Pyridine → 1-{2-(2-Fluoro-phenyl)-2-[hydroxyimino]-ethyl}-3-isopropenyl-1,3-dihydro-benzimidazol-2-one
반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=O)[CH2:9][N:10]1[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=2[N:12]([C:19]([CH3:21])=[CH2:20])[C:11]1=[O:22].Cl.[NH2:25][OH:26].N1C=CC=CC=1>C(O)C>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=[N:25][OH:26])[CH2:9][N:10]1[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][C:13]=2[N:12]([C:19]([CH3:21])=[CH2:20])[C:11]1=[O:22]참가 물질
반응 조건
- 온도
- 80 °C
실험 절차
To a stirred solution of 1-[2-(2-fluoro-phenyl)-2-oxo-ethyl]-3-isopropenyl-1,3-dihydro-benzimidazol-2-one (1.3 g, 4.2 mmol) in ethanol (50 ml) was added hydroxylamine hydrochloride (0.84 g, 12.2 mmol) followed by pyridine (1.7 ml, 21.0 mmol) at ambient temperature. The resulting mixture was warmed to 80° C. for 6 h, cooled to ambient temperature and concentrated. The remaining residue was diluted with water, 1M HCl and ethyl acetate. The layers were separated and the aqueous phase was extracted once more with ethyl acetate. The combined organics were dried (MgSO4), filtered and concentrated to give the crude product which was purified via column chromatography (silica gel, 50% EtOAc/hexanes). The product-containing fractions were combined and concentrated to give 1.0 g (73%) of the desired product as an oil which solidified on standing.
후처리
- temperaturecooled to ambient temperature
- concentrationconcentrated
- additionThe remaining residue was diluted with water, 1M HCl and ethyl acetate
- customThe layers were separated
- extractionthe aqueous phase was extracted once more with ethyl acetate
- dry with materialThe combined organics were dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated
- customto give the crude product which
- customwas purified via column chromatography (silica gel, 50% EtOAc/hexanes)
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-3d71513c1a2c4c63b6c17463a7c809b7
- 출처 데이터셋
- uspto-grants-2015_10
- 특허 번호
- US09150556B2
반응 노트
불러오는 중…