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
No coin nor oath required. For personal study only.
✦ 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.
📜 SIMILAR VOLUMES
## 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