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[C:1]([NH:4][CH:5]([CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([N+:18]([O-:20])=[O:19])[CH:13]=1)[C:6]([O:8][CH2:9][CH3:10])=[O:7])(=[O:3])[CH3:2].C(=O)([O-])O.[NH4+].O>C(#N)C>[C:1]([NH:4][C@H:5]([CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([N+:18]([O-:20])=[O:19])[CH:13]=1)[C:6]([O:8][CH2:9][CH3:10])=[O:7])(=[O:3])[CH3:2]참가 물질
실험 절차
A mixture of 2.8 g of ethyl 2-(acetylamino)-3-(3-nitrophenyl)propanoate in 17 cm3 of acetonitrile [lacuna] to which is added 3.95 g of ammonium hydrogen carbonate and 35 cm3 of water at a pH in the region of 8. 0.017 g of type-II α-chymotrypsin is then introduced and the mixture is left stirring at room temperature for 1 hour 15 min, while measuring the GpH regularly. After this reaction time, the pH is less than 8, a further 0.017 g of type-II α-chymotrypsin is added and stirring of the reaction medium is continued for 2 hours 45 min. The aqueous phase is extracted with 3 times 50 cm3 of ethyl acetate; the combined organic phases are then dried over sodium sulfate, filtered and evaporated under reduced pressure (2 kPa) at a temperature in the region of 40° C. 1.4 g of ethyl (2R)-2-(acetylamino)-3-(3-nitrophenyl)propanoate are obtained in the form of white crystals melting at 110° C.
후처리
- addition0.017 g of type-II α-chymotrypsin is then introduced
- waitthe mixture is left
- additionAfter this reaction time, the pH is less than 8, a further 0.017 g of type-II α-chymotrypsin is added
- stirringstirring of the reaction medium
- waitis continued for 2 hours 45 min
- extractionThe aqueous phase is extracted with 3 times 50 cm3 of ethyl acetate
- dry with materialthe combined organic phases are then dried over sodium sulfate
- filtrationfiltered
- customevaporated under reduced pressure (2 kPa) at a temperature in the region of 40° C
출처 및 근거
- ORD 기록
- ord-12c7a08ff22e4c4288c8ae0051646062
- 출처 데이터셋
- uspto-grants-2002_09
- 특허 번호
- US06451821B1
연결된 노트
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