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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809642Generated: October 30, 2026

8-(Benzyloxy)-[1,2,4]triazolo[4,3-a]pyridine → [1,2,4]Triazolo[4,3-a]pyridin-8-ol

https://huagongshe.com/reaction/1809642

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-(Benzyloxy)-[1,2,4]triazolo[4,3-a]pyridineHCID 20519399—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product[1,2,4]Triazolo[4,3-a]pyridin-8-olHCID 6748771287.7%

Reaction Steps

To a 8-(benzyloxy)-[1,2,4]triazolo[4,3-a]pyridine (8.05 g, 35.7 mmol) dissolved in EtOH 100 ml was added 300 mg 10% Pd/C (Degussa). The reaction vessel was inerted with nitrogen and then purged with hydrogen 3 times, and the reaction was stirred under double balloon pressure of hydrogen overnight. The catalyst was removed by filtration and the filtrate concentrated to give a residue of [1,2,4]triazolo[4,3-a]pyridin-8-ol (4.23 g, 87% yield) that was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362037B2
Source datasetuspto-grants-2013_01
ORD IDord-3f00fba11a584c7882bca786d7609d4a
Source noteuspto-grants-2013_01