N-({(1S)-1-[(benzyloxy)carbonyl]ethyl}aminocarbonyl)-L-phenylalanine methyl ester

Base Information

Chemical Name:N-({(1S)-1-[(benzyloxy)carbonyl]ethyl}aminocarbonyl)-L-phenylalanine methyl ester
CAS No.:1027200-09-4
Molecular Formula:C₂₁H₂₄N₂O₅
Molecular Weight:384.432
Hs Code.:

Synonyms:N-({(1S)-1-[(benzyloxy)carbonyl]ethyl}aminocarbonyl)-L-phenylalanine methyl ester

Suppliers and Price of N-({(1S)-1-[(benzyloxy)carbonyl]ethyl}aminocarbonyl)-L-phenylalanine 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-({(1S)-1-[(benzyloxy)carbonyl]ethyl}aminocarbonyl)-L-phenylalanine methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-({(1S)-1-[(benzyloxy)carbonyl]ethyl}aminocarbonyl)-L-phenylalanine methyl ester

There total 2 articles about N-({(1S)-1-[(benzyloxy)carbonyl]ethyl}aminocarbonyl)-L-phenylalanine 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: 78.0%

: 124-38-9,18923-20-1
carbon dioxide

: 2577-90-4
methyl (2S)-2-amino-3-phenylpropanoate

: 42854-62-6
L-alanine benzyl ester p-toluenesulfonate

: 1027200-09-4
N-({(1S)-1-[(benzyloxy)carbonyl]ethyl}aminocarbonyl)-L-phenylalanine methyl ester

Guidance literature:: carbon dioxide; L-alanine benzyl ester p-toluenesulfonate; With pyridine; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at -20 ℃; for 0.5h;

With thionyl chloride; In dichloromethane; at -20 - 20 ℃; for 2h; Inert atmosphere;

methyl (2S)-2-amino-3-phenylpropanoate; With pyridine; at 20 ℃; for 4h; Inert atmosphere;
DOI:10.1002/ejoc.201500589

Reference yield:

: 42854-62-6
L-alanine benzyl ester p-toluenesulfonate

: 7524-50-7
methyl (2S)-2-amino-3-phenylpropanoate hydrochloride

: 530-62-1
1,1'-carbonyldiimidazole

: 1027200-09-4
N-({(1S)-1-[(benzyloxy)carbonyl]ethyl}aminocarbonyl)-L-phenylalanine methyl ester

Guidance literature:: With 4-methyl-morpholine; Yield given. Multistep reaction; 1) CH₂Cl₂, 5 min; 2) CH₂Cl₂, rt, overnight;
DOI:10.1021/jo970514p