Abstract

N-Methyl-N-(4-chloro-1-phthalazinyl)-(E)-hydrazones of the corresponding carbonyl compounds were obtained by condensation of 1-methyl-1-(4-chloro-1-phthalazinyl)hydrazine with carbonyl compounds. The PMR spectra of the products in a number of solvents at various temperatures and the UV spectra in solution and in the solid form were recorded. It was established that a change in the nature of the substituents in the ylidene fragment leads to a change in the three-dimensional structure and the reaction center (Cpht-Cl, Cpht-N, C=N) in acid hydrolysis reactions.

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