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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229026Generated: October 25, 2026

Ethanol → Ethyl 2-(6,7-dimethoxy-quinolin-4-ylsulfanyl)-5-fluoro-benzoate

https://huagongshe.com/reaction/229026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThionyl ChlorideHCID 24386—
Reactant2-(6,7-Dimethoxy-quinolin-4-ylsulfanyl)-5-fluoro-benzoic acidHCID 23078377—
ProductEthyl 2-(6,7-dimethoxy-quinolin-4-ylsulfanyl)-5-fluoro-benzoateHCID 2307832284%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(6,7-Dimethoxy-quinolin-4-ylsulfanyl)-5-fluoro-benzoic acid (76 mg) was suspended in ethanol (387 mg), and the suspension was cooled at 0° C. Thionyl chloride (50 mg) was gradually added dropwise thereto, and the mixture was then heated under reflux for 20 min. The solvent was removed by distillation under the reduced pressure, water was added to the residue, and the mixture was neutralized with a 20% aqueous sodium hydroxide solution and was then extracted with ethyl acetate. Next, the ethyl acetate layer was washed with water and saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography using acetone-hexane to give the title compound (68 mg, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-ab1cd4f2ce044492810a09c0dc77ac37
Source noteuspto-grants-2009_07