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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274642Generated: October 29, 2026

Trifluoroacetic acid → 4-[3-(Trifluoroacetylamino)propylthio]pyridine hydrochloride

https://huagongshe.com/reaction/274642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
Reactant4-(3-Aminopropylthio)pyridine dihydrochlorideHCID 19079259—
SolventDichloromethaneHCID 6344—
Product4-[3-(Trifluoroacetylamino)propylthio]pyridine hydrochlorideHCID 1907926368.4%

Reaction Steps

To a solution of 1.00 g (4.15 mmol) of 4-(3-aminopropylthio)pyridine dihydrochloride and 2.77 ml (19.8 mmol) of triethylamine in 40 ml of methylene chloride was added 0.70 ml (4.96 mmol) of anhydrous trifluoroacetic acid under ice-cooling with stirring and the mixture was stirred for at room temperature for 30 minutes. The reaction mixture was washed with an aqueous saturated sodium bicarbonate solution and water and dried. The solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain the powder which was washed with hexane and dried to obtain 750 mg of the desired compound (free base) (68.4%, pale yellow prisms).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389658
Source datasetuspto-grants-1995_02
ORD IDord-51834fb593fc4ab78a89f8f120ca7a95
Source noteuspto-grants-1995_02