Formamide → HCID 22313804, compound
Reaction equation
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]=1Participants
Procedure
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).
Workup
- temperaturethe mixture was heated
- temperatureat reflux temperature for 2 hours
- customthe solution was decanted away from solids
- temperaturethe mixture was heated
- temperatureat reflux temperature for 6 hours
- temperatureThe reaction mixture was cooled down to room temperature
- extractionThe whole was extracted with ethyl acetate
- washThe organic layer was washed with brine
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
- customThe residue was purified by flash chromatography
- washeluting with ethyl acetate-hexane (1:4)
Sources & evidence
- ORD record
- ord-5151aee4ce9746a9b951842574964794
- Source dataset
- uspto-grants-2003_08
- Patent number
- US06608095B2
Reaction notes
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