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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896464Generated: October 30, 2026

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

https://huagongshe.com/reaction/1896464

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 NaIO4 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 numberUS08518943B2
Source datasetuspto-grants-2013_08
ORD IDord-e6c4ec8a6d0b43a2b685873404dfaf42
Source noteuspto-grants-2013_08