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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591192Generated: November 1, 2026

6-Chloro-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione → HCID 19045534, compound

https://huagongshe.com/reaction/1591192

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloro-1,3-dimethyl-2,4(1H,3H)-pyrimidinedioneHCID 81442—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 45158372HCID 45158372—
SolventAcetonitrileHCID 6342—
ProductHCID 19045534HCID 1904553461%

Reaction Steps

A solution of 3,4-dihydro-6-methoxyspiro-[(2H)-1-benzopyran-2,4'-piperidin]-4-one hydrochloride (0.568 g, 2 mmol), 6-chloro-1,3-dimethylpyrimidine-2,4-(1H,3H)-dione (0.349 g, 2 mmol) and sodium bicarbonate (0.42 g, 5 mmol) in acetonitrile was heated at reflux for 42 hours. After cooling, the reaction mixture was concentrated in vacuo to dryness. The residue was partitioned between chloroform and water. The chloroform solution was washed twice with water and once with saturated brine solution and then dried over sodium sulfate and concentrated to dryness in vacuo. The solid residue was recrystallized from methanol/ethanol to give the title compound (0.47 g, 61% yield) mp 202°-203° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05206240
Source datasetuspto-grants-1993_04
ORD IDord-1eaad74547d54ee8b55563f22454fa5d
Source noteuspto-grants-1993_04