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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010451Generated: October 30, 2026

Ethyl Acetate → 4-(4-Aminophenoxy)-6-cyano-7-((2R)-oxiran-2-yl)methoxyquinoline

https://huagongshe.com/reaction/1010451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantGlycidyl tosylate, (R)-HCID 154187—
Reactant4-(4-Aminophenoxy)-6-cyano-7-hydroxyquinolineHCID 135829390—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(4-Aminophenoxy)-6-cyano-7-((2R)-oxiran-2-yl)methoxyquinolineHCID 8659148097%

Reaction Steps

After dissolving 4-(4-aminophenoxy)-6-cyano-7-hydroxyquinoline (277 mg, 1.00 mmol) in dimethylformamide (3.0 ml), sodium hydride (40 mg, 1.00 mmol, 60% in oil) was added at room temperature and the mixture was stirred. There was then added (2R)-oxiran-2-ylmethyl 4-methyl-1-benzenesulfonate (228 mg, 1.00 mmol), and the mixture was heated and stirred at 60° C. for 5 hours. After cooling to room temperature, the reaction solution was distributed between ethyl acetate and water. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate, and the solvent was distilled off to obtain the title compound (322 mg, 0.97 mmol, 97%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973160B2
Source datasetuspto-grants-2011_07
ORD IDord-35342a87e2b64fbca81e8c0e8d747b63
Source noteuspto-grants-2011_07