2-Methoxybenzylamine → HCID 178489483, compound

HRID 1170150Notes

Reaction equation

HRID 1170150 reaction equation
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](Cl)=[N:9]2)([O-])=O.[CH3:15][O:16][C:17]1[CH:24]=[CH:23][CH:22]=[CH:21][C:18]=1[CH2:19][NH2:20].[CH3:25][C:26]1[N:27]=[CH:28][NH:29][C:30]=1[CH:31]=O>>[CH3:15][O:16][C:17]1[CH:24]=[CH:23][CH:22]=[CH:21][C:18]=1[CH2:19][NH:20][C:8]1[CH:7]=[CH:6][C:5]2[C:4]([NH:1][CH2:25][C:26]3[NH:27][CH:28]=[N:29][C:30]=3[CH3:31])=[CH:13][CH:12]=[CH:11][C:10]=2[N:9]=1

Participants

4

Reactant 3

HCID 812922-MethoxybenzylamineHCID 3192512-Chloro-5-nitroquinolineHCID 27958875-Methyl-1H-imidazole-4-carbaldehyde

Product 1

HCID 178489483HCID 178489483, compound

Procedure

The title compound, MS: m/e=374.4 (M+H+), was prepared from 5-nitro-2-chloroquinoline, 2-methoxybenzylamine and 4-methyl-5-imidazole-carboxaldehyde as described in example 26.

Sources & evidence

ORD record
ord-0a3cb97c65f941d1b976cb91b452d46f
Source dataset
uspto-grants-2010_11
Patent number
US07825253B2

Reaction notes

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