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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599363Generated: October 31, 2026

Triethylamine → 2-(Quinolin-4-ylmethylthio)-N-(4-trifluoromethoxyphenyl)pyridine-3-carboxamide

https://huagongshe.com/reaction/599363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant4-(Chloromethyl)quinolineHCID 12355701—
Reactant2-mercapto-N-(4-trifluoromethoxyphenyl)pyridine-3-carboxamideHCID 178522235—
SolventDimethylformamideHCID 6228—
Product2-(Quinolin-4-ylmethylthio)-N-(4-trifluoromethoxyphenyl)pyridine-3-carboxamideHCID 1184704452%

Reaction Steps

Triethylamine (66 μL, 0.47 mmol) was added to a solution of 2-mercapto-N-(4-trifluoromethoxyphenyl)pyridine-3-carboxamide (Reference Compound No. 8-3, 52 mg, 0.17 mmol) and 4-(chloromethyl)quinoline (Reference Compound No. 5-1, 28 mg, 0.16 mmol) in anhydrous N,N-dimethylformamide (11.0 mL) at room temperature, and the mixture was stirred for 18 hours. Ethyl acetate (50 mL) was added thereto, then the whole was washed with saturated aqueous sodium hydrogencarbonate solution (5 mL) and brine (50 mL). The organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and then the resulting residue was purified by silica gel column chromatography to give 40 mg of the title compound as a white amorphous (Yield: 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897774B2
Source datasetuspto-grants-2011_03
ORD IDord-ce95029d13354666ae5c0ec456e1fa88
Source noteuspto-grants-2011_03