An efficient synthesis of new class of pyrazolo[3,4-b]pyridine-6-one derivatives by a novel cascade reaction
✍ Scribed by Feng Shi; Junyong Zhang; Shujiang Tu; Runhong Jia; Yan Zhang; Bo Jiang; Hong Jiang
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2007
- Tongue
- English
- Weight
- 335 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
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A novel cascade reaction of 4‐arylidene‐2‐phenyl‐1,3‐oxazol‐5(4__H__)‐one with 3‐methyl‐1‐phenyl‐1__H__‐pyrazol‐5‐amine was described and a number of new pyrazolo[3,4‐b]pyridine‐6‐one derivatives were synthesized. This new protocol has the advantages of shorter time, higher yields, and lower cost as well as easier operation.
📜 SIMILAR VOLUMES
## Abstract A series of 3‐methyl‐1,4‐disubstituted‐4,5‐dihydro‐1__H__‐pyrazolo[3,4‐__b__]pyridine‐6(7__H__)‐ones was synthesized __via__ the three‐component reaction of aldehyde, 3‐methyl‐1‐phenyl‐1__H__‐pyrazol‐5‐amine, and Meldrum's acid catalyzed by L‐proline. This protocol has the advantages of
A series of 4-aryl-3,7,7-trimethyl-1-phenyl-7,8-dihydro-1H-pyrazolo[3,4-b]quinolin-5(6H)-ones were synthesized via the three-component reaction of aromatic aldehydes, 5,5-dimethyl-1,3-cyclohexandione and 5-amino-3-methyl-1-phenylpyrazole in ionic liquid without using any catalyst. This protocol has