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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747690Generated: October 26, 2026

Triethylamine → N-[2-(3-cyanophenoxy)ethyl]-4-[(pyridine-4-yl)amino]benzamide

https://huagongshe.com/reaction/747690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant3-(2-Aminoethoxy)benzonitrile hydrobromideHCID 17788773—
ReactantEthyl 4-[(pyridin-4-yl)amino]benzoateHCID 68830990—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductN-[2-(3-cyanophenoxy)ethyl]-4-[(pyridine-4-yl)amino]benzamideHCID 68832693—

Reaction Conditions

Temperature70 °C

Reaction Steps

180 mg (0.743 mmol) of ethyl 4-[(pyridine-4-yl)amino]benzoate was dissolved in 5 ml of concentrated hydrochloric acid, and the solution was stirred at 70° C. for 15 hours. The solvent was evaporated, and the residue was dissolved in 5 ml of dichloromethane. 0.23 ml (1.64 mmol) of triethylamine, 156 mg (0.82 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 208 mg (0.82 mmol) of 1-hydroxybenzotriazole and 199 mg (0.82 mmol) of 3-(2-aminoethoxy)benzonitrile hydrobromide were added to the solution, and they were stirred for 16 hours. The reaction liquid was diluted with water. After the extraction with ethyl acetate, the organic layer was successively washed with water, 1 N sodium hydroxide and saturated aqueous NaCl solution, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by the silica gel column chromatography to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396844B1
Source datasetuspto-grants-2008_07
ORD IDord-a2848d6062a4443e91d576b536c5acfe
Source noteuspto-grants-2008_07