N-(Benzyloxycarbonyl)-L-alanyl-L-prolyl-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-O-(2-acetamido-4,6-di-O-benzoyl-2-desoxy-α-D-galactopyranosyl)>-L-threonyl-O-tert-butyl-L-seryl-O-tert-butyl-L-serin-tert-butylester

Base Information

• Chemical Name: N-(Benzyloxycarbonyl)-L-alanyl-L-prolyl-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-O-(2-acetamido-4,6-di-O-benzoyl-2-desoxy-α-D-galactopyranosyl)>-L-threonyl-O-tert-butyl-L-seryl-O-tert-butyl-L-serin-tert-butylester
• CAS No.: 120792-22-5
• Molecular Formula: C₇₄H₁₀₀N₆O₂₇
• Molecular Weight: 1505.63

Synonyms:

Chemical Property of N-(Benzyloxycarbonyl)-L-alanyl-L-prolyl-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-O-(2-acetamido-4,6-di-O-benzoyl-2-desoxy-α-D-galactopyranosyl)>-L-threonyl-O-tert-butyl-L-seryl-O-tert-butyl-L-serin-tert-butylester

Chemical Property:

Purity/Quality:

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Useful:

Technology Process of N-(Benzyloxycarbonyl)-L-alanyl-L-prolyl-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-O-(2-acetamido-4,6-di-O-benzoyl-2-desoxy-α-D-galactopyranosyl)>-L-threonyl-O-tert-butyl-L-seryl-O-tert-butyl-L-serin-tert-butylester

There total 1 articles about N-(Benzyloxycarbonyl)-L-alanyl-L-prolyl-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-O-(2-acetamido-4,6-di-O-benzoyl-2-desoxy-α-D-galactopyranosyl)>-L-threonyl-O-tert-butyl-L-seryl-O-tert-butyl-L-serin-tert-butylester 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:

H-Ser(But)-Ser(But)-OBut (120204-24-2) + C56H66N4O23 (120792-21-4) → N-(Benzyloxycarbonyl)-L-alanyl-L-prolyl-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-O-(2-acetamido-4,6-di-O-benzoyl-2-desoxy-α-D-galactopyranosyl)>-L-threonyl-O-tert-butyl-L-seryl-O-tert-butyl-L-serin-tert-butylester (120792-22-5)

Guidance literature:

With N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; In dichloromethane; for 18h; Yield given;

Reference yield:

N-(Benzyloxycarbonyl)-L-alanyl-L-prolyl-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-O-(2-acetamido-4,6-di-O-benzoyl-2-desoxy-α-D-galactopyranosyl)>-L-threonyl-O-tert-butyl-L-seryl-O-tert-butyl-L-serin-tert-butylester (120792-22-5) → L-Alanyl-L-prolyl-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-O-(2-acetamido-4,6-di-O-benzoyl-2-desoxy-α-D-galactopyranosyl)>-L-threonyl-L-seryl-L-serin (120792-23-6)

Guidance literature:

With formic acid; palladium; Yield given. Multistep reaction; 1.) room temp., 18 h;

upstream raw materials:

H-Ser(Bu^t)-Ser(Bu^t)-OBu^t

C₅₆H₆₆N₄O₂₃

Downstream raw materials:

L-Alanyl-L-prolyl-O-<(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1->3)-O-(2-acetamido-4,6-di-O-benzoyl-2-desoxy-α-D-galactopyranosyl)>-L-threonyl-L-seryl-L-serin

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