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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229027Generated: October 30, 2026

4-Chloro-6,7-dimethoxyquinoline → 6,7-Dimethoxy-4-(quinolin-2-ylsulfanyl)-quinoline

https://huagongshe.com/reaction/229027

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
ReactantHCID 178418736HCID 178418736—
SolventAcetonitrileHCID 6342—
Product6,7-Dimethoxy-4-(quinolin-2-ylsulfanyl)-quinolineHCID 2307831910%

Reaction Steps

2-Quinolinethiol (87 mg) and 4-chloro-6,7-dimethoxyquinoline (100 mg) were suspended in acetonitrile (3 ml), and the suspension was stirred at room temperature overnight. The solvent was removed by distillation under the reduced pressure. Water was added to the residue, and the mixture was neutralized with sodium hydrogencarbonate and was then extracted with chloroform. The chloroform layer was washed with water and saturated brine and was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography using acetone-chloroform to give the title compound (15 mg, yield 10%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-88a8020c274944bfa8f874a75297eb2c
Source noteuspto-grants-2009_07