(S)-2-[2-(carboxymethyl-phenethyl-amino)-acetylamino]-3-(1H-imidazol-4-yl)-propionic acid methyl ester

Base Information

Chemical Name:(S)-2-[2-(carboxymethyl-phenethyl-amino)-acetylamino]-3-(1H-imidazol-4-yl)-propionic acid methyl ester
CAS No.:1333226-77-9
Molecular Formula:C₁₉H₂₄N₄O₅
Molecular Weight:388.423
Hs Code.:

Synonyms:(S)-2-[2-(carboxymethyl-phenethyl-amino)-acetylamino]-3-(1H-imidazol-4-yl)-propionic acid methyl ester

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Chemical Property of (S)-2-[2-(carboxymethyl-phenethyl-amino)-acetylamino]-3-(1H-imidazol-4-yl)-propionic acid methyl ester

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Technology Process of (S)-2-[2-(carboxymethyl-phenethyl-amino)-acetylamino]-3-(1H-imidazol-4-yl)-propionic acid methyl ester

There total 3 articles about (S)-2-[2-(carboxymethyl-phenethyl-amino)-acetylamino]-3-(1H-imidazol-4-yl)-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: 52.0%

: 36369-62-7
(carboxymethyl-phenethyl-amino)-acetic acid

: 4467-54-3,5619-10-3,7389-87-9,18684-16-7,22888-60-4,32381-17-2,92742-29-5,100009-20-9
l-histidine methyl ester dihydrochloride

: 1333226-77-9
(S)-2-[2-(carboxymethyl-phenethyl-amino)-acetylamino]-3-(1H-imidazol-4-yl)-propionic acid methyl ester

Guidance literature:: (carboxymethyl-phenethyl-amino)-acetic acid; With acetic anhydride; trifluoroacetic acid; at 40 ℃; for 4h;

l-histidine methyl ester dihydrochloride; With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃; Inert atmosphere;
DOI:10.1016/j.ejmech.2014.04.009

Reference yield:

: 1609485-75-7
C₃₈H₃₈N₄O₅

: 1333226-77-9
(S)-2-[2-(carboxymethyl-phenethyl-amino)-acetylamino]-3-(1H-imidazol-4-yl)-propionic acid methyl ester

Guidance literature:: With chlorotriisopropylsilane; trifluoroacetic acid; at 20 ℃; for 1h;
DOI:10.1016/j.ejmech.2014.04.009

Reference yield:

: 103-63-9
1-phenyl-2-bromoethane

: 1333226-77-9
(S)-2-[2-(carboxymethyl-phenethyl-amino)-acetylamino]-3-(1H-imidazol-4-yl)-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium hydroxide / methanol / Reflux

2.1: trifluoroacetic acid; acetic anhydride / 4 h / 40 °C

2.2: 20 °C / Inert atmosphere

With acetic anhydride; trifluoroacetic acid; potassium hydroxide; In methanol;
DOI:10.1016/j.ejmech.2014.04.009