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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210146Generated: October 25, 2026

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

https://huagongshe.com/reaction/2210146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant4-(3-(N-2-pyridylmethylamino)propylthio]pyridineHCID 19079176—
SolventDichloromethaneHCID 6344—
Product4-[3-(N-2-pyridylmethyl-N-benzoylamino)propylthio]pyridineHCID 1907915058.9%

Reaction Steps

To a solution of 1.60 g (6.17 mmol) of 4-[3-(N-2-Pyridylmethylamino)propylthio)pyridine and 1.05 ml (7.40 mmol) of triethylamine in 10 ml of methylene chloride, 0.86 ml (7.40 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 then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate/methanol=10:1) to obtain 1.32 g of the desired compound (yield: 58.9%, yellow oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457106
Source datasetuspto-grants-1995_10
ORD IDord-bd93a3249d48470eaea0dc8b6c2b5a6e
Source noteuspto-grants-1995_10