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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008329Generated: October 27, 2026

Sodium hydride → 4-{[7-(Benzyloxy)-6-methoxy-4-quinolyl]oxy}-2,3-dimethylaniline

https://huagongshe.com/reaction/1008329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-HydroxyxylidineHCID 76542—
ReactantSodium BicarbonateHCID 516892—
Reactant7-(Benzyloxy)-4-chloro-6-methoxyquinolineHCID 22646562—
SolventDimethyl SulfoxideHCID 679—
Product4-{[7-(Benzyloxy)-6-methoxy-4-quinolyl]oxy}-2,3-dimethylanilineHCID 2266715049%

Reaction Steps

Sodium hydride (60 wt %, 0.32 g) was added to dimethyl sulfoxide (6 ml), and the mixture was stirred at room temperature for 30 min. 4-Amino-2,3-dimethylphenol (1.10 g) was then added thereto, and the mixture was stirred at room temperature for 10 min. Next, 7-(benzyloxy)-4-chloro-6-methoxyquinoline (1.20 g) was added thereto, and the mixture was stirred at 110° C. for 6 hr. A saturated aqueous sodium hydrogencarbonate solution was added to the reaction solution, followed by extraction with chloroform. The chloroform layer was dried over anhydrous magnesium 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 (6/1) to give 0.78 g (yield 49%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797823B1
Source datasetuspto-grants-2004_09
ORD IDord-6c99965b8db74e70a3c2dc5c659be044
Source noteuspto-grants-2004_09