7-Nitro-3-(6-nitroquinol-2-ylmethyl)-1,2,4,5-tetrahydro-3H-3-benzazepine → 7-amino-3-(6-aminoquinol-2-ylmethyl)-1,2,4,5-tetrahydro-3H-3-benzazepine
Reaction equation
[N+:1]([C:4]1[CH:28]=[CH:27][C:7]2[CH2:8][CH2:9][N:10]([CH2:13][C:14]3[CH:23]=[CH:22][C:21]4[C:16](=[CH:17][CH:18]=[C:19]([N+:24]([O-])=O)[CH:20]=4)[N:15]=3)[CH2:11][CH2:12][C:6]=2[CH:5]=1)([O-])=O>C(O)C.[H][H].[Pd]>[NH2:1][C:4]1[CH:28]=[CH:27][C:7]2[CH2:8][CH2:9][N:10]([CH2:13][C:14]3[CH:23]=[CH:22][C:21]4[C:16](=[CH:17][CH:18]=[C:19]([NH2:24])[CH:20]=4)[N:15]=3)[CH2:11][CH2:12][C:6]=2[CH:5]=1Participants
4
Procedure
The title compound was prepared similarly to the procedure of Preparation 5 by the hydrogenation of 7-nitro-3-(6-nitroquinol-2-ylmethyl)-1,2,4,5-tetrahydro-3H-3-benzazepine using H2 /Pd/C in ethanol.
Sources & evidence
- ORD record
- ord-2a12a7d8dccf4af790d947cddcc57da7
- Source dataset
- uspto-grants-1989_04
- Patent number
- US04822793
Reaction notes
Loading…