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