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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615625Generated: November 2, 2026

[1,2,4]Triazolo[1,5-a]pyridin-2-ylmethanol → HCID 72207223, compound

https://huagongshe.com/reaction/1615625

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[1,2,4]Triazolo[1,5-a]pyridin-2-ylmethanolHCID 18406865—
CatalystHCID 178418406HCID 178418406—
SolventEthanolHCID 702—
ProductHCID 72207223HCID 7220722344.3%

Reaction Steps

To a solution of [1,2,4]triazolo[1,5-a]pyridin-2-ylmethanol (0.35 g, 2.3 mmol) in EtOH (50 mL) was added manganese (IV) oxide (1.02 g, 11.5 mmol). The mixture was refluxed for 2 days. After cooling to room temperature, the mixture was filtered through Celite. The filtrate was concentrated, and the residue was purified by reverse phase column chromatography (eluting with 10% v/v acetonitrile in water, with 0.01% NH3.H2O) to afford the title compound (0.15 g, 43% yield) as a white solid. ESI MS: m/z 148 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765760B2
Source datasetuspto-grants-2014_07
ORD IDord-770550ffb68f4471a8d3f521eff936c9
Source noteuspto-grants-2014_07