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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073625Generated: November 3, 2026

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

https://huagongshe.com/reaction/1073625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
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 1942367892.7%

Reaction Conditions

Temperature20 °C

Reaction Steps

A suspension of 4 g of 3-ethoxycarbonyl-7,8,9-trifluoro-1-methyl-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine in 30 cm3 of acetic acid and 30 cm3 of 50% hydrochloric acid is heated at a temperature close to 100° C. for 2 hours. After cooling to about 20° C., 100 cm3 of water are added. The precipitate formed is drained, washed with 3 times 50 cm3 of water and recrystallized from 80 cm3 of dimethylformamide. 3.4 g of 7,8,9-trifluoro-1-methyl-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine-3-carboxylic acid are obtained in the form of a colourless solid melting at 350°-352° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04970213
Source datasetuspto-grants-1990_11
ORD IDord-ee83efbd99de4644a6d49230da47c58c
Source noteuspto-grants-1990_11