104271-33-2

Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 52, p. 1863, 1987 DOI: 10.1021/jo00385a041

Upstream product

• 104271-32-1 5,6-dihydro-8-phenylimidazo<1,2-a>pyridine 
• 107-20-0 2-chloroethanal 
• 87109-10-2 2-amino-3-phenyl pyridine 
• 939-52-6 4-chloro-1-phenylbutan-1-one 

Relevant academic research and scientific papers

Pd-Catalyzed Tandem Cyclization via C-H Arylation and Acylation for the Construction of Polycyclic Scaffolds

The first Pd-catalyzed tandem cyclization of imidazo[1,2-a]pyridines with 2-chlorobenzaldehydes through C-H arylation and acylation is presented for the efficient synthesis of novel 6H-benzo[b]imidazo[5,1,2-de]quinolizin-6-ones. The direct acylation react

Cardiotonic agents. 1. Novel 8-aryl-substituted imidazo[1,2-a]- and -[1,5-a]pyridines and imidazo[1,5-a]pyridinones as potential positive inotropic agents

Several 8-arylimidazo[1,2-a]pyridines, 8-arylimidazo[1,5-a]pyridines, and 8-arylimidazo[1,5-a]pyridinones were prepared and tested in vitro for potential cardiac inotropic and electrophysiological activity. Selected analogues were further tested in vivo i

Imidazo[1,2-a]pyridines, and process for their preparation

This invention relates to novel substituted imidazo[1,2-a]pyridines, most especially novel 8-phenylimidazo[1,2-a]pyridines and a process for their preparation. The compounds of the invention have been found to have cardiotonic antiarrhythmic, CNS stimulant, CNS depressant and other pharmacological effects.