(R)-3-[4-(3-Acetyl-pyrrol-1-yl)-3-fluoro-phenyl]-5-hydroxymethyl-oxazolidin-2-one

Base Information

Chemical Name:(R)-3-[4-(3-Acetyl-pyrrol-1-yl)-3-fluoro-phenyl]-5-hydroxymethyl-oxazolidin-2-one
CAS No.:1025890-48-5
Molecular Formula:C₁₆H₁₅FN₂O₄
Molecular Weight:318.305
Hs Code.:

Synonyms:(R)-3-[4-(3-Acetyl-pyrrol-1-yl)-3-fluoro-phenyl]-5-hydroxymethyl-oxazolidin-2-one

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Chemical Property of (R)-3-[4-(3-Acetyl-pyrrol-1-yl)-3-fluoro-phenyl]-5-hydroxymethyl-oxazolidin-2-one

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Technology Process of (R)-3-[4-(3-Acetyl-pyrrol-1-yl)-3-fluoro-phenyl]-5-hydroxymethyl-oxazolidin-2-one

There total 5 articles about (R)-3-[4-(3-Acetyl-pyrrol-1-yl)-3-fluoro-phenyl]-5-hydroxymethyl-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:

: 60456-26-0
(R)-glycidyl butyrate

: [4-(3-acetyl-pyrrol-1-yl)-3-fluoro-phenyl]-carbamic acid benzyl ester

: 1025890-48-5
(R)-3-[4-(3-Acetyl-pyrrol-1-yl)-3-fluoro-phenyl]-5-hydroxymethyl-oxazolidin-2-one

Guidance literature:: [4-(3-acetyl-pyrrol-1-yl)-3-fluoro-phenyl]-carbamic acid benzyl ester; With lithium hexamethyldisilazane; In tetrahydrofuran; at -78 ℃; for 0.5h;

(R)-glycidyl butyrate; In tetrahydrofuran; at 20 ℃; for 24h; Further stages.;
DOI:10.1021/jm990373e

Reference yield:

: 1072-82-8
3-acetylpyrrole

: 1025890-48-5
(R)-3-[4-(3-Acetyl-pyrrol-1-yl)-3-fluoro-phenyl]-5-hydroxymethyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: K₂CO₃ / dimethylsulfoxide / 50 °C

2.1: H₂ / tetrahydrofuran / 18 h

3.1: NaHCO₃ / tetrahydrofuran / 48 h / 20 °C

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

4.2: tetrahydrofuran / 24 h / 20 °C

With hydrogen; sodium hydrogencarbonate; potassium carbonate; lithium hexamethyldisilazane; In tetrahydrofuran; dimethyl sulfoxide; 1.1: Substitution / 2.1: Reduction / 3.1: Acylation / 4.1: Metallation / 4.2: Ring cleavage;
DOI:10.1021/jm990373e

Reference yield:

: 369-34-6
3,4-difluoronitrobenzene

: 1025890-48-5
(R)-3-[4-(3-Acetyl-pyrrol-1-yl)-3-fluoro-phenyl]-5-hydroxymethyl-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: K₂CO₃ / dimethylsulfoxide / 50 °C

2.1: H₂ / tetrahydrofuran / 18 h

3.1: NaHCO₃ / tetrahydrofuran / 48 h / 20 °C

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

4.2: tetrahydrofuran / 24 h / 20 °C

With hydrogen; sodium hydrogencarbonate; potassium carbonate; lithium hexamethyldisilazane; In tetrahydrofuran; dimethyl sulfoxide; 1.1: Substitution / 2.1: Reduction / 3.1: Acylation / 4.1: Metallation / 4.2: Ring cleavage;
DOI:10.1021/jm990373e