3-Methoxybenzylamine → HCID 25235529, compound

HRID 1949007Notes

Reaction equation

HRID 1949007 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][O:24][C:25]1[CH:26]=[C:27]([CH:30]=[CH:31][CH:32]=1)[CH2:28][NH2:29]>>[CH3:23][O:24][C:25]1[CH:26]=[C:27]([CH:30]=[CH:31][CH:32]=1)[CH2:28][NH:29][C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[N:3]=[C:2]([NH:18][CH2:17][C:16]1[CH:19]=[CH:20][CH:21]=[CH:22][C:15]=1[O:14][CH3:13])[CH:11]=[CH:10]2

Participants

4

Reactant 3

HCID 211563-MethoxybenzylamineHCID 812922-MethoxybenzylamineHCID 6075022,6-Dichloroquinoline

Product 1

HCID 25235529HCID 25235529, compound

Procedure

The title compound, MS: m/e=400.0 (M+H+), was prepared in accordance with the general method of example 1 from 2,6-dichloroquinoline, 2-methoxybenzylamine and 3-methoxybenzylamine.

Sources & evidence

ORD record
ord-2e93282b5b5142a79fb61a6860af06d9
Source dataset
uspto-grants-2013_03
Patent number
US08399674B2

Reaction notes

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