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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-CyanopyridineHCID 7506—
Reactant4-Aminobenzoic acid hydrazideHCID 21450—
ReactantSodiumHCID 5360545—
SolventMethanolHCID 887—
Product4-[5-(Pyridin-4-yl)-1H-1,2,4-triazol-3-yl]anilineHCID 2028581220.9%

Reaction Conditions

Temperature245 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04011218
Source datasetuspto-grants-1977_03
ORD IDord-09efdaa95f984a3985a412bc4cc2fd45
Source noteuspto-grants-1977_03