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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964138Generated: October 30, 2026

Benzoyl chloride → 4-[4-(Benzoylamino)butylthio]pyridine

https://huagongshe.com/reaction/964138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant4-[(Pyridin-4-yl)sulfanyl]butan-1-amineHCID 13557537—
SolventDichloromethaneHCID 6344—
Product4-[4-(Benzoylamino)butylthio]pyridineHCID 1907917034.4%

Reaction Steps

To a solution of 100 g (5.49 mmol) of 4-(4-aminobutylthio)pyridine and 0.92 ml (6.60 mmol) of triethylamine in 30 ml of methylene chloride, 0.67 ml (5.77 mmol) of benzoyl chloride was added with stirring under ice-cooling and the mixture was stirred at room temperature for 13 hours. The mixture was washed with saturated aqueous sodium bicarbonate and saturated saline, and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by column chromatography (eluent: ethyl acetate) to give 0.54 g of the desired compound (34.4% yield, colorless crystals), mp. 75°-77° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05767121
Source datasetuspto-grants-1998_06
ORD IDord-0fc762c5567947859fab1a894a18f11c
Source noteuspto-grants-1998_06