1H-pyrrole-3-carboxylic acid (2-bromo-4-methoxy-phenyl)-(2-trimethylsilanyl-ethoxymethyl)-amide

Base Information

Chemical Name:1H-pyrrole-3-carboxylic acid (2-bromo-4-methoxy-phenyl)-(2-trimethylsilanyl-ethoxymethyl)-amide
CAS No.:324520-82-3
Molecular Formula:C₁₈H₂₅BrN₂O₃Si
Molecular Weight:425.398
Hs Code.:

1<i>H</i>-pyrrole-3-carboxylic acid (2-bromo-4-methoxy-phenyl)-(2-trimethylsilanyl-ethoxymethyl)-amide

Synonyms:1H-pyrrole-3-carboxylic acid (2-bromo-4-methoxy-phenyl)-(2-trimethylsilanyl-ethoxymethyl)-amide

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Chemical Property of 1H-pyrrole-3-carboxylic acid (2-bromo-4-methoxy-phenyl)-(2-trimethylsilanyl-ethoxymethyl)-amide

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Technology Process of 1H-pyrrole-3-carboxylic acid (2-bromo-4-methoxy-phenyl)-(2-trimethylsilanyl-ethoxymethyl)-amide

There total 3 articles about 1H-pyrrole-3-carboxylic acid (2-bromo-4-methoxy-phenyl)-(2-trimethylsilanyl-ethoxymethyl)-amide 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: 57.0%

: 38622-91-2,36635-61-7
[(p-methylphenyl)sulfonylmethyl]isonitrile

: 444166-96-5
N-(2-bromo-4-methoxyphenyl)-N-(2-trimethylsilylethoxymethyl)acrylamide

: 324520-82-3
1H-pyrrole-3-carboxylic acid (2-bromo-4-methoxy-phenyl)-(2-trimethylsilanyl-ethoxymethyl)-amide

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; at 0 ℃; for 1h;
DOI:10.1016/S0040-4020(02)00007-8

Reference yield:

: 32338-02-6
2-bromo-4-methoxyaniline

: 324520-82-3
1H-pyrrole-3-carboxylic acid (2-bromo-4-methoxy-phenyl)-(2-trimethylsilanyl-ethoxymethyl)-amide

Guidance literature:: Multi-step reaction with 3 steps

1: 93 percent / N,N-diisopropylethylamine / diethyl ether / 4 h / 0 - 20 °C

2: 92 percent / NaH / tetrahydrofuran

3: 57 percent / t-BuOK / tetrahydrofuran / 1 h / 0 °C

With potassium tert-butylate; sodium hydride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; diethyl ether;
DOI:10.1016/S0040-4020(02)00007-8

Reference yield:

: 116707-97-2
N-(2-bromo-4-methoxyphenyl)acrylamide

: 324520-82-3
1H-pyrrole-3-carboxylic acid (2-bromo-4-methoxy-phenyl)-(2-trimethylsilanyl-ethoxymethyl)-amide

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / NaH / tetrahydrofuran

2: 57 percent / t-BuOK / tetrahydrofuran / 1 h / 0 °C

With potassium tert-butylate; sodium hydride; In tetrahydrofuran;
DOI:10.1016/S0040-4020(02)00007-8