Dichloromethane → (2R)-2-[(2S)-3-(Benzoylthio)-2-methylpropionylamino]-3-(4-methylbenzylthio)propionic acid

HRID 1003651노트

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HRID 1003651 반응식
C(N(CC)CC)C.[CH3:8][C:9]1[CH:22]=[CH:21][C:12]([CH2:13][S:14][CH2:15][C@@H:16]([C:18]([OH:20])=[O:19])[NH2:17])=[CH:11][CH:10]=1.C(Cl)Cl.[C:26]([S:34][CH2:35][C@@H:36]([CH3:49])[C:37](OC1C=CC([N+]([O-])=O)=CC=1)=[O:38])(=[O:33])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>CN(C)C=O>[C:26]([S:34][CH2:35][C@@H:36]([CH3:49])[C:37]([NH:17][C@@H:16]([CH2:15][S:14][CH2:13][C:12]1[CH:11]=[CH:10][C:9]([CH3:8])=[CH:22][CH:21]=1)[C:18]([OH:20])=[O:19])=[O:38])(=[O:33])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1

참가 물질

6

실험 절차

Triethylamine (0.464 ml) is added to a solution of S-(4-methylbenzyl)-L-cysteine (reference compound No. 2-1, 500 mg) in a mixed solvent of methylene chloride (20 ml)/dimethylformamide (5 ml) under ice-cooling, and the mixture is stirred. 4-Nitrophenyl (2S)-3-benzoylthio-2-methylpropionate (reference compound No. 1-1, 919 mg) is added to the system of reaction, and the system is stirred overnight. The system of reaction is further stirred overnight at 40° to 50° C. After the reaction is completed, the mixture is concentrated under reduced pressure, a 10%, aqueous citric acid solution is added to the residue, and the whole is extracted with ethyl acetate. The organic layer is washed with water and a saturated sodium chloride solution successively, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue is purified by silica gel column chromatography to give 660 mg (68.9%) of the titled compound. (Compound No. 1-1)

후처리

  1. temperaturecooling
  2. stirringthe system is stirred overnight
  3. customThe system of reaction
  4. stirringis further stirred overnight at 40° to 50° C
  5. concentrationthe mixture is concentrated under reduced pressure
  6. additiona 10%, aqueous citric acid solution is added to the residue
  7. extractionthe whole is extracted with ethyl acetate
  8. washThe organic layer is washed with water
  9. dry with materiala saturated sodium chloride solution successively, dried over anhydrous sodium sulfate
  10. concentrationconcentrated under reduced pressure
  11. customThe obtained residue is purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-e19f5ff67c3f446f8bf5238fe557bb84
출처 데이터셋
uspto-grants-2000_04
특허 번호
US06046235

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