HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368416Generated: October 26, 2026
Ethyl 3-(3-chloro-2,4,5-trifluorophenyl)-3-oxopropanoate → Ethyl 8-chloro-1-[3,5-difluoro-6-(p-methoxybenzylamino)-4-methylpyridin-2-yl]-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate
https://huagongshe.com/reaction/368416
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 3-(3-chloro-2,4,5-trifluorophenyl)-3-oxopropanoate | HCID 10934859 | — |
| Reactant | 2-Amino-3,5-difluoro-6-(p-methoxybenzylamino)-4-methylpyridine | HCID 22121271 | — |
| Reactant | Ethyl 3-ethoxy-2-(3-chloro-2,4,5-trifluorobenzoyl)acrylate | HCID 54402571 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 8-chloro-1-[3,5-difluoro-6-(p-methoxybenzylamino)-4-methylpyridin-2-yl]-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate | HCID 22121289 | — |
Reaction Steps
To 3 ml chloroform solution of ethyl 3-ethoxy-2-(3-chloro-2,4,5-trifluorobenzoyl)acrylate prepared from 0.78 g of ethyl 3-chloro-2,4,5-trifluorobenzoylacetate by normal process was added 0.90 g of 2-amino-3,5-difluoro-6-(p-methoxybenzylamino)-4-methylpyridine. The solution was concentrated under reduced pressure, and to the residue were added 1.3 g of anhydrous potassium carbonate and 3 ml of N,N-dimethylformamide, and the mixture was stirred at 90° C. for 15 minutes and allowed to cool. The solution was separated by adding 30 ml of chloroform and 300 ml of distilled water, and the chloroform layer was washed twice with 300 ml of distilled water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to obtain the title compound as a brown crude oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06133284 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-12e86be522d64dbda23a33d1157e4c48 |
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| Source note | uspto-grants-2000_10 |
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