(3S)-3-(4-fluoro-3-nitrophenyl)-2-<(2R)-2-(4-hydroxy-phenyl)-2-<2-(3-hydroxyphenyl)-acetylamino>acetylamino>-propionic acid methyl ester

Base Information

Chemical Name:(3S)-3-(4-fluoro-3-nitrophenyl)-2-<(2R)-2-(4-hydroxy-phenyl)-2-<2-(3-hydroxyphenyl)-acetylamino>acetylamino>-propionic acid methyl ester
CAS No.:199486-35-6
Molecular Formula:C₂₆H₂₄FN₃O₈
Molecular Weight:525.49
Hs Code.:

Synonyms:(3S)-3-(4-fluoro-3-nitrophenyl)-2-<(2R)-2-(4-hydroxy-phenyl)-2-<2-(3-hydroxyphenyl)-acetylamino>acetylamino>-propionic acid methyl ester

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Chemical Property of (3S)-3-(4-fluoro-3-nitrophenyl)-2-<(2R)-2-(4-hydroxy-phenyl)-2-<2-(3-hydroxyphenyl)-acetylamino>acetylamino>-propionic acid methyl ester

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Technology Process of (3S)-3-(4-fluoro-3-nitrophenyl)-2-<(2R)-2-(4-hydroxy-phenyl)-2-<2-(3-hydroxyphenyl)-acetylamino>acetylamino>-propionic acid methyl ester

There total 8 articles about (3S)-3-(4-fluoro-3-nitrophenyl)-2-<(2R)-2-(4-hydroxy-phenyl)-2-<2-(3-hydroxyphenyl)-acetylamino>acetylamino>-propionic acid methyl 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: 89.0%

: 621-37-4
m-hydroxyphenylacetic acid

: (S)-2-[(R)-2-Amino-2-(4-hydroxy-phenyl)-acetylamino]-3-(4-fluoro-3-nitro-phenyl)-propionic acid methyl ester

: 199486-35-6
(3S)-3-(4-fluoro-3-nitrophenyl)-2-<(2R)-2-(4-hydroxy-phenyl)-2-<2-(3-hydroxyphenyl)-acetylamino>acetylamino>-propionic acid methyl ester

Guidance literature:: With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; In dichloromethane;
DOI:10.1016/S0040-4039(97)10217-9

Reference yield:

: 27460-85-1
N-(tert-butoxycarbonyl)-D-(4-hydroxyphenyl)glycine

: 199486-35-6
(3S)-3-(4-fluoro-3-nitrophenyl)-2-<(2R)-2-(4-hydroxy-phenyl)-2-<2-(3-hydroxyphenyl)-acetylamino>acetylamino>-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 77 percent / EDC, HOBt, NEt₃ / CH₂Cl₂

2: TFA / CH₂Cl₂

3: 89 percent / EDC, HOBt, NEt₃ / CH₂Cl₂

With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; trifluoroacetic acid; In dichloromethane;
DOI:10.1016/S0040-4039(97)10217-9

Reference yield:

: 15017-52-4
4-(bromomethyl)-1-fluoro-2-nitrobenzene

: 199486-35-6
(3S)-3-(4-fluoro-3-nitrophenyl)-2-<(2R)-2-(4-hydroxy-phenyl)-2-<2-(3-hydroxyphenyl)-acetylamino>acetylamino>-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) NaH; 2.) HCl / dimethylformamide

2: 1.) SOCl₂; 2.) NEt₃ / 2.) CH₂Cl₂

3: 1.) protease type VIII-A from Bacillus licheniformis; 2.) SOCl₂ / 1.) phosphate buffer pH 7.5, CH₂Cl₂; 2.) MeOH, 0 deg C

4: 77 percent / EDC, HOBt, NEt₃ / CH₂Cl₂

5: TFA / CH₂Cl₂

6: 89 percent / EDC, HOBt, NEt₃ / CH₂Cl₂

With hydrogenchloride; thionyl chloride; protease type VIII-A from Bacillus licheniformis; sodium hydride; benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(97)10217-9