Abstract Condensation reactions ol the “functionalized” pyrroles which were obtained by one pot synthesis of aziridines and acetylenic dipolarophiles were discussed. On treatments of 3,4‐di‐ and 2,3,4‐tribenzoylpyrroles with hydrazine hydrate and phosphorus pentasulfide, the several pyrrolo‐pyridazine derivatives and fused thiophenes, respectively, were prepared. The structure proofs for the products of the reaction of the 2,3,4‐tribenzoylpyrrole ( 9a ) with hydrazine hydrate were based on the 13 C FT‐nmr spectrum of the corresponding 13 C‐enriched compounds.