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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986756Generated: October 30, 2026

Ethyl cyanoacetate → HCID 13728611, compound

https://huagongshe.com/reaction/986756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl cyanoacetateHCID 7764—
ReactantPiperidineHCID 8082—
Reactant6-Acetyl-4-oxo-4H-1-benzopyran-3-carbonitrileHCID 13728610—
SolventEthanolHCID 702—
ProductHCID 13728611HCID 13728611—

Reaction Steps

In ethanol (800 ml) was suspended 6-acetyl-4-oxo-4H-1-benzopyran-3-carbonitrile (32 g). To the suspension were added ethyl cyanoacetate (23.9 ml) and piperidine (23.7 ml). The mixture was refluxed for one hour, then cooled to room temperature. The resulting crystals were collected by filtration, washed with ethanol, then with acetone, followed by drying to give ethyl 7-acetyl-2-amino-5-oxo-5H-[1]benzopyrano[2,3-b]pyridine-3-carboxylate as yellow crystals (46.3 g). Melting point: >300° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04716167
Source datasetuspto-grants-1987_12
ORD IDord-8e835ff05a3c47818bffba484b806547
Source noteuspto-grants-1987_12