Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217674Generated: October 29, 2026

Piperidine → 6-Piperidin-1-yl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine

https://huagongshe.com/reaction/217674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant6-Chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine hydrobromideHCID 86650794—
SolventWaterHCID 962—
Product6-Piperidin-1-yl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamineHCID 15107882—

Reaction Steps

6-Chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine hydrobromide (W2.001; 100 mg) were initially charged in water (1 ml) and admixed with piperidine (260 μl) with stirring. Thereafter, the mixture was heated to reflux for 1 h and, after cooling, freed of the solvent. Subsequently, the mixture was admixed with water and the solid formed was filtered off with suction and dried. The mother liquor was dried and admixed with a little water. The solid obtained was filtered off with suction and dried. The filtrate was then 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. The three resulting solid fractions were combined and gave rise to 56 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198272B2
Source datasetuspto-grants-2012_06
ORD IDord-54e1cb8527cf46c4896cfb1e2f9d958f
Source noteuspto-grants-2012_06