(1S,2R)-{[2-(5-Methyl-1H-indol-3-yl)-1-methyl-2-phenyl-ethyl]-methyl-amino}-acetonitrile

Base Information

Chemical Name:(1S,2R)-{[2-(5-Methyl-1H-indol-3-yl)-1-methyl-2-phenyl-ethyl]-methyl-amino}-acetonitrile
CAS No.:1613740-66-1
Molecular Formula:C₂₁H₂₃N₃
Molecular Weight:317.434
Hs Code.:

Synonyms:(1S,2R)-{[2-(5-Methyl-1H-indol-3-yl)-1-methyl-2-phenyl-ethyl]-methyl-amino}-acetonitrile

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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 (1S,2R)-{[2-(5-Methyl-1H-indol-3-yl)-1-methyl-2-phenyl-ethyl]-methyl-amino}-acetonitrile

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Technology Process of (1S,2R)-{[2-(5-Methyl-1H-indol-3-yl)-1-methyl-2-phenyl-ethyl]-methyl-amino}-acetonitrile

There total 1 articles about (1S,2R)-{[2-(5-Methyl-1H-indol-3-yl)-1-methyl-2-phenyl-ethyl]-methyl-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: 44.0%

: 614-96-0
5-methyl-1H-indole

: 452096-19-4
pseudoephedrine-derived chloride

: 1613740-66-1
(1S,2R)-{[2-(5-Methyl-1H-indol-3-yl)-1-methyl-2-phenyl-ethyl]-methyl-amino}-acetonitrile

Guidance literature:: pseudoephedrine-derived chloride; With silver tetrafluoroborate; In acetonitrile; at 20 ℃; for 0.5h; Inert atmosphere;

5-methyl-1H-indole; In acetonitrile; at 20 ℃; stereoselective reaction; Inert atmosphere;
DOI:10.1016/j.tet.2014.05.009