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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896466Generated: October 31, 2026

Ammonia → HCID 14998298, compound

https://huagongshe.com/reaction/1896466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHCID 14998306HCID 14998306—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 14998298HCID 1499829885%

Reaction Steps

6-chloro-8-methyl-3-phenyl[1,2,4]triazolo[4,3-b]pyridazine x240 is dissolved in ethanol (300 ml), and 10% Pd/C (0.9 g) and 25% aqueous ammonia (60 ml) are added. The mixture is hydrogenated in the Parr apparatus under hydrogen pressure 2.5 atm at room temperature for 1h10. The reaction mixture is filtered through a Celite layer, which is washed with ethanol. The combined filtrates are evaporated, and the residue is dissolved in dichloromethane. The solution is washed with brine and dried over anhydrous Na2SO4. The solvent is removed under reduced pressure to afford 2.9 g of 8-methyl-3-phenyl[1,2,4]triazolo[4,3-b]pyridazine x241.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518943B2
Source datasetuspto-grants-2013_08
ORD IDord-cb605a9971e549909f0973e6465f44bc
Source noteuspto-grants-2013_08