HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381075Generated: November 1, 2026
HCID 46681952, compound → HCID 68499878, compound
https://huagongshe.com/reaction/2381075
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 46681952 | HCID 46681952 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68499878 | HCID 68499878 | 94.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258140B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-8bb61b72e947420db617b223b74fe6a3 |
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| Source note | uspto-grants-2012_09 |
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