(2R,4S)-tert-butyl 4-((4-((2-(allyloxy)pyrimidin-4-yl)carbamoyl)phenyl)carbamoyl)-2-(tert-butyl)-4-methyloxazolidine-3-carboxylate

Base Information

Chemical Name:(2R,4S)-tert-butyl 4-((4-((2-(allyloxy)pyrimidin-4-yl)carbamoyl)phenyl)carbamoyl)-2-(tert-butyl)-4-methyloxazolidine-3-carboxylate
CAS No.:1333077-66-9
Molecular Formula:C₂₈H₃₇N₅O₆
Molecular Weight:539.632
Hs Code.:

Synonyms:(2R,4S)-tert-butyl 4-((4-((2-(allyloxy)pyrimidin-4-yl)carbamoyl)phenyl)carbamoyl)-2-(tert-butyl)-4-methyloxazolidine-3-carboxylate

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Chemical Property of (2R,4S)-tert-butyl 4-((4-((2-(allyloxy)pyrimidin-4-yl)carbamoyl)phenyl)carbamoyl)-2-(tert-butyl)-4-methyloxazolidine-3-carboxylate

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Technology Process of (2R,4S)-tert-butyl 4-((4-((2-(allyloxy)pyrimidin-4-yl)carbamoyl)phenyl)carbamoyl)-2-(tert-butyl)-4-methyloxazolidine-3-carboxylate

There total 6 articles about (2R,4S)-tert-butyl 4-((4-((2-(allyloxy)pyrimidin-4-yl)carbamoyl)phenyl)carbamoyl)-2-(tert-butyl)-4-methyloxazolidine-3-carboxylate 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: 92.0%

: 1333077-64-7
tert-butyl (2R, 4S)-2-(tert-butyl)-4-carbamoyl-4-methyl-4-methyloxazolidine-3-carboxylate

: 1333077-65-8
N-(2-(allyloxy)pyrimidin-4-yl)-4-iodobenzamide

: 1333077-66-9
(2R,4S)-tert-butyl 4-((4-((2-(allyloxy)pyrimidin-4-yl)carbamoyl)phenyl)carbamoyl)-2-(tert-butyl)-4-methyloxazolidine-3-carboxylate

Guidance literature:: With copper(l) iodide; potassium carbonate; N,N`-dimethylethylenediamine; In 1,4-dioxane; at 100 ℃; for 60h; Inert atmosphere;
DOI:10.1021/ol2018196

Reference yield:

: 1179522-58-7,1686957-60-7
(2R,4S)-2-tert-butyl-3-tert-butoxycarbonyl-4-methyl-1,3-oxazolidine-4-carboxylic acid

: 1333077-66-9
(2R,4S)-tert-butyl 4-((4-((2-(allyloxy)pyrimidin-4-yl)carbamoyl)phenyl)carbamoyl)-2-(tert-butyl)-4-methyloxazolidine-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: oxalyl dichloride; triethylamine / dichloromethane; N,N-dimethyl-formamide / 2 h / 0 - 20 °C / Inert atmosphere

1.2: 6 h / 20 °C / Inert atmosphere

2.1: copper(l) iodide; potassium carbonate; N,N`-dimethylethylenediamine / 1,4-dioxane / 60 h / 100 °C / Inert atmosphere

With copper(l) iodide; oxalyl dichloride; potassium carbonate; triethylamine; N,N`-dimethylethylenediamine; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ol2018196

Reference yield:

: (2S,4S)-3-tert-butyl 4-methyl 2-tert-butyl-4-methyl-1,3-oxazolidine-3,4-dicarboxylate

: 1333077-66-9
(2R,4S)-tert-butyl 4-((4-((2-(allyloxy)pyrimidin-4-yl)carbamoyl)phenyl)carbamoyl)-2-(tert-butyl)-4-methyloxazolidine-3-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogenchloride; lithium hydroxide monohydrate / tetrahydrofuran; water / 36 h / 50 °C / Inert atmosphere

2.1: oxalyl dichloride; triethylamine / dichloromethane; N,N-dimethyl-formamide / 2 h / 0 - 20 °C / Inert atmosphere

2.2: 6 h / 20 °C / Inert atmosphere

3.1: copper(l) iodide; potassium carbonate; N,N`-dimethylethylenediamine / 1,4-dioxane / 60 h / 100 °C / Inert atmosphere

With hydrogenchloride; copper(l) iodide; oxalyl dichloride; lithium hydroxide monohydrate; potassium carbonate; triethylamine; N,N`-dimethylethylenediamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1021/ol2018196