1611476-99-3

Basic information

• Product Name: N-(2-bromo-4,5-dimethoxyphenyl)-N-((4,9-dihydro-3H-pyrido[3,4-b]indol-1-yl)methyl)isobutyramide
• Synonyms: N-(2-bromo-4,5-dimethoxyphenyl)-N-((4,9-dihydro-3H-pyrido[3,4-b]indol-1-yl)methyl)isobutyramide
• CAS NO: 1611476-99-3
• Molecular Weight: 484.393
• Mol File: 1611476-99-3.mol

Chemical Properties

• CAS DataBase Reference: N-(2-bromo-4,5-dimethoxyphenyl)-N-((4,9-dihydro-3H-pyrido[3,4-b]indol-1-yl)methyl)isobutyramide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-bromo-4,5-dimethoxyphenyl)-N-((4,9-dihydro-3H-pyrido[3,4-b]indol-1-yl)methyl)isobutyramide(1611476-99-3)
• EPA Substance Registry System: N-(2-bromo-4,5-dimethoxyphenyl)-N-((4,9-dihydro-3H-pyrido[3,4-b]indol-1-yl)methyl)isobutyramide(1611476-99-3)

Safety Data

• Hazardous Substances Data: 1611476-99-3(Hazardous Substances Data)

Upstream product

• 100571-64-0 2-(3-indolyl)ethyl isocyanide 
• 1611476-95-9 N-(2-((2-(1H-indol-3-yl)ethyl)amino)-2-oxoethyl)-N-(2-bromo-4,5-dimethoxyphenyl)isobutyramide 
• 16791-41-6 2-bromo-4,5-dimethoxyaniline 

Relevant articles and documents

Multicomponent access to novel dihydroimidazo[1′,5′:1,2] pyrido[3,4-b]indol-2-ium salts and indoles by means of Ugi/Bischler-Napieralski/ heterocyclization two step strategy

A simple, efficient and general two step procedure, through a sequential Ugi reaction followed by a Bischler-Napieralski/heterocyclization tandem closure, to give novel 6,11-dihydro-5H-imidazo[1′,5′:1,2]pyrido[3,4- b]indol-2-ium salt derivatives, is described. By changing the amine and the acid components with ammonium formate, the same procedure affords 6,11-dihydro-5H-imidazo[1′,5′:1,2]pyrido[3,4-b]indole derivatives.