Open Access1D and 2D NMR spectroscopy for identification of carbamide-containing biologically active compounds
Author(s) -
А. А. Бакибаев,
S. Yu. Panshina,
O.V. Ponomarenko,
Victor S. Malkov,
O.A. Kotelnikov,
А. К. Ташенов
Publication year - 2021
Publication title -
ķaraġandy universitetìnìn̦ habaršysy. himiâ seriâsy
Language(s) - English
Resource type - Journals
eISSN - 2663-4872
pISSN - 2518-718X
DOI - 10.31489/2021ch1/71-81
Subject(s) - chemistry , urea , nuclear magnetic resonance spectroscopy , barbituric acid , spectroscopy , biological activity , nmr spectra database , carbon 13 nmr , proton nmr , molecule , stereochemistry , spectral line , organic chemistry , biochemistry , physics , quantum mechanics , astronomy , in vitro
Urea (carbamide) is the main end product of amino acids' metabolism in mammals. Extensive research in the field of urea chemistryhas contributed to the creation of many biologically active and other compounds based on the carbamide fragment NH–CO–NH. The substituting groups of urea directly affect its properties and characteristics which are reflected in the NMR spectral data and this circumstance can be the basis for the identification of urea derivatives. In this work, chemical shifts in the NMR spectra of urea and its acyclic structure, barbituric series, imidazolidinone series and bicyclic structure derivativeswere studied and identi-fied. A system analysis was carried out to determine the effect of the type of substituents on the positions of signals of the NH-CO-NH fragment in the NMR spectra. The possibility of 2D NMR spectroscopy using to simplify the identification procedurefor complex mixtureswas shown in the paper. The combined use of 1D and 2D NMR spectroscopy is convenient and informative to establishthe structure of biologically active compounds. These methods make it possible to determine the presence and type of impurities, as well as to establish thedestruction processes leading to the corresponding impurities.