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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395872Generated: November 2, 2026

Chloranil → 4-(1,2,4,5-Tetrazin-3-yl)aniline

https://huagongshe.com/reaction/1395872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloranilHCID 8371—
ReactantHydrazineHCID 9321—
Reactant4-Amidinoaniline dihydrochlorideHCID 75626—
ReactantFormamidine acetateHCID 160693—
SolventAcetonitrileHCID 6342—
Product4-(1,2,4,5-Tetrazin-3-yl)anilineHCID 5849021119.1%

Reaction Steps

To a mixture of 4-Aminobenzamidine dihydrochloride (1 mmol, 208 mg) and formamidine acetate (4 mmol, 416 mg) in acetonitrile (25 mL) was added anhydrous hydrazine (10 mmol, 315 uL). The solution was heated to reflux for 1 hour, cooled, and the solvent was removed by rotary evaporation. The residue was resuspended with water (25 mL) and was stirred with solid tetrachloro-1,4-benzoquinone (2 mmol, 492 mg) for 1 hour. After removal of the solids from the pink solution by filtration, the reaction was concentrated by rotary evaporation and purified by preparative HPLC using a gradient from 0-40% buffer B (buffer A is water with 0.1% TFA, and buffer B is acetonitrile with 10% water and 0.1% TFA) to afford pure 4-(1,2,4,5-tetrazin-3-yl)aniline (33 mg, 19%), as a pink solid. LRMS-ESI [M+H]+ calcd. for C8H8N5+: 174.08, found: 173.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08900549B2
Source datasetuspto-grants-2014_12
ORD IDord-7bec7a2f31474e1095b1fd8fd25a7756
Source noteuspto-grants-2014_12