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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1938340Generated: October 29, 2026

3-Nitro-7-(5-methyl-2-phenyl-4-oxazolylmethoxy)quinoline → 3-Amino-7-(5-methyl-2-phenyl-4-oxazolylmethoxy)quinoline

https://huagongshe.com/reaction/1938340

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitro-7-(5-methyl-2-phenyl-4-oxazolylmethoxy)quinolineHCID 21469326—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product3-Amino-7-(5-methyl-2-phenyl-4-oxazolylmethoxy)quinolineHCID 2146927042%

Reaction Steps

In a mixture of ethanol (20 mL) and ethyl acetate (10 mL) was suspended 3-nitro-7-(5-methyl-2-phenyl-4-oxazolylmethoxy)quinoline (740 mg, 2.1 mmol.), and to the suspension was added 10% palladium/carbon (50 mg). Then, catalytic reduction was performed overnight. After the completion of reaction was confirmed, the reaction mixture was filtered over Celite®, and the filtrate was placed under reduced pressure to remove the solvent. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/7 to ethyl acetate), to give 280 mg of the desired compound as brown oil (yield 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05693651
Source datasetuspto-grants-1997_12
ORD IDord-35bc5fa6f6db4664859e78d18e822f26
Source noteuspto-grants-1997_12