Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517809Generated: October 25, 2026

Potassium Carbonate → 3-Chloro-6-(oxetan-2-ylmethoxy)[1,2,4]triazolo[4,3-b]pyridazine

https://huagongshe.com/reaction/517809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazineHCID 1482346—
Reactant(Oxetan-2-yl)methanolHCID 12284142—
SolventDimethylformamideHCID 6228—
Product3-Chloro-6-(oxetan-2-ylmethoxy)[1,2,4]triazolo[4,3-b]pyridazineHCID 67524580—

Reaction Conditions

Temperature100 °C

Reaction Steps

a mixture of 756 mg of commercial 3,6-dichloro[1,2,4]triazolo[4,3-b]pyridazine, 0.352 cm3 of 2-hydroxymethyloxetane and 552 mg of potassium carbonate in 8 cm3 of N,N-dimethylformamide is heated at 100° C. for 6 h and then stirred at 20° C. overnight. The reaction medium is concentrated to dryness under vacuum. The residue obtained is purified by chromatography on a Merck cartridge of 25 g of silica 15-40 μm by solid deposit, elution being carried out with a dichloromethane/methanol gradient of 100/0 to 97/03. 701 mg of 3-chloro-6-(oxetan-2-ylmethoxy)[1,2,4]triazolo[4,3-b]pyridazine are thus obtained in the form of a beige solid, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115134B2
Source datasetuspto-grants-2015_08
ORD IDord-0cf7bdb542bd42b9958625e0d297b56a
Source noteuspto-grants-2015_08