N-(((S)-3-(3-fluoro-4-(4-((1-(4-fluorophenyl)-2-methyl-5-o-tolyl-1H-pyrrol-3-yl)methyl)piperazin-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide

Base Information

Chemical Name:N-(((S)-3-(3-fluoro-4-(4-((1-(4-fluorophenyl)-2-methyl-5-o-tolyl-1H-pyrrol-3-yl)methyl)piperazin-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide
CAS No.:1445874-57-6
Molecular Formula:C₃₅H₃₇F₂N₅O₃
Molecular Weight:613.707
Hs Code.:

Synonyms:N-(((S)-3-(3-fluoro-4-(4-((1-(4-fluorophenyl)-2-methyl-5-o-tolyl-1H-pyrrol-3-yl)methyl)piperazin-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide

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Chemical Property of N-(((S)-3-(3-fluoro-4-(4-((1-(4-fluorophenyl)-2-methyl-5-o-tolyl-1H-pyrrol-3-yl)methyl)piperazin-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide

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Technology Process of N-(((S)-3-(3-fluoro-4-(4-((1-(4-fluorophenyl)-2-methyl-5-o-tolyl-1H-pyrrol-3-yl)methyl)piperazin-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide

There total 5 articles about N-(((S)-3-(3-fluoro-4-(4-((1-(4-fluorophenyl)-2-methyl-5-o-tolyl-1H-pyrrol-3-yl)methyl)piperazin-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)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: 89.0%

: 1445874-39-4
(5S)-5-(aminomethyl)-3-(3-fluoro-4-(4-((1-(4-fluorophenyl)-2-methyl-5-o-tolyl-1H-pyrrol-3-yl)methyl)piperazin-1-yl)phenyl)oxazolidin-2-one

: 75-36-5
acetyl chloride

: 1445874-57-6
N-(((S)-3-(3-fluoro-4-(4-((1-(4-fluorophenyl)-2-methyl-5-o-tolyl-1H-pyrrol-3-yl)methyl)piperazin-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 30 ℃; Inert atmosphere;
DOI:10.1016/j.ejmech.2013.03.027

Reference yield:

: 529-20-4
2-methylphenyl aldehyde

: 1445874-57-6
N-(((S)-3-(3-fluoro-4-(4-((1-(4-fluorophenyl)-2-methyl-5-o-tolyl-1H-pyrrol-3-yl)methyl)piperazin-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / 5 h / 75 - 78 °C

2: gadolinium(III) trifluoromethanesulfonate / acetonitrile / 0.5 h / 30 °C

3: acetic acid / acetonitrile; water / 6 h / 0 - 30 °C

4: palladium on activated charcoal; hydrogen / ethanol / 3 h / 30 °C

5: triethylamine / dichloromethane / 0 - 30 °C / Inert atmosphere

With palladium on activated charcoal; hydrogen; acetic acid; triethylamine; gadolinium(III) trifluoromethanesulfonate; In ethanol; dichloromethane; water; acetonitrile; 1: |Stetter 1,4-Dicarbonyl Synthesis / 2: |Paal-Knorr Pyrrole Synthesis / 3: |Mannich Aminomethylation;
DOI:10.1016/j.ejmech.2013.03.027

Reference yield:

: 908292-44-4
1-(4-fluorophenyl)-2-methyl-5-(2-methylphenyl)-1H-pyrrole

: 1445874-57-6
N-(((S)-3-(3-fluoro-4-(4-((1-(4-fluorophenyl)-2-methyl-5-o-tolyl-1H-pyrrol-3-yl)methyl)piperazin-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: acetic acid / acetonitrile; water / 6 h / 0 - 30 °C

2: palladium on activated charcoal; hydrogen / ethanol / 3 h / 30 °C

3: triethylamine / dichloromethane / 0 - 30 °C / Inert atmosphere

With palladium on activated charcoal; hydrogen; acetic acid; triethylamine; In ethanol; dichloromethane; water; acetonitrile; 1: |Mannich Aminomethylation;
DOI:10.1016/j.ejmech.2013.03.027