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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381079Generated: November 1, 2026

1-[3-(Trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperidin-4-ol → HCID 68499637, compound

https://huagongshe.com/reaction/2381079

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[3-(Trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperidin-4-olHCID 24587632—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 68499637HCID 6849963798%

Reaction Conditions

Temperature50 °C

Reaction Steps

1-[3-(Trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperidin-4-ol (5 g, 17.41 mmol) and 5% palladium on carbon (50% wet, 0.963 g, 0.23 mmol) in MeOH (50 mL) were stirred under an atmosphere of hydrogen at 5 bar and 50° C. for 16 hours. The reaction was incomplete and further 5% palladium on carbon (50% wet, 0.963 g, 0.23 mmol) was added and the mixture was stirred at 50° C. for a further 16 hours. The catalyst was removed by filtration and washed with MeOH/DCM mixtures. The solvents were evaporated to give 1-[3-(trifluoromethyl)-7,8-dihydro-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]piperidin-4-ol (4.93 g, 98%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258140B2
Source datasetuspto-grants-2012_09
ORD IDord-a3c95acaf6b34ab39e1a5fe0bfc48d63
Source noteuspto-grants-2012_09