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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896682Generated: October 31, 2026

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

https://huagongshe.com/reaction/1896682

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 numberUS08518973B2
Source datasetuspto-grants-2013_08
ORD IDord-74a12cae3de74ae7974bcaa3635d7a5a
Source noteuspto-grants-2013_08