Specificity of Alkylation of 5-R-Amino-4-aroyl-1,2,4-triazole-3-thione

Фізер, Максим Михайлович; Сливка, Михайло Васильович; Баумер, Вячеслав М.; Лендєл, Василь Георгійович

Please use this identifier to cite or link to this item: https://dspace.uzhnu.edu.ua/jspui/handle/lib/4968

Title:	Specificity of Alkylation of 5-R-Amino-4-aroyl-1,2,4-triazole-3-thione
Other Titles:	Специфіка алкілування 5-аміно-4-ароїл-1,2,4-триазол-3-тіону
Authors:	Фізер, Максим Михайлович Сливка, Михайло Васильович Баумер, Вячеслав М. Лендєл, Василь Георгійович
Keywords:	Перегрупування Дімрота, 1,2,4-triazole, 1,3,4-thiadiazole, Dimroth rearrangement, alkylation.
Issue Date:	13-Nov-2015
Publisher:	Kharkiv: Ekskluziv Publ. [email protected]
Citation:	Maksym M. Fizer, Mikhailo V. Slivka*, Vjacheslav M. Baumer, Vasil G. Lendel. Specificity of Alkylation of 5-R-Amino-4-aroyl-1,2,4-triazole-3-thione. // Chemistry of Nitrogen Containing Heterocycles, CNCH-2015, 19th - 13th November, 2015, Kharkiv, Ukraine. Book of Abstracts. – Kharkiv: Ekskluziv Publ., 2015. – 124 p.
Series/Report no.:	Тези конференції;2015-11
Abstract:	It was investigated the alkylation reaction of 5-R-amino-4-aroyl-1,2,4-triazole-3-thiones. Initial triazoles had been received after heating of aroyl-bis-thoureas in n-butanol or acetonitrile medium up to full releasing of hydrogen sulfide. Alkylation was carried out in alcoholic medium at base presence. It was shown, that Dimroth rearrangement with 1,3,4-thiadiazole ring formation is realized under above mentioned conditions.
Description:	Department of Organic Chemistry, Faculty of Chemistry, Uzhhorod National University, Fedinca str. 53/1, Uzhhorod, 88000, Ukraine, e-mail: [email protected]
Type:	Text
Publication type:	Тези до статті
URI:	https://dspace.uzhnu.edu.ua/jspui/handle/lib/4968
ISBN:	978-966-2166-81-1
Appears in Collections:	Наукові публікації кафедри органічної хімії

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