Ring closure reactions of 3-arylhydrazonoalkyl-quinolin-2-ones to 1-aryl-pyrazolo[4,3-c]quinolin-2-ones
4‐Hydroxy‐3‐arylhydrazonoalkyl‐2‐quinolones 6 or reactive derivatives such as 3‐arylhydrazonoalkyl‐4‐tosyloxy‐2‐quinolones 7 or 4‐chloro‐3‐arylhydrazonoalkyl‐2‐quinolones 14, which are obtained via 3‐acyl‐4‐hydroxyquinolones 4, 10 or 3‐phenylarrmomethylene‐quinoline‐2,4‐diones 12, cyclize in excelle...
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Veröffentlicht in: | Journal of heterocyclic chemistry 2004-09, Vol.41 (5), p.681-690 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | 4‐Hydroxy‐3‐arylhydrazonoalkyl‐2‐quinolones 6 or reactive derivatives such as 3‐arylhydrazonoalkyl‐4‐tosyloxy‐2‐quinolones 7 or 4‐chloro‐3‐arylhydrazonoalkyl‐2‐quinolones 14, which are obtained via 3‐acyl‐4‐hydroxyquinolones 4, 10 or 3‐phenylarrmomethylene‐quinoline‐2,4‐diones 12, cyclize in excellent yields to 1‐aryl‐pyrazolo[4,3‐c]quinolin‐4‐ones (11). The cyclization conditions were investigated by differential scanning calorimetry (DSC). |
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ISSN: | 0022-152X 1943-5193 |
DOI: | 10.1002/jhet.5570410505 |