Email this article New Method of Synthesis of Biologically Active Get(aryl)chalcogenylacetates of Tris(2-hydroxyethyl)ammonium
- Authors: Adamovich S.N.1, Oborina Е.N.1, Ushakov I.А.2, Mirskova А.N.1
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Affiliations:
- A.E. Favorskii Irkutsk Institute of Chemistry, Siberian Branch
- Irkutsk National Research Technical University
- Issue: Vol 88, No 10 (2018)
- Pages: 2227-2229
- Section: Letters to the Editor
- URL: https://journals.rcsi.science/1070-3632/article/view/222512
- DOI: https://doi.org/10.1134/S1070363218100353
- ID: 222512
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Abstract
Physiologically and pharmacologically active het(aryl)chalcogenylacetates of tris(2-hydroxyethyl)ammonium of pharmacopeial purity have been synthesized by the reaction of het(aryl)chalcogenylacetic acids with sodium (potassium) hydroxide and triethanolamine hydrochloride by one-pot method in quantitative yield (up to 99.8%).
About the authors
S. N. Adamovich
A.E. Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Author for correspondence.
Email: mir@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033
Е. N. Oborina
A.E. Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: mir@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033
I. А. Ushakov
Irkutsk National Research Technical University
Email: mir@irioch.irk.ru
Russian Federation, Irkutsk
А. N. Mirskova
A.E. Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: mir@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033
