An efficient one-pot synthesis of pyrazolo[3,4-b]pyridinone derivatives catalyzed by L-proline
✍ Scribed by Chun-Ling Shi; Hui Chen; Da-Qing Shi
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2010
- Tongue
- English
- Weight
- 120 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.573
No coin nor oath required. For personal study only.
✦ Synopsis
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 easier work‐up, milder reaction conditions, and high yields. J. Heterocyclic Chem., (2011).
📜 SIMILAR VOLUMES
## Abstract L‐Proline is found to be an efficient catalyst for the synthesis of tetrahydrofuro[3,4‐__b__]quinoline‐1,8(3__H__,4__H__)‐dione derivatives. This protocol is novel and has the advantages of mild condition, high yield, and easy operation. J. Heterocyclic Chem., (2012).
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