(4R,5S)-4-methyl-3-((S)-3-oxocyclohexanecarbonyl)-5-phenyloxazolidin-2-one

Base Information

Chemical Name:(4R,5S)-4-methyl-3-((S)-3-oxocyclohexanecarbonyl)-5-phenyloxazolidin-2-one
CAS No.:1374445-29-0
Molecular Formula:C₁₇H₁₉NO₄
Molecular Weight:301.342
Hs Code.:

Synonyms:(4R,5S)-4-methyl-3-((S)-3-oxocyclohexanecarbonyl)-5-phenyloxazolidin-2-one

Suppliers and Price of (4R,5S)-4-methyl-3-((S)-3-oxocyclohexanecarbonyl)-5-phenyloxazolidin-2-one

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (4R,5S)-4-methyl-3-((S)-3-oxocyclohexanecarbonyl)-5-phenyloxazolidin-2-one

Chemical Property:

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Technology Process of (4R,5S)-4-methyl-3-((S)-3-oxocyclohexanecarbonyl)-5-phenyloxazolidin-2-one

There total 1 articles about (4R,5S)-4-methyl-3-((S)-3-oxocyclohexanecarbonyl)-5-phenyloxazolidin-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:

: 77943-39-6
4-methyl-5-phenyloxazolidin-2-one

: 16205-98-4
3-oxo-cyclohexanecarboxylic acid

: 1374445-31-4
(4R,5S)-4-methyl-3-((R)-3-oxocyclohexanecarbonyl)-5-phenyloxazolidin-2-one

: 1374445-29-0
(4R,5S)-4-methyl-3-((S)-3-oxocyclohexanecarbonyl)-5-phenyloxazolidin-2-one

Guidance literature:: 3-oxo-cyclohexanecarboxylic acid; With pivaloyl chloride; triethylamine; In tetrahydrofuran; at -20 ℃; for 1h;

4-methyl-5-phenyloxazolidin-2-one; With lithium chloride; In tetrahydrofuran; at -20 - 20 ℃;

Reference yield:

: 1374445-29-0
(4R,5S)-4-methyl-3-((S)-3-oxocyclohexanecarbonyl)-5-phenyloxazolidin-2-one

: 1374443-95-4
(3R,4S)-3-amino-7-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)chroman-4-ol trifluoroacetate

: 1374445-39-2
(4R,5S)-3-((1S,3R)-3-((3R,4S)-4-hydroxy-7-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)chroman-3-ylamino)cyclohexanecarbonyl)-4-methyl-5-phenyloxazolidin-2-one

: 1374445-42-7
(4R,5S)-3-((1S,3S)-3-((3R,4S)-4-hydroxy-7-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)chroman-3-ylamino)cyclohexanecarbonyl)-4-methyl-5-phenyloxazolidin-2-one

Guidance literature:: With sodium tris(acetoxy)borohydride; triethylamine; In chloroform;

Reference yield:

: 1374445-29-0
(4R,5S)-4-methyl-3-((S)-3-oxocyclohexanecarbonyl)-5-phenyloxazolidin-2-one

: 1374443-95-4
(3R,4S)-3-amino-7-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)chroman-4-ol trifluoroacetate

: 1374444-83-3
(1S,3S)-3-((3R,4S)-4-hydroxy-7-(5-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)chroman-3-ylamino)cyclohexanecarboxylic acid trifluoroacetate

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine; sodium tris(acetoxy)borohydride / chloroform

2.1: lithium hydroxide; dihydrogen peroxide / tetrahydrofuran / 1 h / 0 °C

2.2: 1.5 h / 20 °C / pH 9

With dihydrogen peroxide; sodium tris(acetoxy)borohydride; triethylamine; lithium hydroxide; In tetrahydrofuran; chloroform;