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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926838Generated: November 3, 2026

Methanol → 3-(Trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazine-7-carbaldehyde

https://huagongshe.com/reaction/1926838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant7-Methyl-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazineHCID 53629203—
SolventDichloromethaneHCID 6344—
Product3-(Trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazine-7-carbaldehydeHCID 5362920478%

Reaction Steps

A finely-ground powder of NalO4 is added to a solution of 7-methyl-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazine x233 (0.52 g, 2.0 mmol) in absolute methanol (42 ml). The reaction mixture is stirred at room temperature for 1.5 h and diluted with an equal volume of dichloromethane. The mixture is filtered through the Celite layer, and the solvents are removed under reduced pressure. The residue (0.5 g) is purified by chromatography on silicagel (hexane/ethyl acetate 3/2) to yield 0.34 g of 3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazine-7-carbaldehyde x235 as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183241B2
Source datasetuspto-grants-2012_05
ORD IDord-ee7d2b53e1dc456c9a1fdb2948e669c0
Source noteuspto-grants-2012_05