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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295728Generated: October 31, 2026

Phthalaldehyde → 7-Fluoro-8-(4-phthalidyl-1-piperazinyl)-5-oxo-1,2-dihydro-5H-thiazolo(3,2-a)-quinoline-4-carboxylic acid

https://huagongshe.com/reaction/2295728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalaldehydeHCID 4807—
Reactant7-Fluoro-8-(1-piperazinyl)-5-oxo-1,2-dihydro-5H-thiazolo(3,2-a)quinoline-4-carboxylic acidHCID 13116429—
SolventDimethylformamideHCID 6228—
Product7-Fluoro-8-(4-phthalidyl-1-piperazinyl)-5-oxo-1,2-dihydro-5H-thiazolo(3,2-a)-quinoline-4-carboxylic acidHCID 13116430—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 300 mg (0.9 mmol) of 7-fluoro-8-(1-piperazinyl)-5-oxo-1,2-dihydro-5H-thiazolo(3,2-a)-quinoline-4-carboxylic acid and 13.5 mg (0.9 mmol) of o-phthal aldehyde acid was suspended in 4 ml of dimethyl formamide and the whole mixture was heated with stirring at 120° C. for seven hours in an oil bath. When the reaction was completed, the mixture was allowed to cool to room temperature and, by collecting the crystals separated out therefrom by filtration, the title compound was obtained as powder. Yield 207 mg (47.7 percent). Melting point 261° to 262° C. (decomposition). Elementary analysis calculated as C24H20FN3O5S: C 59.87, H 4.19, N 8.73; Found: C 60.09, H 4.32, N 8.64.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04426381
Source datasetuspto-grants-1984_01
ORD IDord-d85aa68c66044523827de99f139c4860
Source noteuspto-grants-1984_01