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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291359Generated: October 30, 2026

Dimethyl Sulfoxide → 2-[4-(4-Methoxycarbonylbenzoyl)benzyloxy]-3-methyl-4H-pyrido[1,2-a]pyrimidin-4-one

https://huagongshe.com/reaction/1291359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Methylpyrido[1,2-a]pyrimidine-2,4-dioneHCID 5163266—
Reactant4-(4-Methoxycarbonylbenzoyl)benzyl bromideHCID 21218032—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-[4-(4-Methoxycarbonylbenzoyl)benzyloxy]-3-methyl-4H-pyrido[1,2-a]pyrimidin-4-oneHCID 18919341—

Reaction Steps

To a solution of 3-methylpyrido[1,2-a]pyrimidine-2,4-dione (2.20 g, 12.5 mmol) and 4-(4-methoxycarbonylbenzoyl)benzyl bromide (7.04 g, 12.7 mmol) in DMF (40.0 ml)-DMSO (20.0 ml) was added potassium carbonate (3.92 g, 28.4 mmol) and the mixture was stirred at room temperature overnight. This reaction mixture was diluted with water and the resulting crystals were collected by filtration, dissolved in ethyl acetate, and dried over MgSO4. The solvent was then distilled off under reduced pressure and the residue was re-crystallized from ethyl acetate to provide colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753664
Source datasetuspto-grants-1998_05
ORD IDord-c8ec30e8a046440f94ade46fc2101c5f
Source noteuspto-grants-1998_05