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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381075Generated: November 1, 2026

HCID 46681952, compound → HCID 68499878, compound

https://huagongshe.com/reaction/2381075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 46681952HCID 46681952—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 68499878HCID 6849987894.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

10% Palladium on carbon (0.563 g, 0.53 mmol) and tert-butyl 4-(3-(trifluoromethyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)piperazine-1-carboxylate (1.97 g, 5.29 mmol) were stirred in MeOH (30 mL) under an atmosphere of hydrogen at atmospheric temperature and pressure for 3 days. The catalyst was removed by filtration and the solvents evaporated. The residues were re-dissolved in MeOH (50 mL), 5% palladium on carbon (0.4 g, 0.09 mmol) was added and the mixture was stirred under an atmosphere of hydrogen at 50° C. and 5 Bar pressure until complete conversion was obtained. The catalyst was removed by filtration, washed with MeOH then DCM/MeOH and the solvent was evaporated to afford tert-butyl 4-(3-(trifluoromethyl)-7,8-dihydro-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)piperazine-1-carboxylate (1.880 g, 9%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258140B2
Source datasetuspto-grants-2012_09
ORD IDord-8bb61b72e947420db617b223b74fe6a3
Source noteuspto-grants-2012_09