Synthesis of some new 4-(2,4-dimethyl-phenyl)-2H-phthalazinone derivatives

Autor: Mamdouh A. Taha, Ibrahim E. El-Shamy, Asmaa K. Mourad, Ahmed Th. Ali
Jazyk: angličtina
Rok vydání: 2021
Předmět:
Zdroj: Journal of Scientific Research in Science, Vol 38, Iss 1, Pp 233-242 (2021)
Druh dokumentu: article
ISSN: 2356-8364
2356-8372
DOI: 10.21608/JSRS.2021.48596.1039
Popis: Aroylation of m-xylene by phthalic anhydride under Friedel craft’s reaction conditions to afford the corresponding o-aroylbenzoic acid derivative (2), which followed by cyclization reaction with hydroxylamine hydrochloride to produce the correlating benzoxazinone derivative (3), which was utilized as a precursor for the formation of some novel phthalazinone derivatives (4˗6). This transformation was achieved by interactions with thiosemicarbazide, thiocarbohydrazide, and hydrazine monohydrate and/or ammonium acetate under suitable conditions. 4-Substituted-1(2H)- phthalazinone derivative (6), which undergoes N-alkylation using ethyl bromoacetate to produce the phthalazinone acetic acid ethyl ester derivative (7), that followed by the interaction with hydrazine monohydrate to afford the phthalazinone acetic acid hydrazide derivative (8). The latter product was conducted with different aromatic acid compounds in presence of POCl3, to give the correlating oxadiazoles (9,10). The chemical structures of all the synthesized compounds are confirmed using physical and spectral data analyses like FT- IR, 1H-NMR, and mass spectroscopy.
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