5-[4-(6,6-Dimethyl-5,6,7,8-tetrahydroquinazolin-4-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepin-7-yl]-3-nitropyridin-2-amine → 5-[4-(6,6-Dimethyl-5,6,7,8-tetrahydroquinazolin-4-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepin-7-yl]pyridine-2,3-diamine
반응식
[CH3:1][C:2]1([CH3:33])[CH2:11][CH2:10][C:9]2[N:8]=[CH:7][N:6]=[C:5]([N:12]3[CH2:18][C:17]4[CH:19]=[C:20]([C:23]5[CH:24]=[C:25]([N+:30]([O-])=O)[C:26]([NH2:29])=[N:27][CH:28]=5)[CH:21]=[CH:22][C:16]=4[O:15][CH2:14][CH2:13]3)[C:4]=2[CH2:3]1>[Pd].CO>[CH3:1][C:2]1([CH3:33])[CH2:11][CH2:10][C:9]2[N:8]=[CH:7][N:6]=[C:5]([N:12]3[CH2:18][C:17]4[CH:19]=[C:20]([C:23]5[CH:24]=[C:25]([NH2:30])[C:26]([NH2:29])=[N:27][CH:28]=5)[CH:21]=[CH:22][C:16]=4[O:15][CH2:14][CH2:13]3)[C:4]=2[CH2:3]1참가 물질
4
반응물 1
생성물 1
시약·촉매·용매 2
실험 절차
A mixture of 5-[4-(6,6-dimethyl-5,6,7,8-tetrahydroquinazolin-4-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepin-7-yl]-3-nitropyridin-2-amine (0.63 g, 1.4 mmol), 10% palladium on charcoal (0.50 g) in 30 mL of methanol was shaken in a Parr hydrogenation at 38 psi for 18 hours. The reaction mixture was filtered through a pad of celite and concentrated to give to give 5-[4-(6,6-dimethyl-5,6,7,8-tetrahydroquinazolin-4-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepin-7-yl]pyridine-2,3-diamine (0.58 g, 99% yield). MS (EI) for C24H28N6O: 417 (MH+).
후처리
- filtrationThe reaction mixture was filtered through a pad of celite
- concentrationconcentrated
- customto give
출처 및 근거
- ORD 기록
- ord-90663d843ee34125bca8bd9eedb3e59a
- 출처 데이터셋
- uspto-grants-2014_02
- 특허 번호
- US08648066B2
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