methyl 4-[2-(5-chloro-1-(3,4-dichlorobenzyl)-2-{2-[(methylsulfonyl)oxy]ethyl}-1H-indol-3-yl)ethoxy]benzoate

Base Information

Chemical Name:methyl 4-[2-(5-chloro-1-(3,4-dichlorobenzyl)-2-{2-[(methylsulfonyl)oxy]ethyl}-1H-indol-3-yl)ethoxy]benzoate
CAS No.:934286-08-5
Molecular Formula:C₂₈H₂₆Cl₃NO₆S
Molecular Weight:610.943
Hs Code.:

Synonyms:methyl 4-[2-(5-chloro-1-(3,4-dichlorobenzyl)-2-{2-[(methylsulfonyl)oxy]ethyl}-1H-indol-3-yl)ethoxy]benzoate

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Chemical Property of methyl 4-[2-(5-chloro-1-(3,4-dichlorobenzyl)-2-{2-[(methylsulfonyl)oxy]ethyl}-1H-indol-3-yl)ethoxy]benzoate

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Technology Process of methyl 4-[2-(5-chloro-1-(3,4-dichlorobenzyl)-2-{2-[(methylsulfonyl)oxy]ethyl}-1H-indol-3-yl)ethoxy]benzoate

There total 9 articles about methyl 4-[2-(5-chloro-1-(3,4-dichlorobenzyl)-2-{2-[(methylsulfonyl)oxy]ethyl}-1H-indol-3-yl)ethoxy]benzoate 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:

: 124064-21-7
4-(2-oxo-ethoxy)-benzoic acid methyl ester

: 934286-08-5
methyl 4-[2-(5-chloro-1-(3,4-dichlorobenzyl)-2-{2-[(methylsulfonyl)oxy]ethyl}-1H-indol-3-yl)ethoxy]benzoate

Guidance literature:: Multi-step reaction with 3 steps

1: 0.216 g / Et₃SiH; TFA / CH₂Cl₂

2: 0.129 g / TBAF / tetrahydrofuran

3: 0.149 g / Et₃N / tetrahydrofuran / 72 h

With triethylsilane; tetrabutyl ammonium fluoride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm061131z

Reference yield:

: 1025988-82-2
C₁₇H₁₄Cl₃NO

: 934286-08-5
methyl 4-[2-(5-chloro-1-(3,4-dichlorobenzyl)-2-{2-[(methylsulfonyl)oxy]ethyl}-1H-indol-3-yl)ethoxy]benzoate

Guidance literature:: Multi-step reaction with 4 steps

1: 0.420 g / imidazole / dimethylformamide

2: 0.216 g / Et₃SiH; TFA / CH₂Cl₂

3: 0.129 g / TBAF / tetrahydrofuran

4: 0.149 g / Et₃N / tetrahydrofuran / 72 h

With 1H-imidazole; triethylsilane; tetrabutyl ammonium fluoride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm061131z

Reference yield:

: 934286-04-1
4-{5-chloro-2-[(3,4-dichlorobenzyl)amino]phenyl}but-3-yn-1-ol

: 934286-08-5
methyl 4-[2-(5-chloro-1-(3,4-dichlorobenzyl)-2-{2-[(methylsulfonyl)oxy]ethyl}-1H-indol-3-yl)ethoxy]benzoate

Guidance literature:: Multi-step reaction with 5 steps

1: CuI / dimethylformamide / 4 h / Heating

2: 0.420 g / imidazole / dimethylformamide

3: 0.216 g / Et₃SiH; TFA / CH₂Cl₂

4: 0.129 g / TBAF / tetrahydrofuran

5: 0.149 g / Et₃N / tetrahydrofuran / 72 h

With 1H-imidazole; triethylsilane; copper(l) iodide; tetrabutyl ammonium fluoride; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm061131z