(S)-N-(3-(2-ethyl-4-(5-(3-((ethyl(methyl)amino)methyl)-5-methylphenyl)-1,2,4-oxadiazol-3-yl)-6-methylphenoxy)-2-hydroxypropyl)-2-hydroxyacetamide

Base Information

Chemical Name:(S)-N-(3-(2-ethyl-4-(5-(3-((ethyl(methyl)amino)methyl)-5-methylphenyl)-1,2,4-oxadiazol-3-yl)-6-methylphenoxy)-2-hydroxypropyl)-2-hydroxyacetamide
CAS No.:1187028-77-8
Molecular Formula:C₂₇H₃₆N₄O₅
Molecular Weight:496.607
Hs Code.:

Synonyms:(S)-N-(3-(2-ethyl-4-(5-(3-((ethyl(methyl)amino)methyl)-5-methylphenyl)-1,2,4-oxadiazol-3-yl)-6-methylphenoxy)-2-hydroxypropyl)-2-hydroxyacetamide

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Chemical Property of (S)-N-(3-(2-ethyl-4-(5-(3-((ethyl(methyl)amino)methyl)-5-methylphenyl)-1,2,4-oxadiazol-3-yl)-6-methylphenoxy)-2-hydroxypropyl)-2-hydroxyacetamide

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Technology Process of (S)-N-(3-(2-ethyl-4-(5-(3-((ethyl(methyl)amino)methyl)-5-methylphenyl)-1,2,4-oxadiazol-3-yl)-6-methylphenoxy)-2-hydroxypropyl)-2-hydroxyacetamide

There total 7 articles about (S)-N-(3-(2-ethyl-4-(5-(3-((ethyl(methyl)amino)methyl)-5-methylphenyl)-1,2,4-oxadiazol-3-yl)-6-methylphenoxy)-2-hydroxypropyl)-2-hydroxyacetamide 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:

: 624-78-2
N-Ethylmethylamine

: 1187028-55-2
(S)-N-(3-(2-ethyl-4-(5-(3-formyl-5-methylphenyl)-1,2,4-oxadiazol-3-yl)-6-methylphenoxy)-2-hydroxypropyl)-2-hydroxyacetamide

: 1187028-77-8
(S)-N-(3-(2-ethyl-4-(5-(3-((ethyl(methyl)amino)methyl)-5-methylphenyl)-1,2,4-oxadiazol-3-yl)-6-methylphenoxy)-2-hydroxypropyl)-2-hydroxyacetamide

Guidance literature:: With sodium tris(acetoxy)borohydride; acetic acid; In 1-methyl-pyrrolidin-2-one; dichloromethane; at 0 - 20 ℃; for 18h;
DOI:10.1016/j.ejmech.2016.03.048

Reference yield:

: 499-06-9
3,5-dimethylbenzoic acid

: 1187028-77-8
(S)-N-(3-(2-ethyl-4-(5-(3-((ethyl(methyl)amino)methyl)-5-methylphenyl)-1,2,4-oxadiazol-3-yl)-6-methylphenoxy)-2-hydroxypropyl)-2-hydroxyacetamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: 2,2'-azobis(isobutyronitrile); N-Bromosuccinimide / dichloromethane / 18 h / Reflux

2.1: copper nitrate hemi(pentahydrate) / acetonitrile; water / 2 h / Reflux

3.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.5 h / 20 °C

3.2: 18 h / 20 °C

4.1: 1,4-dioxane / 2 h / 100 °C

5.1: sodium tris(acetoxy)borohydride; acetic acid / dichloromethane; 1-methyl-pyrrolidin-2-one / 18 h / 0 - 20 °C

With N-Bromosuccinimide; copper nitrate hemi(pentahydrate); 2,2'-azobis(isobutyronitrile); sodium tris(acetoxy)borohydride; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/j.ejmech.2016.03.048

Reference yield:

: 550367-75-4
3-bromomethyl-5-methylbenzoic acid

: 1187028-77-8
(S)-N-(3-(2-ethyl-4-(5-(3-((ethyl(methyl)amino)methyl)-5-methylphenyl)-1,2,4-oxadiazol-3-yl)-6-methylphenoxy)-2-hydroxypropyl)-2-hydroxyacetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: copper nitrate hemi(pentahydrate) / acetonitrile; water / 2 h / Reflux

2.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.5 h / 20 °C

2.2: 18 h / 20 °C

3.1: 1,4-dioxane / 2 h / 100 °C

4.1: sodium tris(acetoxy)borohydride; acetic acid / dichloromethane; 1-methyl-pyrrolidin-2-one / 18 h / 0 - 20 °C

With copper nitrate hemi(pentahydrate); sodium tris(acetoxy)borohydride; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/j.ejmech.2016.03.048