Synthesis of 1-Substituted 3H-Naphtho[1,2,3-de]quinoline-2,7-diones

A method for preparing 1-tosyl-3 H -naphtho[1,2,3- de ]quinoline-2,7-diones by the reaction of N -(9,10-anthraquinon-1-yl)chloroacetamide with sodium p -toluenesulfinate has been developed. Nucleophilic substitution of the tosyl group by nitrogen and oxygen nucleophiles has been found to proceed und...

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Veröffentlicht in:Doklady. Chemistry 2022-09, Vol.506 (1), p.202-210
Hauptverfasser: Chernenko, S. A., Shatsauskas, A. L., Kostyuchenko, A. S., Fisyuk, A. S.
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Sprache:eng
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Zusammenfassung:A method for preparing 1-tosyl-3 H -naphtho[1,2,3- de ]quinoline-2,7-diones by the reaction of N -(9,10-anthraquinon-1-yl)chloroacetamide with sodium p -toluenesulfinate has been developed. Nucleophilic substitution of the tosyl group by nitrogen and oxygen nucleophiles has been found to proceed under mild conditions. The corresponding 1-substituted 3 H -naphtho[1,2,3- de ]quinoline-2,7-diones have been obtained by the reaction of these compounds with amines, phenol, sodium hydroxide, and sodium azide.
ISSN:0012-5008
1608-3113
DOI:10.1134/S0012500822700112