N-(2-(2-(3,4-dimethoxyphenyl)-1H-indol-3-yl)ethyl)-4-methylbenzenesulfonamide

Base Information

Chemical Name:N-(2-(2-(3,4-dimethoxyphenyl)-1H-indol-3-yl)ethyl)-4-methylbenzenesulfonamide
CAS No.:1616347-86-4
Molecular Formula:C₂₅H₂₆N₂O₄S
Molecular Weight:450.558
Hs Code.:

Synonyms:N-(2-(2-(3,4-dimethoxyphenyl)-1H-indol-3-yl)ethyl)-4-methylbenzenesulfonamide

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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-(2-(2-(3,4-dimethoxyphenyl)-1H-indol-3-yl)ethyl)-4-methylbenzenesulfonamide

Chemical Property:

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Technology Process of N-(2-(2-(3,4-dimethoxyphenyl)-1H-indol-3-yl)ethyl)-4-methylbenzenesulfonamide

There total 5 articles about N-(2-(2-(3,4-dimethoxyphenyl)-1H-indol-3-yl)ethyl)-4-methylbenzenesulfonamide 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:

: 95426-76-9
2-[2-(3,4-dimethoxyphenyl)-1H-indol-3-yl]-ethylamine

: 98-59-9
p-toluenesulfonyl chloride

: 1616347-86-4
N-(2-(2-(3,4-dimethoxyphenyl)-1H-indol-3-yl)ethyl)-4-methylbenzenesulfonamide

Guidance literature:: With triethylamine; In dichloromethane; at 23 ℃; for 18h;
DOI:10.1021/ol501409a

Reference yield:

: 61-54-1
tryptamine

: 1616347-86-4
N-(2-(2-(3,4-dimethoxyphenyl)-1H-indol-3-yl)ethyl)-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: toluene / 13 h / Reflux

2.1: pyridinium hydrobromide perbromide / chloroform; tetrahydrofuran / 1 h / -10 °C

3.1: sodium carbonate monohydrate; lithium chloride / ethanol; water; toluene / 0.5 h / Inert atmosphere

3.2: 6 h / Inert atmosphere; Reflux

4.1: hydrazine hydrate / dichloromethane; methanol / 16 h / Reflux

5.1: triethylamine / dichloromethane / 18 h / 23 °C

With pyridinium hydrobromide perbromide; sodium carbonate monohydrate; hydrazine hydrate; triethylamine; lithium chloride; In tetrahydrofuran; methanol; ethanol; dichloromethane; chloroform; water; toluene;
DOI:10.1021/ol501409a

Reference yield:

: 1616348-02-7
2-(2-(2-(3,4-dimethoxyphenyl)-1H-indol-3-yl)ethyl)isoindoline-1,3-dione

: 1616347-86-4
N-(2-(2-(3,4-dimethoxyphenyl)-1H-indol-3-yl)ethyl)-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: hydrazine hydrate / dichloromethane; methanol / 16 h / Reflux

2: triethylamine / dichloromethane / 18 h / 23 °C

With hydrazine hydrate; triethylamine; In methanol; dichloromethane;
DOI:10.1021/ol501409a