HCID 12843076, compound → HCID 13579654, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:18]([O:19][CH3:20])=[CH:17][C:6]2[CH2:7][C:8](=[O:16])[N:9]([CH2:12][CH2:13][CH2:14]Cl)[CH2:10][CH2:11][C:5]=2[CH:4]=1.[CH3:21][O:22][C:23]1[CH:24]=[C:25]2[C:30](=[CH:31][CH:32]=1)[CH2:29][CH:28]([NH:33][CH3:34])[CH2:27][CH2:26]2>C(N(CC)CC)C>[CH3:1][O:2][C:3]1[C:18]([O:19][CH3:20])=[CH:17][C:6]2[CH2:7][C:8](=[O:16])[N:9]([CH2:12][CH2:13][CH2:14][N:33]([CH3:34])[CH:28]3[CH2:27][CH2:26][C:25]4[C:30](=[CH:31][CH:32]=[C:23]([O:22][CH3:21])[CH:24]=4)[CH2:29]3)[CH2:10][CH2:11][C:5]=2[CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound is prepared analogously to Example 1 by reacting 1-(7,8-dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on-3-yl)-3-chloropropane, triethylamine and 6-methoxy-2-methylamino-1,2,3,4-tetrahydronaphthalene. Mp: 122°-123° C. (decomp.).
Sources & evidence
- ORD record
- ord-e346dba586e64621a15a6b026038f229
- Source dataset
- uspto-grants-1986_04
- Patent number
- US04584293
Reaction notes
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