Abstract
A new class of thiazole‐fused diazepinones has been synthesized by the application of intramolecular hydrazonolysis, wherein 2‐arylamino‐4‐coumarinyl‐5‐formyl thiazoles were treated with hydrazine hydrate in refluxing ethanol to yield the rearranged products via an interesting ring‐opening and cyclization process.
Acknowledgment
Authors thank C. S. Mahajanshetti, former chairman, Department of Chemistry, Karnatak University, Dharwad, India, for valuable suggestions and encouragement.