N-tert-butoxycarbonyl-L-tryptophyl-L-leucyl-β-benzyl-L-asparaginic acid α-amide

Base Information

Chemical Name:N-tert-butoxycarbonyl-L-tryptophyl-L-leucyl-β-benzyl-L-asparaginic acid α-amide
CAS No.:94236-38-1
Molecular Formula:C₃₃H₄₃N₅O₇
Molecular Weight:621.734
Hs Code.:

Synonyms:N-tert-butoxycarbonyl-L-tryptophyl-L-leucyl-β-benzyl-L-asparaginic acid α-amide

Suppliers and Price of N-tert-butoxycarbonyl-L-tryptophyl-L-leucyl-β-benzyl-L-asparaginic acid α-amide

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

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Total 3 raw suppliers

Chemical Property of N-tert-butoxycarbonyl-L-tryptophyl-L-leucyl-β-benzyl-L-asparaginic acid α-amide

Chemical Property:

Purity/Quality:

Safty Information:

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Technology Process of N-tert-butoxycarbonyl-L-tryptophyl-L-leucyl-β-benzyl-L-asparaginic acid α-amide

There total 1 articles about N-tert-butoxycarbonyl-L-tryptophyl-L-leucyl-β-benzyl-L-asparaginic acid α-amide 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:

: 3392-11-8
2,5-dioxopyrrolidin-1-yl N-(tert-butoxycarbonyl)-L-tryptophanate

: 129280-61-1
L-leucyl-β-benzyl-L-asparaginic acid α-amide trifluoroacetate

: 94236-38-1
N-tert-butoxycarbonyl-L-tryptophyl-L-leucyl-β-benzyl-L-asparaginic acid α-amide

Guidance literature:: With triethylamine; Yield given. Multistep reaction; 1.) DMF, 20 deg C, 20 min, 2.) a) 0 deg C, 1 h, b) 20 deg C, 1 d;
DOI:10.1007/BF00766860

Reference yield: 100.0%

: 94236-38-1
N-tert-butoxycarbonyl-L-tryptophyl-L-leucyl-β-benzyl-L-asparaginic acid α-amide

: L-tryptophyl-L-leucyl-β-benzyl-L-asparaginic acid α-amide hydrochloride

Guidance literature:: With hydrogenchloride; methoxybenzene; In 1,4-dioxane; at 20 ℃; for 2h;
DOI:10.1007/BF00766860

Reference yield:

: 94236-38-1
N-tert-butoxycarbonyl-L-tryptophyl-L-leucyl-β-benzyl-L-asparaginic acid α-amide

: 129280-53-1
N^γ-tert-butoxycarbonylaminobutyryl-L-tryptophyl-L-leucyl-β-benzyl-L-asparaginic acid α-amide

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / 6.3 N HCl, anisole / dioxane / 2 h / 20 °C

2: 1.) Et₃N / 1.) DMF, 20 deg C, 20 min, 2.) a) 0 deg C, 1 h, b) 20 deg C, 1 d

With hydrogenchloride; methoxybenzene; triethylamine; In 1,4-dioxane;
DOI:10.1007/BF00766860