tert-butyl ((S)-1-((S)-3-(4-methylbenzyl)-2-oxooxazolidine-4-carbonyl)piperidin-3-yl)methylcarbamate

Base Information

Chemical Name:tert-butyl ((S)-1-((S)-3-(4-methylbenzyl)-2-oxooxazolidine-4-carbonyl)piperidin-3-yl)methylcarbamate
CAS No.:1615250-02-6
Molecular Formula:C₂₃H₃₃N₃O₅
Molecular Weight:431.532
Hs Code.:

Synonyms:tert-butyl ((S)-1-((S)-3-(4-methylbenzyl)-2-oxooxazolidine-4-carbonyl)piperidin-3-yl)methylcarbamate

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Chemical Property of tert-butyl ((S)-1-((S)-3-(4-methylbenzyl)-2-oxooxazolidine-4-carbonyl)piperidin-3-yl)methylcarbamate

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Technology Process of tert-butyl ((S)-1-((S)-3-(4-methylbenzyl)-2-oxooxazolidine-4-carbonyl)piperidin-3-yl)methylcarbamate

There total 3 articles about tert-butyl ((S)-1-((S)-3-(4-methylbenzyl)-2-oxooxazolidine-4-carbonyl)piperidin-3-yl)methylcarbamate 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: 75.0%

: 879275-33-9
(R)-1-piperidin-3-ylmethyl-carbamic acid tert-butyl ester

: 1629057-56-2
(S)-3-(4-methylbenzyl)-2-oxooxazolidine-4-carboxylic acid

: 1615250-02-6
tert-butyl ((S)-1-((S)-3-(4-methylbenzyl)-2-oxooxazolidine-4-carbonyl)piperidin-3-yl)methylcarbamate

Guidance literature:: With benzotriazol-1-ol; dicyclohexyl-carbodiimide; In dichloromethane;
DOI:10.1016/j.ejmech.2014.05.017

Reference yield:

: 104-81-4
4-Methylbenzyl bromide

: 1615250-02-6
tert-butyl ((S)-1-((S)-3-(4-methylbenzyl)-2-oxooxazolidine-4-carbonyl)piperidin-3-yl)methylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -20 °C / Inert atmosphere

1.2: 4 h / 0 - 20 °C / Inert atmosphere

2.1: sodium carbonate; water / methanol / 5 h / 0 - 20 °C

3.1: benzotriazol-1-ol; dicyclohexyl-carbodiimide / dichloromethane

With water; sodium carbonate; benzotriazol-1-ol; dicyclohexyl-carbodiimide; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1016/j.ejmech.2014.05.017

Reference yield:

: C₁₃H₁₅NO₄

: 1615250-02-6
tert-butyl ((S)-1-((S)-3-(4-methylbenzyl)-2-oxooxazolidine-4-carbonyl)piperidin-3-yl)methylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: sodium carbonate; water / methanol / 5 h / 0 - 20 °C

2: benzotriazol-1-ol; dicyclohexyl-carbodiimide / dichloromethane

With water; sodium carbonate; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In methanol; dichloromethane;
DOI:10.1016/j.ejmech.2014.05.017