{benzyl[(1S,2S)-2-(5-methoxy-1H-indol-3-yl)-1-methyl-2-phenylethyl]amino}acetonitrile

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Chemical Name:{benzyl[(1S,2S)-2-(5-methoxy-1H-indol-3-yl)-1-methyl-2-phenylethyl]amino}acetonitrile
CAS No.:1613740-54-7
Molecular Formula:C₂₇H₂₇N₃O
Molecular Weight:409.531
Hs Code.:

Synonyms:{benzyl[(1S,2S)-2-(5-methoxy-1H-indol-3-yl)-1-methyl-2-phenylethyl]amino}acetonitrile

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Chemical Property of {benzyl[(1S,2S)-2-(5-methoxy-1H-indol-3-yl)-1-methyl-2-phenylethyl]amino}acetonitrile

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Technology Process of {benzyl[(1S,2S)-2-(5-methoxy-1H-indol-3-yl)-1-methyl-2-phenylethyl]amino}acetonitrile

There total 2 articles about {benzyl[(1S,2S)-2-(5-methoxy-1H-indol-3-yl)-1-methyl-2-phenylethyl]amino}acetonitrile 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: 51.0%

: 1006-94-6
5-methoxylindole

: 613688-63-4
[benzyl[(1S,2R)-2-chloro-1-methyl-2-phenylethyl]amino]acetonitrile

: 1613740-54-7
{benzyl[(1S,2S)-2-(5-methoxy-1H-indol-3-yl)-1-methyl-2-phenylethyl]amino}acetonitrile

Guidance literature:: [benzyl[(1S,2R)-2-chloro-1-methyl-2-phenylethyl]amino]acetonitrile; With silver tetrafluoroborate; In acetonitrile; at 20 ℃; for 0.5h; Inert atmosphere;

5-methoxylindole; In acetonitrile; at 20 ℃; for 2.5h; Inert atmosphere;
DOI:10.1016/j.tet.2014.05.009

Reference yield:

: 1006-94-6
5-methoxylindole

: 613688-63-4
[benzyl[(1S,2R)-2-chloro-1-methyl-2-phenylethyl]amino]acetonitrile

: 1613740-54-7
{benzyl[(1S,2S)-2-(5-methoxy-1H-indol-3-yl)-1-methyl-2-phenylethyl]amino}acetonitrile

: 1613740-55-8
{benzyl[(1S,2R)-2-(5-methoxy-1H-indol-3-yl)-1-methyl-2-phenylethyl]amino}acetonitrile

Guidance literature:: [benzyl[(1S,2R)-2-chloro-1-methyl-2-phenylethyl]amino]acetonitrile; With silver tetrafluoroborate; In dichloromethane; at 20 ℃; for 0.5h; Inert atmosphere;

5-methoxylindole; In dichloromethane; at 20 ℃; for 2.5h; Overall yield = 41 %; Overall yield = 102 mg; stereoselective reaction; Inert atmosphere;
DOI:10.1016/j.tet.2014.05.009