((4R,5R)-3-(3-fluoro-4-morpholinophenyl)-4-(4-methoxyphenyl)-2-oxooxazolidin-5-yl)methyl benzoate

Base Information

Chemical Name:((4R,5R)-3-(3-fluoro-4-morpholinophenyl)-4-(4-methoxyphenyl)-2-oxooxazolidin-5-yl)methyl benzoate
CAS No.:1613057-73-0
Molecular Formula:C₂₈H₂₇FN₂O₆
Molecular Weight:506.531
Hs Code.:

Synonyms:((4R,5R)-3-(3-fluoro-4-morpholinophenyl)-4-(4-methoxyphenyl)-2-oxooxazolidin-5-yl)methyl benzoate

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Chemical Property of ((4R,5R)-3-(3-fluoro-4-morpholinophenyl)-4-(4-methoxyphenyl)-2-oxooxazolidin-5-yl)methyl benzoate

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Technology Process of ((4R,5R)-3-(3-fluoro-4-morpholinophenyl)-4-(4-methoxyphenyl)-2-oxooxazolidin-5-yl)methyl benzoate

There total 6 articles about ((4R,5R)-3-(3-fluoro-4-morpholinophenyl)-4-(4-methoxyphenyl)-2-oxooxazolidin-5-yl)methyl benzoate 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: 90.0%

: 1613057-71-8
(4R,5R)-3-(3-fluoro-4-morpholinophenyl)-5-(hydroxymethyl)-4-(4-methoxyphenyl)oxazolidin-2-one

: 93-97-0
benzoic acid anhydride

: 1613057-73-0
((4R,5R)-3-(3-fluoro-4-morpholinophenyl)-4-(4-methoxyphenyl)-2-oxooxazolidin-5-yl)methyl benzoate

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 0 - 20 ℃; for 1h;
DOI:10.1016/j.ejmech.2014.04.062

Reference yield:

: 1250999-09-7
4-(2-fluoro-4-iodophenyl)morpholine

: 1613057-73-0
((4R,5R)-3-(3-fluoro-4-morpholinophenyl)-4-(4-methoxyphenyl)-2-oxooxazolidin-5-yl)methyl benzoate

Guidance literature:: Multi-step reaction with 3 steps

1: copper(l) iodide; caesium carbonate; N,N`-dimethylethylenediamine / 1,4-dioxane / 3 h / 110 °C / Inert atmosphere

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

3: dmap; triethylamine / dichloromethane / 1 h / 0 - 20 °C

With dmap; copper(l) iodide; tetrabutyl ammonium fluoride; caesium carbonate; triethylamine; N,N`-dimethylethylenediamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane;
DOI:10.1016/j.ejmech.2014.04.062

Reference yield:

: 254761-52-9
(4R,5R)-5-(((tert-butyldimethylsilyl)oxy)methyl)-4-(4-methoxyphenyl)oxazolidin-2-one

: 1613057-73-0
((4R,5R)-3-(3-fluoro-4-morpholinophenyl)-4-(4-methoxyphenyl)-2-oxooxazolidin-5-yl)methyl benzoate

Guidance literature:: Multi-step reaction with 3 steps

1: copper(l) iodide; caesium carbonate; N,N`-dimethylethylenediamine / 1,4-dioxane / 3 h / 110 °C / Inert atmosphere

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

3: dmap; triethylamine / dichloromethane / 1 h / 0 - 20 °C

With dmap; copper(l) iodide; tetrabutyl ammonium fluoride; caesium carbonate; triethylamine; N,N`-dimethylethylenediamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane;
DOI:10.1016/j.ejmech.2014.04.062