1175675-65-6

Basic information

• Product Name: 9-benzenesulfonyl-6-bromo-4-chloro-9H-pyrido[2,3-b]-indole
• Synonyms: 9-benzenesulfonyl-6-bromo-4-chloro-9H-pyrido[2,3-b]-indole
• CAS NO: 1175675-65-6
• Molecular Weight: 421.702
• Mol File: 1175675-65-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 9-benzenesulfonyl-6-bromo-4-chloro-9H-pyrido[2,3-b]-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 9-benzenesulfonyl-6-bromo-4-chloro-9H-pyrido[2,3-b]-indole(1175675-65-6)
• EPA Substance Registry System: 9-benzenesulfonyl-6-bromo-4-chloro-9H-pyrido[2,3-b]-indole(1175675-65-6)

Safety Data

• Hazardous Substances Data: 1175675-65-6(Hazardous Substances Data)

Upstream product

• 1175675-60-1 6-bromo-4-chloro-9-H-pyrido[2,3-b]indole 
• 98-09-9 benzenesulfonyl chloride 
• 25208-32-6 4-chloro-9-H-pyrido[2,3-b]indole 

Downstream Products

• 1175675-75-8 9-benzenesulfonyl-4-chloro-6-(styryl)-9H-pyrido[2,3-b]indole 
• 1175675-82-7 9-benzenesulfonyl-6-(4-methoxyphenyl)-4-styryl-9H-pyrido[2,3-b]indole 
• 1175675-71-4 9-benzenesulfonyl-4-chloro-6-(4-methoxyphenyl)-9H-pyrido[2,3-b]indole 
• 1175675-91-8 9-benzenesulfonyl-4,6-di(4-methoxyphenyl)-9H-pyrido[2,3-b]indole 

Relevant articles and documents

NOVEL TRICYCLIC COMPOUND AS IRAK4 INHIBITOR

The present invention relates to a pharmaceutical composition for preventing or treating autoimmune diseases or tumors, containing, as an active ingredient, a tricyclic compound represented by the following Chemical Formula 1 or a pharmaceutically acceptable salt thereof, and a health food composition for preventing or alleviating autoimmune diseases or tumors, containing the tricyclic compound as an active ingredient. The tricyclic compound represented by Chemical Formula 1 of the present invention has an excellent inhibitory activity against IRAK4, and thus can be usefully used for the prevention, treatment, or alleviation of autoimmune diseases or tumors.

Chemoselective functionalization of α-carbolines at the C-2, C-3, C-4, and C-6 positions using Suzuki-Miyaura reactions

The synthesis of 2-, 3-, 4-, and 6-substituted pyrido[2,3-b]indoles (α-carbolines) by palladium-catalyzed cross-coupling reactions from the corresponding halopyrido[2,3-b]indoles is described. A sequential and a one-pot chemoselective double Suzuki-Miyaur