Acetic Acid → (R)-4-chloro-8-oxo-9-(2,2,2-trifluoroethyl)-3,6,7,8,9,10-hexahydroazepino[3,4-e]indazol-7-yl benzoate
반응식
[C:1]([O:9][C@H:10]([CH2:15][C:16]1[C:17]([CH2:26][NH:27][CH2:28][C:29]([F:32])([F:31])[F:30])=[C:18]2[C:22](=[C:23]([Cl:25])[CH:24]=1)[NH:21][N:20]=[CH:19]2)[C:11]([O:13]C)=O)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1(C)C=CC=CC=1.C(O)(=O)C>>[C:1]([O:9][C@H:10]1[C:11](=[O:13])[N:27]([CH2:28][C:29]([F:31])([F:32])[F:30])[CH2:26][C:17]2[C:18]3[CH:19]=[N:20][NH:21][C:22]=3[C:23]([Cl:25])=[CH:24][C:16]=2[CH2:15]1)(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1참가 물질
4
실험 절차
(R)-3-(7-chloro-4-((2,2,2-trifluoroethylamino)methyl)-1H-indazol-5-yl)-1-methoxy-1-oxopropan-2-yl benzoate (7.75 g, 16.5 mmol) in toluene (70.00 ml, 657 mmol) was added acetic acid (1.2 ml, 20.96 mmol) and refluxed for 12 h. The solvent was evaporated and the crude product was dissolved in EtOAc, washed with aqueous NaHCO3. The solvent was removed and the crude product was purified by flash chromatography using 50% EtOAc in hexane to give (R)-4-chloro-8-oxo-9-(2,2,2-trifluoroethyl)-3,6,7,8,9,10-hexahydroazepino[3,4-e]indazol-7-yl benzoate in 74% yield. MS (ESI) 438 (M+H); Rf=2.60.
후처리
- temperaturerefluxed for 12 h
- customThe solvent was evaporated
- dissolutionthe crude product was dissolved in EtOAc
- washwashed with aqueous NaHCO3
- customThe solvent was removed
- customthe crude product was purified by flash chromatography
출처 및 근거
- ORD 기록
- ord-3fab6a3c21bd4de5b4da048f2a154cb6
- 출처 데이터셋
- uspto-grants-2008_12
- 특허 번호
- US07470679B2
반응 노트
불러오는 중…