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HRID 1850167作成日:2026年10月26日

Water → (R)-N-((S)-1-(2,3-difluorophenyl)ethyl)-2-methylpropane-2-sulfinamide

https://huagongshe.com/reaction/1850167

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物(NE,R)-N-[(2,3-difluorophenyl)methylidene]-2-methylpropane-2-sulfinamideHCID 89479281—
反応物HCID 178418689HCID 178418689—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物(R)-N-((S)-1-(2,3-difluorophenyl)ethyl)-2-methylpropane-2-sulfinamideHCID 8673019792.3%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08957068B2
出典データセットuspto-grants-2015_02
ORD IDord-8e914af5bebb4bb0823b02a60d6342f7
出典メモuspto-grants-2015_02