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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964118Generated: October 26, 2026

Benzoyl chloride → 4-[3-(N-(2-thienylmethyl)-N-benzoylamino)propylthio]pyridine

https://huagongshe.com/reaction/964118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant4-(3-(N-(2-thienylmethyl)amino)propylthio]pyridineHCID 19079184—
SolventDichloromethaneHCID 6344—
Product4-[3-(N-(2-thienylmethyl)-N-benzoylamino)propylthio]pyridineHCID 1907911735.9%

Reaction Steps

To a solution of 2.5 g (9.45 mmol) of 4-(3-(N-(2-thienylmethyl)amino)propylthio]pyridine and 1.32 ml (9.45 mmol) of triethylamine in 50 ml of methylene chloride, 1.1 ml (9.45 mmol) of benzoyl chloride was added under ice-cooling with stirring. The mixture was stirred at room temperature for 30 minutes. The reaction mixture was washed with a saturated aqueous solution of sodium bicarbonate and water and dried, and the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 1.25 g of the desired compound (yield: 35.9%, yellow oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05767121
Source datasetuspto-grants-1998_06
ORD IDord-cdfde7f2dccf46dd8434528a6caa65bb
Source noteuspto-grants-1998_06