Bromoacetyl bromide → 2-[1-(3,4-Dimethoxy-benzyl)-6-methoxy-7-isopropoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(5,7-dimethyl-1,2,3,4-tetrahydronaphthalen-1-yl)-acetamide

HRID 48695Notes

Reaction equation

HRID 48695 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:23]=[CH:24][C:25]=1[O:26][CH3:27])[CH2:6][CH:7]1[C:16]2[C:11](=[CH:12][C:13]([O:21][CH3:22])=[C:14]([O:17][CH:18]([CH3:20])[CH3:19])[CH:15]=2)[CH2:10][CH2:9][NH:8]1.Br[CH2:29][C:30](Br)=[O:31].[CH3:33][C:34]1[CH:43]=[C:42]([CH3:44])[CH:41]=[C:40]2[C:35]=1[CH2:36][CH2:37][CH2:38][CH:39]2[NH2:45]>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:23]=[CH:24][C:25]=1[O:26][CH3:27])[CH2:6][CH:7]1[C:16]2[C:11](=[CH:12][C:13]([O:21][CH3:22])=[C:14]([O:17][CH:18]([CH3:20])[CH3:19])[CH:15]=2)[CH2:10][CH2:9][N:8]1[CH2:29][C:30]([NH:45][CH:39]1[C:40]2[C:35](=[C:34]([CH3:33])[CH:43]=[C:42]([CH3:44])[CH:41]=2)[CH2:36][CH2:37][CH2:38]1)=[O:31]

Participants

4

Reactant 3

HCID 61147Bromoacetyl bromideHCID 111267915,7-Dimethyl-1,2,3,4-tetrahydronaphthalen-1-amineHCID 227427201-(3,4-Dimethoxy-benzyl)-6-methoxy-7-isopropoxy-1,2,3,4-tetrahydroisoquinoline

Product 1

HCID 227426812-[1-(3,4-Dimethoxy-benzyl)-6-methoxy-7-isopropoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(5,7-dimethyl-1,2,3,4-tetrahydronaphthalen-1-yl)-acetamide

Procedure

prepared by reaction of 1-(3,4-Dimethoxy-benzyl)-6-methoxy-7-isopropoxy-1,2,3,4-tetrahydroisoquinoline and 2-bromoacetyl bromide with 5,7-dimethyl-1,2,3,4-tetrahydro-1-naphthylamine

Sources & evidence

ORD record
ord-853089d1ac0d4cfcab3b7d79763d33b9
Source dataset
uspto-grants-2004_03
Patent number
US06703392B2

Reaction notes

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