentrated

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07211545B2uspto-grants-2007_05