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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035775Generated: October 26, 2026

3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine → 3-Chloro-6-ethoxy[1,2,4]triazolo[4,3-b]pyridazine

https://huagongshe.com/reaction/1035775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazineHCID 1482346—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
Solvent1,4-DioxaneHCID 31275—
Product3-Chloro-6-ethoxy[1,2,4]triazolo[4,3-b]pyridazineHCID 67524522—

Reaction Steps

The 3-chloro-6-ethoxy[1,2,4]triazolo[4,3-b]pyridazine was prepared according to the method described in Example 16b, but using 1 g of commercial 3,6-dichloro[1,2,4]triazolo[4,3-b]pyridazine, 1.71 g of a solution at 21% of sodium ethoxide in ethanol and 30 cm3 of dioxane, after reaction at reflux for 5.5 h. 874 mg of 3-chloro-6-ethoxy[1,2,4]triazolo[4,3-b]pyridazine are thus obtained in the form of a whitish powder, the characteristics are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546393B2
Source datasetuspto-grants-2013_10
ORD IDord-9cd2a2120d904369acf3fdb703edcc80
Source noteuspto-grants-2013_10