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On triazoles XLV [1]. synthesis of 5,7-diamino-1,2,4-triazolo[1,5-a] [1,3,5]triazines

✍ Scribed by Gábor Berecz; László Pongó; István Kövesdi; József Reiter


Publisher
Journal of Heterocyclic Chemistry
Year
2002
Tongue
English
Weight
84 KB
Volume
39
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

Dedicated to Professor András Messmer on the occasion of his 80^th^ birthday

The reaction of differently substituted 5‐amino‐1,2,4‐triazoles (5) with isothiourea derivatives (3) to yield isomeric 5,7‐diamino‐1,2,4‐triazolo[1,5‐a][1,3,5]triazines (6 and 7), previously described as not proceeding in melt, was performed in different solvents as well as in the melt at 150‐160°. It was proved that the above reaction had rather general validity. The structure of isomers 6 and 7 were proved spectroscopically. The structure of 6/5 (Q = ethylamino) was corroborated with single crystal X‐ray diffraction determination, as well.


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Synthesis of Triazolo[1,5-a]triazin-7-on
✍ Montserrat Heras; David Font; Anthony Linden; José M. Villalgordo 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 German ⚖ 161 KB

## Abstract The synthesis of novel triazolo[1,5‐__a__]triazin‐7‐ones is presented. Starting from 3‐amino‐5‐sulfanyl‐1,2,4‐triazole, the synthetic sequence involved alkylation with benzyl bromide, reaction with __p__‐nitrophenyl chloroformate followed by treatment with a primary amine, and condensat