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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 6-Chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine hydrobromide | HCID 86650794 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Piperidin-1-yl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198272B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-54e1cb8527cf46c4896cfb1e2f9d958f |
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| Source note | uspto-grants-2012_06 |
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