2-Benzylamino-6,7-dimethoxy-1,2,3,4-tetrahydronaphthalene → 1-[7,8-Dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on-3-yl]-3-[N-benzyl-N-(6,7-dimethoxy-1,2,3,4-tetrahydronaphth-2-yl)-amino]-propane
Reaction equation
[CH2:1]([NH:8][CH:9]1[CH2:18][CH2:17][C:16]2[C:11](=[CH:12][C:13]([O:21][CH3:22])=[C:14]([O:19][CH3:20])[CH:15]=2)[CH2:10]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:23][O:24][C:25]1[C:40]([O:41][CH3:42])=[CH:39][C:28]2[CH2:29][C:30](=[O:38])[N:31]([CH2:34][CH2:35][CH2:36]Cl)[CH2:32][CH2:33][C:27]=2[CH:26]=1>C(Cl)Cl>[CH3:23][O:24][C:25]1[C:40]([O:41][CH3:42])=[CH:39][C:28]2[CH2:29][C:30](=[O:38])[N:31]([CH2:34][CH2:35][CH2:36][N:8]([CH2:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)[CH:9]3[CH2:18][CH2:17][C:16]4[C:11](=[CH:12][C:13]([O:21][CH3:22])=[C:14]([O:19][CH3:20])[CH:15]=4)[CH2:10]3)[CH2:32][CH2:33][C:27]=2[CH:26]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound is prepared analogously to Example 1 by reacting 2-benzylamino-6,7-dimethoxy-1,2,3,4-tetrahydronaphthalene with 1-(7,8-dimethoxy-1,3,4,5-tetra hydro-2H-3-benzazepin-2-on-3-yl)-3-chloropropane. IR spectrum (methylene chloride): 1645 cm-1 (C=O).
Sources & evidence
- ORD record
- ord-8cdfe36a18fb474f997856eb5335c954
- Source dataset
- uspto-grants-1986_04
- Patent number
- US04584293
Reaction notes
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