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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloranil | HCID 8371 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 4-Amidinoaniline dihydrochloride | HCID 75626 | — |
| Reactant | Formamidine acetate | HCID 160693 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(1,2,4,5-Tetrazin-3-yl)aniline | HCID 58490211 | 19.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08900549B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-7bec7a2f31474e1095b1fd8fd25a7756 |
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| Source note | uspto-grants-2014_12 |
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