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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415927Generated: October 30, 2026

Acetonitrile → Ethyl 7-methyl-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylate

https://huagongshe.com/reaction/415927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
Reactant2-Amino-5-methylpyridineHCID 15348—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductEthyl 7-methyl-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carboxylateHCID 22852658%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of diethyl 2-(ethoxymethylene)malonate (0.60 g, 3 mmol), 5-methylpyridin-2-amine (0.20 g, 2 mmol), DBU (0.1 ml, 0.9 mmol) in acetonitrile (2 g, 49 mmol) was heated under Microwave (CEM) at 150° C. (150 W) for 20 min. The resultant was diluted with dichloromethane and water, and the organic layer was dried over sodium sulfate. The organic solution was concentrated, and the residue was crystallized in dichloromethane and diethyl ether to give the title compound as a pale yellow solid (0.25 g, 58%): MS (ESI pos. ion) m/z: 233 (MH+). Calc'd exact mass for C12H12N2O3: 232.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088794B2
Source datasetuspto-grants-2012_01
ORD IDord-f7c9d175a6fc498dab69ecda00f36815
Source noteuspto-grants-2012_01