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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743660Generated: October 30, 2026

3-Ethoxycarbonyl-7,8,9-trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine → 7,8,9-Trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/743660

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Ethoxycarbonyl-7,8,9-trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridineHCID 19423688—
SolventAcetic AcidHCID 176—
SolventHydrochloric AcidHCID 313—
Product7,8,9-Trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acidHCID 1942367893%

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of 0.88 g of 3-ethoxycarbonyl-7,8,9-trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo-[b][1,8]naphthyridine in a mixture of 10 cm3 of 17.5% aqueous hydrochloric acid solution and 10 cm3 of acetic acid is heated with stirring to a temperature in the region of 100° C. for 3 hours. After cooling to approximately 20° C., the product is drained and washed with 3 times 10 cm3 of water. 0.75 g of 7,8,9-trifluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3carboxylic acid is obtained in the form of a pale yellow solid, which decomposes at 352° C. and which is used without further purification for the subsequent steps.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05556861
Source datasetuspto-grants-1996_09
ORD IDord-6f56098e7f87448cb26483e4e2d65b9c
Source noteuspto-grants-1996_09