Preview

Fine Chemical Technologies

Advanced search

Synthesis and properties of arylheteroaliphatic aminoamides

Full Text:

Abstract

The preparative synthesis of bioactive arylheteroaliphatic N-substitued aminoamides based on the opening of epoxide ring of styrene oxide followed by acylation of diaminoalcohols with acyl chlorides, was developed.

About the Authors

A. Kh. Mohammed
M.V. Lomonosov Moscow State University of Fine Chemical Technologies, 86, Vernadskogo pr., Moscow 119571
Russian Federation


N. Yu. Borisova
M.V. Lomonosov Moscow State University of Fine Chemical Technologies, 86, Vernadskogo pr., Moscow 119571
Russian Federation


E. Ya. Borisova
M.V. Lomonosov Moscow State University of Fine Chemical Technologies, 86, Vernadskogo pr., Moscow 119571
Russian Federation


References

1. Машковский М. Д. Лекарственные средства. - М.: Новая волна, 2002. Т. 1, 608 с. Т. 2, 539 c.

2. Meguro M., Asao N., Yamamoto Y. Ytterbium triflate and high pressure-mediated ring opening of epoxides with amines // J. Chem. Soc. Perkin Trans. 1994. V. 1. № 18. P. 2597-2601.

3. Kitchen L.J., Polard C.B. Monoalkylalklation of ethylenediamine with alkene oxide // J. Org. Chem. 1943. V. 8 (4). P. 342-343.

4. Мохаммед А.Х., Борисова Е.Я., Егорова В.В., Крылов А.В., Борисова Н.Ю. Региоселективность раскрытия эпоксидного цикла окиси стирола этилендиаминами в различных средах // Вестник МИТХТ. 2011. Т. 6. № 5. С. 140-142.


For citation:


Mohammed A.K., Borisova N.Yu., Borisova E.Y. Synthesis and properties of arylheteroaliphatic aminoamides. Fine Chemical Technologies. 2011;6(6):69-71. (In Russ.)

Views: 52


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2410-6593 (Print)
ISSN 2686-7575 (Online)