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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422938Generated: October 30, 2026

Hydrogen Peroxide → 3-Benzyloxy-6-methoxy-[1,5]naphthyridine-4-carboxylic acid amide

https://huagongshe.com/reaction/1422938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
Reactant3-Benzyloxy-6-methoxy-[1,5]naphthyridine-4-carbonitrileHCID 67257004—
CatalystHCID 178418406HCID 178418406—
SolventMethanolHCID 887—
Product3-Benzyloxy-6-methoxy-[1,5]naphthyridine-4-carboxylic acid amideHCID 6725398175%

Reaction Conditions

Temperature70 °C

Reaction Steps

30% Hydrogen peroxide (17.2 mmol, 5.0 eq) is added dropwise at room temperature to a stirred suspension of 3-benzyloxy-6-methoxy-[1,5]naphthyridine-4-carbonitrile (1.0 g, 3.43 mmol, 1.0 eq) and sodium hydroxide (69 mg, 0.17 mmol, 0.05 eq) in methanol (100 mL). After 1 hour stirring at 70° C., a catalytic amount of manganese dioxide is added to the reaction mixture that is concentrated to give a crude that is purified by column chromatography (silica gel, eluent: petroleum ether:ethyl acetate, 1:1, v/v) to afford 3-benzyloxy-6-methoxy-[1,5]naphthyridine-4-carboxylic acid amide as a white solid (800 mg, 75% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927541B2
Source datasetuspto-grants-2015_01
ORD IDord-351f8f2aa16745a0bef44f96a1d9293d
Source noteuspto-grants-2015_01