Unexpected Reaction of Ethyl 4-(Chloromethyl)pyrazolo- [5,1-c][1,2,4]triazine-3-carboxylates with Thiourea and Its Mechanism

The reaction of ethyl 4-(chloromethyl)pyrazolo[5,1-c][1,2,4]triazine-3-carboxylates with thiourea in dimethylformamide involves ANRORC rearrangement (Addition of the Nucleophile, Ring Opening, and Ring Closure) followed by N-formylation to give N-{5-(4-oxo-8-phenyl-1,4-dihydropyrazolo[5,1-c][1,2,4]-triazin-3-yl)-1,3-triazol-2-yl}formamides whose structure was confirmed by X-ray analysis. The reaction mechanism has been studied by HPLC/MS.

Авторы
Ledenyova I.V. 1 , Falaleev A.V. 1 , Shikhaliev K.S. 1 , Ryzhkova E.A. 2 , Zubkov F.I. 2
Издательство
Pleiades Publishing, Ltd. (Плеадес Паблишинг, Лтд)
Номер выпуска
1
Язык
English
Страницы
73-79
Статус
Published
Том
88
Год
2018
Организации
  • 1 Voronezh State University
  • 2 Peoples’ Friendship University of Russia
Ключевые слова
ethyl 4-(chloromethyl)pyrazolo[5,1-c][1,2,4]triazine-3-carboxylate; thiourea; ANRORC rearrangement; formylation
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