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[F:1][C:2]1[C:15]([F:16])=[CH:14][CH:13]=[CH:12][C:3]=1/[CH:4]=[N:5]/[S@@:6]([C:8]([CH3:11])([CH3:10])[CH3:9])=[O:7].O.[CH3:18][Mg+].[Br-]>C(Cl)Cl.C(OCC)C>[F:1][C:2]1[C:15]([F:16])=[CH:14][CH:13]=[CH:12][C:3]=1[C@@H:4]([NH:5][S@@:6]([C:8]([CH3:11])([CH3:10])[CH3:9])=[O:7])[CH3:18]참가 물질
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- 온도
- 0 °C
실험 절차
To a solution of (R,E)-N-(2,3-difluorobenzylidene)-2-methylpropane-2-sulfinamide (0.800 g, 3.26 mmol) in DCM (32.6 mL), cooled to 0° C. (water/icebath) under N2, was added 3M MeMgBr (4.35 mL, 13.05 mmol) in diethyl ether. Reaction mixture allowed to stir for 30 min at 0° C. Then gradually allowed to warm to room temperature and stirred for 30 min at room temperature. Reaction mixture was cooled to 0° C. then quenched with the slow addition of a saturated solution of NH4Cl and diluted with EtOAc. Phases partitioned aqueous phase extracted with EtOAc and the organic layers combined washed with water, brine, dried with MgSO4, filtered and concentrated to afford (R)—N—((S)-1-(2,3-difluorophenyl)ethyl)-2-methylpropane-2-sulfinamide (0.7868 g, 3.01 mmol, 92% yield) as yellow solid. LCMS m/z 262.0 (M+H)+, Rt 0.70 min.
후처리
- customReaction mixture
- temperatureto warm to room temperature
- stirringstirred for 30 min at room temperature
- customReaction mixture
- temperaturewas cooled to 0° C.
- customthen quenched with the slow addition of a saturated solution of NH4Cl
- additiondiluted with EtOAc
- customPhases partitioned aqueous phase
- extractionextracted with EtOAc
- washthe organic layers combined washed with water, brine
- dry with materialdried with MgSO4
- filtrationfiltered
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-8e914af5bebb4bb0823b02a60d6342f7
- 출처 데이터셋
- uspto-grants-2015_02
- 특허 번호
- US08957068B2
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