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

Base Information

• Chemical Name: 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
• CAS No.: 120792-23-6
• Molecular Formula: C₅₄H₇₀N₆O₂₅
• Molecular Weight: 1203.17

Synonyms:

Chemical Property of 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

Chemical Property:

Purity/Quality:

Safty Information:

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Useful:

Technology Process of 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

There total 1 articles about 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 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:

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;

Reference yield: 29.0%

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) → L-Alanyl-L-prolyl-O-<(β-D-galactopyranosyl)-(1->3)-O-(2-acetamido-2-desoxy-α-D-galactopyranosyl)>-L-threonyl-L-seryl-L-serin (120792-30-5)

Guidance literature:

With sodium methylate; In methanol; for 5h;

upstream raw materials:

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

Downstream raw materials:

L-Alanyl-L-prolyl-O-<(β-D-galactopyranosyl)-(1->3)-O-(2-acetamido-2-desoxy-α-D-galactopyranosyl)>-L-threonyl-L-seryl-L-serin

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