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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phthalaldehyde | HCID 4807 | — |
| Reactant | 7-Fluoro-8-(1-piperazinyl)-5-oxo-1,2-dihydro-5H-thiazolo(3,2-a)quinoline-4-carboxylic acid | HCID 13116429 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Fluoro-8-(4-phthalidyl-1-piperazinyl)-5-oxo-1,2-dihydro-5H-thiazolo(3,2-a)-quinoline-4-carboxylic acid | HCID 13116430 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04426381 |
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| Source dataset | uspto-grants-1984_01 |
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| ORD ID | ord-d85aa68c66044523827de99f139c4860 |
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| Source note | uspto-grants-1984_01 |
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