반응식
[C:1](OC(=O)C)(=[O:3])[CH3:2].C(N(CC)C(C)C)(C)C.[C:17]([O:21][C:22]([N:24]1[C@@H:29]([C@@H:30]([OH:41])[C@@H:31]([NH2:40])[CH2:32][C:33]2[CH:38]=[CH:37][CH:36]=[C:35]([OH:39])[CH:34]=2)[CH2:28][O:27][C@@H:26]([O:42][CH2:43][C:44]([CH3:47])([CH3:46])[CH3:45])[C@@H:25]1[CH3:48])=[O:23])([CH3:20])([CH3:19])[CH3:18]>C(OCC)(=O)C>[C:17]([O:21][C:22]([N:24]1[CH:29]([C@@H:30]([OH:41])[C@@H:31]([NH:40][C:1](=[O:3])[CH3:2])[CH2:32][C:33]2[CH:38]=[CH:37][CH:36]=[C:35]([OH:39])[CH:34]=2)[CH2:28][O:27][C@@H:26]([O:42][CH2:43][C:44]([CH3:47])([CH3:46])[CH3:45])[C@@H:25]1[CH3:48])=[O:23])([CH3:19])([CH3:18])[CH3:20]참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
Add acetic anhydride (320 μL, 3.4 mmol) and N,N-diisopropylethylamine (590 μL, 3.4 mmol) to a solution of 5-(R)-[2-(S)-amino-1-(S)-hydroxy-3-(3-hydroxyphenyl)-propyl]-2-(R)-(2,2-dimethylpropoxy)-3-(S)-methylmorpholine-4-carboxylic acid tert-butyl ester (770 mg, 1.70 mmol). Stir for 2.5 hours. Dilute with ethyl acetate, wash with 1 N hydrochloric acid (twice), saturated aqueous sodium bicarbonate, saturated aqueous sodium chloride, dry (magnesium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 20:80 to 25:75 ethyl acetate:hexanes) to give the desired compound (292 mg).
후처리
- washwash with 1 N hydrochloric acid (twice), saturated aqueous sodium bicarbonate, saturated aqueous sodium chloride
- dry with materialdry (magnesium sulfate)
- filtrationfilter
- concentrationconcentrate
- custompurify
- wash(silica gel chromatography, eluting with 20:80 to 25:75 ethyl acetate:hexanes)
출처 및 근거
- ORD 기록
- ord-fbe26c185e70421fb7475c93b15b63c2
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07745438B2
연결된 노트
불러오는 중…