HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085783Generated: November 1, 2026
tert-Butanol → 6,8-Difluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid
https://huagongshe.com/reaction/1085783
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | ethyl 6,8-difluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate | HCID 10000764 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6,8-Difluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid | HCID 10248380 | 92.6% |
Reaction Steps
To 0.5 g of ethyl 6,8-difluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate was added 10 ml of 5% solution of potassium hydroxide in a 3:1 mixture of tert-butanol and water and the mixture was stirred at 60° C. for 30 minutes. tert-Butanol was evaporated therefrom in vacuo and the residue was neutralized with acetic acid. After cooling, the crystals separated out therefrom were collected by filtration, washed with water and then washed with acetone and ether to give 0.43 g of the title product, m.p. 260° C. (decompn.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05011831 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-3f8bc9ea90af4344b2e23845e1db3f16 |
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| Source note | uspto-grants-1991_04 |
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