Formamide → HCID 22313804, 화합물

HRID 396786노트

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HRID 396786 반응식
P12(SP3(SP(SP(S3)(S1)=S)(=S)S2)=S)=S.C(N)=O.Br[CH2:19][C:20]([C:22]1[CH:27]=[CH:26][C:25]([OH:28])=[CH:24][C:23]=1[F:29])=O.[CH:30]([NH2:32])=[S:31].[OH-].[Na+]>O1CCOCC1>[F:29][C:23]1[CH:24]=[C:25]([OH:28])[CH:26]=[CH:27][C:22]=1[C:20]1[N:32]=[CH:30][S:31][CH:19]=1

참가 물질

7

실험 절차

To a stirred solution of phosphorus pentasulfide (4.0 g, 9.0 mmol) in dioxane (40 ml) was added formamide (4.8 g, 106 mmol), and the mixture was heated at reflux temperature for 2 hours. The reaction mixture was cooled down to room temperature, and the solution was decanted away from solids. To a stirred solution of 2-bromo-1-(2-fluoro-4-hydroxyphenyl)-1-ethanone (1.2 g, 5.15 mmol) in dioxane (14 ml) was added the thioformamide solution, and the mixture was heated at reflux temperature for 6 hours. The reaction mixture was cooled down to room temperature, and made basic by addition of 2N NaOH aqueous solution. The whole was extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography eluting with ethyl acetate-hexane (1:4) to give title compound (864 mg, 86% yield).

후처리

  1. temperaturethe mixture was heated
  2. temperatureat reflux temperature for 2 hours
  3. customthe solution was decanted away from solids
  4. temperaturethe mixture was heated
  5. temperatureat reflux temperature for 6 hours
  6. temperatureThe reaction mixture was cooled down to room temperature
  7. extractionThe whole was extracted with ethyl acetate
  8. washThe organic layer was washed with brine
  9. dry with materialdried over MgSO4
  10. concentrationconcentrated in vacuo
  11. customThe residue was purified by flash chromatography
  12. washeluting with ethyl acetate-hexane (1:4)

출처 및 근거

ORD 기록
ord-5151aee4ce9746a9b951842574964794
출처 데이터셋
uspto-grants-2003_08
특허 번호
US06608095B2

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