N-(4-bromobenzyl)-5-methoxy-1-(phenylsulfonyl)-1H-indole-2-sulfonamide

Base Information

Chemical Name:N-(4-bromobenzyl)-5-methoxy-1-(phenylsulfonyl)-1H-indole-2-sulfonamide
CAS No.:1394431-47-0
Molecular Formula:C₂₂H₁₉BrN₂O₅S₂
Molecular Weight:535.439
Hs Code.:

Synonyms:N-(4-bromobenzyl)-5-methoxy-1-(phenylsulfonyl)-1H-indole-2-sulfonamide

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Chemical Property of N-(4-bromobenzyl)-5-methoxy-1-(phenylsulfonyl)-1H-indole-2-sulfonamide

Chemical Property:

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Technology Process of N-(4-bromobenzyl)-5-methoxy-1-(phenylsulfonyl)-1H-indole-2-sulfonamide

There total 8 articles about N-(4-bromobenzyl)-5-methoxy-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:

: 3959-07-7
4-Bromobenzylamine

: 100632-26-6
5-methoxy-1-(phenylsulfonyl)-1H-indole-2-sulfonyl chloride

: 1394431-47-0
N-(4-bromobenzyl)-5-methoxy-1-(phenylsulfonyl)-1H-indole-2-sulfonamide

Guidance literature:: In dichloromethane; Cooling with ice;
DOI:10.1016/j.bmcl.2016.08.018

Reference yield:

: 1006-94-6
5-methoxylindole

: 1394431-47-0
N-(4-bromobenzyl)-5-methoxy-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: dichloromethane / Cooling with ice

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

Reference yield:

: 56995-12-1
1-benzenesulfonyl-5-methoxy-1H-indole

: 1394431-47-0
N-(4-bromobenzyl)-5-methoxy-1-(phenylsulfonyl)-1H-indole-2-sulfonamide

Guidance literature:: Multi-step reaction with 3 steps

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

1.2: 2.25 h / -70 - 20 °C / Inert atmosphere

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

3.1: dichloromethane / Cooling with ice

With N-chloro-succinimide; n-butyllithium; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.bmcl.2016.08.018