(S)-(tert-butyl) 3-(2-(1-phenylethylamino)ethyl)-1H-indole-1-carboxylate

Base Information

Chemical Name:(S)-(tert-butyl) 3-(2-(1-phenylethylamino)ethyl)-1H-indole-1-carboxylate
CAS No.:1431767-73-5
Molecular Formula:C₂₃H₂₈N₂O₂
Molecular Weight:364.488
Hs Code.:

Synonyms:(S)-(tert-butyl) 3-(2-(1-phenylethylamino)ethyl)-1H-indole-1-carboxylate

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Chemical Property of (S)-(tert-butyl) 3-(2-(1-phenylethylamino)ethyl)-1H-indole-1-carboxylate

Chemical Property:

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Technology Process of (S)-(tert-butyl) 3-(2-(1-phenylethylamino)ethyl)-1H-indole-1-carboxylate

There total 3 articles about (S)-(tert-butyl) 3-(2-(1-phenylethylamino)ethyl)-1H-indole-1-carboxylate 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: 94.0%

: 2627-86-3
(S)-1-phenyl-ethylamine

: 131829-28-2
3-(2-bromoethyl)indole-1-carboxylic acid tert-butyl ester

: 1431767-73-5
(S)-(tert-butyl) 3-(2-(1-phenylethylamino)ethyl)-1H-indole-1-carboxylate

Guidance literature:: With potassium carbonate; In acetonitrile; for 4h; Reflux;
DOI:10.1016/j.tetlet.2013.03.068

Reference yield:

: 3389-21-7
3-(2-bromoethyl)-1H-indole

: 1431767-73-5
(S)-(tert-butyl) 3-(2-(1-phenylethylamino)ethyl)-1H-indole-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: dmap; triethylamine / dichloromethane / 3 h / 20 °C

2: potassium carbonate / acetonitrile / 20 °C / Reflux

With dmap; potassium carbonate; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1055/s-0032-1316893

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1431767-73-5
(S)-(tert-butyl) 3-(2-(1-phenylethylamino)ethyl)-1H-indole-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: dmap; triethylamine / dichloromethane / 3 h / 20 °C

2: potassium carbonate / acetonitrile / 20 °C / Reflux

With dmap; potassium carbonate; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1055/s-0032-1316893