2-Methoxybenzylamine → HCID 68434986, compound

HRID 1170080Notes

Reaction equation

HRID 1170080 reaction equation
Br[C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][C:6](Cl)=[N:7]2.[CH3:13][O:14][C:15]1[CH:22]=[CH:21][CH:20]=[CH:19][C:16]=1[CH2:17][NH2:18].[CH3:23][N:24]1[C:28]([CH2:29][NH2:30])=[CH:27][N:26]=[CH:25]1>>[CH3:13][O:14][C:15]1[CH:22]=[CH:21][CH:20]=[CH:19][C:16]=1[CH2:17][NH:18][C:6]1[CH:5]=[CH:4][C:3]2[C:2]([NH:30][CH2:29][C:28]3[N:24]([CH3:23])[CH:25]=[N:26][CH:27]=3)=[CH:11][CH:10]=[CH:9][C:8]=2[N:7]=1

Participants

4

Reactant 3

HCID 812922-MethoxybenzylamineHCID 27954241-Methyl-5-aminomethylimidazoleHCID 142210335-Bromo-2-chloroquinoline

Product 1

HCID 68434986HCID 68434986, compound

Procedure

The title compound, MS: m/e=374.4 (M+H+), was prepared in accordance with the general method of example 1 from 5-bromo-2-chloroquinoline, 2-methoxybenzylamine and (1-methyl-1H-imidazol-5-yl)methylamine.

Sources & evidence

ORD record
ord-7ae2ee14c2a046a9a13cf6835761ce31
Source dataset
uspto-grants-2010_11
Patent number
US07825253B2

Reaction notes

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