Dichloromethane → (2R)-2-[(2S)-3-(Benzoylthio)-2-methylpropionylamino]-3-(4-methylbenzylthio)propionic acid
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]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 1
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
- temperaturecooling
- stirringthe system is stirred overnight
- customThe system of reaction
- stirringis further stirred overnight at 40° to 50° C
- concentrationthe mixture is concentrated under reduced pressure
- additiona 10%, aqueous citric acid solution is added to the residue
- extractionthe whole is extracted with ethyl acetate
- washThe organic layer is washed with water
- dry with materiala saturated sodium chloride solution successively, dried over anhydrous sodium sulfate
- concentrationconcentrated under reduced pressure
- 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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