| Autor: |
Deev SL; Ural Federal University, 19 Mira Street, 620002 Yekaterinburg, Russia., Paramonov AS; Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 16/10 Miklukho-Maklaya Street, 117997 Moscow, Russia., Shestakova TS; Ural Federal University, 19 Mira Street, 620002 Yekaterinburg, Russia., Khalymbadzha IA; Ural Federal University, 19 Mira Street, 620002 Yekaterinburg, Russia., Chupakhin ON; Ural Federal University, 19 Mira Street, 620002 Yekaterinburg, Russia.; I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 22 S. Kovalevskoy Street, 620219 Yekaterinburg, Russia., Subbotina JO; Ural Federal University, 19 Mira Street, 620002 Yekaterinburg, Russia., Eltsov OS; Ural Federal University, 19 Mira Street, 620002 Yekaterinburg, Russia., Slepukhin PA; Ural Federal University, 19 Mira Street, 620002 Yekaterinburg, Russia.; I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 22 S. Kovalevskoy Street, 620219 Yekaterinburg, Russia., Rusinov VL; Ural Federal University, 19 Mira Street, 620002 Yekaterinburg, Russia., Arseniev AS; Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 16/10 Miklukho-Maklaya Street, 117997 Moscow, Russia., Shenkarev ZO; Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 16/10 Miklukho-Maklaya Street, 117997 Moscow, Russia. |
| Abstrakt: |
Determining the accurate chemical structures of synthesized compounds is essential for biomedical studies and computer-assisted drug design. The unequivocal determination of N-adamantylation or N-arylation site(s) in nitrogen-rich heterocycles, characterized by a low density of hydrogen atoms, using NMR methods at natural isotopic abundance is difficult. In these compounds, the heterocyclic moiety is covalently attached to the carbon atom of the substituent group that has no bound hydrogen atoms, and the connection between the two moieties of the compound cannot always be established via conventional 1 H- 1 H and 1 H- 13 C NMR correlation experiments (COSY and HMBC, respectively) or nuclear Overhauser effect spectroscopy (NOESY or ROESY). The selective incorporation of 15 N-labelled atoms in different positions of the heterocyclic core allowed for the use of 1 H- 15 N ( J HN ) and 13 C- 15 N ( J CN ) coupling constants for the structure determinations of N-alkylated nitrogen-containing heterocycles in solution. This method was tested on the N-adamantylated products in a series of azolo-1,2,4-triazines and 1,2,4-triazolo[1,5- a ]pyrimidine. The syntheses of adamantylated azolo-azines were based on the interactions of azolo-azines and 1-adamatanol in TFA solution. For azolo-1,2,4-triazinones, the formation of mixtures of N -adamantyl derivatives was observed. The J HN and J CN values were measured using amplitude-modulated 1D 1 H spin-echo experiments with the selective inversion of the 15 N nuclei and line-shape analysis in the 1D 13 С spectra acquired with selective 15 N decoupling, respectively. Additional spin-spin interactions were detected in the 15 N-HMBC spectra. NMR data and DFT (density functional theory) calculations permitted to suggest a possible mechanism of isomerization for the adamantylated products of the azolo-1,2,4-triazines. The combined analysis of the J HN and J CN couplings in 15 N-labelled compounds provides an efficient method for the structure determination of N-alkylated azolo-azines even in the case of isomer formation. The isomerization of adamantylated tetrazolo[1,5- b ][1,2,4]triazin-7-ones in acidic conditions occurs through the formation of the adamantyl cation. |
