Elemental Sulfur‐Promoted Annulative Coupling of 2‐Aminobenzamides and 2‐Aminobenzylamines with Sulfoxonium Ylides: Access to Quinazolinones and Quinazolines

A novel and straightforward approach for synthesizing quinazolinones and quinazoline derivatives employing sulfur‐mediated annulative coupling of 2‐aminobenzamides and 2‐aminobenzylamines in conjunction with sulfoxonium ylides has been described. This method demonstrates a broad substrate range and...

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Veröffentlicht in:European journal of organic chemistry 2024-12, Vol.27 (47), p.n/a
Hauptverfasser: Chaubey, Trayambek Nath, Borpatra, Paran J., Pandey, Satyendra Kumar
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Sprache:eng
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Zusammenfassung:A novel and straightforward approach for synthesizing quinazolinones and quinazoline derivatives employing sulfur‐mediated annulative coupling of 2‐aminobenzamides and 2‐aminobenzylamines in conjunction with sulfoxonium ylides has been described. This method demonstrates a broad substrate range and exhibits excellent tolerance towards various functional groups. Finally, this protocol has been successfully applied to synthesize pyrazino‐fused quinazolinone derivative with adjustable fluorescence properties and tryptanthrin, a compound known for its potent antitubercular activity. A novel and straightforward approach to synthesize quinazolinones and quinazoline derivatives employing sulfur‐mediated annulative coupling of 2‐aminobenzamides and 2‐aminobenzylamines with readily accessible sulfoxonium ylides has been developed.
ISSN:1434-193X
1099-0690
DOI:10.1002/ejoc.202400889