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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964116Generated: October 25, 2026

Triethylamine → 4-(3-Nicotinoylaminopropyloxy)pyridine

https://huagongshe.com/reaction/964116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Pyridinecarbonyl chloride, hydrochloride (1:1)HCID 88438—
Reactant4-(3-Aminopropoxy)pyridineHCID 14994125—
SolventDichloromethaneHCID 6344—
Product4-(3-Nicotinoylaminopropyloxy)pyridineHCID 1907916788.7%

Reaction Steps

To a solution of 700 mg (4.60 mmol) of 4-(3-aminopropyloxy)pyridine and 1.54 ml (11.0 mmol) of triethylamine in 30 ml of methylene chloride, 830 mg (4.66 mmol) of nicotinoyl chloride hydrochloride 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 then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethanol/ethyl acetate=1:10 to 1:5) to obtain 1.05 g of the desired compound (yield: 85.8%, colorless crystals). mp: 117°-119° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05767121
Source datasetuspto-grants-1998_06
ORD IDord-425e28fb64d1440b96f383f1a0a90ccd
Source noteuspto-grants-1998_06