HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901494Generated: October 31, 2026
Water → Ethyl 1-cyclopropyl-5-ethinyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylate
https://huagongshe.com/reaction/1901494
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | Ethyl 1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-5-trimethylsilylethinyl-4-oxo-3-quinolinecarboxylate | HCID 22924385 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 1-cyclopropyl-5-ethinyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylate | HCID 22924399 | 76.6% |
Reaction Steps
1 g of the product of Example E and 0.45 g of potassium fluoride are stirred for 1 hour at room temperature in a mixture of 20 ml of dimethylformamide, 10 ml of chloroform and 1 ml of water. After chloroform has been added, the organic phase is separated off, extracted by shaking with water, dried over sodium sulphate and concentrated. The residue is boiled briefly in 20 ml of methanol. When the mixture has cooled to 0° C., the solid obtained is filtered off with suction and dried. 0.63 g of the title compound is obtained (77% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05578604 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-30c3076ae1864948bdf7e00a87fa3d8e |
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| Source note | uspto-grants-1996_11 |
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