(R)-3-(3-fluoro-4-(2-(2-methyl-2H-tetrazol-5-yl) isoindolin-5-yl)phenyl)-5-(hydroxylmethyl)oxazolidin-2-one

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Chemical Name:(R)-3-(3-fluoro-4-(2-(2-methyl-2H-tetrazol-5-yl) isoindolin-5-yl)phenyl)-5-(hydroxylmethyl)oxazolidin-2-one
CAS No.:1428738-42-4
Molecular Formula:C₂₀H₁₉FN₆O₃
Molecular Weight:410.408
Hs Code.:

Synonyms:(R)-3-(3-fluoro-4-(2-(2-methyl-2H-tetrazol-5-yl) isoindolin-5-yl)phenyl)-5-(hydroxylmethyl)oxazolidin-2-one

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Chemical Property of (R)-3-(3-fluoro-4-(2-(2-methyl-2H-tetrazol-5-yl) isoindolin-5-yl)phenyl)-5-(hydroxylmethyl)oxazolidin-2-one

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Technology Process of (R)-3-(3-fluoro-4-(2-(2-methyl-2H-tetrazol-5-yl) isoindolin-5-yl)phenyl)-5-(hydroxylmethyl)oxazolidin-2-one

There total 7 articles about (R)-3-(3-fluoro-4-(2-(2-methyl-2H-tetrazol-5-yl) isoindolin-5-yl)phenyl)-5-(hydroxylmethyl)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: 31.0%

: 504438-22-6
(R)‐3‐(3‐fluoro‐4‐(4,4,5,5‐tetramethyl‐1,3,2‐dioxaborolan‐2‐yl)phenyl)‐5‐(hydroxymethyl)‐oxazolidin‐2‐one

: 1428738-33-3
5-bromo-2-(2-methyl-2H-tetrazol-5-yl)isoindoline

: 1428738-42-4
(R)-3-(3-fluoro-4-(2-(2-methyl-2H-tetrazol-5-yl) isoindolin-5-yl)phenyl)-5-(hydroxylmethyl)oxazolidin-2-one

Guidance literature:: With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; caesium carbonate; In 1,4-dioxane; water; at 100 ℃; for 3h;

Reference yield:

: 510729-01-8
(4-bromo-3-fluorophenyl)carbamic acid benzyl ester

: 1428738-42-4
(R)-3-(3-fluoro-4-(2-(2-methyl-2H-tetrazol-5-yl) isoindolin-5-yl)phenyl)-5-(hydroxylmethyl)oxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hexamethyldisilazane; ammonium chloride / tetrahydrofuran / 1.25 h / -78 °C

1.2: 61 h / 20 °C

2.1: potassium acetate; bis-triphenylphosphine-palladium(II) chloride / 1,4-dioxane / 90 °C

3.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; caesium carbonate / 1,4-dioxane; water / 3 h / 100 °C

With bis-triphenylphosphine-palladium(II) chloride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; ammonium chloride; caesium carbonate; lithium hexamethyldisilazane; In tetrahydrofuran; 1,4-dioxane; water;

Reference yield:

: 444335-16-4,1369530-77-7
(R)-3-(4-bromo-3-fluorophenyl)-5-(hydroxylmethyl)oxazolidin-2-one

: 1428738-42-4
(R)-3-(3-fluoro-4-(2-(2-methyl-2H-tetrazol-5-yl) isoindolin-5-yl)phenyl)-5-(hydroxylmethyl)oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: potassium acetate; bis-triphenylphosphine-palladium(II) chloride / 1,4-dioxane / 90 °C

2: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; caesium carbonate / 1,4-dioxane; water / 3 h / 100 °C

With bis-triphenylphosphine-palladium(II) chloride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; caesium carbonate; In 1,4-dioxane; water;