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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210109Generated: October 30, 2026

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

https://huagongshe.com/reaction/2210109

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 numberUS05457106
Source datasetuspto-grants-1995_10
ORD IDord-ea646328c0314f2b9785379cbdab0a4d
Source noteuspto-grants-1995_10