Pathways for Activating Isotope Exchange of Dopamine with D2O

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Various methods of introducing deuterium into dopamine using isotope exchange are considered. The best result is achieved by isotope exchange with deuterated water at 190°C for 30 min using (a) trifluoroacetic acid as a catalyst and (b) 5% Pd/Al2O3 catalyst presaturated with deuterium gas. In the first case, the yield of deuterated dopamine was 65–70%, and the average deuterium content was 2.4–2.5 at./molecule. In the second case, the yield decreased to 35–40%, but the deuterium content increased to 3.50–3.60 at./molecule. The obtained result highlights the effectiveness of an integrated approach to introducing hydrogen isotopes into organic molecules, when activated hydrogen isotope species are formed on the catalyst and the substance deposited on it, which contribute to increasing the efficiency of isotope exchange with deuterated water when heated.

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V. Shevchenko

National Research Centre Kurchatov Institute

Email: nagaev.img@yandex.ru
俄罗斯联邦, pl. Kurchatova 2, Moscow, 123182

I. Nagaev

National Research Centre Kurchatov Institute

编辑信件的主要联系方式.
Email: nagaev.img@yandex.ru
俄罗斯联邦, pl. Kurchatova 2, Moscow, 123182

N. Myasoedov

National Research Centre Kurchatov Institute

Email: nagaev.img@yandex.ru
俄罗斯联邦, pl. Kurchatova 2, Moscow, 123182

参考

  1. Катунина Е. А. // Consilium Medicum. Приложение к журн. «Неврология и ревматология». 2010. № 2. С. 46–49.
  2. Преображенская И. С. // Consilium Medicum. Приложение к журн. «Неврология и ревматология». 2008. № 1. С. 53–58.
  3. Wenzel J. M., Rauscher N. A., Cheer J. F., Oleson E. B. // ACS Chem. Neurosci. 2015. Vol. 6. N1. P. 16–26. https://doi.org/10.1021/cn500255p
  4. Mehta M. A., Riedel W. J. // Curr. Pharm. Des. 2006. Vol. 12. N20. P. 2487–2500. https://doi.org/10.2174/138161206777698891
  5. Шевченко В. П., Нагаев И. Ю., Шевченко К. В., Мясоедов Н. Ф. // Радиохимия. 2023. Т. 65. № 4. С. 349–354. https://doi.org/10.31857/S0033831123040068
  6. Bhering D. L., Ramirez-Solis A., Mota C. J.A. // J. Phys. Chem. B. 2003. Vol. 107. N18. P. 4342–4347. https://doi.org/10.1021/jp022331z
  7. Kresse G., Furthmuller J. // Comput. Mater. Sci. 1996. Vol. 6. N1. P. 15–50. https://doi.org/10.1016/0927-0256(96)00008-0
  8. Zheng A., Li Sh., Liu S.-B., Deng F. // Acc. Chem. Res. 2016. Vol. 49. N4. P. 655–663. https://doi.org/10.1021/acs.accounts.6b00007
  9. Esaki H., Ito N., Sakai Sh., Maegawa T., Monguchi Y., Sajiki H. // Tetrahedron. 2006. Vol. 62. N47. P. 10954–10961. https://doi.org/10.1016/j.tet.2006.08.088
  10. Chiesa M., Giamello E., Murphy D. M., Pacchioni G., Paganini M. C., Soave R., Sojka Z. // J. Phys. Chem. B. 2001. Vol. 105. N2. P. 497–505. https://doi.org/10.1021/jp002794+
  11. Chiesa M., Giamello E., Paganini M. C. // J. Chem. Phys. 2002. Vol. 116. N10. P. 4266–4274. https://doi.org/10.1063/1.1447907
  12. Chiesa M., Paganini M. C., Spoto G., Giamello E., Di Valentin C., Del Vitto A., Pacchioni G. // J. Phys. Chem. B. 2005. Vol. 109. N15. P. 7314–7322. https://doi.org/10.1021/jp044783c
  13. Chiesa M., Paganini M. C., Giamello E., Murphy D. M., Di Valentin C., Pacchioni G. // Acc. Chem. Res. 2006. Vol. 39. N11. P. 861–867. https://doi.org/10.1021/ar068144r

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2. Fig. 1. Analysis of the reaction mixture on a Milichrome A-02 chromatograph after conducting preparative experiments (the first peak is dopamine): a – activation of isotopic exchange of TFA; b – activation of isotopic exchange of 5% Pd/Al2O3.

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3. 2. Isotopomers in [D]dopamine after conducting preparative experiments: a – activation of isotopic exchange of TFA; b – activation of isotopic exchange of 5% Pd/Al2O3.

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