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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043687Generated: October 30, 2026

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

https://huagongshe.com/reaction/2043687

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 NaI4 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 numberUS08586623B2
Source datasetuspto-grants-2013_11
ORD IDord-37a5fbae97884f46a2db07ed3ec2128b
Source noteuspto-grants-2013_11