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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287241Generated: October 26, 2026

Water → 1-(m-nitrophenyl)-3-allylpyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/1287241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAllyl iodideHCID 11166—
ReactantSodium hydrideHCID 24758—
Reactant1-(m-nitrophenyl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 12760301—
SolventDimethylformamideHCID 6228—
Product1-(m-nitrophenyl)-3-allylpyrido[2,3-d]pyrimidine-2,4(1H,3H)-dioneHCID 1276418172%

Reaction Steps

2.8 g of 1-(m-nitrophenyl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione was dissolved in 30 ml of dry dimethylformamide. To the solution was added 0.6 g of approximately 50 % sodium hydride and stirring was performed for 30 minutes. To this was added 3.4 g of allyl iodide and the mixture was reacted for 3 hours at room temperature. Then the solvent was evaporated from the mixture under reduced pressure. To the residue obtained was added water to precipitate a crude product. Recrystallization of this product from methanol gave 2.3 g of 1-(m-nitrophenyl)-3-allylpyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione as pale yellow prisms, melting at 188-189°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03984415
Source datasetuspto-grants-1976_10
ORD IDord-dea5f694724e4ea6ae8c555e40e0ce5d
Source noteuspto-grants-1976_10