Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 10476611 | HCID 10476611 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 10452425 | HCID 10452425 | 38.6% |
Reaction Steps
To 0.5 g of ethyl 6,8-difluoro-1-methyl-7-(4-methyl-1-piperazinyl)-4-oxo-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate was added 10 ml of 5% solution of potassium hydroxide in 3:1 mixture of tert-butanol and water and stirred at 60° C. for 30 minutes. tert-Butanol was evaporated therefrom in vacuo, the residue was neutralized with acetic acid, extracted with a 3:1 mixture of chloroform and methanol, the extract was washed with saturated sodium chloride solution, dried over magnesium sulfate, the solvent was evaporated therefrom, and the residue was subjected to a silica gel column chromatography (30 g of Wakogel C-300 being used) and eluted with chloroform-methanol (10:1) to give 0.18 g of desired product, m.p. 238° 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-8bf4ab4560ec4fb19e846110fe2b8bbf |
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| Source note | uspto-grants-1991_04 |
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