(R)-3-{4-[2-(2-bromo-4-nitro-imidazol-1-yl)1-hydroxymethyl-ethyl]-3-fluoro-phenyl}-5-(tert-butyl-dimethyl-silanyloxymethyl)-oxazolidin-2-one

Base Information

Chemical Name:(R)-3-{4-[2-(2-bromo-4-nitro-imidazol-1-yl)1-hydroxymethyl-ethyl]-3-fluoro-phenyl}-5-(tert-butyl-dimethyl-silanyloxymethyl)-oxazolidin-2-one
CAS No.:1188337-60-1
Molecular Formula:C₂₂H₃₀BrFN₄O₆Si
Molecular Weight:573.491
Hs Code.:

Synonyms:(R)-3-{4-[2-(2-bromo-4-nitro-imidazol-1-yl)1-hydroxymethyl-ethyl]-3-fluoro-phenyl}-5-(tert-butyl-dimethyl-silanyloxymethyl)-oxazolidin-2-one

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Chemical Property of (R)-3-{4-[2-(2-bromo-4-nitro-imidazol-1-yl)1-hydroxymethyl-ethyl]-3-fluoro-phenyl}-5-(tert-butyl-dimethyl-silanyloxymethyl)-oxazolidin-2-one

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Technology Process of (R)-3-{4-[2-(2-bromo-4-nitro-imidazol-1-yl)1-hydroxymethyl-ethyl]-3-fluoro-phenyl}-5-(tert-butyl-dimethyl-silanyloxymethyl)-oxazolidin-2-one

There total 7 articles about (R)-3-{4-[2-(2-bromo-4-nitro-imidazol-1-yl)1-hydroxymethyl-ethyl]-3-fluoro-phenyl}-5-(tert-butyl-dimethyl-silanyloxymethyl)-oxazolidin-2-one 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:

: 1188337-59-8
3-(2-bromo-4-nitro-imidazol-1-yl)-2-{4-[(R)-5-(tert-butyl-dimethyl-silanyloxymethyl)-2-oxo-oxazolidin-3-yl]-2-fluoro-phenyl}-propionic acid ethyl ester

: 1188337-60-1
(R)-3-{4-[2-(2-bromo-4-nitro-imidazol-1-yl)1-hydroxymethyl-ethyl]-3-fluoro-phenyl}-5-(tert-butyl-dimethyl-silanyloxymethyl)-oxazolidin-2-one

Guidance literature:: With sodium tetrahydroborate; water; In tetrahydrofuran; methanol; at 20 ℃; for 0.666667h;

Reference yield:

: 627541-90-6
(R)-5-(tert-butyl-dimethyl-silanyloxymethyl)-3-[3-fluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-oxazolidin-2-one

: 1188337-60-1
(R)-3-{4-[2-(2-bromo-4-nitro-imidazol-1-yl)1-hydroxymethyl-ethyl]-3-fluoro-phenyl}-5-(tert-butyl-dimethyl-silanyloxymethyl)-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / water; N,N-dimethyl-formamide / 2 h / 60 °C / Inert atmosphere

2.1: triethylamine / 1,4-dioxane / 1 h / 20 °C

2.2: 19 h / 80 °C

3.1: sodium tetrahydroborate; water / tetrahydrofuran; methanol / 0.67 h / 20 °C

With sodium tetrahydroborate; water; potassium carbonate; triethylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; methanol; water; N,N-dimethyl-formamide;

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 1188337-60-1
(R)-3-{4-[2-(2-bromo-4-nitro-imidazol-1-yl)1-hydroxymethyl-ethyl]-3-fluoro-phenyl}-5-(tert-butyl-dimethyl-silanyloxymethyl)-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: 1H-imidazole / tetrahydrofuran

2.1: potassium acetate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / dimethyl sulfoxide / 2.5 h / 80 °C / Inert atmosphere

3.1: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / water; N,N-dimethyl-formamide / 2 h / 60 °C / Inert atmosphere

4.1: triethylamine / 1,4-dioxane / 1 h / 20 °C

4.2: 19 h / 80 °C

5.1: sodium tetrahydroborate; water / tetrahydrofuran; methanol / 0.67 h / 20 °C

With 1H-imidazole; sodium tetrahydroborate; water; potassium acetate; potassium carbonate; triethylamine; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; methanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide;