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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375767Generated: October 27, 2026

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

https://huagongshe.com/reaction/1375767

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 numberUS07169789B2
Source datasetuspto-grants-2007_01
ORD IDord-86d49f0fac4b46edb4730ae31e6ef456
Source noteuspto-grants-2007_01