Hydroxylamine → 5-[2-(2-Amino-1,1-dimethyl-ethyl)-5-pyridin-4-yl-1H-imidazol-4-yl]-indan-1-one Oxime
반응식
[NH2:1][CH2:2][C:3]([C:6]1[NH:7][C:8]([C:21]2[CH:26]=[CH:25][N:24]=[CH:23][CH:22]=2)=[C:9]([C:11]2[CH:12]=[C:13]3[C:17](=[CH:18][CH:19]=2)[C:16](=O)[CH2:15][CH2:14]3)[N:10]=1)([CH3:5])[CH3:4].[NH2:27][OH:28]>C(O)C>[NH2:1][CH2:2][C:3]([C:6]1[NH:7][C:8]([C:21]2[CH:26]=[CH:25][N:24]=[CH:23][CH:22]=2)=[C:9]([C:11]2[CH:12]=[C:13]3[C:17](=[CH:18][CH:19]=2)[C:16](=[N:27][OH:28])[CH2:15][CH2:14]3)[N:10]=1)([CH3:5])[CH3:4]참가 물질
4
실험 절차
To a solution of the product of Step 6 (0.12 g, 0.350 mmol) in ethanol (5 ml) at 80° C. was added aqueous hydroxylamine (0.07 g, 1.04 mmol, 50% in water). After 30 min the mixture was cooled to room temperature and concentrated in vacuo to give the title compound, (0.124 g, 100%) as a yellow solid; MS(AP+) m/e 362 [M+H]+.
후처리
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-25eb1dc8e14145a88e72949322a555dc
- 출처 데이터셋
- uspto-grants-2007_04
- 특허 번호
- US07199137B2
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