N-(4-{4-[(5S)-5-(aminomethyl)-2-oxo-1,3-oxazolidin-3-yl]-2-fluorophenylthio}phenyl)acetamide

Base Information

Chemical Name:N-(4-{4-[(5S)-5-(aminomethyl)-2-oxo-1,3-oxazolidin-3-yl]-2-fluorophenylthio}phenyl)acetamide
CAS No.:771477-22-6
Molecular Formula:C₁₈H₁₈FN₃O₃S
Molecular Weight:375.424
Hs Code.:

Synonyms:N-(4-{4-[(5S)-5-(aminomethyl)-2-oxo-1,3-oxazolidin-3-yl]-2-fluorophenylthio}phenyl)acetamide

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Chemical Property of N-(4-{4-[(5S)-5-(aminomethyl)-2-oxo-1,3-oxazolidin-3-yl]-2-fluorophenylthio}phenyl)acetamide

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Technology Process of N-(4-{4-[(5S)-5-(aminomethyl)-2-oxo-1,3-oxazolidin-3-yl]-2-fluorophenylthio}phenyl)acetamide

There total 8 articles about N-(4-{4-[(5S)-5-(aminomethyl)-2-oxo-1,3-oxazolidin-3-yl]-2-fluorophenylthio}phenyl)acetamide 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:

: 771477-20-4
N-(4-{4-[(5R)-5-(azidomethyl)-2-oxo-1,3-oxazolidin-3-yl]-2-fluorophenylthio}phenyl)acetamide

: 771477-22-6
N-(4-{4-[(5S)-5-(aminomethyl)-2-oxo-1,3-oxazolidin-3-yl]-2-fluorophenylthio}phenyl)acetamide

Guidance literature:: N-(4-{4-[(5R)-5-(azidomethyl)-2-oxo-1,3-oxazolidin-3-yl]-2-fluorophenylthio}phenyl)acetamide; With triphenylphosphine; In acetonitrile; at 45 ℃; for 1h;

With water; at 65 - 70 ℃;
DOI:10.1016/j.bmcl.2004.06.096

Reference yield:

: 369-34-6
3,4-difluoronitrobenzene

: 771477-22-6
N-(4-{4-[(5S)-5-(aminomethyl)-2-oxo-1,3-oxazolidin-3-yl]-2-fluorophenylthio}phenyl)acetamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: K₂CO₃ / dimethylformamide / 80 °C

2.1: HCO₂NH₄; Pd/C / methanol / Heating

3.1: aq. Na₂CO₃ / acetone / 3 h / 0 - 25 °C

4.1: n-butyl lithium / tetrahydrofuran / 12 h / -78 - 25 °C

5.1: TEA / CH₂Cl₂

6.1: sodium azide / dimethylformamide / 80 °C

7.1: PPh₃ / acetonitrile / 1 h / 45 °C

7.2: H₂O / 65 - 70 °C

With palladium on activated charcoal; n-butyllithium; sodium azide; TEA; ammonium formate; sodium carbonate; potassium carbonate; triphenylphosphine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetone; acetonitrile;
DOI:10.1016/j.bmcl.2004.06.096

Reference yield:

: 1126-81-4
4-acetamidothiophenol

: 771477-22-6
N-(4-{4-[(5S)-5-(aminomethyl)-2-oxo-1,3-oxazolidin-3-yl]-2-fluorophenylthio}phenyl)acetamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: K₂CO₃ / dimethylformamide / 80 °C

2.1: HCO₂NH₄; Pd/C / methanol / Heating

3.1: aq. Na₂CO₃ / acetone / 3 h / 0 - 25 °C

4.1: n-butyl lithium / tetrahydrofuran / 12 h / -78 - 25 °C

5.1: TEA / CH₂Cl₂

6.1: sodium azide / dimethylformamide / 80 °C

7.1: PPh₃ / acetonitrile / 1 h / 45 °C

7.2: H₂O / 65 - 70 °C

With palladium on activated charcoal; n-butyllithium; sodium azide; TEA; ammonium formate; sodium carbonate; potassium carbonate; triphenylphosphine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetone; acetonitrile;
DOI:10.1016/j.bmcl.2004.06.096