N-Methylbenzylamine → HCID 22742816, compound

HRID 48767Notes

Reaction equation

HRID 48767 reaction equation
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][CH:12]1[C:21]2[C:16](=[CH:17][C:18]([O:24][CH3:25])=[C:19]([O:22][CH3:23])[CH:20]=2)[CH2:15][CH2:14][NH:13]1.Br[CH2:27][C:28](Br)=[O:29].[CH2:31]([NH:38][CH3:39])[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][CH:12]1[C:21]2[C:16](=[CH:17][C:18]([O:24][CH3:25])=[C:19]([O:22][CH3:23])[CH:20]=2)[CH2:15][CH2:14][N:13]1[CH2:27][C:28]([N:38]([CH2:31][C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)[CH3:39])=[O:29]

Participants

4

Reactant 3

HCID 7669N-MethylbenzylamineHCID 61147Bromoacetyl bromideHCID 100247816,7-Dimethoxy-1-naphthalen-2-ylmethyl-1,2,3,4-tetrahydroisoquinoline

Product 1

HCID 22742816HCID 22742816, compound

Procedure

prepared by reaction of 1-(Naphthalen-2-yl-methyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline and 2-bromoacetyl bromide with N-benzyl-N-methyl-amine

Sources & evidence

ORD record
ord-14b61edd4f5f4067be04711bdbdbcd5b
Source dataset
uspto-grants-2004_03
Patent number
US06703392B2

Reaction notes

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