N-Methylhomoveratrylamine → HCID 20433810, compound

HRID 1154672Notes

Reaction equation

[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[CH:12]=[CH:11][N:10]([CH2:13][CH2:14][CH2:15][Cl:16])[C:9](=[O:17])[CH2:8][C:7]=2[C:18]=1[O:19][CH3:20].[CH3:21][NH:22][CH2:23][CH2:24][C:25]1[CH:30]=[CH:29][C:28]([O:31][CH3:32])=[C:27]([O:33][CH3:34])[CH:26]=1>>[ClH:16].[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[CH:12]=[CH:11][N:10]([CH2:13][CH2:14][CH2:15][N:22]([CH3:21])[CH2:23][CH2:24][C:25]3[CH:30]=[CH:29][C:28]([O:31][CH3:32])=[C:27]([O:33][CH3:34])[CH:26]=3)[C:9](=[O:17])[CH2:8][C:7]=2[C:18]=1[O:19][CH3:20]

Participants

Reactant 2

HCID 77039N-Methylhomoveratrylamine

HCID 20433713HCID 20433713, compound

Product 1

HCID 20433810HCID 20433810, compound

Procedure

This compound was prepared analogous to Example 1(b) by reacting 1-(8,9-dimethoxy-1,3-dihydro-2H-3-benzazepin-2on-3yl)-3-chloro-propane with N-methyl-N-[2-(3,4-dimethoxy-phenyl)-ethyl]-amine.

Workup

customThis compound was prepared analogous to Example 1(b)

Sources & evidence

ORD record: ord-8058ce5473f54a79b9acc2cd5d1e5b4f
Source dataset: uspto-grants-1984_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04490369

Reaction notes

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