Original recyclization of S-phenacyl derivatives of 4-acylamino-2-mercapto-1,3-oxazoles and their analogues

Readily accessible acylamino(chloro)acetophenones, if treated with sodium rhodanide and α‐halogenocarbonyl compounds, provide 4‐acylamino‐5‐aryl‐2‐mercapto‐1,3‐oxazole derivatives which undergo recyclization on heating in polyphosphoric acid to give substituted 1,3‐thiazol‐2(3H)‐ones or 1,3‐thiazoli...

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Veröffentlicht in:Heteroatom chemistry 2007-05, Vol.18 (4), p.432-437
Hauptverfasser: Balia, Andrei G., Belyuga, Aleksandr G., Brovarets, Vladimir S., Vasylenko, Aleksandr N., Turov, Aleksandr V., Gakh, Andrei A., Drach, Boris S.
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Sprache:eng
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Zusammenfassung:Readily accessible acylamino(chloro)acetophenones, if treated with sodium rhodanide and α‐halogenocarbonyl compounds, provide 4‐acylamino‐5‐aryl‐2‐mercapto‐1,3‐oxazole derivatives which undergo recyclization on heating in polyphosphoric acid to give substituted 1,3‐thiazol‐2(3H)‐ones or 1,3‐thiazolidin‐2,4‐diones containing 2‐alkyl(aryl)‐5‐aryl‐1,3‐oxazol‐4‐yl residues at the N3 atom. © 2007 Wiley Periodicals, Inc. Heteroatom Chem 18:432–437, 2007; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20317
ISSN:1042-7163
1098-1071
DOI:10.1002/hc.20317