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New routes to aroylthiadiazolines and arylazothiazoles from phenylglyoxalyl bromide arylhydrazones and phenacyl thiocyanate

1976; Wiley; Volume: 13; Issue: 1 Linguagem: Inglês

10.1002/jhet.5570130108

1943-5193

Ahmad Sami Shawali, Abdou O. Abdelhamid,

Synthesis and Biological Evaluation

Abstract Reaction of phenylglyoxalyl bromide arylhydrazones (III) with thiourea in ethanol produces 2‐amino‐4‐phenyl‐5‐arylazothiazoles (XI) instead of the expected 2‐benzoyl‐4‐aryl‐5‐imino‐Δ 2− 1,3,4‐thiadiazolines (V) obtained from III and potassium thiocyanate. Phenacyl thiocyanate (IV) couples with diazotized anilines to give V. The mechanisms of formation of V and XI from VI and III, respectively, are postulated. Nitrosation of V gives the corresponding N ‐nitroso derivatives (VII), which decompose upon refluxing in xylene to give 2,4‐disubstituted Δ 2 −1,3,4‐thiadiazolin‐5‐ones (VIII). The thiadiazolines V give the respective N ‐aeyl derivatives IX and X with acetic anhydride and benzoyl chloride in pyridine.