145835-09-2Relevant academic research and scientific papers
Pyrazolo[1,5-a]pyridines as p38 kinase inhibitors
Stevens, Kirk L.,Jung, David K.,Alberti, Michael J.,Badiang, Jennifer G.,Peckham, Gregory E.,Veal, Jim M.,Cheung, Mui,Harris, Philip A.,Chamberlain, Stanley D.,Peel, Michael R.
, p. 4753 - 4756 (2007/10/03)
(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
Process optimization and synthesis of 3-(4-fluorophenyl)-4,5-dihydro-N-[4-(trifluoromethyl)phenyl]-4-[5- (trifluoromethyl)-2-pyridyl]-1H-pyrazole-1-carboxamide
Renga, James M.,McLaren, Kevin L.,Ricks, Michael J.
, p. 267 - 271 (2013/09/06)
A convenient, high-yielding synthesis of the insecticide 3-(4-fluorophenyl)-4,5-dihydro-N-[4-(trifluoromethyl)phenyl]-4-[5- (trifluoromethyl)-2-pyridyl]-1H-pyrazole-1-carboxamide is presented. Attempted methenylation of the 2-pyridylacetophenone, obtained
Pyrazolopyridines
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, (2008/06/13)
The invention provides the compounds of formula (I) wherein: R0and R1are independently selected from H, halogen, C1-6alkyl, C1-6alkoxy, or C1-6alkoxy substituted by one or more fluorine atoms; R2
