[6-fluoro-4-(4-isopropylsulfamoyl-phenyl)-3-methyl-naphthalen-2-yl]-acetic acid

Base Information

Chemical Name:[6-fluoro-4-(4-isopropylsulfamoyl-phenyl)-3-methyl-naphthalen-2-yl]-acetic acid
CAS No.:1451094-39-5
Molecular Formula:C₂₂H₂₂FNO₄S
Molecular Weight:415.485
Hs Code.:

Synonyms:[6-fluoro-4-(4-isopropylsulfamoyl-phenyl)-3-methyl-naphthalen-2-yl]-acetic acid

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Chemical Property of [6-fluoro-4-(4-isopropylsulfamoyl-phenyl)-3-methyl-naphthalen-2-yl]-acetic acid

Chemical Property:

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Technology Process of [6-fluoro-4-(4-isopropylsulfamoyl-phenyl)-3-methyl-naphthalen-2-yl]-acetic acid

There total 8 articles about [6-fluoro-4-(4-isopropylsulfamoyl-phenyl)-3-methyl-naphthalen-2-yl]-acetic 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: 83.0%

: 1451094-40-8
[6-fluoro-4-(4-isopropylsulfamoyl-phenyl)-3-methyl-naphthalen-2-yl]-acetic acid methyl ester

: 1451094-39-5
[6-fluoro-4-(4-isopropylsulfamoyl-phenyl)-3-methyl-naphthalen-2-yl]-acetic acid

Guidance literature:: [6-fluoro-4-(4-isopropylsulfamoyl-phenyl)-3-methyl-naphthalen-2-yl]-acetic acid methyl ester; With lithium hydroxide monohydrate; In tetrahydrofuran; water; at 20 ℃; for 16h;

With hydrogenchloride; In water; pH=Ca. 2;

Reference yield:

: 1227258-98-1
4-benzyloxy-6-fluoro-3-methyl-naphthalene-2-carboxylic acid methyl ester

: 1451094-39-5
[6-fluoro-4-(4-isopropylsulfamoyl-phenyl)-3-methyl-naphthalen-2-yl]-acetic acid

Guidance literature:: Multi-step reaction with 7 steps

1.1: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 0 - 20 °C / Inert atmosphere

2.1: triphenylphosphine; tetrachloromethane / tetrahydrofuran / 2 h / Reflux; Inert atmosphere

3.1: potassium carbonate; bis-triphenylphosphine-palladium(II) chloride / tetrahydrofuran / 20 °C / Inert atmosphere

4.1: palladium 10% on activated carbon; hydrogen / methanol

5.1: pyridine / dichloromethane / 3.17 h / 0 - 20 °C

6.1: palladium diacetate; sodium carbonate; triphenylphosphine / water; 1,2-dimethoxyethane / 2 h / Reflux; Inert atmosphere

7.1: lithium hydroxide monohydrate / water; tetrahydrofuran / 16 h / 20 °C

7.2: pH Ca_. 2

With pyridine; tetrachloromethane; bis-triphenylphosphine-palladium(II) chloride; lithium aluminium tetrahydride; lithium hydroxide monohydrate; palladium 10% on activated carbon; hydrogen; palladium diacetate; sodium carbonate; potassium carbonate; triphenylphosphine; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; dichloromethane; water;

Reference yield:

: 1227259-02-0
1-benzyloxy-3-chloromethyl-7-fluoro-2-methyl-naphthalene

: 1451094-39-5
[6-fluoro-4-(4-isopropylsulfamoyl-phenyl)-3-methyl-naphthalen-2-yl]-acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate; bis-triphenylphosphine-palladium(II) chloride / tetrahydrofuran / 20 °C / Inert atmosphere

2.1: palladium 10% on activated carbon; hydrogen / methanol

3.1: pyridine / dichloromethane / 3.17 h / 0 - 20 °C

4.1: palladium diacetate; sodium carbonate; triphenylphosphine / water; 1,2-dimethoxyethane / 2 h / Reflux; Inert atmosphere

5.1: lithium hydroxide monohydrate / water; tetrahydrofuran / 16 h / 20 °C

5.2: pH Ca_. 2

With pyridine; bis-triphenylphosphine-palladium(II) chloride; lithium hydroxide monohydrate; palladium 10% on activated carbon; hydrogen; palladium diacetate; sodium carbonate; potassium carbonate; triphenylphosphine; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; dichloromethane; water;