(2E)-3-[(5-methoxy-2-phenyl)-1H-indol-3-yl]-2-(phenylsulfonyl)acrylonitrile

Base Information

Chemical Name:(2E)-3-[(5-methoxy-2-phenyl)-1H-indol-3-yl]-2-(phenylsulfonyl)acrylonitrile
CAS No.:1519005-46-9
Molecular Formula:C₂₄H₁₈N₂O₃S
Molecular Weight:414.485
Hs Code.:

Synonyms:(2E)-3-[(5-methoxy-2-phenyl)-1H-indol-3-yl]-2-(phenylsulfonyl)acrylonitrile

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Chemical Property of (2E)-3-[(5-methoxy-2-phenyl)-1H-indol-3-yl]-2-(phenylsulfonyl)acrylonitrile

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Technology Process of (2E)-3-[(5-methoxy-2-phenyl)-1H-indol-3-yl]-2-(phenylsulfonyl)acrylonitrile

There total 3 articles about (2E)-3-[(5-methoxy-2-phenyl)-1H-indol-3-yl]-2-(phenylsulfonyl)acrylonitrile 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: 78.0%

: 1519005-64-1
C₁₈H₁₉N₂O⁽¹⁺⁾*Cl^(1-)

: 7605-28-9
2-(phenylsulfonyl)acetonitrile

: 1519005-46-9
(2E)-3-[(5-methoxy-2-phenyl)-1H-indol-3-yl]-2-(phenylsulfonyl)acrylonitrile

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; at 80 - 90 ℃; for 0.75h; stereoselective reaction;
DOI:10.1016/j.tet.2013.10.086

Reference yield: 78.0%

: 5883-96-5
5-methoxy-2-phenylindole

: 68-12-2,33513-42-7
N,N-dimethyl-formamide

: 7605-28-9
2-(phenylsulfonyl)acetonitrile

: 1519005-46-9
(2E)-3-[(5-methoxy-2-phenyl)-1H-indol-3-yl]-2-(phenylsulfonyl)acrylonitrile

Guidance literature:: 5-methoxy-2-phenylindole; N,N-dimethyl-formamide; With benzoyl chloride; at 0 ℃;

2-(phenylsulfonyl)acetonitrile; With triethylamine; In N,N-dimethyl-formamide; at 90 ℃; for 0.75h; stereoselective reaction;
DOI:10.1016/j.ejmech.2015.08.009

Reference yield:

: 5883-96-5
5-methoxy-2-phenylindole

: 1519005-46-9
(2E)-3-[(5-methoxy-2-phenyl)-1H-indol-3-yl]-2-(phenylsulfonyl)acrylonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: benzoyl chloride / 5 - 20 °C

2: triethylamine / N,N-dimethyl-formamide / 0.75 h / 80 - 90 °C

With benzoyl chloride; triethylamine; In N,N-dimethyl-formamide; 2: |Knoevenagel Condensation;
DOI:10.1016/j.tet.2013.10.086