3-Methoxybenzylamine → HCID 25235662, compound

HRID 1949047Notes

Reaction equation

HRID 1949047 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:16]=[C:17]([CH:20]=[CH:21][CH:22]=1)[CH2:18][NH2:19].[N:23]1[CH:28]=[CH:27][CH:26]=[C:25]([CH2:29][NH2:30])[CH:24]=1>>[CH3:13][O:14][C:15]1[CH:16]=[C:17]([CH:20]=[CH:21][CH:22]=1)[CH2:18][NH:19][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([NH:30][CH2:29][C:25]3[CH:24]=[N:23][CH:28]=[CH:27][CH:26]=3)[CH:8]=2)[N:3]=1

Participants

4

Reactant 3

HCID 211563-MethoxybenzylamineHCID 310183-PyridinemethanamineHCID 6075022,6-Dichloroquinoline

Product 1

HCID 25235662HCID 25235662, compound

Procedure

The title compound, MS: m/e=371.4 (M+H+), was prepared in accordance with the general method of example 1 from 2,6-dichloroquinoline, 3-methoxybenzylamine and 3-picolylamine.

Sources & evidence

ORD record
ord-f9b53fb6096543e59216f564a59e75ea
Source dataset
uspto-grants-2013_03
Patent number
US08399674B2

Reaction notes

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