(2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid 1-cyclohexyloxycarbonyloxy-ethyl ester

Base Information

Chemical Name:(2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid 1-cyclohexyloxycarbonyloxy-ethyl ester
CAS No.:1394050-62-4
Molecular Formula:C₂₈H₃₇NO₆
Molecular Weight:483.605
Hs Code.:

Synonyms:(2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid 1-cyclohexyloxycarbonyloxy-ethyl ester

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Chemical Property of (2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid 1-cyclohexyloxycarbonyloxy-ethyl ester

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Technology Process of (2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid 1-cyclohexyloxycarbonyloxy-ethyl ester

There total 3 articles about (2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid 1-cyclohexyloxycarbonyloxy-ethyl ester 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:

: C₃₃H₄₅NO₈

: 1394050-62-4
(2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid 1-cyclohexyloxycarbonyloxy-ethyl ester

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; acetonitrile; for 0.5h; Inert atmosphere;

Reference yield:

: 1383026-42-3
[(S)-2-biphenyl-4-yl-1-(2,2-dimethyl-4,6-dioxo-[1,3]dioxan-5-ylmethyl)ethyl]carbamic acid t-butyl ester

: 1394050-62-4
(2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid 1-cyclohexyloxycarbonyloxy-ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl-formamide / 0 - 23 °C / Inert atmosphere

2: samarium diiodide / water; tetrahydrofuran / 0.25 h / Inert atmosphere

3: triethylamine / acetone / 24 h / Inert atmosphere; Reflux

4: hydrogenchloride / 1,4-dioxane; acetonitrile / 0.5 h / Inert atmosphere

With hydrogenchloride; samarium diiodide; potassium carbonate; triethylamine; In tetrahydrofuran; 1,4-dioxane; water; N,N-dimethyl-formamide; acetone; acetonitrile;

Reference yield:

: 1394050-22-6
[(R)-1-(biphenyl-4-yl)-methyl-2-(2,2,5-trimethyl-4,6-dioxo-[1,3]dioxan-5-yl)-ethyl]-carbamic acid t-butyl ester

: 1394050-62-4
(2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid 1-cyclohexyloxycarbonyloxy-ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: samarium diiodide / water; tetrahydrofuran / 0.25 h / Inert atmosphere

2: triethylamine / acetone / 24 h / Inert atmosphere; Reflux

3: hydrogenchloride / 1,4-dioxane; acetonitrile / 0.5 h / Inert atmosphere

With hydrogenchloride; samarium diiodide; triethylamine; In tetrahydrofuran; 1,4-dioxane; water; acetone; acetonitrile;