Phosphate → 2-(R)-[2-(S)-Benzyl-1-(S)-hydroxy-3-(4-(S)-isopropyl-2-oxo-oxazolidin-3-yl)-3-oxopropyl]-4-(R)-fluoropyrrolidine-1-carboxylic acid tert-butyl ester

HRID 732360노트

반응식

HRID 732360 반응식
[O-]S(C(F)(F)F)(=O)=O.C([B+]CCCC)CCC.[CH:18]([C@H:21]1[CH2:25][O:24][C:23](=[O:26])[N:22]1[C:27](=[O:36])[CH2:28][CH2:29][C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)([CH3:20])[CH3:19].C(N(CC)C(C)C)(C)C.[C:46]([O:50][C:51]([N:53]1[CH2:57][C@H:56]([F:58])[CH2:55][C@@H:54]1[CH:59]=[O:60])=[O:52])([CH3:49])([CH3:48])[CH3:47].P([O-])([O-])([O-])=O>ClCCl>[C:46]([O:50][C:51]([N:53]1[CH2:57][C@H:56]([F:58])[CH2:55][C@@H:54]1[C@@H:59]([OH:60])[C@H:28]([CH2:29][C:30]1[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=1)[C:27]([N:22]1[C@@H:21]([CH:18]([CH3:20])[CH3:19])[CH2:25][O:24][C:23]1=[O:26])=[O:36])=[O:52])([CH3:49])([CH3:48])[CH3:47]

참가 물질

7

반응 조건

온도
-78 °C

실험 절차

Add dibutylboron triflate (1 M in dichloromethane, 11.8 mL, 11.8 mmol) to a solution of 4-(S)-isopropyl-3-(3-phenylpropionyl)-oxazolidin-2-one (2.8 g, 10.7 mmol) in dichloromethane (40 mL) at 0° C. Stir 5 min. Add N,N-diisopropylethylamine (2.25 mL, 12.87 mmol) and stir 90 min. Cool to −78° C. and add 4-(R)-fluoro-2-(R)-formylpyrrolidine-1-carboxylic acid tert-butyl ester (2.53 g, 11.6 mmol) in dichloromethane (15 mL) over 15 min. Stir 90 min and then warm to room temperature over 18 h. Cool in ice bath and add 0.05 M pH 7 phosphate buffer (15 mL). Extract with dichloromethane and concentrate. Dissolve in methanol (50 mL) and cool in ice bath. Add aqueous hydrogen peroxide (15 mL, 30% solution) and remove ice bath. Stir 5 min and concentrate. Extract with ethyl acetate and wash extract with 1 N HCl, saturated aqueous sodium bicarbonate, saturated aqueous sodium chloride, dry (magnesium sulfate), concentrate and purify (silica gel chromatography, eluting with hexanes and ethyl acetate) to give the title compound as a foam (2.68 g, 52%).

후처리

  1. stirringStir 90 min
  2. temperaturewarm to room temperature over 18 h
  3. temperatureCool in ice bath
  4. extractionExtract with dichloromethane
  5. concentrationconcentrate
  6. dissolutionDissolve in methanol (50 mL)
  7. temperaturecool in ice bath
  8. customAdd aqueous hydrogen peroxide (15 mL, 30% solution) and remove ice bath
  9. stirringStir 5 min
  10. concentrationconcentrate
  11. extractionExtract with ethyl acetate
  12. washwash
  13. extractionextract with 1 N HCl, saturated aqueous sodium bicarbonate, saturated aqueous sodium chloride
  14. dry with materialdry (magnesium sulfate)
  15. concentrationconcentrate
  16. custompurify
  17. wash(silica gel chromatography, eluting with hexanes and ethyl acetate)

출처 및 근거

ORD 기록
ord-b742167197d34da1b2af5f73233f34a7
출처 데이터셋
uspto-grants-2009_09
특허 번호
US07585885B2

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