Reaction of (Z)-N-Substituted α,β-Dehydroamino Acids Hydrazides with Oxazolones. Antiradical Activity of Bishydrazides and Bisimidazole-4-ones
摘要
The reaction of (Z)-N-substituted α,β-dehydroamino acid hydrazides with 5(4H)-oxazolones was studied. Optimal reaction conditions were found. It was shown that in addition to the main product, bishydrazide, monoimidazolоne hydrazide was also formed. Substituted bishydrazides, N,N-[(2Z,2′Z)-hydrazine-1,2-diyl-bis(1-oxo-3-phenylprop-2-ene-1,2-diyl)]dibenzamides, were converted into the corresponding bisimidazolones—4,4′-di[(Z)-benzylidene]-2,2′-diphenyl-[1,1′-biimidazole]-5,5′(4H,4′H)-diones. Antiradical properties of the synthesized compounds were studied. It was shown that bishydrazides exhibit higher antiradical activity than the corresponding bisimidazolones and monoimidazolonehydrazide. UV spectra of the synthesized compounds were studied, their molar extinction coefficients at λmax were determined. Structure of 4,4′-di[(Z)-benzylidene]-2,2′-diphenyl-[1,1′-bisimidazole]-5,5′(4H,4′H)-dione was determined by single crystal X-ray diffraction analysis.