Synthesis of some new styryl oxazolophenoxazines
Reductive acetylation of 3‐aminophenoxaz‐2‐one (II) gave 3‐acetylamino‐2‐acetoxy‐phenoxazine (IV). Thermolysis of (IV) gave 2‐methyl‐5 H ‐oxazolo(4,5‐ b )phenoxazine (V). The styryl derivatives (VIII) were synthesised by condensation of (V) with aromatic aldehydes. Quaternisation of (V) was carried...
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Veröffentlicht in: | Journal of applied chemistry and biotechnology 1977, Vol.27 (1), p.11-16 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Reductive acetylation of 3‐aminophenoxaz‐2‐one (II) gave 3‐acetylamino‐2‐acetoxy‐phenoxazine (IV). Thermolysis of (IV) gave 2‐methyl‐5
H
‐oxazolo(4,5‐
b
)phenoxazine (V). The styryl derivatives (VIII) were synthesised by condensation of (V) with aromatic aldehydes. Quaternisation of (V) was carried out giving (VII). Oxidation of (V) using SeO
2
gave 2‐formyl‐5
H
‐oxazolo(4,5‐
b
)phenoxazine (VI). Fragmentation patterns of certain of the products under electron impact are suggested. |
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ISSN: | 0375-9210 1935-0554 |
DOI: | 10.1002/jctb.5020270103 |