Facile and simple synthesis of some new polyfunctionally heterocyclic derivatives incorporating 2‐imino‐2 H ‐chromene moiety
1,2‐Dihydro‐2‐imino‐6‐(2‐imino‐2 H ‐chromen‐3‐yl)‐1,4‐diphenyl‐pyridine‐3‐carbonitrile 4 has been synthesized and reacted with ethyl cyanoacetate to yield the new 5‐amino‐1,7‐dihydro‐2‐(2‐imino‐2 H ‐chromen‐3‐yl)‐7‐oxo‐1,4‐diphenyl‐1,8‐naphthyridine‐6‐carbonitrile 6 , which consider a good and avail...
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Veröffentlicht in: | Journal of heterocyclic chemistry 2012-01, Vol.49 (1), p.135-148 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | 1,2‐Dihydro‐2‐imino‐6‐(2‐imino‐2
H
‐chromen‐3‐yl)‐1,4‐diphenyl‐pyridine‐3‐carbonitrile
4
has been synthesized and reacted with ethyl cyanoacetate to yield the new 5‐amino‐1,7‐dihydro‐2‐(2‐imino‐2
H
‐chromen‐3‐yl)‐7‐oxo‐1,4‐diphenyl‐1,8‐naphthyridine‐6‐carbonitrile
6
, which consider a good and available starting intermediate for synthesis of series of functionalized chromenes. So, the compound
6
was utilized as a key for the synthesis of some new pyrimido[5,4‐
c
][1,8]naphthyridinones, pyrido[2,3‐
c
][1,6]naphthyridinones, triazolo[3′,4′:1,6]triazino][5,4‐
c
][1,8]naphthyridinones, triazolo[2′,3′:1,6]pyrimido[4,5‐
c
][1,8]naphthyridinones, triazepino[6,5‐
c
][1,8]naphthyridinone, and triazino[5,4‐
c
][1,8]naphthyridinones. The structures of these compounds were established by elemental analysis, IR, MS, and NMR spectral analysis. J. Heterocyclic Chem., (2012). |
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ISSN: | 0022-152X 1943-5193 |
DOI: | 10.1002/jhet.716 |