HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596416Generated: October 26, 2026
4-Cyanopyridine → 4-[5-(Pyridin-4-yl)-1H-1,2,4-triazol-3-yl]aniline
https://huagongshe.com/reaction/596416
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Cyanopyridine | HCID 7506 | — |
| Reactant | 4-Aminobenzoic acid hydrazide | HCID 21450 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-[5-(Pyridin-4-yl)-1H-1,2,4-triazol-3-yl]aniline | HCID 20285812 | 20.9% |
Reaction Steps
To 4-cyanopyridine (4.2 g.) in methanol (60 ml.) is added sodium (0.2 g.). The solution is allowed to stand for 0.5 hour at room temperature and is then added to a suspension of p-aminobenzhydrazide (6.4 g.) in 150 ml. of methanol. The resulting solution is heated 20 hours at reflux during which time a solid separates. The solid is filtered and heated to 245° C. over 1 hour and maintained at that temperature for an additional 15 minutes. After cooling the solid is recrystallized from a mixture of acetonitrile and water to yield 3-(p-aminophenyl)-5-(4-pyridyl)-1,2,4-triazole (2 g.) m.p. 251°-252.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04011218 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-09efdaa95f984a3985a412bc4cc2fd45 |
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| Source note | uspto-grants-1977_03 |
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