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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605257Generated: November 2, 2026

1-Methylpiperazine → HCID 22756830, compound

https://huagongshe.com/reaction/1605257

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 numberUS03950338
Source datasetuspto-grants-1976_04
ORD IDord-cad74a84de554274a39fe92fdc4a7f8c
Source noteuspto-grants-1976_04