(+-)-Tetrahydropapaverine → HCID 22742600, compound

HRID 48635Notes

Reaction equation

[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:21]=[CH:22][C:23]=1[O:24][CH3:25])[CH2:6][CH:7]1[C:16]2[C:11](=[CH:12][C:13]([O:19][CH3:20])=[C:14]([O:17][CH3:18])[CH:15]=2)[CH2:10][CH2:9][NH:8]1.Br[CH2:27][C:28](Br)=[O:29].[CH3:31][C:32]1[CH:41]=[C:40]([CH3:42])[CH:39]=[C:38]2[C:33]=1[CH2:34][CH2:35][CH2:36][CH:37]2[NH2:43]>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:21]=[CH:22][C:23]=1[O:24][CH3:25])[CH2:6][CH:7]1[C:16]2[C:11](=[CH:12][C:13]([O:19][CH3:20])=[C:14]([O:17][CH3:18])[CH:15]=2)[CH2:10][CH2:9][N:8]1[CH2:27][C:28]([NH:43][CH:37]1[C:38]2[C:33](=[C:32]([CH3:31])[CH:41]=[C:40]([CH3:42])[CH:39]=2)[CH2:34][CH2:35][CH2:36]1)=[O:29]

Participants

Reactant 3

HCID 5418(+-)-Tetrahydropapaverine

HCID 61147Bromoacetyl bromide

HCID 111267915,7-Dimethyl-1,2,3,4-tetrahydronaphthalen-1-amine

Product 1

HCID 22742600HCID 22742600, compound

Procedure

prepared by reaction of 1-(3,4-Dimethoxy-benzyl)-6,7-dimethoxy-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-708e144e4b894a0781effcd1b71e8021
Source dataset: uspto-grants-2004_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06703392B2

Reaction notes

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