N-Methylhomoveratrylamine → HCID 20433751, compound

HRID 1154652Notes

Reaction equation

[CH2:1]([O:4][C:5]1[CH:6]=[CH:7][C:8]2[CH:14]=[CH:13][N:12]([CH2:15][CH2:16][Cl:17])[C:11](=[O:18])[CH2:10][C:9]=2[CH:19]=1)[CH2:2][CH3:3].[CH3:20][NH:21][CH2:22][CH2:23][C:24]1[CH:29]=[CH:28][C:27]([O:30][CH3:31])=[C:26]([O:32][CH3:33])[CH:25]=1>>[ClH:17].[CH2:1]([O:4][C:5]1[CH:6]=[CH:7][C:8]2[CH:14]=[CH:13][N:12]([CH2:15][CH2:16][N:21]([CH3:20])[CH2:22][CH2:23][C:24]3[CH:29]=[CH:28][C:27]([O:30][CH3:31])=[C:26]([O:32][CH3:33])[CH:25]=3)[C:11](=[O:18])[CH2:10][C:9]=2[CH:19]=1)[CH2:2][CH3:3]

Participants

Reactant 2

HCID 77039N-Methylhomoveratrylamine

HCID 20433728HCID 20433728, compound

Product 1

HCID 20433751HCID 20433751, compound

Procedure

This compound was prepared analogous to Example 1(b) from 1-(8-propoxy-1,3-dihydro-2H-3-benzazepin-2-on-3-yl)-2-chloro-ethane and N-methyl-N-[2-(3,4-dimethoxyphenyl)-ethyl]-amine.

Sources & evidence

ORD record: ord-3097424ac55741d38eddbcf0e29a1cd8
Source dataset: uspto-grants-1984_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04490369

Reaction notes

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