반응식
[CH2:1]([O:8][C:9](=[O:23])[CH2:10][C@@H:11]([C:20](O)=[O:21])[NH:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CN1CCOCC1.ClC(OCC(C)C)=O>C(COC)OC>[C:16]([O:15][C:13]([NH:12][C@H:11]([CH2:20][OH:21])[CH2:10][C:9]([O:8][CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)=[O:23])=[O:14])([CH3:18])([CH3:19])[CH3:17]참가 물질
반응 조건
- 온도
- -5 °C
실험 절차
N-(tert-Butoxycarbonyl)-L-aspartic acid 4-benzyl ester (30 g) was dissolved in dimethoxyethane (90 mL) and the solution was cooled to −5° C. N-Methylmorpholine (10.32 mL) was added followed by a slow addition of isobutyl chloroformate (12.66 mL) such that the reaction temperature was kept below −10° C. The mixture was aged for 0.5 hour. The solids were quickly filtered and washed with dimethoxyethane (90 mL). The filtrate was cooled to −50° C. and a solution of sodium borohydride (4.4 g) in water (45 mL) was added slowly such that the reaction temperature was maintained between −30° C. and −15° C. Water (500 mL) was then added such that the reaction mixture temperature was maintained below −15° C. The suspension was filtered, the solid washed with water (400 μL) and dried to yield benzyl (3S)-3-[(tert-butoxycarbonyl)amino]-4-hydroxybutanoate.
후처리
- customwas kept below −10° C
- filtrationThe solids were quickly filtered
- washwashed with dimethoxyethane (90 mL)
- temperatureThe filtrate was cooled to −50° C.
- additiona solution of sodium borohydride (4.4 g) in water (45 mL) was added slowly such that the reaction temperature
- temperaturewas maintained between −30° C. and −15° C
- additionWater (500 mL) was then added such that the reaction mixture temperature
- temperaturewas maintained below −15° C
- filtrationThe suspension was filtered
- washthe solid washed with water (400 μL)
- customdried
출처 및 근거
- ORD 기록
- ord-a9739360c39a496f931652fe8fc1109d
- 출처 데이터셋
- uspto-grants-2011_07
- 특허 번호
- US07973037B2
연결된 노트
불러오는 중…