76006-15-0

Upstream product

• 271-47-6 1H-pyrazolo[3,4-c]pyridine 

Downstream Products

• 76006-13-8 3-bromo-1H-pyrazolo[3,4-c]pyridine 
• 245325-34-2 3-cyano-1H-pyrazolo[3,4-c]pyridine 
• 76006-17-2 1H-pyrazolo[3,4-c]pyridin-3-amine 
• 76006-22-9 6-benzyl-3-nitro-6H-pyrazolo<3,4-c>pyridine 
• 76006-24-1 2-Benzyl-3-nitro-2H-pyrazolo[3,4-c]pyridine 
• 76006-23-0 1-Benzyl-3-nitro-1H-pyrazolo[3,4-c]pyridine 

Relevant academic research and scientific papers

Synthesis, reactivity and 13C-NMR of 1H-pyrazolo[3,4-c]pyridine derivatives

The synthesis of various 1H-pyrazolo [.-c.]pyridines was reported. 3- Cyano derivatives were obtained from the corresponding nitro compounds by Sandmeyer Reaction using Na3[Cu(CN)4] at pH 1. The 13C-NMR data of this series were also described.

Pyrazolopyridines. Part 5. Preparation and Reactions of Pyrazolopyridines

A series of pyrazolopyridines has been prepared by nitrosation of 3-acetamido-4-methylpyridines and subsequent rearrangement and cyclisation of the N-acetyl-N-nitroso-compounds produced.The reactions of the pyrazolopyridines have been investigated. 1- and 2-Acetyl and 1- and 2-benzyl compounds were obtained and their structures elucidated spectroscopically.The ring system readily undergoes electrophilic substitution in the 3-position. 7-Chloropyrazolopyridine has been shown to be more susceptible to nucleophilic substitution than the isomeric 5-chloro-compound.