(2S)-5-(benzyloxy)-N-[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]-N,2-dimethylpentanamide

Base Information

Chemical Name:(2S)-5-(benzyloxy)-N-[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]-N,2-dimethylpentanamide
CAS No.:851955-70-9
Molecular Formula:C₂₃H₃₁NO₃
Molecular Weight:369.504
Hs Code.:

Synonyms:(2S)-5-(benzyloxy)-N-[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]-N,2-dimethylpentanamide

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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 (2S)-5-(benzyloxy)-N-[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]-N,2-dimethylpentanamide

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Technology Process of (2S)-5-(benzyloxy)-N-[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]-N,2-dimethylpentanamide

There total 3 articles about (2S)-5-(benzyloxy)-N-[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]-N,2-dimethylpentanamide 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%

: 851955-69-6
5-(benzyloxy)-N-[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]-N-methylpentanamide

: 74-88-4
methyl iodide

: 851955-70-9
(2S)-5-(benzyloxy)-N-[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]-N,2-dimethylpentanamide

Guidance literature:: With n-butyllithium; diisopropylamine; lithium chloride; In tetrahydrofuran; hexane; at 0 ℃; for 0.75h;
DOI:10.1016/j.bioorg.2004.11.002

Reference yield:

: 64740-39-2
5-benzyloxypentanoic acid

: 851955-70-9
(2S)-5-(benzyloxy)-N-[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]-N,2-dimethylpentanamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: Et₃N; pivaloyl chloride / acetonitrile; tetrahydrofuran / 0.5 h / 0 °C

1.2: 87 percent / Et₃N / acetonitrile; tetrahydrofuran / 3 h / 0 - 20 °C

2.1: 94 percent / LiCl; iPr₂NH; BuLi / tetrahydrofuran; hexane / 0.75 h / 0 °C

With n-butyllithium; pivaloyl chloride; triethylamine; diisopropylamine; lithium chloride; In tetrahydrofuran; hexane; acetonitrile;
DOI:10.1016/j.bioorg.2004.11.002

Reference yield:

: 90-82-4,7009-81-6,90-83-5,6912-63-6
pseudoephedrine

: 851955-70-9
(2S)-5-(benzyloxy)-N-[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]-N,2-dimethylpentanamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: Et₃N; pivaloyl chloride / acetonitrile; tetrahydrofuran / 0.5 h / 0 °C

1.2: 87 percent / Et₃N / acetonitrile; tetrahydrofuran / 3 h / 0 - 20 °C

2.1: 94 percent / LiCl; iPr₂NH; BuLi / tetrahydrofuran; hexane / 0.75 h / 0 °C

With n-butyllithium; pivaloyl chloride; triethylamine; diisopropylamine; lithium chloride; In tetrahydrofuran; hexane; acetonitrile;
DOI:10.1016/j.bioorg.2004.11.002