Synthesis of unsymmetrical 3,3'-biquinazoline-2,2'-diones by condensation of 3-aminoquinazolinones with benzoxazinones; fortuitous discovery, and further syntheses of 4-H-3-oxo-1,9a,10-triazaanthracen-9-ones

Condensation of 2-alkyl- or 2-aryl-3-aminoquinazolin-4-ones with benz[1,3]oxazin-4-ones gives the unsymmetrical 2,2' disubstituted 3,3' biquinazoline-4,4'-diones. The reaction is tolerant to a range of heteroatom and unsaturated functionality in the quinazolinone 2-position. However,...

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Veröffentlicht in:Organic & biomolecular chemistry 2005-03, Vol.3 (6), p.1134-1139
Hauptverfasser: Coogan, Michael P, Ooi, Li-ling, Pertusati, Fabrizio
Format: Artikel
Sprache:eng
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Zusammenfassung:Condensation of 2-alkyl- or 2-aryl-3-aminoquinazolin-4-ones with benz[1,3]oxazin-4-ones gives the unsymmetrical 2,2' disubstituted 3,3' biquinazoline-4,4'-diones. The reaction is tolerant to a range of heteroatom and unsaturated functionality in the quinazolinone 2-position. However, treatment of 3-amino-2-hydroxymethyl-3H-quinazolin-4-ones with benz[1,3]oxazinone at high temperatures gave 4H-3-oxo-1,9a,10-triazaanthracen-9-ones, an unreported fused heterocyclic system, a more direct synthesis of which, replacing benzoxazinones with orthoesters is presented.
ISSN:1477-0520
1477-0539
DOI:10.1039/b419108k