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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675124Generated: October 30, 2026

HCID 59149722, compound → HCID 59149830, compound

https://huagongshe.com/reaction/1675124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59149722HCID 59149722—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 59149830HCID 5914983029%

Reaction Steps

A mixture of 1′-[3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazin-6-yl]-1′,2′,3′,6′-tetrahydro-3,4′-bipyridine (obtained as described in Example 605) (82 mg, 0.24 mmol) and 10% palladium on carbon (25.2 mg, 0.02 mmol) in MeOH (10 mL) was stirred under an atmosphere of hydrogen at atmospheric pressure for 3 days. The catalyst was removed by filtration and the solvent evaporated to give crude product, which was purified by flash silica chromatography, elution gradient 0 to 3% MeOH in DCM. Fractions containing the desired product were evaporated to dryness to give 6-(4-pyridin-3-ylpiperidin-1-yl)-3-(trifluoromethyl)[1,2,4]triazolo[4,3-b]pyridazine (24 mg, 29%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003649B2
Source datasetuspto-grants-2011_08
ORD IDord-bd3298491b474861ae88cf2f98d67169
Source noteuspto-grants-2011_08