(S)-2-[3-(2,4-Difluoro-phenyl)-1-(2-nitro-benzyl)-ureido]-propionic acid

Base Information

Chemical Name:(S)-2-[3-(2,4-Difluoro-phenyl)-1-(2-nitro-benzyl)-ureido]-propionic acid
CAS No.:351527-54-3
Molecular Formula:C₁₇H₁₅F₂N₃O₅
Molecular Weight:379.32
Hs Code.:

Synonyms:(S)-2-[3-(2,4-Difluoro-phenyl)-1-(2-nitro-benzyl)-ureido]-propionic acid

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S)-2-[3-(2,4-Difluoro-phenyl)-1-(2-nitro-benzyl)-ureido]-propionic acid

Chemical Property:

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Technology Process of (S)-2-[3-(2,4-Difluoro-phenyl)-1-(2-nitro-benzyl)-ureido]-propionic acid

There total 2 articles about (S)-2-[3-(2,4-Difluoro-phenyl)-1-(2-nitro-benzyl)-ureido]-propionic acid 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:

: 612-23-7
2-nitrobenzyl chloride

: 351527-54-3
(S)-2-[3-(2,4-Difluoro-phenyl)-1-(2-nitro-benzyl)-ureido]-propionic acid

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / acetonitrile / 10 h / 20 °C

2: Et₃N / acetone / Heating

With triethylamine; In acetone; acetonitrile;
DOI:10.1021/jm010087e

Reference yield:

: 59025-55-7
2,4-diflurophenylisocyanate

: 351526-76-6
N-2-nitrobenzyl-L-alanine

: 351527-54-3
(S)-2-[3-(2,4-Difluoro-phenyl)-1-(2-nitro-benzyl)-ureido]-propionic acid

Guidance literature:: With triethylamine; In acetone; Heating;
DOI:10.1021/jm010087e

Reference yield:

: 351527-54-3
(S)-2-[3-(2,4-Difluoro-phenyl)-1-(2-nitro-benzyl)-ureido]-propionic acid

: 2-[3-(2,4-difluoro-phenyl)-1-(2-nitro-benzyl)-ureido]-N-hydroxy-propionamide

Guidance literature:: With hydroxylamine hydrochloride; triethylamine; diisopropyl-carbodiimide; In acetonitrile; at 4 ℃; for 12h;
DOI:10.1021/jm010087e