S-[(benzyloxy)carbonyl]-L-alanyl-L-phenylalanyl-N-[(benzyloxy)carbonyl]-L-phenylalanylglycyl-L-cysteine

Base Information

Chemical Name:S-[(benzyloxy)carbonyl]-L-alanyl-L-phenylalanyl-N-[(benzyloxy)carbonyl]-L-phenylalanylglycyl-L-cysteine
CAS No.:1621538-70-2
Molecular Formula:C₄₂H₄₅N₅O₁₀S
Molecular Weight:811.913
Hs Code.:

Synonyms:S-[(benzyloxy)carbonyl]-L-alanyl-L-phenylalanyl-N-[(benzyloxy)carbonyl]-L-phenylalanylglycyl-L-cysteine

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Chemical Property of S-[(benzyloxy)carbonyl]-L-alanyl-L-phenylalanyl-N-[(benzyloxy)carbonyl]-L-phenylalanylglycyl-L-cysteine

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Technology Process of S-[(benzyloxy)carbonyl]-L-alanyl-L-phenylalanyl-N-[(benzyloxy)carbonyl]-L-phenylalanylglycyl-L-cysteine

There total 2 articles about S-[(benzyloxy)carbonyl]-L-alanyl-L-phenylalanyl-N-[(benzyloxy)carbonyl]-L-phenylalanylglycyl-L-cysteine 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: 98.0%

: 1621538-60-0
[(benzyloxy)carbonyl]-L-phenylalanylglycyl-L-cysteine

: 820239-47-2
benzyl ((S)-1-(((S)-1-(1H-benzo[d][1,2,3]triazol-1-yl)-1-oxo-3-phenylpropan-2-yl)amino)-1-oxopropan-2-yl)carbamate

: 1621538-70-2
S-[(benzyloxy)carbonyl]-L-alanyl-L-phenylalanyl-N-[(benzyloxy)carbonyl]-L-phenylalanylglycyl-L-cysteine

Guidance literature:: With potassium hydrogencarbonate; In water; acetonitrile; at 0 - 10 ℃;
DOI:10.1055/s-0033-1340089

Reference yield:

: 1286678-64-5
(S)-benzyl (1-((2-(1H-benzo[d][1,2,3]triazol-1-yl)-2-oxoethyl)amino)-1-oxo-3-phenyl-propan-2-yl)carbamate

: 1621538-70-2
S-[(benzyloxy)carbonyl]-L-alanyl-L-phenylalanyl-N-[(benzyloxy)carbonyl]-L-phenylalanylglycyl-L-cysteine

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / acetonitrile; water / 4 h / 0 °C

2: potassium hydrogencarbonate / acetonitrile; water / 0 - 10 °C

With potassium hydrogencarbonate; triethylamine; In water; acetonitrile;
DOI:10.1055/s-0033-1340089