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Solvent-free microwave synthesis of bis-pyrazolo[3,4-b:4′,3′-e]-pyridines and study of their antifungal properties

✍ Scribed by J. Quiroga; J. Portilla; B. Insuasty; R. Abonía; M. Nogueras; M. Sortino; S. Zacchino


Publisher
Journal of Heterocyclic Chemistry
Year
2005
Tongue
English
Weight
64 KB
Volume
42
Category
Article
ISSN
0022-152X

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✦ Synopsis


The synthesis of a series of bis-pyrazolo [3,4-b:4',3'-e]pyridines (3) in the reaction of 5-amino-3-methyl-1phenylpyrazole (1) with aldehydes (2) under microwave irradiation and solvent-free conditions is described. The structure elucidation of the products is based on detailed nmr analysis of experiments such as 1 H-COSY, NOESY, DEPT, HSQC and HMBC. These compounds showed moderate antifungal in vitro activity against dermatophytes.


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✍ Feng Shi; Shujiang Tu; Bo Jiang; Chunmei Li; Dianxiang Zhou; Qingqing Shao; Long 📂 Article 📅 2008 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 421 KB

## Abstract magnified image A series of furo[3,4‐__e__]pyrazolo[3,4‐__b__]pyridine analogues of podophylloxin were synthesized __via__ three‐component reactions of aldehydes, 3‐methyl‐1‐phenyl‐1__H__‐pyrazol‐5‐amine and tetronic acid in water under microwave irradiation without catalyst. This effi