HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl 6-ethoxy-3-pyridylaminomethylenemalonate → Ethyl 6-ethoxy-1,4-dihydro-4-oxo-1,5-naphthyridine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl 6-ethoxy-3-pyridylaminomethylenemalonate | HCID 621746 | — |
| Solvent | Diphenyl Ether | HCID 7583 | — |
| Product | Ethyl 6-ethoxy-1,4-dihydro-4-oxo-1,5-naphthyridine-3-carboxylate | HCID 604651 | 58% |
Reaction Steps
Diethyl (2-ethoxy-5-pyridylaminomethylene)malonate (6.04 g) was added to diphenyl ether (20 mL) preheated to 230° C. Heating was continued for 0.5 h, the reaction flask removed from the oil bath, and the mixture allowed to cool to ambient temperature. The product was triturated with 1:1 ether:hexanes, collected, rinsed with ether, and dried to give 2.98 g of ethyl 6-ethoxy-4-oxo-1,4-dihydro-1,5-naphthyridine-3-carboxylate as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06399604B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-bbf7a10bd08840efbfd51a89b35aaa72 |
| Source note | uspto-grants-2002_06 |