SYNTHESIS OF FUNCTIONAL DERIVATIVES OF CHLORINE-SUBSTITUTED ISOTHIAZOLES

Optimal procedures have been developed for the synthesis of substituted isothiazoles containing an active chlorine atom in position 5 of the heterocycle and various functional groups in position 3: carboxyl, hydroxymethyl, aldehyde. Based on these methods, previously undescribed compounds were obtained: 5-morpholino-substituted 3-hydroxymethyl-4-chloroisothiazole, 4-chloroisothiazole-3-carboxylic acid and its methyl ester. The resulting substances are reactive building blocks for organic synthesis of compounds with a high potential for biological activity. © 2024, Belaruskaya Navuka. All rights reserved.

Авторы
Margun E.N. , Kolesnik I.A. , Akishina E.A. , Dikusar E.A. , Logvinenko N.A. , Volchkov N.S. , Potkin V.I.
Издательство
Belaruskaya Navuka
Номер выпуска
3
Язык
Русский
Страницы
215-221
Статус
Опубликовано
Том
60
Год
2024
Организации
  • 1 Institute of Physical Organic Chemistry of the National Academy of Sciences of Belarus, 13, Surganov Str., Minsk, 220072, Belarus
  • 2 RUDN University, 6, Mik-lukho-Maklay Str, Moscow, 117198, Russian Federation
Ключевые слова
3-hydroxymethyl-4-chloroisothyazole; 4,5-dichlorisothiazole-3-carbalde-hyde; 4-chlorisothiazole-3-carboxylic acid; Corey method; heterocyclic compounds; pharmacophore compounds; Svern method
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