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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522879Generated: October 25, 2026

4-Chlorobenzoic Acid → 3-(4-Chlorophenyl)-[1,2,4]triazolo[4,3-a]pyrazine

https://huagongshe.com/reaction/522879

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoic AcidHCID 6318—
ReactantAmmonium HydroxideHCID 14923—
Reactant2-HydrazinopyrazineHCID 1487823—
Product3-(4-Chlorophenyl)-[1,2,4]triazolo[4,3-a]pyrazineHCID 67376781—

Reaction Conditions

Temperature110 °C

Reaction Steps

To 2-hydrazinopyrazine (1.60 g, 14.55 mmol) was added 4-chloro-benzoic acid (3 eq) followed by 20 mL of polyphosphoric acid, and the reaction mixture was stirred at 110° C. for 18 h. The hot PPA solution was added to ice and neutralized by the addition of ammonium hydroxide (highly exothermic!). The aqueous solution was extracted with ethyl acetate, washed with brine, and dried over anhydrous sodium sulfate. Concentration followed by flash chromatography (silica gel, 1:1 hexanes: ethyl acetate) afforded 3-(4-chlorophenyl)-[1,2,4]triazolo[4,3-a]pyrazine, as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334269B2
Source datasetuspto-grants-2016_05
ORD IDord-24e9a3bbff2040d09a535fde2c205b07
Source noteuspto-grants-2016_05