Abstract:
An efficient synthesis of 2-amino-1-R-[1,2,4]triazolo[1,5-a]-pyrimidinium or 3-amino-2-R-[1,2,4]triazolo[4,3-a]pyrimidi- nium chloride derivatives by heterocyclization of 3,5-diamino-1-R-1,2,4-triazoles (R=Alk or Ar) with pentane-2,4-diones was developed. The process is promoted by chlorotrimethyl- silane which plays the dual role of carbonyl-activating agent and water scavenger.
Citation:
A. V. Astakhov, K. Yu. Suponitsky, V. M. Chernyshev, “Chlorotrimethylsilane-promoted synthesis of 1,2,4-triazolopyrimidines from 3,5-diamino-1,2,4-triazoles and pentane-2,4-diones”, Mendeleev Commun., 28:4 (2018), 439–441
Linking options:
https://www.mathnet.ru/eng/mendc1794
https://www.mathnet.ru/eng/mendc/v28/i4/p439
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