401815-97-2

Upstream product

• 291743-96-9 2-(4-fluorophenyl)-3-bromopyrazolo[1,5-a]pyridine 
• 401815-98-3 2-fluoropyridin-4-ylboronic acid 
• 291743-95-8 2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine 
• 22282-70-8 2-fluoro-4-iodopyridine 
• 497-19-8 sodium carbonate 
• 766-98-3 1-ethynyl-4-fluorobenzene 
• 401815-64-3 2-(4-fluorophenyl)-pyrazolo[1,5-a]pyridine-3-carboxylic acid 
• 340322-91-0 methyl 2-(4-fluorophenyl)-pyrazolo[1,5-a]pyridine-3-carboxylate 
• 130995-12-9 1-(4-fluorophenyl)-2-trimethylsilylacetylene 
• 42122-44-1 methyl 3-(4-fluorophenyl)propiolate 
• 352-34-1 4-fluoro-1-iodobenzene 

Downstream Products

• 401816-24-8 6-Bromo-2-(4-fluorophenyl)-3-(2-fluoro-4-pyridinyl)pyrazolo[1,5-a]pyridine 

Relevant academic research and scientific papers

Palladium-Catalyzed Regioselective Arylation of Pyrazolo[1,5-a]pyridines via C-H Activation and Synthetic Applications on P38 Kinase Inhibitors

A direct arylation of pyrazolo[1,5-a]pyridines with aryl iodides selectively occurring at the C-3 and C-7 positions via palladium-catalyzed C-H activation is described. In these reactions, (a) cesium(I) fluoride and (b) silver(I) carbonate were employed a

Pyrazolo[1,5-a]pyridines as p38 kinase inhibitors

(Chemical Equation Presented) A convergent synthesis of substituted pyrazolo[1,5-a]pyridines has been achieved either via a regioselective [3 + 2] cycloaddition of N-aminopyridines with alkynes or by thermal cyclization of disubstituted azirines. Subseque

Fused pyrazole derivatives bieng protein kinase inhibitors

Compounds of Formula (I): salts or solvates or physiologically functional derivatives thereof, wherein Z is CH or N, and R1, (R2, and R4 are various substituent groups, are protein kinase inhibitors.