Bromoacetyl bromide → 2-[1-(Diphenyl-methyl)-5,8-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-N-(2-methoxy-benzyl)-acetamide

HRID 48668Notes

Reaction equation

HRID 48668 reaction equation
[C:1]1([CH:7]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[CH:8]2[C:17]3[C:12](=[C:13]([O:20][CH3:21])[CH:14]=[CH:15][C:16]=3[O:18][CH3:19])[CH2:11][CH2:10][NH:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Br[CH2:29][C:30](Br)=[O:31].[CH3:33][O:34][C:35]1[CH:42]=[CH:41][CH:40]=[CH:39][C:36]=1[CH2:37][NH2:38]>>[C:22]1([CH:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[CH:8]2[C:17]3[C:12](=[C:13]([O:20][CH3:21])[CH:14]=[CH:15][C:16]=3[O:18][CH3:19])[CH2:11][CH2:10][N:9]2[CH2:29][C:30]([NH:38][CH2:37][C:36]2[CH:39]=[CH:40][CH:41]=[CH:42][C:35]=2[O:34][CH3:33])=[O:31])[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1

Participants

4

Procedure

prepared by reaction of 1-(Diphenyl-methyl)-5,8-dimethoxy-1,2,3,4-tetrahydroisoquinoline and 2-bromoacetyl bromide with 2-methoxy-benzylamine

Sources & evidence

ORD record
ord-ad5b6b5553fd410c9dd9adca23a12f5e
Source dataset
uspto-grants-2004_03
Patent number
US06703392B2

Reaction notes

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