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

HRID 1850167

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HRID 1850167 반응식
[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

6

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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

  1. customReaction mixture
  2. temperatureto warm to room temperature
  3. stirringstirred for 30 min at room temperature
  4. customReaction mixture
  5. temperaturewas cooled to 0° C.
  6. customthen quenched with the slow addition of a saturated solution of NH4Cl
  7. additiondiluted with EtOAc
  8. customPhases partitioned aqueous phase
  9. extractionextracted with EtOAc
  10. washthe organic layers combined washed with water, brine
  11. dry with materialdried with MgSO4
  12. filtrationfiltered
  13. concentrationconcentrated

출처 및 근거

ORD 기록
ord-8e914af5bebb4bb0823b02a60d6342f7
출처 데이터셋
uspto-grants-2015_02
특허 번호
US08957068B2

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