6-fluoro-2-[(4-methoxybenzyl)amino]-1-benzothiophene-3-carboxylic acid

Base Information

Chemical Name:6-fluoro-2-[(4-methoxybenzyl)amino]-1-benzothiophene-3-carboxylic acid
CAS No.:1209007-74-8
Molecular Formula:C₁₇H₁₄FNO₃S
Molecular Weight:331.367
Hs Code.:

Synonyms:6-fluoro-2-[(4-methoxybenzyl)amino]-1-benzothiophene-3-carboxylic acid

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Chemical Property of 6-fluoro-2-[(4-methoxybenzyl)amino]-1-benzothiophene-3-carboxylic acid

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Technology Process of 6-fluoro-2-[(4-methoxybenzyl)amino]-1-benzothiophene-3-carboxylic acid

There total 5 articles about 6-fluoro-2-[(4-methoxybenzyl)amino]-1-benzothiophene-3-carboxylic acid 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:

: 1209007-73-7
C₁₉H₁₈FNO₃S

: 1209007-74-8
6-fluoro-2-[(4-methoxybenzyl)amino]-1-benzothiophene-3-carboxylic acid

Guidance literature:: C₁₉H₁₈FNO₃S; With sodium hydroxide; In tetrahydrofuran; ethanol; water; for 3h; Reflux;

With hydrogenchloride; In water;
DOI:10.1016/j.bmc.2011.01.041

Reference yield:

: 1209007-72-6
ethyl 2-(4-fluoro-2-nitrophenyl)acetate

: 1209007-74-8
6-fluoro-2-[(4-methoxybenzyl)amino]-1-benzothiophene-3-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydride / dimethyl sulfoxide; mineral oil / 2 h / 20 - 120 °C

2: sodium hydroxide / tetrahydrofuran; ethanol; water / 3 h / Reflux

With sodium hydride; sodium hydroxide; In tetrahydrofuran; ethanol; water; dimethyl sulfoxide; mineral oil;
DOI:10.1016/j.bmc.2011.01.041

Reference yield:

: 3694-57-3
1-(isothiocyanatomethyl)-4-methoxybenzene

: 1209007-74-8
6-fluoro-2-[(4-methoxybenzyl)amino]-1-benzothiophene-3-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydride / dimethyl sulfoxide; mineral oil / 2 h / 20 - 120 °C

2: sodium hydroxide / tetrahydrofuran; ethanol; water / 3 h / Reflux

With sodium hydride; sodium hydroxide; In tetrahydrofuran; ethanol; water; dimethyl sulfoxide; mineral oil;
DOI:10.1016/j.bmc.2011.01.041