반응식
[H-].[Na+].[CH2:3]([O:10][C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.S(O[CH2:29][C@H:30]1[CH2:34][CH2:33][CH2:32][N:31]1[C:35]([O:37][C:38]([CH3:41])([CH3:40])[CH3:39])=[O:36])(C1C=CC(C)=CC=1)(=O)=O>CN(C=O)C>[C:38]([O:37][C:35]([N:31]1[CH2:32][CH2:33][CH2:34][CH:30]1[CH2:29][O:17][C:14]1[CH:13]=[CH:12][C:11]([O:10][CH2:3][C:4]2[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=2)=[CH:16][CH:15]=1)=[O:36])([CH3:41])([CH3:39])[CH3:40]참가 물질
실험 절차
To a 15 mL of anhydrous DMF was added NaH (60% dispersion in oil, 338 mg, 8.44 mmol), and the resulting reaction mixture was cooled to 0° C. p-benzyloxy phenol (1.41 g, 7.03 mmol) was added and the reaction mixture was stirred at rt for 45 min. It was then cooled to −5° C., and (R)-Boc-prolinol tosylate (2.5 g, 7.03 mmol) in anhydrous DMF (5 mL) was cooled in a separate ice-bath and added dropwise to the reaction mixture. It was then allowed to warm to rt and stirred at 92° C. for 5 h and at rt overnight. The resulting mixture was poured into 200 mL ice/water and stirred for an hour. The resulting precipitate was filtered, washed with ether, dried over MgSO4, concentrated, recrystallized with ether/hexane to give shiny yellow crystals (1.5 g, 55%).
후처리
- customthe resulting reaction mixture
- additionwas added
- temperatureIt was then cooled to −5° C.
- additionadded dropwise to the reaction mixture
- temperatureto warm to rt
- stirringstirred at 92° C. for 5 h and at rt overnight
- stirringstirred for an hour
- filtrationThe resulting precipitate was filtered
- washwashed with ether
- dry with materialdried over MgSO4
- concentrationconcentrated
- customrecrystallized with ether/hexane
출처 및 근거
- ORD 기록
- ord-188a746988c84b5d953e1fe0403ef6ff
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07728032B2
연결된 노트
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