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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008319Generated: October 31, 2026

Dimethyl Sulfoxide → 4-((6,7-Dimethoxyquinolin-4-yl)oxy)-2,5-dimethylaniline

https://huagongshe.com/reaction/1008319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
Reactant4-Amino-2,5-dimethylphenolHCID 76544—
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
SolventWaterHCID 962—
Product4-((6,7-Dimethoxyquinolin-4-yl)oxy)-2,5-dimethylanilineHCID 21890421—

Reaction Conditions

Temperature50 °C

Reaction Steps

Sodium hydride (60 wt %, 0.36 g) was added to dimethyl sulfoxide (10 ml), and the mixture was stirred at 50° C. for 30 min and was then cooled to room temperature. 4-Amino-2,5-dimethylphenol (1.23 g) was added to the cooled mixture, and the mixture was stirred at room temperature for 10 min. Next, 4-chloro-6,7-dimethoxyquinoline (1.00 g) was added thereto, and the mixture was stirred at 100° C. overnight. Water was added to the reaction solution, followed by extraction with chloroform. The chloroform layer was then washed with a saturated aqueous sodium hydrogencarbonate solution and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by chromatography on silica gel by development with chloroform/acetone (1/1) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797823B1
Source datasetuspto-grants-2004_09
ORD IDord-1e3154ff2ec24f94afa1827cab384c47
Source noteuspto-grants-2004_09