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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66004Generated: October 26, 2026

1-Phenylpiperazine → 2-(4'-Phenyl-piperazino)-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydro-pyrido(2,3-d)pyrimidine

https://huagongshe.com/reaction/66004

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
Reactant1-Phenylpiperazinium chlorideHCID 75164—
Reactant2-Chloro-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydropyrido(2,3-d)pyrimidineHCID 12266805—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product2-(4'-Phenyl-piperazino)-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydro-pyrido(2,3-d)pyrimidineHCID 1226680784%

Reaction Steps

A solution of 3.2 g (0.02 mol) of N-phenyl-piperazine in 30 cm3 of toluene is added to 2.8 g (0.01 mol) of 2-chloro-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydro-pyrido(2,3-d)-pyrimidine dissolved in 30 cm3 of toluene. Reaction takes place practically instantaneously with evolution of heat and the mixture sets solid due to formation of phenylpiperazine hydrochloride. The mixture is diluted with 100 cm3 of ethyl acetate, the solution is filtered, washed with water and dried (MgSO4) and the solvent is evaporated. The residue is recrystallised from 110 cm3 of isopropanol and yields 3.38 g (84%) of 2-(4'-phenyl-piperazino)-5-oxo-6-carbethoxy-8-ethyl-5,8-dihydro-pyrido(2,3-d)pyrimidine; melting point 186° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04129737
Source datasetuspto-grants-1978_12
ORD IDord-f150f2238b904cbeaf123d9cc6497aa3
Source noteuspto-grants-1978_12