Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893913Generated: October 29, 2026

Malononitrile → 8-Ethyl-7-imino-4-methyl-2-(methylthio)-7,8-dihydropyrido[2,3-d]pyrimidine-6-carbonitrile

https://huagongshe.com/reaction/1893913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMalononitrileHCID 8010—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Ethylamino)-6-methyl-2-(methylthio)pyrimidine-5-carbaldehydeHCID 57606953—
SolventEthanolHCID 702—
Product8-Ethyl-7-imino-4-methyl-2-(methylthio)-7,8-dihydropyrido[2,3-d]pyrimidine-6-carbonitrileHCID 57606989—

Reaction Conditions

Temperature70 °C

Reaction Steps

Potassium carbonate (0.539 g, 3.90 mmol) was added to a suspension of 4-(ethylamino)-6-methyl-2-(methylthio)pyrimidine-5-carbaldehyde (0.413 g, 1.95 mmol) from above, and malononitrile (0.194 g, 2.93 mmol) in absolute ethanol (15.0 mL) and heated to 70° C. After one h, the reaction was allowed to cool to room temperature and concentrated in vacuo. The residue was diluted with ethyl acetate (50 mL) and washed with saturated NaHCO3 (50 mL), and brine. The organic phase was separated and concentrated in vacuo. The residue was precipitated with ethyl acetate and hexanes to give 8-ethyl-7-imino-4-methyl-2-(methylthio)-7,8-dihydropyrido[2,3-d]pyrimidine-6-carbonitrile as a brown solid that was used in the subsequent step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513266B2
Source datasetuspto-grants-2013_08
ORD IDord-cf54140ea40c4cd69277dbbd08ef281c
Source noteuspto-grants-2013_08