HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657361Generated: November 2, 2026
Diethyl (ethoxymethylene)malonate → Ethyl 9-hydroxy-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylate
https://huagongshe.com/reaction/1657361
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | 2-Amino-3-Hydroxypyridine | HCID 28114 | — |
| Solvent | 1,2-Diethylbenzene | HCID 8657 | — |
| Product | Ethyl 9-hydroxy-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylate | HCID 616445 | 93% |
Reaction Steps
Diethylbenzene Process: A mixture of 66.0 g of 2-amino-3-pyridinol, 220.0 g of diethyl ethoxymethylenemalonate, and 1.0 liter of diethylbenzene was heated so that the internal temperature reached 140° in 1 hour, was kept for 1 hour at 140°, then heated so that the temperature rose to 180° in 1 hour, and then kept 1 hour at 180°. During this entire heating period, 50 ml. of distillate was collected. The solution was allowed to cool spontaneously, was cooled at 0°, filtered, and the solid washed with diisopropyl ether to give 130.0 g of product, after drying at 56° in vacuo. The m.p. was 175°-177° and a mixture m.p. with the product isolated in (a) above was 175°-177°. The ir and pmr spectra of the two samples were superimposable. The yield was 93%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03960847 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-6637efd088204bffa4fb3ab6d65a2c2b |
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| Source note | uspto-grants-1976_06 |
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