(S)-N-((3-(3,5-difluoro-4-(4-methyl-4-phenyl-1,4-azasilinan-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide

Base Information

Chemical Name:(S)-N-((3-(3,5-difluoro-4-(4-methyl-4-phenyl-1,4-azasilinan-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide
CAS No.:1430321-61-1
Molecular Formula:C₂₃H₂₇F₂N₃O₃Si
Molecular Weight:459.568
Hs Code.:

Synonyms:(S)-N-((3-(3,5-difluoro-4-(4-methyl-4-phenyl-1,4-azasilinan-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide

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Chemical Property of (S)-N-((3-(3,5-difluoro-4-(4-methyl-4-phenyl-1,4-azasilinan-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide

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Technology Process of (S)-N-((3-(3,5-difluoro-4-(4-methyl-4-phenyl-1,4-azasilinan-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide

There total 10 articles about (S)-N-((3-(3,5-difluoro-4-(4-methyl-4-phenyl-1,4-azasilinan-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: 72.0%

: 1430321-60-0
(S)-5-(aminomethyl)-3-(3,5-difluoro-4-(4-methyl-4-phenyl-1,4-azasilinan-1-yl)phenyl)oxazolidin-2-one

: 75-36-5
acetyl chloride

: 1430321-61-1
(S)-N-((3-(3,5-difluoro-4-(4-methyl-4-phenyl-1,4-azasilinan-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 0 - 20 ℃; for 3h; Inert atmosphere;
DOI:10.1021/acsmedchemlett.5b00213

Reference yield:

: 1430321-70-2
1-(2,6-difluoro-4-nitrophenyl)-4-methyl-4-phenyl-1,4-azasilinane

: 1430321-61-1
(S)-N-((3-(3,5-difluoro-4-(4-methyl-4-phenyl-1,4-azasilinan-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: palladium on activated charcoal; hydrogen / tetrahydrofuran / 1810.07 Torr

2: sodium hydrogencarbonate / tetrahydrofuran / 5 h / 25 °C

3: lithium tert-butoxide / N,N-dimethyl-formamide / 45 h / 0 - 25 °C

4: trifluoroacetic acid / dichloromethane / 3 h / 25 °C

5: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 3 h / 0 - 25 °C

With palladium on activated charcoal; hydrogen; sodium hydrogencarbonate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; lithium tert-butoxide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1430321-71-3
benzyl (3,5-difluoro-4-(4-methyl-4-phenyl-1,4-azasilinan-1-yl)phenyl)carbamate

: 1430321-61-1
(S)-N-((3-(3,5-difluoro-4-(4-methyl-4-phenyl-1,4-azasilinan-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: lithium tert-butoxide / N,N-dimethyl-formamide / 45 h / 0 - 25 °C

2: trifluoroacetic acid / dichloromethane / 3 h / 25 °C

3: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 3 h / 0 - 25 °C

With N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; lithium tert-butoxide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;