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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258692Generated: October 29, 2026

1-Methylpiperazine → HCID 22756830, compound

https://huagongshe.com/reaction/258692

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 22756847HCID 22756847—
SolventEthanolHCID 702—
ProductHCID 22756830HCID 2275683058%

Reaction Steps

1.5 g of N-methylpiperazine are added to a stirred suspension of 2 g of 2-chloro-5-oxo-6-carbethoxy-8-methyl-5, 8-dihydro-pyrido(2,3-d)pyrimidine in 20 cm3 of absolute ethanol. The reaction takes place with evolution of heat. After standing for 2 hours at room temperature, the solvent is evaporated in vacuo, the residue is taken up in water and the precipitate is filtered off, washed, dried in vacuo and recrystallised from benzene: 1.4 g (58%) of 2-(4'-methyl-piperazino)-5-oxo-6-carbethoxy-8-methyl-5,8 -dihydro-pyrido(2,3-d)pyrimidine are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04034094
Source datasetuspto-grants-1977_07
ORD IDord-98c5ed11a1d748838722edc849d8b867
Source noteuspto-grants-1977_07