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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346512Generated: October 29, 2026

1,4-Dioxane → HCID 23057947, compound

https://huagongshe.com/reaction/346512

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 23057944HCID 23057944—
ProductHCID 23057947HCID 23057947—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 6-chloro-3-(6-chloropyridin-2-yl)-1,2,4-triazolo[4,3-b]pyridazine (620 mg), heptamethylenimine (1.32 g) and 1,4-dioxane (20 ml) was stirred at 100° C. for 9 hours. After allowing to cool to room temperature, the reaction solution was concentrated under reduced pressure, and the resultant residue was extracted with ethyl acetate. The extract was washed successively with 5% aqueous solution of citric acid, water, saturated aqueous solution of sodium hydrogen carbonate and brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resultant crude crystal was recrystallized from ethanol, to obtain 6-azocan-1-yl -3-(6-chloropyridin-2-yl)-1,2,4-triazolo[4,3-b]pyridazine (370 mg) as grayish white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173033B2
Source datasetuspto-grants-2007_02
ORD IDord-2571f2ac621549bc8747bd408ef3e3b7
Source noteuspto-grants-2007_02