1527501-76-3

Basic information

• Product Name: N-benzyl-N-(5,7-dichloro-1H-indol-2-yl)-4-methylbenzenesulfonamide
• Synonyms: N-benzyl-N-(5,7-dichloro-1H-indol-2-yl)-4-methylbenzenesulfonamide
• CAS NO: 1527501-76-3
• Molecular Weight: 445.369
• Mol File: 1527501-76-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-benzyl-N-(5,7-dichloro-1H-indol-2-yl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-N-(5,7-dichloro-1H-indol-2-yl)-4-methylbenzenesulfonamide(1527501-76-3)
• EPA Substance Registry System: N-benzyl-N-(5,7-dichloro-1H-indol-2-yl)-4-methylbenzenesulfonamide(1527501-76-3)

Safety Data

• Hazardous Substances Data: 1527501-76-3(Hazardous Substances Data)

Upstream product

• 1527502-03-9 C₈H₅Br₂Cl₂N 
• 98-59-9 p-toluenesulfonyl chloride 
• 100-46-9 benzylamine 
• 1576-37-0 N-benzyl-p-toluenesulfonamide 
• 1527501-62-7 N-(2,4-dichloro-6-(2,2-dibromovinyl)phenyl)acetamide 
• 59178-12-0 3,5-dichloro-2-nitrobenzaldehyde 

Relevant articles and documents

CuI-catalyzed coupling of gem-dibromovinylanilides and sulfonamides: An efficient method for the synthesis of 2-amidoindoles and indolo[1,2-a] quinazolines

A Cu(I)-catalyzed, intermolecular protocol for the synthesis of 2-amidoindoles and tetrahydroindolo[1,2-a]quinazolines in shorter time and high yields is reported. The key highlight of this disclosure is the formation of 2-amidoindole and tetrahydroindolo[1,2-a]quinazoline moieties directly from gem-dibromovinylanilides and sulfonamides in a one-pot fashion through the in situ formation of ynamides followed by a base-promoted intramolecular hydroamidation.