Water → (S)-3-(4-bromo-2-hydroxy-phenyl)-pyrrolidine-1-carboxylic acid tert-butyl ester

HRID 503924노트

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HRID 503924 반응식
C([S-])C.[Na+].[C:5]([O:9][C:10]([N:12]1[CH2:16][CH2:15][C@@H:14]([C:17]2[CH:22]=[CH:21][C:20]([Br:23])=[CH:19][C:18]=2[O:24]C)[CH2:13]1)=[O:11])([CH3:8])([CH3:7])[CH3:6].OS([O-])(=O)=O.[K+].[O-]S([O-])(=O)=O.[Na+].[Na+].O>CN(C=O)C>[C:5]([O:9][C:10]([N:12]1[CH2:16][CH2:15][C@@H:14]([C:17]2[CH:22]=[CH:21][C:20]([Br:23])=[CH:19][C:18]=2[OH:24])[CH2:13]1)=[O:11])([CH3:8])([CH3:6])[CH3:7]

참가 물질

6

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온도
105 °C

실험 절차

Sodium ethanethiolate (80%, 218.7 mg, 1.704 mmol) was added to a solution of (S)-3-(4-bromo-2-methoxy-phenyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (303 mg, 0.8505 mmol) in DMF (3.1 mL) under argon atmosphere. The reaction mixture was heated at 105° C. for 3.5 hours, then cooled to 5° C. A solution of 10% KHSO4/Na2SO4 was added until pH reached 2-3. Water was added, and the resulting mixture was extracted with EtOAc. The combined organic extracts were washed with water and brine, dried over Na2SO4, filtered, and evaporated under reduced pressure. The residue was purified via flash chromatography (hexane/EtOAc, with a gradient from 90/10 to 85/15) to give 236 mg (81% yield) of (S)-3-(4-bromo-2-hydroxy-phenyl)-pyrrolidine-1-carboxylic acid tert-butyl ester as a foam.

후처리

  1. temperaturecooled to 5° C
  2. extractionthe resulting mixture was extracted with EtOAc
  3. washThe combined organic extracts were washed with water and brine
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. customevaporated under reduced pressure
  7. customThe residue was purified via flash chromatography (hexane/EtOAc

출처 및 근거

ORD 기록
ord-f026644fd6714ffe8ed5dce0271dbc28
출처 데이터셋
uspto-grants-2010_08
특허 번호
US07776910B2

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