One-step route to fluorinated furo[2,3- b]quinoxalines

The reaction of 6,7-difluoro-1-ethylquinoxalinium salts with 2,4-pentanedione, ethyl and bornyl acetoacetates and other β-keto esters results in the formation of 6,7-difluoro-3a,4,9,9a-tetrahydrofuro[2,3- b]quinoxalines. In addition, asymmetric 6-fluoro-7-morpholino and 6-fluoro-7-thiomorpholino sub...

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Veröffentlicht in:Mendeleev communications 1998, Vol.8 (4), p.133-134
Hauptverfasser: Charushin, Valerii N., Mokrushina, Galina A., Petrova, Galina M., Alexandrov, Grigori G., Chupakhin, Oleg N.
Format: Artikel
Sprache:eng
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Zusammenfassung:The reaction of 6,7-difluoro-1-ethylquinoxalinium salts with 2,4-pentanedione, ethyl and bornyl acetoacetates and other β-keto esters results in the formation of 6,7-difluoro-3a,4,9,9a-tetrahydrofuro[2,3- b]quinoxalines. In addition, asymmetric 6-fluoro-7-morpholino and 6-fluoro-7-thiomorpholino substituted 1-ethylquinoxalinium salts react with alkyl acetoacetates in a regio- and stereoselective manner, thus giving exclusively the corresponding alkyl 2-methyl-6-fluoro-7-substituted 3a,4,9,9a-tetrahydrofuro[2,3- b]quinoxalin-3-carboxylates.
ISSN:0959-9436
DOI:10.1070/MC1998v008n04ABEH000973