{1-[2-fluoro-4-(5-hydroxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-1H-pyrazol-3-yl}-carbamic acid tert-butyl ester

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Chemical Name:{1-[2-fluoro-4-(5-hydroxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-1H-pyrazol-3-yl}-carbamic acid tert-butyl ester
CAS No.:1027839-28-6
Molecular Formula:C₁₈H₂₁FN₄O₅
Molecular Weight:392.387
Hs Code.:

{1-[2-fluoro-4-(5-hydroxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-1<i>H</i>-pyrazol-3-yl}-carbamic acid <i>tert</i>-butyl ester

Synonyms:{1-[2-fluoro-4-(5-hydroxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-1H-pyrazol-3-yl}-carbamic acid tert-butyl ester

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Chemical Property of {1-[2-fluoro-4-(5-hydroxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-1H-pyrazol-3-yl}-carbamic acid tert-butyl ester

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Technology Process of {1-[2-fluoro-4-(5-hydroxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-1H-pyrazol-3-yl}-carbamic acid tert-butyl ester

There total 5 articles about {1-[2-fluoro-4-(5-hydroxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-1H-pyrazol-3-yl}-carbamic acid tert-butyl 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

: 1027839-28-6
{1-[2-fluoro-4-(5-hydroxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-1H-pyrazol-3-yl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 43 percent / K₂CO₃ / acetonitrile / 48 h / 20 °C

2.1: 51 percent / NEt₃; (dimethylamino)pyridine / dimethylformamide

3.1: H₂ / 10percent Pd/C / methanol / 3 h / 1034.32 Torr

4.1: NaHCO₃ / tetrahydrofuran / 0 - 20 °C

5.1: lithium bis(trimethylsilyl)amide / tetrahydrofuran / 0.75 h / -78 °C

5.2: tetrahydrofuran / -78 - 20 °C

With dmap; hydrogen; sodium hydrogencarbonate; potassium carbonate; triethylamine; lithium hexamethyldisilazane; 10percent Pd/C; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetonitrile; 1.1: Substitution / 2.1: Acylation / 3.1: Reduction / 4.1: Acylation / 5.1: Metallation / 5.2: Ring cleavage;
DOI:10.1021/jm990373e

Reference yield:

: 266327-62-2
3-fluoro-1-nitro-4-(1H-3-amino-pyrazol-1-yl)benzene

: 1027839-28-6
{1-[2-fluoro-4-(5-hydroxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-1H-pyrazol-3-yl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: 51 percent / NEt₃; (dimethylamino)pyridine / dimethylformamide

2.1: H₂ / 10percent Pd/C / methanol / 3 h / 1034.32 Torr

3.1: NaHCO₃ / tetrahydrofuran / 0 - 20 °C

4.1: lithium bis(trimethylsilyl)amide / tetrahydrofuran / 0.75 h / -78 °C

4.2: tetrahydrofuran / -78 - 20 °C

With dmap; hydrogen; sodium hydrogencarbonate; triethylamine; lithium hexamethyldisilazane; 10percent Pd/C; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; 1.1: Acylation / 2.1: Reduction / 3.1: Acylation / 4.1: Metallation / 4.2: Ring cleavage;
DOI:10.1021/jm990373e

Reference yield:

: 266327-63-3
3-fluoro-1-nitro-4-(1H-3-tert-butoxycarbonylaminopyrazol-1-yl)benzene

: 1027839-28-6
{1-[2-fluoro-4-(5-hydroxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-1H-pyrazol-3-yl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: H₂ / 10percent Pd/C / methanol / 3 h / 1034.32 Torr

2.1: NaHCO₃ / tetrahydrofuran / 0 - 20 °C

3.1: lithium bis(trimethylsilyl)amide / tetrahydrofuran / 0.75 h / -78 °C

3.2: tetrahydrofuran / -78 - 20 °C

With hydrogen; sodium hydrogencarbonate; lithium hexamethyldisilazane; 10percent Pd/C; In tetrahydrofuran; methanol; 1.1: Reduction / 2.1: Acylation / 3.1: Metallation / 3.2: Ring cleavage;
DOI:10.1021/jm990373e