N-benzyloxycarbonyl-γ,γ-di-tert-butyl-L-γ-carboxyglutamyl-γ-tert-butyl-L-glutamylleucine methyl ester

Base Information

Chemical Name:N-benzyloxycarbonyl-γ,γ-di-tert-butyl-L-γ-carboxyglutamyl-γ-tert-butyl-L-glutamylleucine methyl ester
CAS No.:74193-67-2
Molecular Formula:C₃₈H₅₉N₃O₁₂
Molecular Weight:749.899
Hs Code.:

Synonyms:N-benzyloxycarbonyl-γ,γ-di-tert-butyl-L-γ-carboxyglutamyl-γ-tert-butyl-L-glutamylleucine methyl ester

Suppliers and Price of N-benzyloxycarbonyl-γ,γ-di-tert-butyl-L-γ-carboxyglutamyl-γ-tert-butyl-L-glutamylleucine methyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of N-benzyloxycarbonyl-γ,γ-di-tert-butyl-L-γ-carboxyglutamyl-γ-tert-butyl-L-glutamylleucine methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-benzyloxycarbonyl-γ,γ-di-tert-butyl-L-γ-carboxyglutamyl-γ-tert-butyl-L-glutamylleucine methyl ester

There total 3 articles about N-benzyloxycarbonyl-γ,γ-di-tert-butyl-L-γ-carboxyglutamyl-γ-tert-butyl-L-glutamylleucine 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:

: 7517-19-3
methyl (L)-leucinate hydrochloride

: 74193-67-2
N-benzyloxycarbonyl-γ,γ-di-tert-butyl-L-γ-carboxyglutamyl-γ-tert-butyl-L-glutamylleucine methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / 1-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 4 °C

2: 1.) H₂, 2.) 1-hydroxybenzotriazole, dicyclohexylcarbodiimide / 1.) 10percent palladium/carbon / 1.) acetonitrile, room temperature, 2.) 4 deg C

With hydrogen; benzotriazol-1-ol; dicyclohexyl-carbodiimide; palladium on activated charcoal; In N,N-dimethyl-formamide;
DOI:10.1021/ja00530a017

Reference yield:

: 3967-21-3
N-benzyloxycarbonyl-γ-tert-butyl-L-glutamic acid dicyclohexylamine salt

: 74193-67-2
N-benzyloxycarbonyl-γ,γ-di-tert-butyl-L-γ-carboxyglutamyl-γ-tert-butyl-L-glutamylleucine methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / 1-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 4 °C

2: 1.) H₂, 2.) 1-hydroxybenzotriazole, dicyclohexylcarbodiimide / 1.) 10percent palladium/carbon / 1.) acetonitrile, room temperature, 2.) 4 deg C

With hydrogen; benzotriazol-1-ol; dicyclohexyl-carbodiimide; palladium on activated charcoal; In N,N-dimethyl-formamide;
DOI:10.1021/ja00530a017

Reference yield:

: 60686-50-2,60686-52-4
N-(benzyloxycarbonyl)-γ,γ-di-tert-butyl-L-γ-carboxyglutamic acid

: 24181-32-6
N-benzyloxycarbonyl-γ-tert-butyl-L-glutamyl-L-leucine methyl ester

: 74193-67-2
N-benzyloxycarbonyl-γ,γ-di-tert-butyl-L-γ-carboxyglutamyl-γ-tert-butyl-L-glutamylleucine methyl ester

Guidance literature:: With hydrogen; benzotriazol-1-ol; dicyclohexyl-carbodiimide; palladium on activated charcoal; Yield given. Multistep reaction; 1.) acetonitrile, room temperature, 2.) 4 deg C;
DOI:10.1021/ja00530a017