(R)-2-(4-Fluoro-benzenesulfonylamino)-3-methyl-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester

Base Information

Chemical Name:(R)-2-(4-Fluoro-benzenesulfonylamino)-3-methyl-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester
CAS No.:190275-61-7
Molecular Formula:C₁₅H₁₇FN₂O₆S
Molecular Weight:372.374
Hs Code.:

Synonyms:(R)-2-(4-Fluoro-benzenesulfonylamino)-3-methyl-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester

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Chemical Property of (R)-2-(4-Fluoro-benzenesulfonylamino)-3-methyl-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester

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Technology Process of (R)-2-(4-Fluoro-benzenesulfonylamino)-3-methyl-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester

There total 3 articles about (R)-2-(4-Fluoro-benzenesulfonylamino)-3-methyl-butyric acid 2,5-dioxo-pyrrolidin-1-yl 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:

: 6066-82-6
1-hydroxy-pyrrolidine-2,5-dione

: 190275-60-6
N-(4-fluorophenylsulfonyl)-D-valine

: 190275-61-7
(R)-2-(4-Fluoro-benzenesulfonylamino)-3-methyl-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester

Guidance literature:: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; dichloromethane; at 20 ℃; for 4h;
DOI:10.1021/jm0201924

Reference yield:

: 640-68-6,25609-85-2,7004-03-7,921-10-8
D-Val-OH

: 190275-61-7
(R)-2-(4-Fluoro-benzenesulfonylamino)-3-methyl-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaOH / tetrahydrofuran / 18 h / 20 °C

2: 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride / tetrahydrofuran; CH₂Cl₂ / 4 h / 20 °C

With sodium hydroxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; dichloromethane; 1: Schotten-Baumann reaction;
DOI:10.1021/jm0201924

Reference yield:

: 349-88-2
4-Fluorobenzenesulfonyl chloride

: 190275-61-7
(R)-2-(4-Fluoro-benzenesulfonylamino)-3-methyl-butyric acid 2,5-dioxo-pyrrolidin-1-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaOH / tetrahydrofuran / 18 h / 20 °C

2: 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride / tetrahydrofuran; CH₂Cl₂ / 4 h / 20 °C

With sodium hydroxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; dichloromethane; 1: Schotten-Baumann reaction;
DOI:10.1021/jm0201924