(4S,5R,2'R)-3-(2-azido-2-(2-methoxy-6-methylphenyl)acetyl)-4-methyl-5-phenyl-1,3-oxazolidin-2-one

Base Information

Chemical Name:(4S,5R,2'R)-3-(2-azido-2-(2-methoxy-6-methylphenyl)acetyl)-4-methyl-5-phenyl-1,3-oxazolidin-2-one
CAS No.:151858-73-0
Molecular Formula:C₂₀H₂₀N₄O₄
Molecular Weight:380.403
Hs Code.:

Synonyms:(4S,5R,2'R)-3-(2-azido-2-(2-methoxy-6-methylphenyl)acetyl)-4-methyl-5-phenyl-1,3-oxazolidin-2-one

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Chemical Property of (4S,5R,2'R)-3-(2-azido-2-(2-methoxy-6-methylphenyl)acetyl)-4-methyl-5-phenyl-1,3-oxazolidin-2-one

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Technology Process of (4S,5R,2'R)-3-(2-azido-2-(2-methoxy-6-methylphenyl)acetyl)-4-methyl-5-phenyl-1,3-oxazolidin-2-one

There total 5 articles about (4S,5R,2'R)-3-(2-azido-2-(2-methoxy-6-methylphenyl)acetyl)-4-methyl-5-phenyl-1,3-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:

: 151858-71-8
(2-methoxy-6-methylphenyl)acetic acid

: 151858-73-0
(4S,5R,2'R)-3-(2-azido-2-(2-methoxy-6-methylphenyl)acetyl)-4-methyl-5-phenyl-1,3-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: Et₃N / tetrahydrofuran / 1.) -78 deg C, 15 min, 2.) 0 deg C, 45 min

2: 1.) n-BuLi / 1.) THF, -78 deg C, 15 min, 2.) THF, a) -78 deg C, 15 min, b) RT, 9 h

3: 1.) KN(SiMe₃)2, 2.) trisyl azide, 3.) AcOH

With n-butyllithium; 2,4,6-Triisopropylbenzenesulfonyl azide; potassium hexamethylsilazane; acetic acid; triethylamine; In tetrahydrofuran;
DOI:10.1021/ja00076a036

Reference yield:

: 1-(methylsulfinyl)-1-(methylthio)-2-(2-methoxy-6-methylphenyl)ethylene

: 151858-73-0
(4S,5R,2'R)-3-(2-azido-2-(2-methoxy-6-methylphenyl)acetyl)-4-methyl-5-phenyl-1,3-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: 72 percent / aq. HCl / diethyl ether / 72 h / Heating

2: Et₃N / tetrahydrofuran / 1.) -78 deg C, 15 min, 2.) 0 deg C, 45 min

3: 1.) n-BuLi / 1.) THF, -78 deg C, 15 min, 2.) THF, a) -78 deg C, 15 min, b) RT, 9 h

4: 1.) KN(SiMe₃)2, 2.) trisyl azide, 3.) AcOH

With hydrogenchloride; n-butyllithium; 2,4,6-Triisopropylbenzenesulfonyl azide; potassium hexamethylsilazane; acetic acid; triethylamine; In tetrahydrofuran; diethyl ether;
DOI:10.1021/ja00076a036

Reference yield:

: 151858-72-9
(4S,5R)-3-(2-(2-methoxy-6-methylphenyl)acetyl)-4-methyl-5-phenyl-1,3-oxazolidin-2-one

: 151858-73-0
(4S,5R,2'R)-3-(2-azido-2-(2-methoxy-6-methylphenyl)acetyl)-4-methyl-5-phenyl-1,3-oxazolidin-2-one

Guidance literature:: With 2,4,6-Triisopropylbenzenesulfonyl azide; potassium hexamethylsilazane; acetic acid; Yield given. Multistep reaction;
DOI:10.1021/ja00076a036