(S)-2-[(S)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-3-oxo-1-trifluoromethyl-propylamino]-N-benzyloxy-3-methyl-butyramide

Base Information

Chemical Name:(S)-2-[(S)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-3-oxo-1-trifluoromethyl-propylamino]-N-benzyloxy-3-methyl-butyramide
CAS No.:347383-72-6
Molecular Formula:C₂₆H₃₀F₃N₃O₅
Molecular Weight:521.537
Hs Code.:

Synonyms:(S)-2-[(S)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-3-oxo-1-trifluoromethyl-propylamino]-N-benzyloxy-3-methyl-butyramide

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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 (S)-2-[(S)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-3-oxo-1-trifluoromethyl-propylamino]-N-benzyloxy-3-methyl-butyramide

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Technology Process of (S)-2-[(S)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-3-oxo-1-trifluoromethyl-propylamino]-N-benzyloxy-3-methyl-butyramide

There total 1 articles about (S)-2-[(S)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-3-oxo-1-trifluoromethyl-propylamino]-N-benzyloxy-3-methyl-butyramide 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:

: 243121-08-6
(S)-4-benzyl-3-[(E)-4,4,4-trifluorobut-2-enoyl]oxazolidin-2-one

: 2-amino-N-benzyloxy-3-methyl-butyramide; compound with trifluoro-acetic acid

: 347383-72-6
(S)-2-[(S)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-3-oxo-1-trifluoromethyl-propylamino]-N-benzyloxy-3-methyl-butyramide

: (S)-2-[(R)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-3-oxo-1-trifluoromethyl-propylamino]-N-benzyloxy-3-methyl-butyramide

Guidance literature:: With 2,4,6-trimethyl-pyridine; In dichloromethane; at 20 ℃; for 72h;
DOI:10.1016/S0040-4039(01)00375-6

Reference yield: 60.0%

: 347383-72-6
(S)-2-[(S)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-3-oxo-1-trifluoromethyl-propylamino]-N-benzyloxy-3-methyl-butyramide

: 347383-76-0
(S)-3-((S)-1-Benzyloxycarbamoyl-2-methyl-propylamino)-4,4,4-trifluoro-butyric acid

Guidance literature:: With lithium hydroxide; dihydrogen peroxide; at 0 ℃; for 0.5h;
DOI:10.1016/S0040-4039(01)00375-6

Reference yield:

: 347383-72-6
(S)-2-[(S)-3-((S)-4-Benzyl-2-oxo-oxazolidin-3-yl)-3-oxo-1-trifluoromethyl-propylamino]-N-benzyloxy-3-methyl-butyramide

: (S)-3-Phenyl-2-[(S)-4,4,4-trifluoro-3-((S)-1-hydroxycarbamoyl-2-methyl-propylamino)-butyrylamino]-propionic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 60 percent / aq. H₂O₂; LiOH*H₂O / tetrahydrofuran / 0.5 h / 0 °C

2: sym-collidine; HOAt; HATU / dimethylformamide

3: 85 percent / H₂ / Pd(OH)2/C / ethanol / 20 °C

With 2,4,6-trimethyl-pyridine; lithium hydroxide; 1-hydroxy-7-aza-benzotriazole; hydrogen; dihydrogen peroxide; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; palladium dihydroxide; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide;
DOI:10.1002/1099-0690(20022)2002:3<428::AID-EJOC428<3.0.CO;2-J