(1R,2S,3S,4'S)-[1-benzyl-2-hydroxy-4-(4'-isopropyl-2'-oxo-oxazolidin-3'-yl)-3-methyl-4-oxobutyl]carbamic acid tert-butyl ester

Base Information

Chemical Name:(1R,2S,3S,4'S)-[1-benzyl-2-hydroxy-4-(4'-isopropyl-2'-oxo-oxazolidin-3'-yl)-3-methyl-4-oxobutyl]carbamic acid tert-butyl ester
CAS No.:574012-06-9
Molecular Formula:C₂₃H₃₄N₂O₆
Molecular Weight:434.533
Hs Code.:

Synonyms:(1R,2S,3S,4'S)-[1-benzyl-2-hydroxy-4-(4'-isopropyl-2'-oxo-oxazolidin-3'-yl)-3-methyl-4-oxobutyl]carbamic acid tert-butyl ester

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Chemical Property of (1R,2S,3S,4'S)-[1-benzyl-2-hydroxy-4-(4'-isopropyl-2'-oxo-oxazolidin-3'-yl)-3-methyl-4-oxobutyl]carbamic acid tert-butyl ester

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Technology Process of (1R,2S,3S,4'S)-[1-benzyl-2-hydroxy-4-(4'-isopropyl-2'-oxo-oxazolidin-3'-yl)-3-methyl-4-oxobutyl]carbamic acid tert-butyl ester

There total 4 articles about (1R,2S,3S,4'S)-[1-benzyl-2-hydroxy-4-(4'-isopropyl-2'-oxo-oxazolidin-3'-yl)-3-methyl-4-oxobutyl]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:

: 77877-19-1,165657-81-8
N-isopropyl oxazolidinone

: 77119-85-8
N-(tert-butoxycarbonyl)-D-phenylalaninal

: 574012-06-9
(1R,2S,3S,4'S)-[1-benzyl-2-hydroxy-4-(4'-isopropyl-2'-oxo-oxazolidin-3'-yl)-3-methyl-4-oxobutyl]carbamic acid tert-butyl ester

Guidance literature:: N-isopropyl oxazolidinone; With di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine; In dichloromethane; for 1h;

N-(tert-butoxycarbonyl)-D-phenylalaninal; In dichloromethane; at -78 - 20 ℃;

With dihydrogen peroxide; In methanol; for 4h;
DOI:10.1021/ja021388w

Reference yield:

: 18942-49-9
Boc-D-Phe-OH

: 574012-06-9
(1R,2S,3S,4'S)-[1-benzyl-2-hydroxy-4-(4'-isopropyl-2'-oxo-oxazolidin-3'-yl)-3-methyl-4-oxobutyl]carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine / dichloromethane / Inert atmosphere

1.2: Inert atmosphere

1.3: Inert atmosphere

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 °C / Inert atmosphere

3.1: di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine / dichloromethane / -78 °C / Inert atmosphere

With lithium aluminium tetrahydride; di-n-butylboryl trifluoromethanesulfonate; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.bmc.2011.04.047

Reference yield:

: 17016-83-0
(4S)-4-isopropyl-1,3-oxazolidin-2-one

: 574012-06-9
(1R,2S,3S,4'S)-[1-benzyl-2-hydroxy-4-(4'-isopropyl-2'-oxo-oxazolidin-3'-yl)-3-methyl-4-oxobutyl]carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-butyllithium / tetrahydrofuran / -78 - 25 °C / Inert atmosphere

1.2: -78 - 25 °C / Inert atmosphere

2.1: di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine / dichloromethane / -78 °C / Inert atmosphere

With n-butyllithium; di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.bmc.2011.04.047