NH-Polyfluoroalkyl іminophosphonates in the synthesis of α-amino-α-polyfluoroalkyl- γ-oxobutylphosphonic acids

Authors

  • O. V. Stanko Institute of Organic Chemistry of the NAS of Ukraine, Ukraine
  • Y. P. Yelenich Institute of Organic Chemistry of the NAS of Ukraine, Ukraine
  • P. P. Onys’ko Institute of Organic Chemistry of the NAS of Ukraine, Ukraine
  • Yu. V. Rassukana Institute of Organic Chemistry of the NAS of Ukraine; National Technical University of Ukraine "Igor Sikorsky Kyiv Polytechnic Institute", Ukraine

DOI:

https://doi.org/10.24959/ophcj.19.967

Keywords:

оptically active a-aminophosphonates, рolyfluoroalkylated aminophosphonic acids, іminophosphonates, stereoselective synthesis

Abstract

Aim. To develop the preparative method for the synthesis of optically active α-amino-α-polyfluoroalkyl-γ-oxobutylphosphonic acids as new promising chiral building blocks.
Results and discussion. It has been shown that the reaction of NH-polyfluoroalkyl aminophosphonates with acetone in the presence of a catalytic amount of L- or D-proline occurs stereoselectively to give enantiomerically enriched (R)- or (S)-α-amino-γ-oxophosphonates, respectively. The resulting optically active phosphonates were converted into water-soluble α-amino-γ-oxophosphonic acids isolated in the individual form as hydrochlorides.
Experimental part. By the reaction of рolyfluoroacetonitriles with diethyl phosphite in the presence of triethylamine the series of NH-рolyfluoroalkyl іminophosphonates were synthesized. They undergo the prolinecatalysed reaction with acetone to form optically active α-amino-α-polyfluoroalkyl-γ-oxobutyl phosphonates. The latter were converted into the corresponding phosphonic acids by the reaction with hydrogen chloride. The structures of the compounds synthesized were confirmed by analytical and spectral NMR (1Н, 13С, 19F, 31Р) methods.
Conclusions. Based on the proline-catalyzed reaction of NH-рolyfluoroalkyl іminophosphonates with acetone the preparative
synthesis method for new chiral building blocks – α-amino-α-polyfluoroalkyl-γ-oxobuthylphosphonates and phosphonic acids has been developed.

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References

  1. Kukhar, V. P., Hudson, H. R. (2000). Aminophosphonic and Aminophosphinic Acids : Chemistry and Biological Activity. John Wiley & Sons : Chichester.
  2. Kafarski, P., Lejczak, B. (1991). Biological activity of aminophosphonic acids. Phosphorus, Sulfur, Silicon and related elements, 63 (1–2), 193–215. https://doi.org/10.1080/10426509108029443
  3. Mucha, A., Kafarski, P., Berlicki, L. (2011). Remarkable potential of the β–aminophosphonate/phosphinate structural motif in medicinal chemistry. Journal of Medicinal Chemistry, 54 (17), 5955–5980. https://doi.org/10.1021/jm200587f
  4. Romanenko, V. D., Kukhar, V. P. (2012). 1–Amino–1,1–bisphosphonates. Fundamental syntheses and new developments. Arkivoc, 2012 (4), 127–166. https://doi.org/10.3998/ark.5550190.0013.411
  5. Rassukana, Yu. V., Yelenich, I. P., Synytsya, A. D., Onys`ko, P. P. (2014). Fluorinated NH–iminophosphonates and iminocarboxylates : novel synthons for the preparation of biorelevant a-aminophosphonates and carboxylates. Tetrahedron, 70 (18), 2928–2937. https://doi.org/10.1016/j.tet.2014.03.030
  6. Onys’ko, P., Rassukana, Y., Kolotylo, M., Sinitsa, O., & Pirozhenko, V. (2007). α–Iminotrifluoroethylphosphonates: The First Representatives of N–H Imidoyl Phosphonates. Synthesis, 2007 (17), 2627–2630. https://doi.org/10.1055/s-2007-983838
  7. Rassukana, Y. V., Yelenich, I. P., Vlasenko, Y. G., & Onys’ko, P. P. (2014). Asymmetric synthesis of phosphonotrifluoroalanine derivatives via proline–catalyzed direct enantioselective CC bond formation reactions of NH trifluoroacetimidoyl phosphonate. Tetrahedron: Asymmetry, 25 (16-17), 1234–1238. https://doi.org/10.1016/j.tetasy.2014.07.007

Published

2019-06-14

How to Cite

(1)
Stanko, O. V.; Yelenich, Y. P.; Onys’ko, P. P.; Rassukana, Y. V. NH-Polyfluoroalkyl іminophosphonates in the Synthesis of α-Amino-α-Polyfluoroalkyl- γ-Oxobutylphosphonic Acids. J. Org. Pharm. Chem. 2019, 17, 5-10.

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Original Researches