Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257787Generated: October 26, 2026

Potassium Carbonate → 1-(3-Nitrophenyl)-3-[(pyridin-4-yl)methyl]pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/257787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Chloromethyl)pyridinium chlorideHCID 74570—
Reactant1-(m-nitrophenyl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 12760301—
SolventAcetoneHCID 180—
Product1-(3-Nitrophenyl)-3-[(pyridin-4-yl)methyl]pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 984255663%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(3-Nitrophenyl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione (12.0 g, 42.2 mmoles) was added into 2 liters of acetone and warmed with stirring until a solution was formed. To the solution was added powdered potassium carbonate (23.4 g, 169.3 mmoles) and 4-chloromethylpyridine hydrochloride (10.4 g, 63.4 mmoles). The solution was stirred at reflux temperature for 18 hours. The solution was filtered while hot. Three quarters of the solvent was removed resulting in the formation of a precipitate. The solution was cooled to 0° C. and the precipitate was removed by filtration. The precipitate was washed with ethyl ether and air dried yielding 10.0 g (26.6 mmole, 63% yield) of 1-(3-nitrophenyl)-3-(4-pyridylmethyl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione (mp 207°-209° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05264437
Source datasetuspto-grants-1993_11
ORD IDord-b1b9e512781043e2bfd7eec8c5be498f
Source noteuspto-grants-1993_11