2-(4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-yl)-2-((trimethylsilyl)oxy)-acetonitrile

Base Information

Chemical Name:2-(4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-yl)-2-((trimethylsilyl)oxy)-acetonitrile
CAS No.:1422975-81-2
Molecular Formula:C₂₂H₂₆N₂O₃Si
Molecular Weight:394.546
Hs Code.:

Synonyms:2-(4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-yl)-2-((trimethylsilyl)oxy)-acetonitrile

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Chemical Property of 2-(4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-yl)-2-((trimethylsilyl)oxy)-acetonitrile

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Technology Process of 2-(4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-yl)-2-((trimethylsilyl)oxy)-acetonitrile

There total 1 articles about 2-(4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-yl)-2-((trimethylsilyl)oxy)-acetonitrile 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: 64.0%

: 7677-24-9
trimethylsilyl cyanide

: 1220960-48-4
4,6-dimethoxy-3-(4-methylphenyl)-1H-indole-7-carbaldehyde

: 1422975-81-2
2-(4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-yl)-2-((trimethylsilyl)oxy)-acetonitrile

Guidance literature:: In acetonitrile; Reflux;
DOI:10.1016/j.tet.2012.12.084

Reference yield: 80.0%

: 1422975-81-2
2-(4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-yl)-2-((trimethylsilyl)oxy)-acetonitrile

: 1422975-85-6
4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-carbonyl cyanide

Guidance literature:: With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In 1,4-dioxane; at 20 ℃;
DOI:10.1016/j.tet.2012.12.084

Reference yield:

: 1422975-81-2
2-(4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-yl)-2-((trimethylsilyl)oxy)-acetonitrile

: 2-amino-1-(4,6-dimethoxy-3-(p-tolyl)-1H-indol-7-yl)-ethanone monoacetate

Guidance literature:: Multi-step reaction with 2 steps

1: 2,3-dicyano-5,6-dichloro-p-benzoquinone / 1,4-dioxane / 20 °C

2: hydrogen; palladium 10% on activated carbon / ethyl acetate / 20 h / 20 °C

With palladium 10% on activated carbon; hydrogen; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In 1,4-dioxane; ethyl acetate;
DOI:10.1016/j.tet.2012.12.084