[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-1-(3-isopropoxy-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester

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Chemical Name:[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-1-(3-isopropoxy-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester
CAS No.:185112-29-2
Molecular Formula:C₂₆H₃₂N₂O₆
Molecular Weight:468.55
Hs Code.:

Synonyms:[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-1-(3-isopropoxy-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester

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Chemical Property of [(S)-2-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-1-(3-isopropoxy-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester

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Technology Process of [(S)-2-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-1-(3-isopropoxy-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester

There total 4 articles about [(S)-2-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-1-(3-isopropoxy-phenyl)-2-oxo-ethyl]-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: 92.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 185112-28-1
(S)-3-[(S)-2-Azido-2-(3-isopropoxy-phenyl)-acetyl]-4-benzyl-oxazolidin-2-one

: 185112-29-2
[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-1-(3-isopropoxy-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethyl acetate; for 2h; under 760 Torr;
DOI:10.1021/jo961412m

Reference yield:

: C₁₆H₂₂O₄

: 185112-29-2
[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-1-(3-isopropoxy-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / Et₃N / tetrahydrofuran / 0.25 h / -78 °C

2: 1.) KHDMS, 2.) trisyl azide / 1.) THF_. -78 deh C, 30 min, 2.) THF, -78 deg C, 4 min

3: 92 percent / H₂ / Pd/C / ethyl acetate / 2 h / 760 Torr

With 2,4,6-Triisopropylbenzenesulfonyl azide; hydrogen; potassium hexamethylsilazane; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethyl acetate;
DOI:10.1021/jo961412m

Reference yield:

: 185112-27-0
(S)-4-Benzyl-3-[2-(3-isopropoxy-phenyl)-acetyl]-oxazolidin-2-one

: 185112-29-2
[(S)-2-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-1-(3-isopropoxy-phenyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) KHDMS, 2.) trisyl azide / 1.) THF_. -78 deh C, 30 min, 2.) THF, -78 deg C, 4 min

2: 92 percent / H₂ / Pd/C / ethyl acetate / 2 h / 760 Torr

With 2,4,6-Triisopropylbenzenesulfonyl azide; hydrogen; potassium hexamethylsilazane; palladium on activated charcoal; In ethyl acetate;
DOI:10.1021/jo961412m