Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345763Generated: October 27, 2026

Pyridine → 2,6-Di-tert-butyl-4-[(pyrazin-2-yl)imino]cyclohexa-2,5-dien-1-one

https://huagongshe.com/reaction/345763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,6-Di-t-butyl-p-benzoquinoneHCID 12867—
ReactantAminopyrazineHCID 78747—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,1-DichloroethaneHCID 6365—
Product2,6-Di-tert-butyl-4-[(pyrazin-2-yl)imino]cyclohexa-2,5-dien-1-oneHCID 1437366658.3%

Reaction Steps

A 1.62 ml quantity of pyridine was dissolved in 60 ml of dichloroethane. To the solution was added 0.89 g of aluminum chloride powder, and the mixture was refluxed with heating for 15 minutes. Then to the mixture were added 2.20 g of 2,6-di-tert-butyl-1,4-benzoquinone and 0.95 g of aminopyrazine, and the mixture was refluxed under heating for 17.5 hours. The reaction mixture was cooled to room temperature and filtered through a Celite pad and the insoluble materials were washed there with dicloromethane. The filtrate was concentrated, and the resulting crude product was purified by silica gel column chromatography (eluent: diethyl ether-hexane=3:7), giving 1.73 g of Compound 1a.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05059598
Source datasetuspto-grants-1991_10
ORD IDord-3dd159d9b0b8427183d52d987c187d70
Source noteuspto-grants-1991_10