2-(N-benzyloxycarbonyl)-aminoethyl (methyl 2,3-di-O-benzyl-α-D-glucopyranosyluronate)-(1->3)-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)-(2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Base Information

• Chemical Name: 2-(N-benzyloxycarbonyl)-aminoethyl (methyl 2,3-di-O-benzyl-α-D-glucopyranosyluronate)-(1->3)-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)-(2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside
• CAS No.: 648904-03-4
• Molecular Formula: C₁₀₀H₁₀₈N₂O₂₄
• Molecular Weight: 1721.96

Synonyms:2-(N-benzyloxycarbonyl)-aminoethyl (methyl 2,3-di-O-benzyl-α-D-glucopyranosyluronate)-(1->3)-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)-(2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

Chemical Property of 2-(N-benzyloxycarbonyl)-aminoethyl (methyl 2,3-di-O-benzyl-α-D-glucopyranosyluronate)-(1->3)-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)-(2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

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Technology Process of 2-(N-benzyloxycarbonyl)-aminoethyl (methyl 2,3-di-O-benzyl-α-D-glucopyranosyluronate)-(1->3)-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)-(2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside

There total 1 articles about 2-(N-benzyloxycarbonyl)-aminoethyl (methyl 2,3-di-O-benzyl-α-D-glucopyranosyluronate)-(1->3)-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)-(2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 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: 76.0%

C102H109ClN2O25 → 2-(N-benzyloxycarbonyl)-aminoethyl (methyl 2,3-di-O-benzyl-α-D-glucopyranosyluronate)-(1->3)-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)-(2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside (648904-03-4)

Guidance literature:

With hydrazinium monoacetate; In methanol;

DOI:10.1016/S0008-6215(03)00271-4

Reference yield: 45.0%

1-deoxy-1-(S-ethyl)-2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside (74666-83-4,105990-37-2,125354-46-3,125354-47-4,125411-99-6,108739-67-9) + 2-(N-benzyloxycarbonyl)-aminoethyl (methyl 2,3-di-O-benzyl-α-D-glucopyranosyluronate)-(1->3)-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)-(2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside (648904-03-4) → C134H142N2O29 + C134H142N2O29

Guidance literature:

With dimethyl-(methylthio)-sulphonium trifluoromethanesulphonate; In diethyl ether; at 20 ℃; for 6h;

DOI:10.1016/S0008-6215(03)00271-4

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