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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210174Generated: October 30, 2026

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

https://huagongshe.com/reaction/2210174

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 1.00 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 numberUS05457106
Source datasetuspto-grants-1995_10
ORD IDord-60db8ed9768d4eca8062ff52bab03fc6
Source noteuspto-grants-1995_10