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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433737Generated: October 25, 2026

Ethyl Acetate → N6-Ethyl-4-(4-amino-3-chlorophenoxy)-7-benzyloxy-6-quinolinecarboxamide

https://huagongshe.com/reaction/1433737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant4-Amino-3-chlorophenolHCID 87184—
ReactantN6-Ethyl-7-benzyloxy-4-chloro-6-quinolinecarboxamideHCID 22936981—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductN6-Ethyl-4-(4-amino-3-chlorophenoxy)-7-benzyloxy-6-quinolinecarboxamideHCID 2293631792%

Reaction Conditions

Temperature100 °C

Reaction Steps

After dissolving 4-amino-3-chlorophenol (379 mg, 2.64 mmol) in dimethylsulfoxide (10 ml), sodium hydride (106 mg, 2.64 mmol) was gradually added at room temperature and the mixture was stirred for 30 minutes. N6-Ethyl-7-benzyloxy-4-chloro-6-quinolinecarboxamide (720 mg, 2.11 mmol) was added, and the mixture was heated at 100° C. for 2 hours while stirring. Upon cooling to room temperature, the reaction solution was distributed between ethyl acetate and water, and the organic layer was washed with ammonia water, water and saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off, suspended in ethyl acetate and diluted with hexane, and the crystals were filtered out and blow-dried to obtain the title compound (870 mg, 1.94 mmol, 92%) as brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612092B2
Source datasetuspto-grants-2009_11
ORD IDord-6d15e80a6b83484799cc9a1178f2f1a2
Source noteuspto-grants-2009_11