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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700352Generated: October 30, 2026

Ethyl Acetate → 2-Cyanoethyl 4-(3-chlorophenyl)-2,6-dimethyl-5-(phenylcarbamoylmethylcarbamoyl)-1,4-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/1700352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2-AminoacetanilideHCID 208384—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantMono(2-cyanoethyl) 4-(3-chlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylateHCID 86757801—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2-Cyanoethyl 4-(3-chlorophenyl)-2,6-dimethyl-5-(phenylcarbamoylmethylcarbamoyl)-1,4-dihydropyridine-3-carboxylateHCID 18318257—

Reaction Steps

179 mg (0.49 mmol) of mono(2-cyanoethyl) 4-(3-chlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate, 245mg (1.63 mmol) of 2-amino-N-phenylacetamide, 129 mg (0.67 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 11 mg (0.09 mmol) of 4-dimethylaminopyridine were stirred in 10 ml of dichloromethane at room temperature overnight. Ethyl acetate was added to the reaction mixture, and the product was washed with 1 N hydrochloric acid and then with a saturated aqueous sodium hydrogencarbonate solution. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was purified by the silica gel chromatography (chloroform/methanol=100/1) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350762B1
Source datasetuspto-grants-2002_02
ORD IDord-f085719675364f2ebc4637a93ffbc420
Source noteuspto-grants-2002_02