155601-71-1

Usage

Uses

Used in Pharmaceutical Industry:
TERT-BUTYL 6-FLUORO-1H-PYRAZOLO[3,4-B]PYRIDINE-3-CARBOXYLATE is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a key component in the development of new drugs and medications.
Used in Chemical Synthesis:
TERT-BUTYL 6-FLUORO-1H-PYRAZOLO[3,4-B]PYRIDINE-3-CARBOXYLATE is used as a building block in the synthesis of other complex chemical compounds. Its high reactivity with various substances allows for the creation of a wide range of products in the chemical industry.
Used in Research and Development:
TERT-BUTYL 6-FLUORO-1H-PYRAZOLO[3,4-B]PYRIDINE-3-CARBOXYLATE is used as a research compound for studying its properties and potential applications in various fields. Its stability and low toxicity make it an ideal candidate for further investigation and experimentation.

InChI:InChI=1/C11H12FN3O2/c1-11(2,3)17-10(16)8-6-4-5-7(12)13-9(6)15-14-8/h4-5H,1-3H3,(H,13,14,15)

Upstream product

• 7732-18-5 water 
• 155601-70-0 2,6-Difluoropyridine-3-(α-oxo)acetic acid, t-butyl ester 
• 75716-83-5 tert-butyl α-oxo-1H-imidazole-1-acetate 
• 1513-65-1 2,6-difluoro pyridine 

Downstream Products

• 932702-22-2 tert-butyl 6-phenyl-1H-pyrazolo[3,4-b]pyridine-3-carboxylate 
• 1034474-26-4 tert-butyl 6-fluoro-1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridine-3-carboxylate 
• 1345337-09-8 tert-butyl 6-fluoro-2-(4-methoxybenzyl)-2H-pyrazolo[3,4-b]pyridine-3-carboxylate 
• 1034474-27-5 tert-butyl 1-(4-methoxybenzyl)-6-[(4-methoxybenzyl)amino]-1H-pyrazolo[3,4-b]pyridine-3-carboxylate 
• 1034474-34-4 3-chloro-5-{[5-chloro-1-({1-(4-methoxybenzyl)-6-[(4-methoxybenzyl)amino]-1H-pyrazolo[3,4-b]pyridin-3-yl}methyl)-1H-indazol-4-yl]oxy}benzonitrile 
• 1345337-17-8 3-chloro-5-{[5-chloro-2-({1-(4-methoxybenzyl)-6-[(4-methoxybenzyl)amino]-1H-pyrazolo[3,4-b]pyridin-3-yl}methyl)-2H-indazol-4-yl]oxy}benzonitrile 
• 1034474-20-8 3-{[5-chloro-4-(3-chloro-5-cyanophenoxy)-1H-indazol-1-yl]methyl}-1H-pyrazolo[3,4-b]pyridin-6-aminium chloride 
• 1034474-35-5 3-({1-[(6-amino-1H-pyrazolo[3,4-b]pyridin-3-yl)methyl]-5-chloro-1H-indazol-4-yl}oxy)-5-chlorobenzonitrile 
• 1345337-24-7 3-chloro-5-{[5-chloro-1-({2-(4-methoxybenzyl)-6-[(4-methoxybenzyl)amino]-2H-pyrazolo[3,4-b]pyridin-3-yl}methyl)-1H-1,2,3-benzotriazol-4-yl]oxy}benzonitrile 
• 1345337-21-4 3-(chloromethyl)-N,2-bis(4-methoxybenzyl)-2H-pyrazolo[3,4-b]pyridin-6-amine 
• 1345337-40-7 3-{[5-chloro-4-(3-chloro-5-cyanophenoxy)-1H-1,2,3-benzotriazol-1-yl]methyl}-1H-pyrazolo[3,4-b]pyridin-6-aminium chloride 
• 1345336-22-2 3-({1-[(6-amino-1H-pyrazolo[3,4-b]pyridin-3-yl)methyl]-5-chloro-1H-1,2,3-benzotriazol-4-yl}oxy)-5-chlorobenzonitrile 
• 1034474-28-6 {1-(4-methoxybenzyl)-6-[(4-methoxybenzyl)amino]-1H-pyrazolo[3,4-b]pyridin-3-yl}methanol 
• 1034474-25-3 3-(chloromethyl)-N,1-bis(methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-6-amine 

Relevant academic research and scientific papers

Synthesis of some piperazinylpyrazolo[3,4-b]pyridines as selective serotonin re-uptake inhibitors

A number of 3-substituted 6-piperazinylpyrazolo[3,4-b]pyridines were synthesized from 2,6-difluoropyridine by directed ortho metallation and sequential intra- and intermolecular displacement of fluorine. Three derivatives with a cyano group in the 3-position showed activity as selective serotonin re-uptake inhibitors.