Abstract
Under the action of concentrated sulfuric acid, a number of arylhydrazides of diarylglycolic acids are converted into 4,4-diaryl-3-oxo-1, 2, 3, 4-tetrahydrocinnolines. The cyclization reaction takes place through the intermediate formation of a halochromic salt. The UV and IR spectra of the cinnoline derivatives have been studied.
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For part XLV, see [1].
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Berdinskii, I.S. Substituted hydrazides of hydroxycarboxylic acids. Chem Heterocycl Compd 5, 659–661 (1969). https://doi.org/10.1007/BF00957384
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DOI: https://doi.org/10.1007/BF00957384