In this paper, two of the new antipyrine heterocyclic derivatives have been synthesized via the formation of Schiff bases. The Schiff bases compounds were generated from the reaction of 4-Ameno-antipyrine (4-AAP) with 3-hydroxybenzaldehyde and 4-nitrobenzaldehyde, which was converted to imidazolidinone compounds by reaction with glycine. The reactions were monitored by Thin Layer Chromatography (TLC). The structure of the prepared compounds was confirmed by physical and available spectroscopic data, i.e., FTIR, 1 HNMR, 13 C-NMR, GC-Mass and HRMs.