Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375765Generated: October 30, 2026

Dimethyl Sulfoxide → 4-{[7-(Benzyloxy)-6-methoxy-4-quinolyl]oxy}-2-chloroaniline

https://huagongshe.com/reaction/1375765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium hydrideHCID 24758—
Reactant4-Amino-3-chlorophenol hydrochlorideHCID 12598190—
Reactant7-(Benzyloxy)-4-chloro-6-methoxyquinolineHCID 22646562—
SolventWaterHCID 962—
Product4-{[7-(Benzyloxy)-6-methoxy-4-quinolyl]oxy}-2-chloroanilineHCID 2266706266%

Reaction Conditions

Temperature60 °C

Reaction Steps

Sodium hydride (60 wt %, 320 mg) was added to dimethyl sulfoxide (3.6 ml), and the mixture was stirred at 60° C. for 30 min and was then cooled to room temperature. Next, 4-amino-3-chlorophenol hydrochloride (720 mg) was added thereto, and the mixture was stirred at room temperature for 10 min. 7-(Benzyloxy)-4-chloro-6-methoxyquinoline (600 mg) was then added thereto, and the mixture was stirred at 105° C. for 22 hr. 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 to prepare a suspension. The precipitated crystal was collected by suction filtration to give 533 mg (yield 66%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169789B2
Source datasetuspto-grants-2007_01
ORD IDord-e1fbd803baef4e2cabf077a7465f830c
Source noteuspto-grants-2007_01