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 |
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Format: | Artikel |
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. |
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ISSN: | 1434-193X 1099-0690 |
DOI: | 10.1002/ejoc.202400889 |