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Treatment of 1-hydroxy-2,3-dihydro-1H-pyrazolo[1,2-a]pyridazine-5,8-diones and -1H-pyrazolo[1,2-b]phthalazine-5,10-diones with hydrazides produces corresponding acylhydrazino derivatives. In this work, ten new hydrazino derivatives were synthesized, and their properties were studied by 1 H and 13 C NMR spectroscopy. These compounds exhibited several types of structural variation, including ring-chain tautomerism, cis-trans isomerism with respect to the substituents in the pyrazole ring, and (E)/(Z) rotamerism with respect to the nitrogen−carbon hydrazide bond with partial double-

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