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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295725Generated: November 1, 2026

Ethanol → 8-chloro-7-fluoro-5-oxo-1,2-dihydro-5H-thiazolo(3,2-a)quinoline-4-carboxylic acid

https://huagongshe.com/reaction/2295725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactantethyl 8-chloro-7-fluoro-5-oxo-1,2-dihydro-5H-thiazolo(3,2-a)-quinoline-4-carboxylateHCID 10404195—
SolventWaterHCID 962—
Product8-chloro-7-fluoro-5-oxo-1,2-dihydro-5H-thiazolo(3,2-a)quinoline-4-carboxylic acidHCID 1047004591.4%

Reaction Steps

Six hundred mg (1.83 mmol) of ethyl 8-chloro-7-fluoro-5-oxo-1,2-dihydro-5H-thiazolo(3,2-a)-quinoline-4-carboxylate obtained in Example 15 was added to a mixed solvent of ethanol and water (1:1), then 2 ml of 2 N aqueous solution of sodium hydroxide was added thereto, and the mixture was heated to reflux for two hours. When the reaction was completed, ethanol was evaporated therefrom, the residual aqueous solution was adjusted to pH nearly 7.0 with 1 N aqueous solution of acetic acid and, after stirring for a while, crystals separated out therefrom were collected by filtration, successively washed with ethanol, acetone and ether and air dried to give 501 mg (91.4 percent) of the title compound, melting point 318° C. (decomposition). Elementary analysis calculated as C12H7FClNO3S: C 48.09, H 2.35, N. 4.67; Found: C 48.28, H 2.14, N 4.37.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04426381
Source datasetuspto-grants-1984_01
ORD IDord-0f23ade7236f4960a96ab9ab7d482156
Source noteuspto-grants-1984_01