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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6143Generated: October 25, 2026

Triethylamine → 4-[3-(2-Thenoylamino)propyloxy]pyridine

https://huagongshe.com/reaction/6143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Thiophenecarbonyl chlorideHCID 78928—
Reactant4-(3-Aminopropoxy)pyridineHCID 14994125—
SolventDichloromethaneHCID 6344—
Product4-[3-(2-Thenoylamino)propyloxy]pyridineHCID 1523149570.4%

Reaction Steps

To a solution of 700 mg (4.60 mmol) of 4-(3-aminopropyloxy)pyridine and 0.77 ml (5.52 mmol) of triethylamine in 30 ml of methylene chloride, 0.50 ml (4.68 mmol) of thenoyl chloride was added under ice-cooling with stirring. The mixture was stirred at room temperature for 1.5 hours. The reaction mixture was washed successively with a saturated aqueous solution of sodium bicarbonate and brine and dried over anhydrous magnesium sulfate, and the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 850 mg of the desired compound (yield: 70.0%, colorless crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246948
Source datasetuspto-grants-1993_09
ORD IDord-6aaafa271c764cd7bffa5143f19ab4b3
Source noteuspto-grants-1993_09