[4,4′-Bi-1H-pyrazolo[3,4-b]pyridine] aus 1,6-Diaryl-1,3,4,6-hexantetronen
✍ Scribed by Sušnik-Rybarski, Ivana ;Džanić, Husein ;Laćan, Marijan ;Mesić, Vladimir
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 184 KB
- Volume
- 1982
- Category
- Article
- ISSN
- 0947-3440
No coin nor oath required. For personal study only.
✦ Synopsis
[4,4′‐Bi‐1__H__‐pyrazolo[3,4‐b]pyridines] from 1,6‐Diaryl‐1,3,4,6‐hexanetetrones
Reaction of 1,6‐diaryl‐1,3,4,6‐hexanetetrones 1a–c (Ar = phenyl, p‐tolyl or 2‐thienyl) with 3‐amino‐1‐phenyl‐5‐pyrazolone (2) in the presence of piperidine leads to 6,6′‐diaryl‐2,2′‐diphenyl[4,4′‐bi‐1__H__‐pyrazolo[3,4‐b]pyridine]‐3,3′(2__H__,2′H)diones 3a‐c, which are transformed into the acetates 4a–c.
📜 SIMILAR VOLUMES
## Abstract This review describe the synthesis and reactions of 3‐amino‐4,6‐dimethyl‐1__H__‐pyrazolo[3,4‐__b__]pyridine as building block for the synthesis of polyfunctionalized heterocyclic compounds with pharmacological interest. J. Heterocyclic Chem., 2011.
## Abstract magnified image Reaction of 6‐methyl‐4‐oxo‐4__H__‐[1]‐benzopyran‐3‐carboxaldehyde **1** with 5‐amino‐3‐methyl‐1‐phenylpyrazole **2** in alcoholic reaction media in the presence of 4‐toluenesulfonic acid as catalyst afforded 5‐(2‐hydroxy‐5‐methylbenzoyl)‐3‐methyl‐1‐phenyl‐1__H__‐pyrazol