HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243054Generated: November 4, 2026
Water → Ethyl 1-(2,2-difluoroethyl)-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylate
https://huagongshe.com/reaction/2243054
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,2-Difluoroethanamine | HCID 136274 | — |
| Reactant | Ethyl 3-(dimethylamino)-2-(2-fluoro-5-iodobenzoyl)acrylate | HCID 58801734 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 1-(2,2-difluoroethyl)-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylate | HCID 59208381 | — |
Reaction Steps
A suspension of ethyl 3-(dimethylamino)-2-(2-fluoro-5-iodobenzoyl)acrylate (335 mg, 0.86 mmol) and 2,2-difluoroethylamine (76 mg, 0.94 mmol) in ethanol (3 mL) was stirred at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure and dissolved in DMF (3 mL). Potassium carbonate (178 mg, 1.28 mmol) was added to the reaction mixture and the reaction was heated to 70° C. for 3 h, then cooled to room temperature and poured into water. The title compound formed a precipitate which was collected by filtration and placed upon lyophilizer overnight to remove residual water. MS (ESP): 408 (M+H+) for C14H12F2INO3; NMR: 1.29 (t, J=7 Hz, 3H), 4.25 (q, J=7 Hz, 2H), 4.96 (m, 2H), 6.50 (t, J=20 Hz, 1H), 7.73 (m, 1H), 8.08 (m, 1H), 8.50 (m, 1H), 8.70 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07674801B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-ba5a3d2bba154d6fa2322e147ba64ecf |
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| Source note | uspto-grants-2010_03 |
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