1001736-32-8

Basic information

• Product Name: 6-bromo-N-tert-butyl-2-(4-chlorophenyl) imidazo[1,2-a]pyridin-3-amine
• Synonyms: 6-bromo-N-tert-butyl-2-(4-chlorophenyl) imidazo[1,2-a]pyridin-3-amine
• CAS NO: 1001736-32-8
• Molecular Formula: C₁₇H₁₇BrClN₃
• Molecular Weight: 379
• Mol File: 1001736-32-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6-bromo-N-tert-butyl-2-(4-chlorophenyl) imidazo[1,2-a]pyridin-3-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 6-bromo-N-tert-butyl-2-(4-chlorophenyl) imidazo[1,2-a]pyridin-3-amine(1001736-32-8)
• EPA Substance Registry System: 6-bromo-N-tert-butyl-2-(4-chlorophenyl) imidazo[1,2-a]pyridin-3-amine(1001736-32-8)

Safety Data

• Hazardous Substances Data: 1001736-32-8(Hazardous Substances Data)

Upstream product

• 1072-97-5 5-bromo-2-pyridylamine 
• 119072-55-8 tert-butylisonitrile 
• 104-83-6 1-Chloro-4-(chloromethyl)benzene 
• 104-88-1 4-chlorobenzaldehyde 

Relevant articles and documents

One-pot synthesis of imidazo[1,2-a]pyridines from benzyl halides or benzyl tosylates, 2-aminopyridines and isocyanides

A one-pot synthesis of imidazo[1,2-a]pyridines is described. Benzyl halides or benzyl tosylates are oxidized to aldehydes under mild Kornblum conditions which then undergo a three-component reaction with various 2-aminopyridines and isocyanides to afford the imidazo[1,2-a]pyridines in excellent yields.

Catalytic activity of aqueous cationic polyurethane dispersions: A novel feature of polyurethanes

Polyurethane ionomers are well-known and user-friendly polymers. Here, we introduce their catalytic activity for organic reactions as a novel aspect of these polymers. We selected an isocyanide-based multicomponent reaction for proving the catalytic activity of polyurethane ionomers. Therefore, a convenient and very mild methodology is described for the preparation of 3-aminoimidazo[1,2-a]pyridines via a three component reaction between 2-aminopyridines, aldehydes and isocyanides in the presence of a cationic polyurethane dispersion at low reaction temperatures, in short reaction times and excellent yields.