Methanesulfonic acid (R)-3-[4-(benzyl-benzyloxycarbonyl-amino)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl ester

Base Information

Chemical Name:Methanesulfonic acid (R)-3-[4-(benzyl-benzyloxycarbonyl-amino)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl ester
CAS No.:219664-27-4
Molecular Formula:C₂₆H₂₅FN₂O₇S
Molecular Weight:528.558
Hs Code.:

Synonyms:Methanesulfonic acid (R)-3-[4-(benzyl-benzyloxycarbonyl-amino)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl ester

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Chemical Property of Methanesulfonic acid (R)-3-[4-(benzyl-benzyloxycarbonyl-amino)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl ester

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Technology Process of Methanesulfonic acid (R)-3-[4-(benzyl-benzyloxycarbonyl-amino)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl ester

There total 7 articles about Methanesulfonic acid (R)-3-[4-(benzyl-benzyloxycarbonyl-amino)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl ester 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:

: 369-34-6
3,4-difluoronitrobenzene

: 219664-27-4
Methanesulfonic acid (R)-3-[4-(benzyl-benzyloxycarbonyl-amino)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 77 percent / N,N-diisopropylethylamine / acetonitrile / 6 h / 90 °C

2.1: H₂ / 5percent Pt/C / tetrahydrofuran / 6 h

3.1: N,N-dimethylaniline / tetrahydrofuran / 17 h / 20 °C

4.1: lithium bis(trimethylsilyl)amide / tetrahydrofuran / 0.5 h / -78 °C

4.2: 77 percent / tetrahydrofuran / 24 h / -78 - 20 °C

5.1: NEt₃ / CH₂Cl₂ / 0.75 h / 0 °C

With hydrogen; N,N-dimethyl-aniline; triethylamine; N-ethyl-N,N-diisopropylamine; lithium hexamethyldisilazane; 5percent Pt/C; In tetrahydrofuran; dichloromethane; acetonitrile; 1.1: Substitution / 2.1: Reduction / 3.1: Acylation / 4.1: Metallation / 4.2: Ring cleavage / 5.1: mesylation;
DOI:10.1021/jm990373e

Reference yield:

: 181997-28-4
N-benzyl-2-fluoro-4-nitroaniline

: 219664-27-4
Methanesulfonic acid (R)-3-[4-(benzyl-benzyloxycarbonyl-amino)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: H₂ / 5percent Pt/C / tetrahydrofuran / 6 h

2.1: N,N-dimethylaniline / tetrahydrofuran / 17 h / 20 °C

3.1: lithium bis(trimethylsilyl)amide / tetrahydrofuran / 0.5 h / -78 °C

3.2: 77 percent / tetrahydrofuran / 24 h / -78 - 20 °C

4.1: NEt₃ / CH₂Cl₂ / 0.75 h / 0 °C

With hydrogen; N,N-dimethyl-aniline; triethylamine; lithium hexamethyldisilazane; 5percent Pt/C; In tetrahydrofuran; dichloromethane; 1.1: Reduction / 2.1: Acylation / 3.1: Metallation / 3.2: Ring cleavage / 4.1: mesylation;
DOI:10.1021/jm990373e