2-((1-(3-bromobenzyl)-4,6-difluoro-1H-indol-3-yl)sulfonyl)-N-(pyridin-2-yl)acetamide

Base Information

Chemical Name:2-((1-(3-bromobenzyl)-4,6-difluoro-1H-indol-3-yl)sulfonyl)-N-(pyridin-2-yl)acetamide
CAS No.:1353015-84-5
Molecular Formula:C₂₂H₁₆BrF₂N₃O₃S
Molecular Weight:520.354
Hs Code.:

Synonyms:2-((1-(3-bromobenzyl)-4,6-difluoro-1H-indol-3-yl)sulfonyl)-N-(pyridin-2-yl)acetamide

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Chemical Property of 2-((1-(3-bromobenzyl)-4,6-difluoro-1H-indol-3-yl)sulfonyl)-N-(pyridin-2-yl)acetamide

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Technology Process of 2-((1-(3-bromobenzyl)-4,6-difluoro-1H-indol-3-yl)sulfonyl)-N-(pyridin-2-yl)acetamide

There total 5 articles about 2-((1-(3-bromobenzyl)-4,6-difluoro-1H-indol-3-yl)sulfonyl)-N-(pyridin-2-yl)acetamide 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:

: 504-29-0
2-aminopyridine

: 1353016-19-9
2-((1-(3-bromobenzyl)-4,6-difluoro-1H-indol-3-yl)sulfonyl)acetic acid

: 1353015-84-5
2-((1-(3-bromobenzyl)-4,6-difluoro-1H-indol-3-yl)sulfonyl)-N-(pyridin-2-yl)acetamide

Guidance literature:: With chloro-N,N,N',N'-bis(tetramethylene)formamidinium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In 1,1-dichloroethane; at 110 ℃; for 0.5h;

Reference yield:

: 199526-97-1
4,6-difluoro-1H-indole

: 1353015-84-5
2-((1-(3-bromobenzyl)-4,6-difluoro-1H-indol-3-yl)sulfonyl)-N-(pyridin-2-yl)acetamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium iodide; iodine / water; methanol / 60 h / 20 °C / 760.05 Torr

2.1: sodium hydride / N,N-dimethyl-formamide / 0.25 h / 0 °C / 760.05 Torr

2.2: 3 h / 0 - 20 °C / 760.05 Torr

3.1: Oxone / water; methanol / 20 °C / 760.05 Torr

4.1: water; lithium hydroxide / tetrahydrofuran / 20 °C / 760.05 Torr

4.2: 760.05 Torr

5.1: N-ethyl-N,N-diisopropylamine; chloro-N,N,N',N'-bis(tetramethylene)formamidinium hexafluorophosphate / 1,1-dichloroethane / 0.5 h / 110 °C

With Oxone; water; iodine; sodium hydride; chloro-N,N,N',N'-bis(tetramethylene)formamidinium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; potassium iodide; lithium hydroxide; In tetrahydrofuran; methanol; 1,1-dichloroethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1353016-17-7
methyl 2-((1-(3-bromobenzyl)-4,6-difluoro-1H-indol-3-yl)thio)acetate

: 1353015-84-5
2-((1-(3-bromobenzyl)-4,6-difluoro-1H-indol-3-yl)sulfonyl)-N-(pyridin-2-yl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: Oxone / water; methanol / 20 °C / 760.05 Torr

2.1: water; lithium hydroxide / tetrahydrofuran / 20 °C / 760.05 Torr

2.2: 760.05 Torr

3.1: N-ethyl-N,N-diisopropylamine; chloro-N,N,N',N'-bis(tetramethylene)formamidinium hexafluorophosphate / 1,1-dichloroethane / 0.5 h / 110 °C

With Oxone; water; chloro-N,N,N',N'-bis(tetramethylene)formamidinium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; methanol; 1,1-dichloroethane; water;