Methanesulfonic acid (R)-3-(3-fluoro-4-pyrazol-1-yl-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester

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Chemical Name:Methanesulfonic acid (R)-3-(3-fluoro-4-pyrazol-1-yl-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester
CAS No.:226220-37-7
Molecular Formula:C₁₄H₁₄FN₃O₅S
Molecular Weight:355.347
Hs Code.:

Synonyms:Methanesulfonic acid (R)-3-(3-fluoro-4-pyrazol-1-yl-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester

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Chemical Property of Methanesulfonic acid (R)-3-(3-fluoro-4-pyrazol-1-yl-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester

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Technology Process of Methanesulfonic acid (R)-3-(3-fluoro-4-pyrazol-1-yl-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester

There total 5 articles about Methanesulfonic acid (R)-3-(3-fluoro-4-pyrazol-1-yl-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:

: 124-63-0
methanesulfonyl chloride

: 226220-36-6
[3-[3-fluoro-4-(1H-pyrazol-1-yl)phenyl]-2-oxo-5-oxazolidinyl]methanol

: 226220-37-7
Methanesulfonic acid (R)-3-(3-fluoro-4-pyrazol-1-yl-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 0.5h;
DOI:10.1021/jm990373e

Reference yield:

: 369-34-6
3,4-difluoronitrobenzene

: 226220-37-7
Methanesulfonic acid (R)-3-(3-fluoro-4-pyrazol-1-yl-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 87 percent / K₂CO₃ / dimethylsulfoxide / 18 h / 90 °C

2.1: H₂ / W-2 Raney Nickel / tetrahydrofuran / 16 h / 2068.65 Torr

3.1: 5.92 g / NaHCO₃ / tetrahydrofuran / 48 h / -20 - 20 °C

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

4.2: 85 percent / tetrahydrofuran / 24 h / -78 - 20 °C

5.1: NEt₃ / CH₂Cl₂ / 0.5 h / 0 °C

With hydrogen; sodium hydrogencarbonate; potassium carbonate; triethylamine; lithium hexamethyldisilazane; W-2 Raney nickel; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide; 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:

: 226220-35-5
3-fluoro-1-nitro-4-(1H-pyrazol-1-yl)benzene

: 226220-37-7
Methanesulfonic acid (R)-3-(3-fluoro-4-pyrazol-1-yl-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: H₂ / W-2 Raney Nickel / tetrahydrofuran / 16 h / 2068.65 Torr

2.1: 5.92 g / NaHCO₃ / tetrahydrofuran / 48 h / -20 - 20 °C

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

3.2: 85 percent / tetrahydrofuran / 24 h / -78 - 20 °C

4.1: NEt₃ / CH₂Cl₂ / 0.5 h / 0 °C

With hydrogen; sodium hydrogencarbonate; triethylamine; lithium hexamethyldisilazane; W-2 Raney nickel; In tetrahydrofuran; dichloromethane; 1.1: Reduction / 2.1: Acylation / 3.1: Metallation / 3.2: Ring cleavage / 4.1: mesylation;
DOI:10.1021/jm990373e