반응식
[F:1][C:2]([F:28])([F:27])[C:3]([NH:5][CH:6]1[C:14]2[C:9](=[CH:10][C:11]([CH2:15][N:16]3[CH:20]=[C:19]([CH2:21][OH:22])[C:18]([C:23]([F:26])([F:25])[F:24])=[N:17]3)=[CH:12][CH:13]=2)[CH2:8][CH2:7]1)=O.B#B.Cl>C1COCC1>[F:28][C:2]([F:1])([F:27])[CH2:3][NH:5][CH:6]1[C:14]2[C:9](=[CH:10][C:11]([CH2:15][N:16]3[CH:20]=[C:19]([CH2:21][OH:22])[C:18]([C:23]([F:24])([F:25])[F:26])=[N:17]3)=[CH:12][CH:13]=2)[CH2:8][CH2:7]1참가 물질
5
실험 절차
To a solution of 2,2,2-trifluoro-N-(5-((4-(hydroxymethyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)methyl)-2,3-dihydro-1H-inden-1-yl)acetamide (0.172 mmol, 70 mg) in THF (2 mL) was added diborane (1.719 mmol, 1.719 mL) and the whole heated to reflux for 6 h. The reaction mixture was allowed to cool to room temperature before being treated with 2N HCl (3 mL) and left to stand overnight. After this time the crude mixture was applied to an SCX column & eluted with 2N NH3/MeOH. After evaporation, the residue was further purified by prep LCMS to give a clear film (11 mg, 0.028 mmol, 16.3%). MS (ESI): m/z [M+H]+ 394.1.
후처리
- temperaturethe whole heated
- temperatureto reflux for 6 h
- waitleft
- washeluted with 2N NH3/MeOH
- customAfter evaporation
- customthe residue was further purified by prep LCMS
- customto give a clear film (11 mg, 0.028 mmol, 16.3%)
출처 및 근거
- ORD 기록
- ord-f7027af75a864385b6ed2b3a6210bce6
- 출처 데이터셋
- uspto-grants-2013_09
- 특허 번호
- US08536214B2
연결된 노트
불러오는 중…