Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
Reactant2-Amino-3-HydroxypyridineHCID 28114—
Solvent1,2-DiethylbenzeneHCID 8657—
ProductEthyl 9-hydroxy-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylateHCID 61644593%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03960847
Source datasetuspto-grants-1976_06
ORD IDord-6637efd088204bffa4fb3ab6d65a2c2b
Source noteuspto-grants-1976_06