(R)-1-(5-(2-(1H-indol-3-yl)ethyl)-4-(2,4-dimethoxybenzyl)-4H-1,2,4-triazol-3-yl)-2-(1H-indol-3-yl)ethanamine

Base Information

Chemical Name:(R)-1-(5-(2-(1H-indol-3-yl)ethyl)-4-(2,4-dimethoxybenzyl)-4H-1,2,4-triazol-3-yl)-2-(1H-indol-3-yl)ethanamine
CAS No.:925239-13-0
Molecular Formula:C₃₁H₃₂N₆O₂
Molecular Weight:520.634
Hs Code.:

Synonyms:(R)-1-(5-(2-(1H-indol-3-yl)ethyl)-4-(2,4-dimethoxybenzyl)-4H-1,2,4-triazol-3-yl)-2-(1H-indol-3-yl)ethanamine

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Chemical Property of (R)-1-(5-(2-(1H-indol-3-yl)ethyl)-4-(2,4-dimethoxybenzyl)-4H-1,2,4-triazol-3-yl)-2-(1H-indol-3-yl)ethanamine

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Technology Process of (R)-1-(5-(2-(1H-indol-3-yl)ethyl)-4-(2,4-dimethoxybenzyl)-4H-1,2,4-triazol-3-yl)-2-(1H-indol-3-yl)ethanamine

There total 9 articles about (R)-1-(5-(2-(1H-indol-3-yl)ethyl)-4-(2,4-dimethoxybenzyl)-4H-1,2,4-triazol-3-yl)-2-(1H-indol-3-yl)ethanamine 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:

: 937247-23-9
tert-butyl (R)-1-(5-(2-(1H-indol-3-yl)ethyl)-4-(2,4-dimethoxybenzyl)-4H-1,2,4-triazol-3-yl)-2-(1H-indol-3-yl)ethylcarbamate

: 925239-13-0
(R)-1-(5-(2-(1H-indol-3-yl)ethyl)-4-(2,4-dimethoxybenzyl)-4H-1,2,4-triazol-3-yl)-2-(1H-indol-3-yl)ethanamine

Guidance literature:: With hydrogenchloride; In ethyl acetate;
DOI:10.1016/j.bmcl.2007.10.113

Reference yield:

: 937247-19-3
(R)-tert-butyl 1-(2,4-dimethoxybenzylamino)-3-(1H-indol-3-yl)-1-thioxopropan-2-ylcarbamate

: 925239-13-0
(R)-1-(5-(2-(1H-indol-3-yl)ethyl)-4-(2,4-dimethoxybenzyl)-4H-1,2,4-triazol-3-yl)-2-(1H-indol-3-yl)ethanamine

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / mercury(II) acetate / tetrahydrofuran / 48 h / 20 °C

2: HCl / ethyl acetate / 1 h / 20 °C

With hydrogenchloride; mercury(II) diacetate; In tetrahydrofuran; ethyl acetate;
DOI:10.1021/jm070024h

Reference yield:

: 956489-57-9
(R)-tert-butyl 1-(2,4-dimethoxybenzylamino)-3-(1H-indol-3-yl)-1-oxopropan-2-ylcarbamate

: 925239-13-0
(R)-1-(5-(2-(1H-indol-3-yl)ethyl)-4-(2,4-dimethoxybenzyl)-4H-1,2,4-triazol-3-yl)-2-(1H-indol-3-yl)ethanamine

Guidance literature:: Multi-step reaction with 3 steps

1: Lawesson's reagent / 1,2-dimethoxy-ethane / 2 h / 85 °C

2: 65 percent / mercury(II) acetate / tetrahydrofuran / 48 h / 20 °C

3: HCl / ethyl acetate / 1 h / 20 °C

With Lawessons reagent; hydrogenchloride; mercury(II) diacetate; In tetrahydrofuran; 1,2-dimethoxyethane; ethyl acetate;
DOI:10.1021/jm070024h