HCID 12381618, compound → 1-[7,8-Ethylenedioxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on-3-yl]-3-[N-methyl-N-(6,7-dimethoxy-1,2,3,4-tetrahydronaphth-2-yl)-amino]-propane

HRID 1380898Notes

Reaction equation

HRID 1380898 reaction equation
[CH2:1]1[CH2:20][O:19][C:18]2[C:3](=[CH:4][C:5]3[CH2:11][CH2:10][N:9]([CH2:12][CH2:13][CH2:14]Cl)[C:8](=[O:16])[CH2:7][C:6]=3[CH:17]=2)[O:2]1.[CH3:21][O:22][C:23]1[CH:24]=[C:25]2[C:30](=[CH:31][C:32]=1[O:33][CH3:34])[CH2:29][CH:28]([NH:35][CH3:36])[CH2:27][CH2:26]2>>[CH2:1]1[CH2:20][O:19][C:18]2[C:3](=[CH:4][C:5]3[CH2:11][CH2:10][N:9]([CH2:12][CH2:13][CH2:14][N:35]([CH3:36])[CH:28]4[CH2:27][CH2:26][C:25]5[C:30](=[CH:31][C:32]([O:33][CH3:34])=[C:23]([O:22][CH3:21])[CH:24]=5)[CH2:29]4)[C:8](=[O:16])[CH2:7][C:6]=3[CH:17]=2)[O:2]1

Participants

3

Procedure

The title compound is prepared from 1-[7,8-ethylenedioxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-on-3-yl]-3-chloropropane and 6,7-dimethoxy-2-methylamino-1,2,3,4-tetrahydronaphthalene analogously to Example 1. Mp: 152°-157° C.

Sources & evidence

ORD record
ord-1dbd4960a207443fbe0daa3804abbdc3
Source dataset
uspto-grants-1986_04
Patent number
US04584293

Reaction notes

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