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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853563Generated: October 29, 2026

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

https://huagongshe.com/reaction/853563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
Reactant4-Amino-3-chlorophenolHCID 87184—
ReactantN6-Methyl-7-(benzyloxy)-4-chloro-6-quinolinecarboxamideHCID 22936745—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductN6-Methyl-4-(4-amino-3-chlorophenoxy)-7-(benzyloxy)-6-quinolinecarboxamideHCID 2293633787.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

After dissolving 4-amino-3-chlorophenol (624 mg, 4.35 mmol) in dimethylsulfoxide (15ml), sodiumhydride (174 mg, 4.35 mmol) was gradually added at room temperature and the mixture was stirred for 30 minutes. N6-Methyl-7-(benzyloxy)-4-chloro-6-quinolinecarboxamide (947 mg, 2.90 mmol) was added, and the mixture was heated at 100° C. while stirring for 2 hours. After cooling to room temperature, the reaction solution was distributed between ethyl acetate and water, and the organic layer was washed with 1N aqueous sodium hydroxide, water and saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled off, the residue was suspended in ethyl acetate, the suspension was diluted with hexane and the crystals were filtered out and blow-dried to obtain the title compound (1.098 g, 2.53 mmol, 87.3%) as light brown crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253286B2
Source datasetuspto-grants-2007_08
ORD IDord-8b610e0d254649daa6a83f3083853a2d
Source noteuspto-grants-2007_08