Dimethylformamide → HCID 53783583, 화합물
반응식
[C:1]([C:4]1[CH:5]=[C:6]([C:10]2[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][CH:11]=2)[CH:7]=[CH:8][CH:9]=1)(=[O:3])[CH3:2].[H-].[Na+].F.[OH-:20].[Na+].[CH3:22][N:23]([CH3:26])C=O>C(#N)C.O>[C:1]([C:4]1[CH:5]=[C:6]([C:10]2[CH:11]=[CH:12][C:13]([O:16][CH2:6][C@H:7]([OH:20])[CH2:8][CH2:9][C:4]3[CH:26]=[N:23][CH:22]=[CH:2][CH:1]=3)=[CH:14][CH:15]=2)[CH:7]=[CH:8][CH:9]=1)(=[O:3])[CH3:2]참가 물질
실험 절차
Prepared according to method described in Example 26e) from 3'-acetylbiphenyl-4-ol (Example 55b), 0.59 g), (2R)-4-(tert-butyldimethylsilyloxy)-4-(3-pyridyl)-1-(4-toluenesulfonyloxy)butane (1.0 g) and sodium hydride (60% dispersion in mineral oil, 0.12 g) in dry N,N-dimethylformamide (10 ml). Crude material from this reaction was dissolved in acetonitrile (15 ml) and treated with hydrofluoric acid (40%, 5 ml). The reaction mixture was stirred at room temperature for 18 hours and then poured into water (25 ml). The pH was adjusted to 9 by adding sodium hydroxide solution (2 M). The mixture was then extracted with ethyl acetate (3×100 ml) and the combined extracts dried over anhydrous magnesium sulfate. The solution was filtered and then concentrated under reduced pressure. The residue was purified by column chromatography over silica eluting with ethyl acetate to give the title compound as a white solid (0.25 g).
후처리
- customPrepared
- extractionThe mixture was then extracted with ethyl acetate (3×100 ml)
- dry with materialthe combined extracts dried over anhydrous magnesium sulfate
- filtrationThe solution was filtered
- concentrationconcentrated under reduced pressure
- customThe residue was purified by column chromatography over silica eluting with ethyl acetate
출처 및 근거
- ORD 기록
- ord-184c5c9528b34d6a8fd95ef4792b7da6
- 출처 데이터셋
- uspto-grants-1999_11
- 특허 번호
- US05977105
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