(S)-tert-butyl 1-(4-acetyl-2-fluorophenyl)ethylcarbamate → HCID 131736959, 화합물

HRID 57439노트

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HRID 57439 반응식
[C:1]([O:5][C:6](=[O:20])[NH:7][C@H:8]([C:10]1[CH:15]=[CH:14][C:13]([C:16](=[O:18])[CH3:17])=[CH:12][C:11]=1[F:19])[CH3:9])([CH3:4])([CH3:3])[CH3:2].[CH3:21][Mg+].[Br-]>C(Cl)Cl.C(OCC)C>[C:1]([O:5][C:6](=[O:20])[NH:7][C@H:8]([C:10]1[CH:15]=[CH:14][C:13]([C:16]([OH:18])([CH3:21])[CH3:17])=[CH:12][C:11]=1[F:19])[CH3:9])([CH3:2])([CH3:3])[CH3:4]

참가 물질

5

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온도
0 °C

실험 절차

To a solution of (S)-tert-butyl(1-(4-acetyl-2-fluorophenyl)ethyl)carbamate (200 mg, 0.71 mmol) in DCM (7.1 mL), cooled to 0° C. (water/ice bath) under N2, was added 3M MeMgBr (10.95 mL, 2.84 mmol) in diethyl ether. Reaction mixture allowed to stir for 5 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 DCM. Phases partitioned, aqueous phase extracted with DCM and the organic layers combined washed with water, brine, dried (Na2SO4), filtered and concentrated to (S)-tert-butyl(1-(2-fluoro-4-(2-hydroxypropan-2-yl)phenyl)ethyl)carbamate (184 mg, 0.62 mmol, 87% yield) afford as a colorless oil which slowly crystallizes upon standing. 1H NMR (400 MHz, CDCl3) δ 1.39-1.48 (m, 12H) 1.57 (s, 6H) 7.15-7.25 (m, 2H) 7.31-7.36 (m, 1H).

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 DCM
  8. customPhases partitioned
  9. extractionaqueous phase extracted with DCM
  10. washthe organic layers combined washed with water, brine
  11. dry with materialdried (Na2SO4)
  12. filtrationfiltered

출처 및 근거

ORD 기록
ord-1175839d694d45008522fd37dc12344d
출처 데이터셋
uspto-grants-2016_09
특허 번호
US09434719B2

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