5-bromo-N-((5-(4-fluorophenyl)pyridin-2-yl)methyl)-1-(phenylsulfonyl)-1H-indole-2-sulfonamide

Base Information

Chemical Name:5-bromo-N-((5-(4-fluorophenyl)pyridin-2-yl)methyl)-1-(phenylsulfonyl)-1H-indole-2-sulfonamide
CAS No.:1394431-50-5
Molecular Formula:C₂₆H₁₉BrFN₃O₄S₂
Molecular Weight:600.489
Hs Code.:

Synonyms:5-bromo-N-((5-(4-fluorophenyl)pyridin-2-yl)methyl)-1-(phenylsulfonyl)-1H-indole-2-sulfonamide

Suppliers and Price of 5-bromo-N-((5-(4-fluorophenyl)pyridin-2-yl)methyl)-1-(phenylsulfonyl)-1H-indole-2-sulfonamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 5-bromo-N-((5-(4-fluorophenyl)pyridin-2-yl)methyl)-1-(phenylsulfonyl)-1H-indole-2-sulfonamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 5-bromo-N-((5-(4-fluorophenyl)pyridin-2-yl)methyl)-1-(phenylsulfonyl)-1H-indole-2-sulfonamide

There total 9 articles about 5-bromo-N-((5-(4-fluorophenyl)pyridin-2-yl)methyl)-1-(phenylsulfonyl)-1H-indole-2-sulfonamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 914349-75-0
5-(4-fluorophenyl)picolinonitrile

: 1394431-50-5
5-bromo-N-((5-(4-fluorophenyl)pyridin-2-yl)methyl)-1-(phenylsulfonyl)-1H-indole-2-sulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 20 °C / Cooling with ethanol-dry ice

2: tetrahydrofuran / 20 °C / Cooling with ethanol-dry ice

With lithium aluminium tetrahydride; In tetrahydrofuran;
DOI:10.1016/j.bmcl.2016.08.018

Reference yield:

: 16732-70-0
ethyl 5-bromoindolecarboxylate

: 1394431-50-5
5-bromo-N-((5-(4-fluorophenyl)pyridin-2-yl)methyl)-1-(phenylsulfonyl)-1H-indole-2-sulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydroxide / ethanol / 40 °C

1.2: 0.42 h / 250 °C / Microwave irradiation

2.1: sodium hydride / N,N-dimethyl-formamide / 18 h / 20 °C

3.1: n-butyllithium / tetrahydrofuran / 0.5 h / -70 °C / Inert atmosphere

3.2: 2.25 h / -70 - 20 °C / Inert atmosphere

4.1: N-chloro-succinimide / dichloromethane / 2 h / 5 °C

5.1: tetrahydrofuran / 20 °C / Cooling with ethanol-dry ice

With N-chloro-succinimide; n-butyllithium; sodium hydride; sodium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2016.08.018

Reference yield:

: 10075-50-0
5-bromo-1H-indole

: 1394431-50-5
5-bromo-N-((5-(4-fluorophenyl)pyridin-2-yl)methyl)-1-(phenylsulfonyl)-1H-indole-2-sulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 18 h / 20 °C

2.1: n-butyllithium / tetrahydrofuran / 0.5 h / -70 °C / Inert atmosphere

2.2: 2.25 h / -70 - 20 °C / Inert atmosphere

3.1: N-chloro-succinimide / dichloromethane / 2 h / 5 °C

4.1: tetrahydrofuran / 20 °C / Cooling with ethanol-dry ice

With N-chloro-succinimide; n-butyllithium; sodium hydride; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2016.08.018