6,7,8,9-tetrahydro-5H-benzo(7)annulen-5-amine → HCID 22742690, compound

HRID 48708Notes

Reaction equation

HRID 48708 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].[CH:33]1[C:38]2[CH2:39][CH2:40][CH2:41][CH2:42][CH:43]([NH2:44])[C:37]=2[CH:36]=[CH:35][CH:34]=1>>[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:44][CH:43]1[C:37]2[CH:36]=[CH:35][CH:34]=[CH:33][C:38]=2[CH2:39][CH2:40][CH2:41][CH2:42]1)=[O:31]

Participants

4

Reactant 3

HCID 252446,7,8,9-tetrahydro-5H-benzo(7)annulen-5-amineHCID 61147Bromoacetyl bromideHCID 227427201-(3,4-Dimethoxy-benzyl)-6-methoxy-7-isopropoxy-1,2,3,4-tetrahydroisoquinoline

Product 1

HCID 22742690HCID 22742690, compound

Procedure

prepared by reaction of 1-(3,4-Dimethoxy-benzyl)-6-methoxy-7-isopropoxy-1,2,3,4-tetrahydroisoquinoline and 2-bromoacetyl bromide with 6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ylamine

Sources & evidence

ORD record
ord-c841511f022649c58e1a68da68648083
Source dataset
uspto-grants-2004_03
Patent number
US06703392B2

Reaction notes

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