𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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

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


An efficient one-pot three-component syn
✍ Chun-Ling Shi; Hui Chen; Daqing Shi 📂 Article 📅 2011 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 85 KB

## 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).

An efficient synthesis of pyrazolo[3,4-b
✍ Da-Qing Shi; Fang Yang 📂 Article 📅 2010 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 82 KB

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