benzyloxycarbonyl-γ-L-glutamyl-(glycine benzyl ester)-α-L-leucine benzyl ester

Base Information

Chemical Name:benzyloxycarbonyl-γ-L-glutamyl-(glycine benzyl ester)-α-L-leucine benzyl ester
CAS No.:78578-01-5
Molecular Formula:C₃₅H₄₁N₃O₈
Molecular Weight:631.726
Hs Code.:

Synonyms:benzyloxycarbonyl-γ-L-glutamyl-(glycine benzyl ester)-α-L-leucine benzyl ester

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Chemical Property of benzyloxycarbonyl-γ-L-glutamyl-(glycine benzyl ester)-α-L-leucine benzyl ester

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Technology Process of benzyloxycarbonyl-γ-L-glutamyl-(glycine benzyl ester)-α-L-leucine benzyl ester

There total 4 articles about benzyloxycarbonyl-γ-L-glutamyl-(glycine benzyl ester)-α-L-leucine benzyl 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: 88.0%

: 1738-69-8
L-Leucine benzyl ester

: 78578-00-4
benzyloxycarbonyl-γ-L-glutamyl-(glycine benzyl ester) α-p-nitrophenyl ester

: 78578-01-5
benzyloxycarbonyl-γ-L-glutamyl-(glycine benzyl ester)-α-L-leucine benzyl ester

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

Reference yield:

: 1738-68-7
Gly-OBz

: 78578-01-5
benzyloxycarbonyl-γ-L-glutamyl-(glycine benzyl ester)-α-L-leucine benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

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

2: 88 percent / Et₃N / dimethylformamide

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

Reference yield:

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

: 78578-01-5
benzyloxycarbonyl-γ-L-glutamyl-(glycine benzyl ester)-α-L-leucine benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

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

2: 88 percent / Et₃N / dimethylformamide

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