tert-butyl (S)-(3-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-(4-chlorophenyl)-3-oxopropyl)(2,4-dimethoxybenzyl)carbamate

Base Information

• Chemical Name: tert-butyl (S)-(3-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-(4-chlorophenyl)-3-oxopropyl)(2,4-dimethoxybenzyl)carbamate
• CAS No.: 1396257-04-7
• Molecular Formula: C₃₂H₃₅ClN₂O₆
• Molecular Weight: 579.093
• Mol file: 1396257-04-7.mol

Synonyms:tert-butyl (S)-(3-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-(4-chlorophenyl)-3-oxopropyl)(2,4-dimethoxybenzyl)carbamate

Chemical Property of tert-butyl (S)-(3-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-(4-chlorophenyl)-3-oxopropyl)(2,4-dimethoxybenzyl)carbamate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of tert-butyl (S)-(3-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-(4-chlorophenyl)-3-oxopropyl)(2,4-dimethoxybenzyl)carbamate

There total 2 articles about tert-butyl (S)-(3-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-(4-chlorophenyl)-3-oxopropyl)(2,4-dimethoxybenzyl)carbamate 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: 66.0%

tert-butyl (4-methoxybenzyl)(methoxymethyl)carbamate (1396257-27-4) + (R)-4-benzyl-3-(2-(4-chlorophenyl)acetyl)oxazolidin-2-one (220041-96-3) → tert-butyl (S)-(3-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-(4-chlorophenyl)-3-oxopropyl)(2,4-dimethoxybenzyl)carbamate (1396257-04-7)

Guidance literature:

(R)-4-benzyl-3-(2-(4-chlorophenyl)acetyl)oxazolidin-2-one; With titanium tetrachloride; N-ethyl-N,N-diisopropylamine; In dichloromethane; toluene; at -78 ℃; for 0.333333h;

tert-butyl (4-methoxybenzyl)(methoxymethyl)carbamate; In dichloromethane; toluene; at -78 - -10 ℃; for 3.16667h;

DOI:10.1021/jm301024w

Reference yield:

(R)-4-(phenylmethyl)-2-oxazolidinone (40217-17-2,90719-32-7,120574-96-1,102029-44-7) → tert-butyl (S)-(3-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-(4-chlorophenyl)-3-oxopropyl)(2,4-dimethoxybenzyl)carbamate (1396257-04-7)

Guidance literature:

Multi-step reaction with 2 steps

1.1: n-butyllithium / tetrahydrofuran; toluene / 1 h / -78 - -20 °C

1.2: -78 - 20 °C

2.1: N-ethyl-N,N-diisopropylamine; titanium tetrachloride / dichloromethane; toluene / 0.25 h / -78 °C

2.2: 1.75 h / -78 - 20 °C

With n-butyllithium; titanium tetrachloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; toluene; 2.2: |Mannich Aminomethylation;

DOI:10.1021/jm301024w

Reference yield: 100.0%

tert-butyl (S)-(3-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-(4-chlorophenyl)-3-oxopropyl)(2,4-dimethoxybenzyl)carbamate (1396257-04-7) → tert-butyl (S)-(3-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-(4-chlorophenyl)-3-oxopropyl)carbamate (1001180-01-3)

Guidance literature:

With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane; water; at 20 ℃; for 19h;

DOI:10.1021/jm301024w

upstream raw materials:

tert-butyl (4-methoxybenzyl)(methoxymethyl)carbamate

(R)-4-benzyl-3-(2-(4-chlorophenyl)acetyl)oxazolidin-2-one

(R)-4-(phenylmethyl)-2-oxazolidinone

Downstream raw materials:

tert-butyl ((S)-2-(4-chlorophenyl)-3-(4-((5R,7R)-7-hydroxy-5-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)piperazin-1-yl)-3-oxopropyl)carbamate

tert-butyl (S)-(3-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-(4-chlorophenyl)-3-oxopropyl)carbamate