A new ten heterocyclic compounds were prepared starting from aniline derivatives which underwent diazotization reaction with salicylaldehyde affording 5-tolyl azo salicylaldehyde 2 which further reacted with 2-isocyanoacetohydrazide to produce 2-cyano-N'-(2-hydroxy-5-(4-methyl phenyldiazenyl)benzylidene)acetohydrazide 4 in yield 82%. In order to obtain 2-Cyano-N'-(2-hydroxy-5-(p-tolyldiazenyl)benzylidene 6a-e, component 4 underwent condensation reaction with several aldehydes, including benzaldehyde, 4-methoxy benzaldehyde, 2,5-dimethoxy benzaldehyde, 4-chloro benzaldehyde, and 2,5-dichloro benzaldehyde. 2-Cyano-N'-(2-hydroxy-5-(p-tolyldiazenyl)benzylidene) (6a) in yield 83%, 3-phenylacrylo hydrazide acrylohydrazide-3-(4-methoxyphenyl) (6b) in yield 82%, 2-Cyano-3-(2,5-dimethoxyphenyl) acrylohydrazide N'-(2-hydroxy-5-(p-tolyldiazenyl)benzylide,3-(Chlorophenol) (6c) in yield 75%, 2-Cyano-3-(2,4-dichlorophenyl)- N' -(2-hydroxy-5-(p-tolyldiazenyl) benzylidene) (6d) in yield 78% and 2-cyano- N' -(2-hydroxy-5-(p-tolyldiazenyl) benzylidene) acrylohydrazide (6e) in yield 85%, respectively. Moreover, compound 4 combined with para toluedene and/or aniline to produce 2-Cyano-N'- (2-hydroxy-5-p-tolyldiazenyl) benzylidene-2- (phenyldiazenyl) aceto-hydrazide (8a) in yield 64% and 3.1.3.2.2-Cyano-N'- (2-hydroxy-5-p-tolyldiazenyl) benzylidene-2- (p-tolyldiazenyl) acetohydrazide (8b) in yield 67% respectively. In the end, compound 4 gave rise to N'-(2-hydroxy-5-(p-tolyldiazenyl)benzylidene)-2-oxo-2H-chromene-3-carbohydrazide (11a) in yield 69% and 6-Hydroxy-N'-(2-hydroxy-5-(p-tolyldiazenyl) benzylidene)-2-oxo-2H-chromene-3-carbohydrazide (11b) in yield 72% via reactions with o-hydroxybenzaldehydes and 2,4-dihydroxybenzaldehyde. Several analytical and spectroscopic techniques, including mass spectroscopy, infrared spectroscopy, carbon thirteen magnetic resonance spectroscopy, proton magnetic resonance spectroscopy, and elemental analysis, were used to illustrate the structures of all produced compounds.