4-[[1-[[3-(1-methylethyl)phenyl]sulfonyl]-5-(trifluoromethyl)-1H-indol-2-yl]methyl]benzoic acid, methyl ester

Base Information

Chemical Name:4-[[1-[[3-(1-methylethyl)phenyl]sulfonyl]-5-(trifluoromethyl)-1H-indol-2-yl]methyl]benzoic acid, methyl ester
CAS No.:1272718-40-7
Molecular Formula:C₂₇H₂₄F₃NO₄S
Molecular Weight:515.553
Hs Code.:

Synonyms:4-[[1-[[3-(1-methylethyl)phenyl]sulfonyl]-5-(trifluoromethyl)-1H-indol-2-yl]methyl]benzoic acid, methyl ester

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Chemical Property of 4-[[1-[[3-(1-methylethyl)phenyl]sulfonyl]-5-(trifluoromethyl)-1H-indol-2-yl]methyl]benzoic acid, methyl ester

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Technology Process of 4-[[1-[[3-(1-methylethyl)phenyl]sulfonyl]-5-(trifluoromethyl)-1H-indol-2-yl]methyl]benzoic acid, methyl ester

There total 4 articles about 4-[[1-[[3-(1-methylethyl)phenyl]sulfonyl]-5-(trifluoromethyl)-1H-indol-2-yl]methyl]benzoic acid, methyl 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: 78.0%

: 1272718-39-4
4-[(RS)-hydroxy[1-[[3-(1-methylethyl)phenyl]sulfonyl]-5-(trifluoro-methyl)-1H-indol-2-yl]methyl]benzoic acid, methyl ester

: 1272718-40-7
4-[[1-[[3-(1-methylethyl)phenyl]sulfonyl]-5-(trifluoromethyl)-1H-indol-2-yl]methyl]benzoic acid, methyl ester

Guidance literature:: 4-[(RS)-hydroxy[1-[[3-(1-methylethyl)phenyl]sulfonyl]-5-(trifluoro-methyl)-1H-indol-2-yl]methyl]benzoic acid, methyl ester; With triethylsilane; boron trifluoride diethyl etherate; trifluoroacetic acid; In dichloromethane; at 20 ℃; for 1h;

With water; In dichloromethane; Cooling with ice;

Reference yield:

: 163444-17-5
2-iodo-4-(trifluoromethyl)aniline

: 1272718-40-7
4-[[1-[[3-(1-methylethyl)phenyl]sulfonyl]-5-(trifluoromethyl)-1H-indol-2-yl]methyl]benzoic acid, methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: pyridine / 21 h / 20 °C

1.2: 77 h / 20 °C / Reflux

1.3: Cooling with ice

2.1: diethylamine / copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 0.5 h / Reflux

3.1: trifluoroacetic acid; boron trifluoride diethyl etherate; triethylsilane / dichloromethane / 1 h / 20 °C

3.2: Cooling with ice

With pyridine; triethylsilane; boron trifluoride diethyl etherate; diethylamine; trifluoroacetic acid; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In dichloromethane; N,N-dimethyl-formamide; 2.1: Sonogashira Coupling;

Reference yield:

: 71530-58-0
m-cumenesulfonyl chloride

: 1272718-40-7
4-[[1-[[3-(1-methylethyl)phenyl]sulfonyl]-5-(trifluoromethyl)-1H-indol-2-yl]methyl]benzoic acid, methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: pyridine / 21 h / 20 °C

1.2: 77 h / 20 °C / Reflux

1.3: Cooling with ice

2.1: diethylamine / copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 0.5 h / Reflux

3.1: trifluoroacetic acid; boron trifluoride diethyl etherate; triethylsilane / dichloromethane / 1 h / 20 °C

3.2: Cooling with ice

With pyridine; triethylsilane; boron trifluoride diethyl etherate; diethylamine; trifluoroacetic acid; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In dichloromethane; N,N-dimethyl-formamide; 2.1: Sonogashira Coupling;