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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605256Generated: November 1, 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/1605256

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 numberUS03950338
Source datasetuspto-grants-1976_04
ORD IDord-d7e2c8b59f9043cb83a6ddc18c8db07e
Source noteuspto-grants-1976_04