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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375248Generated: October 29, 2026

Ethanol → 3-Ethoxy-7,8-difluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine

https://huagongshe.com/reaction/375248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHydrogen PeroxideHCID 784—
ReactantSodium ThiosulfateHCID 24477—
Reactant3-Ethoxycarbonyl-7,8-difluoro-1-methyl-4-oxo-1,2,3,4-tetrahydrobenzo[b][1,8]naphthyridineHCID 9883542—
CatalystPotassium IodideHCID 4875—
SolventWaterHCID 962—
Product3-Ethoxy-7,8-difluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridineHCID 18994605—

Reaction Conditions

Temperature77 °C

Reaction Steps

A solution of 3.78 g of potassium iodide in 20 cm3 of water is added with stirring at approximately 20° C. to a suspension of 71 g of 3-ethoxycarbonyl-7,8-difluoro-1-methyl-4-oxo-1,2,3,4-tetrahydrobenzo[b][1,8]naphthyridine in 1,000 cm3 of ethanol. The suspension is heated to 77° C. and 30 cm3 33% by weight hydrogen peroxide are added in the course of 60 minutes at this temperature. The reaction mixture is kept refluxing for a further 30 minutes and is then cooled to approximately 20° C. A solution of 11.4 g of sodium thiosulphate in 50 cm3 of water is introduced in the course of 5 minutes at this temperature. The precipitate obtained is drained at approximately 20° C. and washed with twice 300 cm3 of water. The wet product obtained is dried under reduced pressure (20 kPa) at approximately 60° C. 73 g of 3-ethoxy-7,8-difluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine are isolated in the form of a white solid, melting point above 270° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484921
Source datasetuspto-grants-1996_01
ORD IDord-4652b245e1e34bce9fe57b1b15f88e97
Source noteuspto-grants-1996_01