HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 375254Erstellt: 23. Oktober 2026
Water → 3-ethoxycarbonyl-6,7-difluoro-2-[N-cyclopropyl-N-(beta-ethoxycarbonylethyl)amino]quinoline
https://huagongshe.com/de/reaction/375254
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 2-Chloro-3-ethoxycarbonyl-6,7-difluoroquinoline | HCID 9795461 | — |
| Edukt | Ethyl 3-(cyclopropylamino)propanoate | HCID 13456042 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 3-ethoxycarbonyl-6,7-difluoro-2-[N-cyclopropyl-N-(beta-ethoxycarbonylethyl)amino]quinoline | HCID 18994585 | 65,6% |
Reaktionsschritte
3 g of sodium carbonate are added to a solution of 3.48 g of 2-chloro-3-ethoxycarbonyl-6,7-difluoroquinoline and 3 g of N-cyclopropyl-N-(β-ethoxycarbonylethyl)amine in 10 cm3 of toluene. The suspension obtained is heated to reflux and then stirred for 15 hours at this temperature. The reaction mixture is then cooled to approximately 20° C. and 30 cm3 of water and 4.5 cm3 of acetic acid are thereafter added. After settling has taken place, the reaction mixture is separated and washed with twice 10 cm3 of water. The organic phase is concentrated to dryness under reduced pressure (20 kPa) at approximately 50° C. 3.3 g of crude 3-ethoxycarbonyl-6,7-difluoro-2-[N-cyclopropyl-N-(β-ethoxycarbonylethyl)amino]quinoline are obtained in the form of an oil, which is used without further purification for the subsequent step.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05484921 |
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| Quelldatensatz | uspto-grants-1996_01 |
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| ORD ID | ord-b734297800dd43688690a6e9911a857b |
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| Quellennotiz | uspto-grants-1996_01 |
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