반응식
[Br:1][CH:2]([C:4]1[C:5](=O)[NH:6][C:7]2[C:12]([N:13]=1)=[CH:11][CH:10]=[C:9]([F:14])[CH:8]=2)[CH3:3].P(Cl)(Cl)([Cl:18])=O>>[Br:1][CH:2]([C:4]1[C:5]([Cl:18])=[N:6][C:7]2[C:12](=[CH:11][CH:10]=[C:9]([F:14])[CH:8]=2)[N:13]=1)[CH3:3]참가 물질
반응 조건
- 온도
- 100 °C
실험 절차
A heterogeneous mixture of 3-(1-bromoethyl)-7-fluoroquinoxalin-2(1H)-one (58.86 g, 217.1 mmol) and phosphorous oxychloride (198.8 ml, 2171 mmol) in a 1 L round bottom flask was stirred at 100° C. for 2 h. The mixture was heterogeneous in the beginning of the reaction and then homogeneous black solution over 1 h. After 2 h, the mixture was cooled to rt and concentrated under reduced pressure. To the black residue was carefully added ice (˜400 ml) in portions and then water (200 ml) with stirring. The mixture was neutralized with NH4OH (200 ml) and ice (˜200 ml) with stirring. The resulting precipitate was collected by filtration, rinsed with water (1 L), and dried under high vacuum overnight to give 2-(1-bromoethyl)-3-chloro-6-fluoroquinoxaline (58.31 g, 92.8% yield) including 3-chloro-2-(1-chloroethyl)-6-fluoroquinoxaline as a brown solid. 1H NMR (400 MHz, DMSO-d6), ratio of bromoethyl analog and chloroethyl analog=2.5:1 Mass Spectrum (ESI) m/e=288.9 [M+H(79Br)]+ and 291.0 [M+H (81Br)]+
후처리
- customThe mixture was heterogeneous in the beginning of the reaction
- waithomogeneous black solution over 1 h
- waitAfter 2 h
- temperaturethe mixture was cooled to rt
- concentrationconcentrated under reduced pressure
- stirringwater (200 ml) with stirring
- stirringwith stirring
- filtrationThe resulting precipitate was collected by filtration
- washrinsed with water (1 L)
- customdried under high vacuum overnight
출처 및 근거
- ORD 기록
- ord-86e02f9c3a284b659a42addacb36b686
- 출처 데이터셋
- uspto-grants-2014_05
- 특허 번호
- US08716290B2
연결된 노트
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