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

Base Information

Chemical Name:(S)-2-[2-(benzyl-carboxymethyl-amino)-acetylamino]-3-(1H-imidazol-4-yl)-propionic acid methyl ester
CAS No.:1333226-73-5
Molecular Formula:C₁₈H₂₂N₄O₅
Molecular Weight:374.396
Hs Code.:

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

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

Chemical Property:

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

There total 6 articles about (S)-2-[2-(benzyl-carboxymethyl-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:

: 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

: 67305-69-5
N-benzyliminodiacetic anhydride acid

: 1333226-73-5
(S)-2-[2-(benzyl-carboxymethyl-amino)-acetylamino]-3-(1H-imidazol-4-yl)-propionic acid methyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/j.ejmech.2014.04.009

Reference yield:

: 3987-53-9
N-benzyliminodiacetic acid

: 1333226-73-5
(S)-2-[2-(benzyl-carboxymethyl-amino)-acetylamino]-3-(1H-imidazol-4-yl)-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: acetic anhydride; trifluoroacetic anhydride / 5 h / 20 - 70 °C

2: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide; tetrahydrofuran / 20 °C

With acetic anhydride; N-ethyl-N,N-diisopropylamine; trifluoroacetic anhydride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2014.04.009

Reference yield:

: 100-39-0
benzyl bromide

: 1333226-73-5
(S)-2-[2-(benzyl-carboxymethyl-amino)-acetylamino]-3-(1H-imidazol-4-yl)-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: methanol / 20 °C

2: acetic anhydride; trifluoroacetic anhydride / 5 h / 20 - 70 °C

3: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide; tetrahydrofuran / 20 °C

With acetic anhydride; N-ethyl-N,N-diisopropylamine; trifluoroacetic anhydride; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2014.04.009