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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66005Generated: October 28, 2026

1-Methylpiperazine → HCID 22756830, compound

https://huagongshe.com/reaction/66005

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 numberUS04129737
Source datasetuspto-grants-1978_12
ORD IDord-cff2fbb5070b4dd7923b8424a085d970
Source noteuspto-grants-1978_12