Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443513Generated: October 25, 2026

Hydrazinecarboxaldehyde → 6-(2-Pyridyl)-1,2,4-triazolo[4,3-b]pyridazine

https://huagongshe.com/reaction/443513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazinecarboxaldehydeHCID 12229—
Reactant3-Chloro-6-(pyridin-2-yl)pyridazineHCID 6417960—
Solvent1-ButanolHCID 263—
Product6-(2-Pyridyl)-1,2,4-triazolo[4,3-b]pyridazineHCID 23467576—

Reaction Steps

A mixture of 1.0 g. of 3-chloro-6-(2-pyridyl)pyridazine and 0.6 g. of formic acid hydrazide in 50 ml. of n-butyl alcohol is heated at the reflux temperature for 18 hours. The volatiles are removed in vacuo and the residue is partitioned between dilute aqueous sodium hydroxide and methylene chloride. The organic layer is dried over sodium sulfate and filtered. The filtrate is evaporated and the residue is crystallized from methylene chloride-hexane to afford 1.0 g. of the desired product as off-white to yellow crystals, m.p. 191°-192° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04260756
Source datasetuspto-grants-1981_04
ORD IDord-e58587e3d57a455e90a9cbde34758b4a
Source noteuspto-grants-1981_04