Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431598Generated: November 2, 2026

Tetrahydrofuran → 4-Chloro-5,7-difluoro-3-methyl-2-(5-(methylsulfonyl)pyridin-3-yl)quinoline

https://huagongshe.com/reaction/1431598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant4-Chloro-5,7-difluoro-3-methyl-2-(5-(methylthio)pyridin-3-yl)quinolineHCID 59631284—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product4-Chloro-5,7-difluoro-3-methyl-2-(5-(methylsulfonyl)pyridin-3-yl)quinolineHCID 67285711—

Reaction Steps

To a stirring suspension of 4-chloro-5,7-difluoro-3-methyl-2-(5-(methylthio)pyridin-3-yl)quinoline (200 mg, 0.594 mmol) in THF (4.4 mL) and water (1.4 mL) was added oxone (913 mg, 1.49 mmol). The reaction was stirred at rt for 18 h, then poured into 15 mL water and stirred for ten min. The resulting precipitate was isolated by filtration, then dissolved in EtOAc, dried over magnesium sulfate, and cond, affording 4-chloro-5,7-difluoro-3-methyl-2-(5-(methylsulfonyl)pyridin-3-yl)quinoline. Mass Spectrum (ESI) m/e=369.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-b063933084ff4d108ff5cf161cd6dfb0
Source noteuspto-grants-2015_01