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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1949153Generated: October 25, 2026

Potassium Carbonate → 2-(2-(Phenylsulfonyl)ethylthio)-6-(trifluoromethyl)quinoline-3-carboxylic acid

https://huagongshe.com/reaction/1949153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Phenylsulfonyl)ethanethiolHCID 447093—
Reactant2-Chloro-6-(trifluoromethyl)quinoline-3-carboxylic acidHCID 86645339—
SolventAcetoneHCID 180—
Product2-(2-(Phenylsulfonyl)ethylthio)-6-(trifluoromethyl)quinoline-3-carboxylic acidHCID 6713367672%

Reaction Conditions

Temperature70 °C

Reaction Steps

206 mg (1.5 mmol) K2CO3 and 303 mg (1.5 mmol) 2-(phenylsulfonyl)ethanethiol were added to a solution of 827 mg (1.0 mmol) 2-chloro-6-(trifluoromethyl)quinoline-3-carboxylic acid (precursor VVV03) in acetone (3 ml) and the mixture was heated for 5 h at 70° C. Then it was filtered and the filtrate was concentrated to small volume under vacuum. The residue was dissolved in water and acidified with a 1N hydrochloric acid. It was then extracted with EE and the organic phase was dried over Na2SO4, filtered and concentrated to small volume under vacuum. Crystallisation (DCM/hexane) of the residue yielded 316 mg (0.7 mmol, 72%) 2-(2-(phenylsulfonyl)ethylthio)-6-(trifluoromethyl)quinoline-3-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399673B2
Source datasetuspto-grants-2013_03
ORD IDord-88758ace43f74dcdb759344c5a002fd1
Source noteuspto-grants-2013_03