benzyloxycarbonyl-γ-L-glutamyl-(glycyl-L-alanine 2,4,6-trimethylbenzyl ester)-α-L-alanine 2,4,6-trimethylbenzyl ester

Base Information

Chemical Name:benzyloxycarbonyl-γ-L-glutamyl-(glycyl-L-alanine 2,4,6-trimethylbenzyl ester)-α-L-alanine 2,4,6-trimethylbenzyl ester
CAS No.:78596-96-0
Molecular Formula:C₄₁H₅₂N₄O₉
Molecular Weight:744.885
Hs Code.:

Synonyms:benzyloxycarbonyl-γ-L-glutamyl-(glycyl-L-alanine 2,4,6-trimethylbenzyl ester)-α-L-alanine 2,4,6-trimethylbenzyl ester

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Chemical Property of benzyloxycarbonyl-γ-L-glutamyl-(glycyl-L-alanine 2,4,6-trimethylbenzyl ester)-α-L-alanine 2,4,6-trimethylbenzyl ester

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Technology Process of benzyloxycarbonyl-γ-L-glutamyl-(glycyl-L-alanine 2,4,6-trimethylbenzyl ester)-α-L-alanine 2,4,6-trimethylbenzyl ester

There total 3 articles about benzyloxycarbonyl-γ-L-glutamyl-(glycyl-L-alanine 2,4,6-trimethylbenzyl ester)-α-L-alanine 2,4,6-trimethylbenzyl 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: 93.0%

: (S)-2-Amino-propionic acid 2,4,6-trimethyl-benzyl ester; hydrochloride

: 78578-05-9
benzyloxycarbonyl-γ-L-glutamyl-(glycine p-nitrophenyl ester) α-p-nitrophenyl ester

: 78596-96-0
benzyloxycarbonyl-γ-L-glutamyl-(glycyl-L-alanine 2,4,6-trimethylbenzyl ester)-α-L-alanine 2,4,6-trimethylbenzyl ester

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide;

Reference yield:

: 25126-09-4
benzyloxycarbonyl-L-glutamic acid α-p-nitrophenyl ester

: 78596-96-0
benzyloxycarbonyl-γ-L-glutamyl-(glycyl-L-alanine 2,4,6-trimethylbenzyl ester)-α-L-alanine 2,4,6-trimethylbenzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) N-methylmorpholine, isobutyl chloroformate / 1.) acetonitrile, -15 deg C

2: 93 percent / Et₃N / dimethylformamide

With 4-methyl-morpholine; triethylamine; isobutyl chloroformate; In N,N-dimethyl-formamide;

Reference yield:

: benzyloxycarbonyl-L-glutamic acid α-p-nitrophenyl γ-2,4,6-trimethylbenzylester

: 78596-96-0
benzyloxycarbonyl-γ-L-glutamyl-(glycyl-L-alanine 2,4,6-trimethylbenzyl ester)-α-L-alanine 2,4,6-trimethylbenzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / trifluoroacetic acid, anisole / 1 h / Ambient temperature

2: 1.) N-methylmorpholine, isobutyl chloroformate / 1.) acetonitrile, -15 deg C

3: 93 percent / Et₃N / dimethylformamide

With 4-methyl-morpholine; methoxybenzene; triethylamine; trifluoroacetic acid; isobutyl chloroformate; In N,N-dimethyl-formamide;