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
Hauptverfasser: Metwally, Saoud A. M., Youssef, Mohamed S. K.
Format: Artikel
Sprache:eng
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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.
ISSN:0375-9210
1935-0554
DOI:10.1002/jctb.5020270103