HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl cyanoacetate → HCID 13851039, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl cyanoacetate | HCID 7764 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 13851038 | HCID 13851038 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13851039 | HCID 13851039 | — |
Reaction Steps
A mixture of 6-isopropenyl-4-oxo-4H-1-benzopyran-3-carbonitrile (800 mg), ethanol (40 ml), piperidine (0.6 ml) and ethyl cyanoacetate (0.7 ml) was subjected to reflux for three hours, which was then left standing at room temperature overnight. Precipitating crystals were collected by filtration, which were recrystallized from ethanol to afford colorless crystals (1.09 g) of ethyl 2-amino-7-isopropenyl-5-oxo-5H-[1]benzopyrano[2,3-b]pyridine-3-carboxylate, m.p. 227°-230° C. (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04716167 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-e6462487f8dc4a68a7751baf9905daa2 |
| Source note | uspto-grants-1987_12 |