Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658114Generated: November 2, 2026

1-Acetylpiperazine → Ethyl 2-(4-acetyl-1-piperazinyl)-5,8-dihydro-8-ethyl-5-oxopyrido[2,3-d]pyrimidine-6-carboxylate

https://huagongshe.com/reaction/1658114

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-AcetylpiperazineHCID 83795—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Chloro-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydropyrido(2,3-d)pyrimidineHCID 12266805—
SolventDimethyl SulfoxideHCID 679—
ProductEthyl 2-(4-acetyl-1-piperazinyl)-5,8-dihydro-8-ethyl-5-oxopyrido[2,3-d]pyrimidine-6-carboxylateHCID 12917682—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture containing 1.0 g of ethyl 2-chloro-5,8-dihydro-8-ethyl-5-oxopyrido[2,3-d]pyrimidine-6-carboxylate, 0.60 g of sodium bicarbonate, 20 ml of dimethyl sulfoxide, and 0.60 g of 1-acetylpiperazine was heated at 120°C for 1.5 hours with stirring. The dimethylsulfoxide was distilled off in vacuo and the residue was taken up in chloroform. The chloroform solution was washed with water, dried over anhydrous magnesium sulfate, and concentrated to dryness. The residual solid was recrystallized from a mixture of n-hexane and acetone to yield 1.21 of the product, m.p. 208°- 210°C with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03962443
Source datasetuspto-grants-1976_06
ORD IDord-3ae73c3b426b4aa3bb910352a0f60cc0
Source noteuspto-grants-1976_06