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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36023Generated: October 29, 2026

Ethyl 7-chloro-6-fluoro-1-(1,2,4-thiadiazol-5-yl)-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylate → 7-Chloro-6-fluoro-1-(1,2,4-thiadiazol-5-yl)-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/36023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 7-chloro-6-fluoro-1-(1,2,4-thiadiazol-5-yl)-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylateHCID 15229391—
SolventTetrahydrofuranHCID 8028—
Product7-Chloro-6-fluoro-1-(1,2,4-thiadiazol-5-yl)-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acidHCID 15229392—

Reaction Conditions

Temperature80 °C

Reaction Steps

Compound No. 164 (1.1 g) obtained in Example 99 was dissolved in a mixture of tetrahydrofuran (40 ml) and c-HCl (10 ml). The solution was stirred at 80° C. for 1.5 hour. After the solvent was removed in vacuo, the precipitate was filtrated and washed with ethanol, ether and n-hexane. The title compound No. 165 was obtained as a slightly yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05412098
Source datasetuspto-grants-1995_05
ORD IDord-c65a6d6409614695970fd6ca70748059
Source noteuspto-grants-1995_05