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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532321Generated: October 31, 2026

Water → 6-Cyclobutoxy-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine

https://huagongshe.com/reaction/532321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantCyclobutanolHCID 76218—
Reactant6-Chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine hydrobromideHCID 86650794—
Product6-Cyclobutoxy-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamineHCID 58136790—

Reaction Conditions

Temperature0 °C

Reaction Steps

Cyclobutanol (2.43 ml) was initially charged at RT with stirring and cooled almost to 0° C. with an ice bath. Subsequently, the mixture was admixed with portions of sodium hydride (146 mg). The suspension formed was heated to 55° C. for 30 min and admixed with portions of 6-chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine hydrobromide (W2.001, 200 mg), suspended in cyclobutanol (5 ml). After stirring at 55° C. for 1.5 h, the mixture was left to stand at RT overnight and then admixed with water and extracted three times with dichloromethane. The combined organic phases were dried over sodium sulfate and, after the desiccant had been filtered off, dried under reduced pressure. 136 mg of the title compound were obtained in solid form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853206B2
Source datasetuspto-grants-2014_10
ORD IDord-322bc79a605d4870aa6fc117c10581d9
Source noteuspto-grants-2014_10