[2S,4S,1'S,2'S]-(+)-N,2-dimethyl-4-phenyl-N-(2'-phenyl-2'-hydroxy-1'-methylethyl)-4-(p-toluenesulfonylamino)butamide

Base Information

Chemical Name:[2S,4S,1'S,2'S]-(+)-N,2-dimethyl-4-phenyl-N-(2'-phenyl-2'-hydroxy-1'-methylethyl)-4-(p-toluenesulfonylamino)butamide
CAS No.:362495-81-6
Molecular Formula:C₂₈H₃₄N₂O₄S
Molecular Weight:494.655
Hs Code.:

Synonyms:[2S,4S,1'S,2'S]-(+)-N,2-dimethyl-4-phenyl-N-(2'-phenyl-2'-hydroxy-1'-methylethyl)-4-(p-toluenesulfonylamino)butamide

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Chemical Property of [2S,4S,1'S,2'S]-(+)-N,2-dimethyl-4-phenyl-N-(2'-phenyl-2'-hydroxy-1'-methylethyl)-4-(p-toluenesulfonylamino)butamide

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Technology Process of [2S,4S,1'S,2'S]-(+)-N,2-dimethyl-4-phenyl-N-(2'-phenyl-2'-hydroxy-1'-methylethyl)-4-(p-toluenesulfonylamino)butamide

There total 1 articles about [2S,4S,1'S,2'S]-(+)-N,2-dimethyl-4-phenyl-N-(2'-phenyl-2'-hydroxy-1'-methylethyl)-4-(p-toluenesulfonylamino)butamide 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: 67.0%

: 24395-14-0,149769-84-6,151003-26-8,62596-62-7
(R)-2-phenyl-N-tosylaziridine

: 159213-03-3
N-[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]-N-methylpropionamide

: 362495-81-6
[2S,4S,1'S,2'S]-(+)-N,2-dimethyl-4-phenyl-N-(2'-phenyl-2'-hydroxy-1'-methylethyl)-4-(p-toluenesulfonylamino)butamide

: (2R,4S)-N-((1S,2S)-2-Hydroxy-1-methyl-2-phenyl-ethyl)-2,N-dimethyl-4-phenyl-4-(toluene-4-sulfonylamino)-butyramide

Guidance literature:: With lithium chloride; lithium diisopropyl amide; In tetrahydrofuran;
DOI:10.1021/jo0103571

Reference yield: 82.0%

: 362495-81-6
[2S,4S,1'S,2'S]-(+)-N,2-dimethyl-4-phenyl-N-(2'-phenyl-2'-hydroxy-1'-methylethyl)-4-(p-toluenesulfonylamino)butamide

: 362495-91-8
[2S,4S]-(+)-2-methyl-4-phenyl-4-(p-toluenesulfonylamino)butanoic acid

Guidance literature:: With sulfuric acid; In 1,4-dioxane; Heating;
DOI:10.1021/jo0103571

Reference yield:

: 362495-81-6
[2S,4S,1'S,2'S]-(+)-N,2-dimethyl-4-phenyl-N-(2'-phenyl-2'-hydroxy-1'-methylethyl)-4-(p-toluenesulfonylamino)butamide

: [3S,5S]-(+)-3-methyl-5-phenyl-1-(p-toluenesulfonyl)pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 82 percent / aq. H₂SO₄ / dioxane / Heating

2: 92 percent / conc. HCl / Heating

3: 71 percent / (Me₃Si)2NLi / tetrahydrofuran / -20 °C

With hydrogenchloride; sulfuric acid; lithium hexamethyldisilazane; In tetrahydrofuran; 1,4-dioxane;
DOI:10.1021/jo0103571