A simple and efficient preparation of pyrazolo[3,4-b]-pyridine derivatives through an unexpected reaction of cyanothioacetamide under microwave irradiation
โ Scribed by Xuesen Fan; Xia Wang; Xinying Zhang; Xiaoyan Li; Guirong Qu
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 166 KB
- Volume
- 19
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20497
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
An unexpected multicomponent reaction of cyanothioacetamide with aromatic aldehydes and aminopyrazole under MWI was found and reported. It turned out to be an efficient and simple procedure for the preparation of pyrazolo[3,4โb]pyridine derivatives. The structure of the product was characterized by IR, MS, ^1^H and ^13^C NMR, COSY and NOESY spectroscopy, Xโray crystallographic analysis, and by comparison with the authentic sample prepared with the known procedure. ยฉ 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:694โ699, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20497
๐ SIMILAR VOLUMES
## Abstract magnified image A practical, inexpensive, and rapid method for the stereoselective synthesis of pyrazolo[4,3โ__c__]pyridine derivatives __via__ microwaveโassisted reactions of 3,5โdiarylidenepiperidinโ4โones with phenylhydrazine in ethylene glycol. This method has the advantages of goo
## Abstract magnified image A series of furo[3,4โ__e__]pyrazolo[3,4โ__b__]pyridine analogues of podophylloxin were synthesized __via__ threeโcomponent reactions of aldehydes, 3โmethylโ1โphenylโ1__H__โpyrazolโ5โamine and tetronic acid in water under microwave irradiation without catalyst. This effi