반응 #90289

ord-6365eebc110043db9bb3f4a65d5db8ff

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONthe reaction mixture was poured onto water (50 mL)
  2. 2
    여과The resulting precipitate was filtered off
  3. 3
    세척washed with water (25 mL)
  4. 4
    기타dried
  5. 5
    기타Recrystallisation from dichloromethane/isopropanol

실험 절차

A mixture of 2-(trifluoromethyl)pyridine-3-carbothioamide (0.227 g, 1.10 mmol) and 1-[3,4-bis(benzyloxy)-5-nitrophenyl]-2-bromoethanone (0.50 g, 1.10 mmol) were refluxed overnight in absolute ethanol (5 mL). After cooling to room temperature, the reaction mixture was poured onto water (50 mL). The resulting precipitate was filtered off, washed with water (25 mL) and dried. Recrystallisation from dichloromethane/isopropanol afforded 4-(3,4-bis(benzyloxy)-5-nitrophenyl)-2-(2-(trifluoromethyl)pyridin-3-yl)thiazole, 0.539 g (87%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09446012B2uspto-grants-2016_09