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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274671Generated: October 25, 2026

Triethylamine → 4-(3-(N-(2-thienylmethyl)amino)propylthio]pyridine

https://huagongshe.com/reaction/274671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(2-Thienylmethyl)amineHCID 34005—
Reactant4-(3-Hydroxypropylthio)pyridineHCID 19079134—
SolventDichloromethaneHCID 6344—
Product4-(3-(N-(2-thienylmethyl)amino)propylthio]pyridineHCID 1907918429.1%

Reaction Steps

In 200 ml of methylene chloride were dissolved 10.34 g (61.1 mmol) of 4-(3-hydroxypropylthio)pyridine and 10.2 ml (73.3 mmol) of triethylamine, methanesulfonyl chloride [5.7 ml (73.3 mmol)] was added, and the mixture was stirred as room temperature for 30 minutes. The reaction mixture was washed with a saturated aqueous solution of sodium bicarbonate and water and dried. Then the solvent was distilled off. To 8.05 g of the residue was added 3.3 ml (32.5 mmol) of 2-thiophenemethylamine. The mixture was heated at 80° C. for 3 hours. After cooling, the mixture was purified by column chromatography (eluent: chloroform/methanol=25:1) to obtain 2.5 g of the desired compound (yield: 29.1%, yellow oil).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389658
Source datasetuspto-grants-1995_02
ORD IDord-8457de51d7784f48a4edc044ecd0b664
Source noteuspto-grants-1995_02