(E)-1-(2-(2-(6-nitrobenzo[d][1,3]dioxol-5-yl)vinyl)-1-(phenylsulfonyl)-1H-indol-3-yl)ethanone

Base Information

Chemical Name:(E)-1-(2-(2-(6-nitrobenzo[d][1,3]dioxol-5-yl)vinyl)-1-(phenylsulfonyl)-1H-indol-3-yl)ethanone
CAS No.:1445973-86-3
Molecular Formula:C₂₅H₁₈N₂O₇S
Molecular Weight:490.493
Hs Code.:

Synonyms:(E)-1-(2-(2-(6-nitrobenzo[d][1,3]dioxol-5-yl)vinyl)-1-(phenylsulfonyl)-1H-indol-3-yl)ethanone

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Chemical Property of (E)-1-(2-(2-(6-nitrobenzo[d][1,3]dioxol-5-yl)vinyl)-1-(phenylsulfonyl)-1H-indol-3-yl)ethanone

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Technology Process of (E)-1-(2-(2-(6-nitrobenzo[d][1,3]dioxol-5-yl)vinyl)-1-(phenylsulfonyl)-1H-indol-3-yl)ethanone

There total 6 articles about (E)-1-(2-(2-(6-nitrobenzo[d][1,3]dioxol-5-yl)vinyl)-1-(phenylsulfonyl)-1H-indol-3-yl)ethanone 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: 90.0%

: 1445973-83-0
C₃₅H₂₈NO₃PS

: 712-97-0
6-nitro-1,3-benzodioxole-5-carbaldehyde

: 1445973-86-3
(E)-1-(2-(2-(6-nitrobenzo[d][1,3]dioxol-5-yl)vinyl)-1-(phenylsulfonyl)-1H-indol-3-yl)ethanone

Guidance literature:: In 1,2-dichloro-ethane; for 6h; Reflux; Inert atmosphere;
DOI:10.1021/ol4015738

Reference yield:

: 113685-33-9
3-acetyl-2-methyl-1-(phenylsulfonyl)indole

: 1445973-86-3
(E)-1-(2-(2-(6-nitrobenzo[d][1,3]dioxol-5-yl)vinyl)-1-(phenylsulfonyl)-1H-indol-3-yl)ethanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 3 h / Reflux; Inert atmosphere

2.1: tetrahydrofuran / 2 h / Reflux; Inert atmosphere

2.2: 12 h / 20 °C / Inert atmosphere

3.1: 1,2-dichloro-ethane / 6 h / Reflux; Inert atmosphere

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrahydrofuran; tetrachloromethane; 1,2-dichloro-ethane;
DOI:10.1021/ol4015738

Reference yield:

: 143774-55-4
1-(2-(bromomethyl)-1-(phenylsulfonyl)-1H-indol-3-yl)ethanone

: 1445973-86-3
(E)-1-(2-(2-(6-nitrobenzo[d][1,3]dioxol-5-yl)vinyl)-1-(phenylsulfonyl)-1H-indol-3-yl)ethanone

Guidance literature:: Multi-step reaction with 2 steps

1.1: tetrahydrofuran / 2 h / Reflux; Inert atmosphere

1.2: 12 h / 20 °C / Inert atmosphere

2.1: 1,2-dichloro-ethane / 6 h / Reflux; Inert atmosphere

In tetrahydrofuran; 1,2-dichloro-ethane;
DOI:10.1021/ol4015738