AbstractA novel series of 1,3,5‐trisubstituted pyrazoles was synthesized. Thus, ethyl 2,4‐dioxo‐6‐phenylhex‐5‐enoate (I) was condensed with phenylhydrazine to afford 3‐ethoxycarbonyl‐1‐phenyl‐5‐styrylpyrazole (II) which on fusion with hydrazine hydrate gave the corresponding acid hydrazide (III). Reaction of III with the appropriate isothiocyanate yielded the disubstituted thiosemicarbazides (IVa‐e) which were cyclized into thiotriazoles (Va‐e), thiadiazoles (Vla‐e) and oxadiazoles (VIIa‐). The structure of the newly synthesized compounds was elucidated by elemental a