4-Chlorobenzylamine → (4-Chlorobenzyl)-(2-methyl-8-methoxyquinolin-4-yl)amine

HRID 1966547Notes

Reaction equation

Cl[C:2]1[C:11]2[C:6](=[C:7]([O:12][CH3:13])[CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([CH3:14])[CH:3]=1.[Cl:15][C:16]1[CH:23]=[CH:22][C:19]([CH2:20][NH2:21])=[CH:18][CH:17]=1>>[Cl:15][C:16]1[CH:23]=[CH:22][C:19]([CH2:20][NH:21][C:2]2[C:11]3[C:6](=[C:7]([O:12][CH3:13])[CH:8]=[CH:9][CH:10]=3)[N:5]=[C:4]([CH3:14])[CH:3]=2)=[CH:18][CH:17]=1

Participants

Reactant 2

HCID 660364-Chlorobenzylamine

HCID 8075834-Chloro-8-methoxy-2-methylquinoline

Product 1

HCID 59474794(4-Chlorobenzyl)-(2-methyl-8-methoxyquinolin-4-yl)amine

Procedure

Preparation was made using a similar procedure as described in example 1, method 1.3. Starting materials were 4-chloro-2-methyl-8-methoxyquinoline and 4-chlorobenzylamine.

Workup

customPreparation

Sources & evidence

ORD record: ord-ab2921d1ce5a49d9a4c91a71f7957be9
Source dataset: uspto-grants-2013_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08420670B2

Reaction notes

Loading…