5-bromo-2-(4-fluoro-phenyl)-6-methanesulfonylamino-benzofuran-3-carboxylic acid ethyl ester

Base Information

Chemical Name:5-bromo-2-(4-fluoro-phenyl)-6-methanesulfonylamino-benzofuran-3-carboxylic acid ethyl ester
CAS No.:1333340-16-1
Molecular Formula:C₁₈H₁₅BrFNO₅S
Molecular Weight:456.289
Hs Code.:

Synonyms:5-bromo-2-(4-fluoro-phenyl)-6-methanesulfonylamino-benzofuran-3-carboxylic acid ethyl ester

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Chemical Property of 5-bromo-2-(4-fluoro-phenyl)-6-methanesulfonylamino-benzofuran-3-carboxylic acid ethyl ester

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Technology Process of 5-bromo-2-(4-fluoro-phenyl)-6-methanesulfonylamino-benzofuran-3-carboxylic acid ethyl ester

There total 5 articles about 5-bromo-2-(4-fluoro-phenyl)-6-methanesulfonylamino-benzofuran-3-carboxylic acid ethyl ester 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: 82.0%

: 1333340-15-0
ethyl 6-amino-5-bromo-2-(4-fluorophenyl)benzofuran-3-carboxylate

: 124-63-0
methanesulfonyl chloride

: 1333340-16-1
5-bromo-2-(4-fluoro-phenyl)-6-methanesulfonylamino-benzofuran-3-carboxylic acid ethyl ester

Guidance literature:: With pyridine; In dichloromethane; at 0 - 25 ℃;
DOI:10.1016/j.tetlet.2014.02.051

Reference yield:

: 1333340-13-8
ethyl 5-bromo-2-(4-fluorophenyl)benzofuran-3-carboxylate

: 1333340-16-1
5-bromo-2-(4-fluoro-phenyl)-6-methanesulfonylamino-benzofuran-3-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: nitric acid / chloroform / 0.5 h / -15 °C

2: iron; ammonium chloride / tetrahydrofuran; methanol; water / 3 h / Reflux

3: pyridine / dichloromethane / 0 - 25 °C

With pyridine; nitric acid; iron; ammonium chloride; In tetrahydrofuran; methanol; dichloromethane; chloroform; water;
DOI:10.1016/j.tetlet.2014.02.051

Reference yield:

: 403-42-9
1-(4-fluorophenyl)ethanone

: 1333340-16-1
5-bromo-2-(4-fluoro-phenyl)-6-methanesulfonylamino-benzofuran-3-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydride / tetrahydrofuran; mineral oil / 3 h / 70 °C

2: di-tert-butyl peroxide; iron(III) chloride hexahydrate / 1,2-dichloro-ethane / 6 h / Inert atmosphere; Reflux

3: nitric acid / chloroform / 0.5 h / -15 °C

4: iron; ammonium chloride / tetrahydrofuran; methanol; water / 3 h / Reflux

5: pyridine / dichloromethane / 0 - 25 °C

With pyridine; di-tert-butyl peroxide; iron(III) chloride hexahydrate; nitric acid; iron; sodium hydride; ammonium chloride; In tetrahydrofuran; methanol; dichloromethane; chloroform; water; 1,2-dichloro-ethane; mineral oil;
DOI:10.1016/j.tetlet.2014.02.051