N-((4-bromophenyl)(2-(thiophen-2-yl)-1H-indol-3-yl)methyl)toluenesulfonamide

Base Information

Chemical Name:N-((4-bromophenyl)(2-(thiophen-2-yl)-1H-indol-3-yl)methyl)toluenesulfonamide
CAS No.:1426243-76-6
Molecular Formula:C₂₆H₂₁BrN₂O₂S₂
Molecular Weight:537.501
Hs Code.:

Synonyms:N-((4-bromophenyl)(2-(thiophen-2-yl)-1H-indol-3-yl)methyl)toluenesulfonamide

Suppliers and Price of N-((4-bromophenyl)(2-(thiophen-2-yl)-1H-indol-3-yl)methyl)toluenesulfonamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-((4-bromophenyl)(2-(thiophen-2-yl)-1H-indol-3-yl)methyl)toluenesulfonamide

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Technology Process of N-((4-bromophenyl)(2-(thiophen-2-yl)-1H-indol-3-yl)methyl)toluenesulfonamide

There total 6 articles about N-((4-bromophenyl)(2-(thiophen-2-yl)-1H-indol-3-yl)methyl)toluenesulfonamide 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: 93.0%

: 55968-16-6
2-(2-thienyl)indole

: 36176-90-6
N-(4-bromobenzylidene)-4-methylbenzenesulfonamide

: 1426243-76-6
N-((4-bromophenyl)(2-(thiophen-2-yl)-1H-indol-3-yl)methyl)toluenesulfonamide

Guidance literature:: With [Ir(COD)(SnCl3)Cl(μ-Cl)]2; In 1,2-dichloro-ethane; at 20 ℃; for 0.5h; Inert atmosphere; Schlenk technique;
DOI:10.1016/j.tet.2013.01.074

Reference yield:

: 70-55-3
toluene-4-sulfonamide

: 1426243-76-6
N-((4-bromophenyl)(2-(thiophen-2-yl)-1H-indol-3-yl)methyl)toluenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: amberlite H⁺ resin IR-120 / toluene / 12 h / 120 °C / Dean-Stark; Molecular sieve

2: [Ir(COD)(SnCl3)Cl(μ-Cl)]2 / 1,2-dichloro-ethane / 0.5 h / 20 °C / Inert atmosphere; Schlenk technique

With [Ir(COD)(SnCl3)Cl(μ-Cl)]2; In 1,2-dichloro-ethane; toluene;
DOI:10.1016/j.tet.2013.01.074

Reference yield:

: 100-63-0
phenylhydrazine

: 1426243-76-6
N-((4-bromophenyl)(2-(thiophen-2-yl)-1H-indol-3-yl)methyl)toluenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / 5 h / Reflux

2: polyphosphoric acid / 0.42 h / 100 - 120 °C

3: [Ir(COD)(SnCl3)Cl(μ-Cl)]2 / 1,2-dichloro-ethane / 0.5 h / 20 °C / Inert atmosphere; Schlenk technique

With [Ir(COD)(SnCl3)Cl(μ-Cl)]2; In ethanol; 1,2-dichloro-ethane;
DOI:10.1016/j.tet.2013.01.074