1353511-55-3

Basic information

• Product Name: 2-phenyl-3-(pyridin-4-yl)imidazo[1,2-a]pyridine
• Synonyms: 2-phenyl-3-(pyridin-4-yl)imidazo[1,2-a]pyridine
• CAS NO: 1353511-55-3
• Molecular Weight: 271.321
• Mol File: 1353511-55-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-phenyl-3-(pyridin-4-yl)imidazo[1,2-a]pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-3-(pyridin-4-yl)imidazo[1,2-a]pyridine(1353511-55-3)
• EPA Substance Registry System: 2-phenyl-3-(pyridin-4-yl)imidazo[1,2-a]pyridine(1353511-55-3)

Safety Data

• Hazardous Substances Data: 1353511-55-3(Hazardous Substances Data)

Upstream product

• 1692-15-5 4-pyridylboronic acid 
• 4105-21-9 2-phenylimidazo[1,2-a]pyridine 
• 98-80-6 phenylboronic acid 
• 1373338-15-8 2-iodoimidazo[1,2-a]pyridine 
• 19524-06-2 4-bromopyridine hydrochloride 
• 74129-11-6 4-bromopyridine hydrobromide salt 
• 3999-05-1 2-chloroimidazo[1,2-a]pyridine 
• 4044-95-5 2-Phenyl-3-bromoimidazo<1,2-a>pyridine 
• 181219-01-2 4-pyridineboronic acid pinacol ester 
• 1021019-74-8 imidazo[1,2-a]pyridin-2-yl trifluoromethanesulfonate 
• 126202-06-0 2-(2-imino-1,2-dihydropyridin-1-yl)acetic acid 
• 112581-95-0 2-Bromoimidazo[1,2-a]pyridine 
• 504-29-0 2-aminopyridine 
• 1120-87-2 4-bromopyridin 

Relevant articles and documents

Regiocontrolled functionalization of 2,3-dihalogenoimidazo[1,2-a]pyridines by Suzuki-Miyaura and Sonogashira cross-coupling reactions

An efficient method for regiocontrolled functionalization of 2,3-dihalogenoimidazo[1,2-a]pyridine was developed. This sequence allowed the selective introduction of aryl, heteroaryl, alkyl and alkynyl substituents at both 2- and 3-positions, by using Suzu

Efficient access to 2,3-diarylimidazo[1,2-a ]pyridines via a one-pot, ligand-free, palladium-catalyzed three-component reaction under microwave irradiation

An expeditious one-pot, ligand-free, Pd(OAc)2-catalyzed, three-component reaction for the synthesis of 2,3-diarylimidazo[1,2-a]pyridines was developed under microwave irradiation. With the high availability of commercial reagents and great efficiency in expanding molecule diversity, this methodology is superior to the existing procedures for the synthesis of 2,3-diarylimidazo[1,2-a]pyridines analogues.

An efficient access to 2,3-diarylimidazo[1,2-a]pyridines via imidazo[1,2-a]pyridin-2-yl triflate through a Suzuki cross-coupling reaction-direct arylation sequence

An efficient method to prepare 2,3-diarylimidazo[1,2-a]pyridines is described. The procedure involves a Suzuki cross-coupling reaction followed by a direct arylation at position 3. Imidazo[1,2-a]pyridin-2-yl triflate was identified as a suitable coupling partner, permitting access to a variety of highly functionalized 2,3-diarylimidazo[1,2-a]pyridines.