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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593870Generated: October 26, 2026

Hydrochloric Acid → Ethyl 5-cyano-4-methyl-6-oxo-1,6-dihydropyridine-2-carboxylate

https://huagongshe.com/reaction/593870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCyanoacetamideHCID 7898—
ReactantPotassium CarbonateHCID 11430—
ReactantCID 275522HCID 275522—
SolventAcetoneHCID 180—
ProductEthyl 5-cyano-4-methyl-6-oxo-1,6-dihydropyridine-2-carboxylateHCID 27552365.8%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of ethyl 4-ethoxy-2-oxopent-3-enoate (22.5 g, 121 mmol) and 2-cyanoacetamide (9.0 g, 107 mmol) in acetone (250 mL) was added potassium carbonate (15.8 g, 114 mmol). The reaction was refluxed (85° C. oil bath) for 10 hr (the reaction formed a thick ppt. in a deep red solution). The slurry was added to cold 1N HCl (230 mL) in ice. After stirring for 30 min. the suspension was filtered, washed with water and dried under vacuum to give the product ethyl 5-cyano-4-methyl-6-oxo-1,6-dihydropyridine-2-carboxylate (14.51 g, 70.4 mmol, 65.7% yield) as a light pink solid. 1H NMR (400 MHz, DMSO-d6) δ12.60 (br. s., 1H), 7.05 (br. s., 1H), 4.34 (q, J=7.1 Hz, 2H), 2.45 (s, 3H), 1.32 (t, J=7.1 Hz, 3H). MS(ES)+ m/e 206.8 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242962B2
Source datasetuspto-grants-2016_01
ORD IDord-952798e87ea34fe590227fa907cd7ca1
Source noteuspto-grants-2016_01