4-Chlorobenzylamine → HCID 59474761, compound

HRID 1966546Notes

Reaction equation

HRID 1966546 reaction equation
Cl[C:2]1[C:11]2[C:6](=[C:7]([S: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]([S: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

3

Reactant 2

HCID 660364-ChlorobenzylamineHCID 2331984-chloro-2-methyl-8-methylsulfanylquinoline

Product 1

HCID 59474761HCID 59474761, compound

Procedure

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

Workup

  1. customPreparation

Sources & evidence

ORD record
ord-499409afbfec41679a71293e63d7f384
Source dataset
uspto-grants-2013_04
Patent number
US08420670B2

Reaction notes

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