437384-09-3

Upstream product

• 108-24-7 acetic anhydride 
• 637775-52-1 cyclopentyl-[2-(4-fluoro-phenyl)-pyrazolo[1,5-a]pyridin-7-yl]-amine 
• 1003-03-8 Cyclopentamine 
• 437384-08-2 1-[7-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-3-yl]ethanone 
• 437384-06-0 2-(6-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone oxime 
• 637775-51-0 2-chloro-6-[3-(4-fluoro-phenyl)-2H-azirin-2-yl]-pyridine 
• 437384-05-9 2-(6-chloro-2-pyridinyl)-1-(4-fluorophenyl)ethanone 
• 451-46-7 4-fluorobenzoic acid ethyl ester 
• 437384-07-1 7-chloro-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine 

Downstream Products

• 437384-10-6 (2E)-1-[7-(cyclopentylamino)-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridin-3-yl]-3-(dimethylamino)-2-propen-1-one 
• 942937-98-6 C₂₀H₁₉FN₃OBr 

Relevant academic research and scientific papers

Pyrazolopyridine antiherpetics: SAR of C2′ and C7 amine substituents

A novel series of potent pyrazolo[1,5-a]pyridine inhibitors of herpes simplex virus 1 replication have been identified. Several complimentary synthetic methods were developed to allow facile access to a diverse set of analogs from common late stage interm

Therapeutic compounds

The present invention provides compounds of formula (I): wherein all variables are as defined herein, pharmaceutical compositions containing the same, processes for preparing the same and their use as pharmaceutical agents. 1

Pyrazolo[1,5-a]pyridines: Synthetic approaches to a novel class of antiherpetics

Synthesis of a novel class of 7-amino-3-pyrimidinyl-pyrazolo[1,5-a] pyridine antiherpetic compounds is described. The synthetic methodology is designed to allow for rapid analog synthesis around the C-3 and C-7 positions of the pyrazolo[1,5-a]pyridine. Th