2-(3,4-Dimethoxyphenylamino)-ethylamine → N-[3-(7,8-Dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-1,2-dion-3-yl)-propyl]-2-(3,4-dimethoxyphenylamino)-ethylamine
Reaction equation
[CH3:1][O:2][C:3]1[C:19]([O:20][CH3:21])=[CH:18][C:6]2[C:7](=[O:17])[C:8](=[O:16])[N:9]([CH2:12][CH2:13][CH2:14]Cl)[CH2:10][CH2:11][C:5]=2[CH:4]=1.[CH3:22][O:23][C:24]1[CH:25]=[C:26]([NH:32][CH2:33][CH2:34][NH2:35])[CH:27]=[CH:28][C:29]=1[O:30][CH3:31]>>[CH3:1][O:2][C:3]1[C:19]([O:20][CH3:21])=[CH:18][C:6]2[C:7](=[O:17])[C:8](=[O:16])[N:9]([CH2:12][CH2:13][CH2:14][NH:35][CH2:34][CH2:33][NH:32][C:26]3[CH:27]=[CH:28][C:29]([O:30][CH3:31])=[C:24]([O:23][CH3:22])[CH:25]=3)[CH2:10][CH2:11][C:5]=2[CH:4]=1Participants
3
Procedure
The title compound is prepared from 3-(7,8-dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-1,2-dion-3-yl)-propyl chloride and 2-(3,4-dimethoxyphenylamino)-ethylamine analogously to Example 6.
Sources & evidence
- ORD record
- ord-d74dd6f7b05748f0a9ceb6f64d54c02b
- Source dataset
- uspto-grants-1986_08
- Patent number
- US04604389
Reaction notes
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