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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253543Generated: November 1, 2026

4-(benzyloxy)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine → HCID 67374373, compound

https://huagongshe.com/reaction/1253543

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(benzyloxy)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridineHCID 67374956—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
ProductHCID 67374373HCID 67374373—

Reaction Steps

4-(benzyloxy)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridine (185 mg, 0.608 mmol) and palladium hydroxide on carbon (85 mg, 0.122 mmol, 20 wt %) were suspended in EtOH (10 ml) and placed under an atmosphere of hydrogen (balloon). After 2 h, additional palladium hydroxide on carbon (85 mg, 0.122 mmol, 20 wt %) was added and the mixture was allowed to stir overnight. The reaction mixture was filtered through a 45 μm syringe filter and the filtrate was concentrated. The residue was purified by column chromatography on silica gel (methanol/ethyl acetate gradient) to afford 6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyridin-4-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455477B2
Source datasetuspto-grants-2013_06
ORD IDord-e3378b1708fb4106b12f6eb166928497
Source noteuspto-grants-2013_06