2-Methoxybenzylamine → HCID 68574735, compound

HRID 1949012Notes

Reaction equation

HRID 1949012 reaction equation
Cl[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7](Cl)[CH:8]=2)[N:3]=1.[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:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([NH:30][CH2:29][C:28]3[N:24]([CH3:23])[CH:25]=[N:26][CH:27]=3)[CH:8]=2)[N:3]=1

Participants

4

Reactant 3

HCID 812922-MethoxybenzylamineHCID 6075022,6-DichloroquinolineHCID 27954241-Methyl-5-aminomethylimidazole

Product 1

HCID 68574735HCID 68574735, compound

Procedure

The title compound, MS: m/e=374.1 (M+H+), was prepared in accordance with the general method of example 1 from 2,6-dichloroquinoline, 2-methoxybenzylamine and (1-methyl-1H-imidazol-5-yl)methylamine.

Sources & evidence

ORD record
ord-d5e9ddc530c947c68f8d548b4050e6d2
Source dataset
uspto-grants-2013_03
Patent number
US08399674B2

Reaction notes

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