HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525889Generated: October 30, 2026
Triethyl Phosphate → Ethyl 1-ethyl-8-fluoro-6,7-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate
https://huagongshe.com/reaction/525889
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethyl Phosphate | HCID 6535 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 8-fluoro-6,7-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate | HCID 86732753 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 1-ethyl-8-fluoro-6,7-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate | HCID 86732754 | 57.9% |
Reaction Steps
A mixture of ethyl 8-fluoro-6,7-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate (41 g, 139 mmol) and potassium carbonate (28.8 g, 208 mmol) in triethyl phosphate (118 ml, 694 mmol) was stirred at 120° C. for 5 h. LCMS indicated completion of the reaction. Then the reaction mixture was cooled down and diluted with water, extracted with DCM, dried over sodium sulfate and evaporated in vacuo. The crude material was purified by reverse phase automatic C-18 column chromatography (Combiflash RF, 130 g column), eluting with Acetonitrile/Water (10-80%) to afford ethyl 1-ethyl-8-fluoro-6,7-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate (26 g, 80 mmol, 57.9% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340556B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-7de7bb11a00e4b05b59380038dbb7c14 |
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| Source note | uspto-grants-2016_05 |
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