HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1421411Erstellt: 26. Oktober 2026
Diethyl Malonate → Ethyl 2-(3-chloro-2,4-difluorobenzoyl)-3-ethoxy-acrylate
https://huagongshe.com/reaction/1421411
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Malonate | HCID 7761 | — |
| Edukt | 3-Chloro-2,4-difluorobenzoyl chloride | HCID 2773538 | — |
| Edukt | Diethyl (3-chloro-2,4-difluorobenzoyl)malonate | HCID 22077280 | — |
| Edukt | Ethyl (3-chloro-2,4-difluoro-benzoyl)-acetate | HCID 54232984 | — |
| Edukt | Ethyl orthoformate acetic anhydride | HCID 86583744 | — |
| Produkt | Ethyl 2-(3-chloro-2,4-difluorobenzoyl)-3-ethoxy-acrylate | HCID 54286793 | — |
Reaktionsschritte
Reaction of 3-chloro-2,4-difluoro-benzoyl chloride with diethyl malonate gives diethyl (3-chloro-2,4-difluoro-benzoyl)-malonate, and partial hydrolysis and decarboxylation lead to ethyl (3-chloro-2,4-difluoro-benzoyl)-acetate, which is reacted with ethyl orthoformate/acetic anhydride to give ethyl 2-(3-chloro-2,4-difluorobenzoyl)-3-ethoxy-acrylate; further reaction with cyclopropylamine leads to ethyl 2-(3-chloro-2,4-difluoro-benzoyl)-3-cyclopropylaminoacrylate, which is cyclized with potassium carbonateldimethylformamide to give ethyl 8-chloro-1-cyclopropyl-7-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylate; hydrolysis then finally leads to the corresponding carboxylic acid. The reaction sequence described can be represented by the following equation: ##STR4## The quinolonecarboxylic acid obtained in the 6th stage can be converted by reaction with compounds Z--H of the formulae ##STR5## wherein R1 represents hydrogen, straight-chain or branched C1 -C3 -alkyl or cyclopropyl,
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06075165 |
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| Quelldatensatz | uspto-grants-2000_06 |
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| ORD ID | ord-6b9919477f6547a1aa499d6f7d465975 |
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| Quellennotiz | uspto-grants-2000_06 |
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