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Cesium carbonate → HCID 86665194, 화합물

HRID 1404484
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HRID 1404484 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5](=[O:9])[NH:6][C:7]=1[CH3:8].C(=O)([O-])[O-].[Cs+].[Cs+].CS(O[CH2:21][C:22]([F:25])([F:24])[F:23])(=O)=O.F[B-](F)(F)F.[O:31]=[N+:32]=[O:33]>O1CCOCC1.ClCCl>[Br:1][C:2]1[CH:3]=[C:4]([N+:32]([O-:33])=[O:31])[C:5](=[O:9])[N:6]([CH2:21][C:22]([F:25])([F:24])[F:23])[C:7]=1[CH3:8]
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참가 물질

7

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HCID 10796Cesium carbonateHCID 5565652,2,2-Trifluoroethyl MethanesulfonateHCID 27344173-Bromo-6-hydroxy-2-methylpyridineHCID 11073463Nitronium tetrafluoroborate

생성물 1

HCID 86665194HCID 86665194, 화합물

시약·촉매·용매 2

HCID 6344Dichloromethane용매
HCID 312751,4-Dioxane용매

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온도
66 °C

실험 절차

A mixture of 5-bromo-6-methylpyridin-2(1H)-one (10.0 g, 53.2 mmol), cesium carbonate (20.8 g, 63.8 mmol), and 2,2,2-trifluoroethyl methanesulfonate (18.5 g, 80.0 mmol) in dioxane (266 mL) was heated at 66° C. for 1.5 h. The mixture was allowed to cool to 23° C., then diluted with dichloromethane (266 mL). Nitronium tetrafluoroborate (21.2 g, 160 mmol) was added and the resulting mixture was stirred for 16 h. The mixture was then partitioned between half-saturated aqueous sodium chloride solution (500 mL) and ethyl acetate (1 L). The organic layer was washed with brine, dried over sodium sulfate and concentrated. The residue was purified by flash column chromatography on silica gel, eluting with hexane initially, grading to 50% EtOAc in hexane to provide the title compound. MS: m/z=315.0 (M+1).

후처리

  1. temperatureto cool to 23° C.
  2. customThe mixture was then partitioned between half-saturated aqueous sodium chloride solution (500 mL) and ethyl acetate (1 L)
  3. washThe organic layer was washed with brine
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated
  6. customThe residue was purified by flash column chromatography on silica gel
  7. washeluting with hexane initially

출처 및 근거

ORD 기록
ord-503050c34c20492c866c32f618114198
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08912210B2

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