HETEROCYCLIZATION REACTIONS OF 3-METHYLISOXAZOL-5-AMINE WITH PYRUVIC ACID DERIVATIVES USING CLASSICAL AND NON-CLASSICAL ACTIVATION METHODS

Authors

  • Алиса Д. Морозова Scientific-Technological Complex ''Institute of Single Crystals'', National Academy of Sciences of Ukraine, 60 Nauky Ave., Kharkiv 61072
  • Елена А. Муравьева Scientific-Technological Complex ''Institute of Single Crystals'', National Academy of Sciences of Ukraine, 60 Nauky Ave., Kharkiv 61072
  • Сергей М. Десенко Scientific-Technological Complex ''Institute of Single Crystals'', National Academy of Sciences of Ukraine, 60 Nauky Ave., Kharkiv 61072
  • Владимир И. Мусатов Scientific-Technological Complex ''Institute of Single Crystals'', National Academy of Sciences of Ukraine, 60 Nauky Ave., Kharkiv 61072
  • Дарья В. Едаменко Scientific-Technological Complex ''Institute of Single Crystals'', National Academy of Sciences of Ukraine, 60 Nauky Ave., Kharkiv 61072
  • Валентин А. Чебанов Scientific-Technological Complex ''Institute of Single Crystals'', National Academy of Sciences of Ukraine, 60 Nauky Ave., Kharkiv 61072

DOI:

https://doi.org/10.1007/3464

Keywords:

isoxazolo[5, 4-b]pyridine, Lewis acid, 3-methylisoxazol-5-amine, pyruvic acid derivatives, ultrasonication, heterocyclization, microwave irradiation, non-classical method of activation

Abstract

Two- and multicomponent interactions between 3-methylisoxazol-5-amine and pyruvic acid derivatives were studied both by using classical methods of activation, as well as under microwave irradiation and ultrasonication. It was shown that the reactions with esters of arylidene pyruvic acids could lead to the formation of three different types of heterocyclic systems, while in the case of arylidene pyruvic acid a very insignificant conversion of the starting compounds to isoxazolo[5,4-b]pyridine carboxylic acids was observed, due to the low stability of 3-methylisoxazol-5-amine.

Authors: Alisa D. Morozova, Elena A. Muravyova, Sergey M. Desenko, Vladimir I. Musatov, Daria V. Yedamenko, Valentin A. Chebanov

 

Published

2016-12-06