반응 #2000855

ord-74df6f667add46f188820196f37c26df

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출followed by extraction with ethyl acetate twice
  2. 2
    세척The combined organic layers were washed with water
  3. 3
    건조a saturated sodium chloride solution, dried over anhydrous magnesium sulfate
  4. 4
    농축concentrated under reduced pressure

실험 절차

A mixture of 0.50 g of 4-[5-(trifluoromethyl)benzoxazole-2-yl]pyridin-3-ol, 1.23 g of potassium carbonate and 14 ml of DMF was stirred while heating at 70° C. for three hours with chlorodifluoromethane gas injected. By stopping injection of gas, the mixture was cooled to room temperature and allowed to stand overnight. Water was added to the reaction mixture, followed by extraction with ethyl acetate twice. The combined organic layers were washed with water and a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.11 g of 2-(3-difluoromethoxypyridin-4-yl)-5-(trifluoromethyl)benzoxazole (hereinafter, referred to as “active compound 126”).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08609705B2uspto-grants-2013_12