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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345762Generated: October 30, 2026

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

https://huagongshe.com/reaction/345762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,6-Di-t-butyl-p-benzoquinoneHCID 12867—
ReactantAminopyrazineHCID 78747—
CatalystTitanium TetrachlorideHCID 24193—
Solvent1,1-DichloroethaneHCID 6365—
Product2,6-Di-tert-butyl-4-[(pyrazin-2-yl)imino]cyclohexa-2,5-dien-1-oneHCID 1437366646.4%

Reaction Steps

A 97.1 ml quantity of pyridine was dissolved in 944 ml of dichloroethane, and 32.9 ml of titanium tetrachloride was added thereto. The resulting mixture was refluxed with heating for 15 minutes. To the mixture were then added 132.2 g of 2,6-di-tert-butyl-1,4-benzoquinone and 57.1 g of aminopyrazine, and the mixture was refluxed with heating for 42 hours. The reaction mixture was cooled to room temperature and filtered through a Celite pad and the insoluble materials were washed there with dichloromethane. The filtrate was concentrated, and the resulting crude product was purified by silica gel column chromatography (eluent: diethyl ether-hexane=3:7), giving 82.8 g of Compound 1a.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05059598
Source datasetuspto-grants-1991_10
ORD IDord-aebe2d2b4a1e45d49b6a2f85040e0619
Source noteuspto-grants-1991_10