반응 #43434
ord-37d3299f2cea443e921cc4d0be63dbbe
반응 방정식
3,8-difluoro-4-methylidene-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one
tert-butanol water
sodium sulphite
→
solid
수율 82.0%
(4R/S)-3,8-Difluoro-4-liydroxy-4-(hydroxymethyl)-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one
수율 82.0%
반응물
시약
없음
반응 조건
상세 조건
See reaction.notes.procedure_details.
후처리
- 1workup.ADDITIONmix alpha/beta (0.75 g/0.75 g)
- 2추출After 10 minutes the mixture was extracted with 20% methanol in dichloromethane (3×200 ml)
- 3농축The aqueous phase was concentrated (to ca 20 ml)
- 4추출further extracted with 20% methanol in dichloromethane (3×200 ml)
- 5기타The organic extracts were dried
- 6기타evaporated
실험 절차
A solution of 3,8-difluoro-4-methylidene-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one (219 mg, 1 mmol) in tert-butanol/water (10 ml/10 ml) was treated with AD mix alpha/beta (0.75 g/0.75 g). After 6 hours the reaction mixture was treated with saturated sodium sulphite solution (10 ml). After 10 minutes the mixture was extracted with 20% methanol in dichloromethane (3×200 ml). The aqueous phase was concentrated (to ca 20 ml) and further extracted with 20% methanol in dichloromethane (3×200 ml). The organic extracts were dried and evaporated affording a white solid (206 mg, 82%).