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1,2,3-Triazolo[4,5-e]-1,2,4-triazolo[3,4-c]pyrimidines

✍ Scribed by Giuliana Biagi; Irene Giorgi; Oreste Livi; Clementina Manera; Valerio Scartoni


Publisher
Journal of Heterocyclic Chemistry
Year
1999
Tongue
English
Weight
301 KB
Volume
36
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

Some new 1,2,3‐triazolo[4,5‐e]‐1,2,4‐triazolo[3,4‐c]pyrimidmes were prepared starting from the corresponding 1,2,3‐triazolo[4,5‐d]pyrimidines via the formation of the 1,2,4‐triazole ring. Thus suitable hydrazino derivatives 6 were condensed with triethyl orthoformate, triethyl orthoacetate and triethyl orthobenzoate to give the expected tricyclic derivatives 7, 8 and 9. Intramolecular cyclization of the ethoxycarbonylhydrazino derivatives 10 gave the tricyclic compounds 11 bearing an hydroxyl group in the 3 position. The v‐triazolo‐s‐triazolopyrimidine derivatives were tested towards the A~1~ and A~2A~ adenosine receptors in binding assays, but they did not show any receptor affinity.


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✍ Giuliana Biagi; Irene Giorgi; Oreste Livi; Federica Pacchini; Valerio Scartoni 📂 Article 📅 2002 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 32 KB

## Abstract The 7‐chloro‐3‐(2‐chlorobenzyl)‐ and 7‐chloro‐3‐(2‐fluorobenzyl)‐1,2,3‐triazolo[4,5‐__d__]pyrimidines (**1** and **4**), by nucleophilic replacement with some hydrazides, gave the corresponding 7‐hydrazidoderivatives (**2a‐e** and **5a‐e**). These, by heating in Dowtherm, underwent an i