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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112943Generated: October 31, 2026

1-Ethyl-3-(5-hydroxymethyl-7-pyridin-3-yl-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-urea → 1-Ethyl-3-(5-formyl-7-pyridin-3-yl-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-urea

https://huagongshe.com/reaction/2112943

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(5-hydroxymethyl-7-pyridin-3-yl-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-ureaHCID 68834808—
CatalystManganese dioxideHCID 14801—
SolventTetrahydrofuranHCID 8028—
Product1-Ethyl-3-(5-formyl-7-pyridin-3-yl-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-ureaHCID 86618022—

Reaction Steps

The product of Step 1 (154 mg, 0.50 mmol) was dissolved in THF (50 mL), to which was added MnO2 (250 mg). This mixture was heated at reflux for 18 h., at which point two further portions (50 mg each) were added over the next 8 hours. Finally, the mixture was heated at reflux for 18 h., allowed to cool, then the MnO2 removed by filtration over celite which was washed with THF and MeOH/CH2Cl2. The solvent was removed under reduced pressure to afford 1-ethyl-3-(5-formyl-7-pyridin-3-yl-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-urea as a crude solid. LCMS (APCI+) 311.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524860B2
Source datasetuspto-grants-2009_04
ORD IDord-8b21061d454c4793b89cf04555bcf3b2
Source noteuspto-grants-2009_04