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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385556Generated: October 31, 2026

Water → HCID 57815351, compound

https://huagongshe.com/reaction/385556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-Dioxolane, 2-(bromomethyl)-HCID 78068—
Reactant2-Methoxypyrido[2,3-d]pyrimidin-7(8H)-oneHCID 57815329—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductHCID 57815351HCID 57815351—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a suspension of 0.50 g of 2-methoxypyrido(2,3-d)pyrimidin-7(8H)-one in 7.5 mL of N,N-dimethylformamide, 0.59 g of potassium carbonate was added at room temperature, the temperature was increased to 60 to 80° C., and the mixture was stirred for 1 hour. Thereto was added 0.35 mL of 2-bromomethyl-1,3-dioxolan at 80° C., the temperature of the reaction mixture was increased to 103° C., and the mixture was stirred for 3 hours 30 minutes. The reaction mixture was cooled to room temperature, and water and chloroform were added thereto. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, the resultant solution was washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The resultant residue was purified by silica gel column chromatography using an eluent of chloroform:methanol=75:1 to obtain 0.60 g of 8-(1,3-dioxolan-2-ylmethyl)-2-methoxypyrido(2,3-d)pyrimidin-7(8H)-one as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367831B2
Source datasetuspto-grants-2013_02
ORD IDord-a4221fef090948738f99f29c7ee86332
Source noteuspto-grants-2013_02