Triethylamine → (4RS,5SR)-5-(3-chlorophenyl)-4-[4-(2,2,3,3,3-pentafluoropropyl)benzyl]-1,3-oxazolidin-2-one

HRID 1610756노트

반응식

HRID 1610756 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]([OH:28])[CH:9]([CH2:13][C:14]2[CH:19]=[CH:18][C:17]([CH2:20][C:21]([F:27])([F:26])[C:22]([F:25])([F:24])[F:23])=[CH:16][CH:15]=2)C(O)=O)[CH:5]=[CH:6][CH:7]=1.C([N:31]([CH2:34]C)CC)C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=[O:43])C=CC=CC=1>O1CCCC1>[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]2[O:28][C:34](=[O:43])[NH:31][CH:9]2[CH2:13][C:14]2[CH:15]=[CH:16][C:17]([CH2:20][C:21]([F:26])([F:27])[C:22]([F:25])([F:24])[F:23])=[CH:18][CH:19]=2)[CH:5]=[CH:6][CH:7]=1

참가 물질

5

실험 절차

To a solution of (2RS,3RS)-3-(3-chlorophenyl)-3-hydroxy-2-[4-(2,2,3,3,3-pentafluoropropyl)benzyl]propionic acid (2.75 g, 6.50 mmol) in tetrahydrofuran (70 ml) were added triethylamine (1.36 ml, 9.75 mmol) and diphenylphosphoryl azide (1.54 ml, 7.15 mmol), and the mixture was heated under reflux for 4 hrs. The solvent was evaporated and the residue was diluted with ethyl acetate, washed with water, saturated. aqueous sodium hydrogen carbonate and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The residue as recrystallized from hexane-ethyl acetate to give (4RS,5SR)-5-(3-chlorophenyl)-4-[4-(2,2,3,3,3-pentafluoropropyl)benzyl]-1,3-oxazolidin-2-one (2.54 g, 93%) as colorless crystals.

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 4 hrs
  3. customThe solvent was evaporated
  4. additionthe residue was diluted with ethyl acetate
  5. washwashed with water
  6. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customThe residue as recrystallized from hexane-ethyl acetate

출처 및 근거

ORD 기록
ord-e99d7f5fa7cb423fb6cff27aac897866
출처 데이터셋
uspto-grants-2006_01
특허 번호
US06982348B2

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