[2-(4-{4-[(S)-5-(Acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluoro-phenoxy}-piperidin-1-yl)-2-oxo-ethyl]-carbamic acid benzyl ester

Base Information

• Chemical Name: [2-(4-{4-[(S)-5-(Acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluoro-phenoxy}-piperidin-1-yl)-2-oxo-ethyl]-carbamic acid benzyl ester
• CAS No.: 346664-54-8
• Molecular Formula: C₂₇H₃₁FN₄O₇
• Molecular Weight: 542.564

Synonyms:[2-(4-{4-[(S)-5-(Acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluoro-phenoxy}-piperidin-1-yl)-2-oxo-ethyl]-carbamic acid benzyl ester

Chemical Property of [2-(4-{4-[(S)-5-(Acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluoro-phenoxy}-piperidin-1-yl)-2-oxo-ethyl]-carbamic acid benzyl ester

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Technology Process of [2-(4-{4-[(S)-5-(Acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluoro-phenoxy}-piperidin-1-yl)-2-oxo-ethyl]-carbamic acid benzyl ester

There total 1 articles about [2-(4-{4-[(S)-5-(Acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluoro-phenoxy}-piperidin-1-yl)-2-oxo-ethyl]-carbamic acid benzyl 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: 91.0%

Z-glycine fluoride (133010-18-1) + N-{3-[3-fluoro-4-(piperidin-4-yloxy)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide; compound with trifluoro-acetic acid → [2-(4-{4-[(S)-5-(Acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluoro-phenoxy}-piperidin-1-yl)-2-oxo-ethyl]-carbamic acid benzyl ester (346664-54-8)

Guidance literature:

With triethylamine; In dichloromethane; at 20 ℃; for 1.5h;

DOI:10.1016/S0968-0896(02)00065-2

Reference yield: 73.0%

[2-(4-{4-[(S)-5-(Acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluoro-phenoxy}-piperidin-1-yl)-2-oxo-ethyl]-carbamic acid benzyl ester (346664-54-8) → N-((S)-3-{4-[1-(2-Amino-acetyl)-piperidin-4-yloxy]-3-fluoro-phenyl}-2-oxo-oxazolidin-5-ylmethyl)-acetamide

Guidance literature:

With hydrogen; palladium on activated charcoal; In ethanol; under 2585.74 Torr;

DOI:10.1016/S0968-0896(02)00065-2

Reference yield:

[2-(4-{4-[(S)-5-(Acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2-fluoro-phenoxy}-piperidin-1-yl)-2-oxo-ethyl]-carbamic acid benzyl ester (346664-54-8) → N-((S)-3-{3-Fluoro-4-[1-(2-methanesulfonylamino-acetyl)-piperidin-4-yloxy]-phenyl}-2-oxo-oxazolidin-5-ylmethyl)-acetamide

Guidance literature:

Multi-step reaction with 2 steps

1: 73 percent / H₂ / 10 percent Pd-C / ethanol / 2585.74 Torr

2: 32 percent / Et₃N / CH₂Cl₂ / 18 h / 20 °C

With hydrogen; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane;

DOI:10.1016/S0968-0896(02)00065-2

upstream raw materials:

Z-glycine fluoride

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