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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493238Generated: November 1, 2026

Potassium Carbonate → 2-(4-Pyridylmethylthio)-N-(4-trifluoromethylsulfonylphenyl)pyridine-3-carboxamide

https://huagongshe.com/reaction/493238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-chloro-N-(4-trifluoromethylsulfonylphenyl)pyridine-3-carboxamideHCID 23093777—
Reactant4-Pyridinemethanethiol hydrochlorideHCID 23093873—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product2-(4-Pyridylmethylthio)-N-(4-trifluoromethylsulfonylphenyl)pyridine-3-carboxamideHCID 2309381437%

Reaction Steps

4-Pyridinemethanethiol hydrochloride (0.32 g, 2.0 mmol) and potassium carbonate (0.63 g, 4.5 mmol) were added to a solution of 2-chloro-N-(4-trifluoromethylsulfonylphenyl)pyridine-3-carboxamide (0.65 g, 1.8 mmol, Reference compound No. 2-2) in ethanol (10 mL) under a nitrogen atmosphere, then the mixture was stirred at 65° C. for 8 hours. The reaction mixture was diluted with ethyl acetate (100 mL), then the ethyl acetate layer was washed with a saturated aqueous sodium hydrogencarbonate solution (100 mL) and brine (100 mL), and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, then the resulting residue was purified by silica gel column chromatography to give 0.29 g of the target compound as a white solid. (Yield 37%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534802B2
Source datasetuspto-grants-2009_05
ORD IDord-9809cc5e082c48e981cd85cc9b2e1d8f
Source noteuspto-grants-2009_05