945933-92-6

Basic information

• Product Name: 6-(4-nitrophenyl)pyrido[2',1':2,3]imidazo[4,5-c]quinoline
• Synonyms: 6-(4-nitrophenyl)pyrido[2',1':2,3]imidazo[4,5-c]quinoline
• CAS NO: 945933-92-6
• Molecular Weight: 340.341
• Mol File: 945933-92-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6-(4-nitrophenyl)pyrido[2',1':2,3]imidazo[4,5-c]quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(4-nitrophenyl)pyrido[2',1':2,3]imidazo[4,5-c]quinoline(945933-92-6)
• EPA Substance Registry System: 6-(4-nitrophenyl)pyrido[2',1':2,3]imidazo[4,5-c]quinoline(945933-92-6)

Safety Data

• Hazardous Substances Data: 945933-92-6(Hazardous Substances Data)

Upstream product

• 504-29-0 2-aminopyridine 
• 253684-24-1 1-(2,2-dibromovinyl)-2-nitrobenzene 
• 126267-63-8 2-(2-nitro-phenyl)-imidazo[1,2-a]pyridine 
• 555-16-8 4-nitrobenzaldehdye 
• 552-89-6 2-nitro-benzaldehyde 
• 6851-99-6 2-bromo-1-(2-nitrophenyl)ethanone 
• 115769-03-4 2-(2-bromophenyl)imidazo[1,2-α]pyridine 
• 49851-55-0 2,2'-dibromoacetophenone 

Relevant articles and documents

An expeditious microwave assisted one-pot sequential route to pyrido fused imidazo[4,5-c] quinolines in green media

An expeditious microwave assisted one-pot sequential route to synthesize pyrido fused imidazo[4,5-c]quinolinesviathe Pictet-Spengler cyclization strategy has been developed. In this study, substituted 2-amino pyridines are condensed with 2-bromo-2′-nitroa

Synthesis of biologically active pyridoimidazole/imidazobenzothiazole annulated polyheterocycles using cyanuric chloride in water

An efficient and mild protocol for rapid access to N-fused polyheterocycles via Pictet-Spengler type 6-endo cyclization using cyanuric chloride in an aqueous reaction medium has been developed. The protocol was successfully applied to a wide range of compounds including aryl/heteroaryl aldehydes (8a-o), ketones (10a-e), an electron-rich metallocene aldehyde (8e) and indoline-2,3-diones (12a-c) using cyanuric chloride (15-20 mol%) with tetra-n-butylammonium bromide (TBAB) (2.0 eq.) as an additive at 80-90 °C to give a good to excellent yield (66-92%) of polyheterocycles. Some of the synthesized compounds were found to exhibit antiplasmodial activity against chloroquine-sensitive (CQ-S) 3D7 and chloroquine-resistant (CQ-R) K1 strains of Plasmodium falciparum. This journal is the Partner Organisations 2014.