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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290331Generated: October 28, 2026

1-(2-Furoyl)piperazine → HCID 20232070, compound

https://huagongshe.com/reaction/2290331

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Furoyl)piperazineHCID 550206—
ReactantHCID 15586342HCID 15586342—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
ProductHCID 20232070HCID 2023207029%

Reaction Steps

A mixture of 5-methyl-3-methylthio-6-phenyl-1,2,4-triazine (9 g) and N-(2-furoyl)piperazine (10 g) was heated at 150° to 160° C. for 89 hours with stirring. The reaction mixture was dissolved in benzene (300 ml) and subjected to chromatography on silica gel (300 g) using a mixture of benzene and ethyl acetate (3:2) as an eluent. The eluate was concentrated to dryness and the resulting solid was recrystallized from a mixture of chloroform and diisopropyl ether to give crystals of 3-[4-(2-furoyl)-1-piperazinyl]-5-methyl-6-phenyl-1,2,4-triazine (4.20 g), mp 141.5°~142.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04616014
Source datasetuspto-grants-1986_10
ORD IDord-2a3dcf6c72064815a8b2eed8b9b6bcc0
Source noteuspto-grants-1986_10