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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375756Generated: November 1, 2026

Dimethyl Sulfoxide → 4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,3-dimethylaniline

https://huagongshe.com/reaction/1375756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Reactant4-Amino-2,3-xylenol hydrochlorideHCID 22667220—
SolventWaterHCID 962—
Product4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,3-dimethylanilineHCID 2189043965%

Reaction Conditions

Temperature50 °C

Reaction Steps

Sodium hydride (60 wt %, 0.72 g) was added to dimethyl sulfoxide (10 ml). The mixture was stirred at 50° C. for 30 min and was then cooled to room temperature. 4-Amino-2,3-dimethylphenol hydrochloride (1.55 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 methanol was added to the residue. The precipitated crystal was collected by suction filtration to give 0.94 g (yield 65%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169789B2
Source datasetuspto-grants-2007_01
ORD IDord-3ee77c3ad2454349b0aae4e73b63683a
Source noteuspto-grants-2007_01