Cesium carbonate → HCID 86665194, compound
Reaction equation
[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]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 66 °C
Procedure
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).
Workup
- temperatureto cool to 23° C.
- customThe mixture was then partitioned between half-saturated aqueous sodium chloride solution (500 mL) and ethyl acetate (1 L)
- washThe organic layer was washed with brine
- dry with materialdried over sodium sulfate
- concentrationconcentrated
- customThe residue was purified by flash column chromatography on silica gel
- washeluting with hexane initially
Sources & evidence
- ORD record
- ord-503050c34c20492c866c32f618114198
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08912210B2
Reaction notes
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