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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375755Generated: November 1, 2026

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

https://huagongshe.com/reaction/1375755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Reactant4-Amino-3-chlorophenol hydrochlorideHCID 12598190—
SolventWaterHCID 962—
Product4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2-chloroanilineHCID 1122122360.2%

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-3-chlorophenol hydrochloride (1.61 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 0.89 g (yield 60%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169789B2
Source datasetuspto-grants-2007_01
ORD IDord-0223e6b405c54bc992cb8e2e16a8f982
Source noteuspto-grants-2007_01