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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433730Generated: October 26, 2026

Ethyl Acetate → 4-(4-Amino-2,3-dimethylphenoxy)-7-benzyloxy-6-cyanoquinoline

https://huagongshe.com/reaction/1433730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant4-HydroxyxylidineHCID 76542—
Reactant7-Benzyloxy-4-chloro-6-cyanoquinolineHCID 22646519—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product4-(4-Amino-2,3-dimethylphenoxy)-7-benzyloxy-6-cyanoquinolineHCID 2293651642.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-Amino-2,3-xylenol (2.80 g) purchased from Tokyo Chemical Industries was dissolved in dimethylsulfoxide (15 ml), and after gradually adding sodium hydride (816 mg) at room temperature, the mixture was stirred for 20 minutes. 7-Benzyloxy-4-chloro-6-cyanoquinoline (3.0 g) was added, and the mixture was heated at 100° C. for 4 hours while stirring. After cooling to room temperature, the reaction solution was distributed between ethyl acetate and water, and the organic layer was washed with water, 1N aqueous sodium hydroxide and saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off, and the obtained crude product was washed with ethyl acetate to obtain the title compound (1.72 g) as light brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612092B2
Source datasetuspto-grants-2009_11
ORD IDord-13848e6ed9fd4848965176d703f9b343
Source noteuspto-grants-2009_11