p-methoxyphenyl (2,6-di-O-benzyl-α-D-galactopyranosyl)-(1→6)-(2,3,4-tri-O-benzoyl-β-D-glucopyranosyl)-(1→3)-4-O-acetyl-6-O-benzyl-2-deoxy-2-N-phthalimido-β-D-galactopyranoside

Base Information

• Chemical Name: p-methoxyphenyl (2,6-di-O-benzyl-α-D-galactopyranosyl)-(1→6)-(2,3,4-tri-O-benzoyl-β-D-glucopyranosyl)-(1→3)-4-O-acetyl-6-O-benzyl-2-deoxy-2-N-phthalimido-β-D-galactopyranoside
• CAS No.: 1453085-87-4
• Molecular Formula: C₇₇H₇₃NO₂₂
• Molecular Weight: 1364.42

Synonyms:p-methoxyphenyl (2,6-di-O-benzyl-α-D-galactopyranosyl)-(1→6)-(2,3,4-tri-O-benzoyl-β-D-glucopyranosyl)-(1→3)-4-O-acetyl-6-O-benzyl-2-deoxy-2-N-phthalimido-β-D-galactopyranoside

Chemical Property of p-methoxyphenyl (2,6-di-O-benzyl-α-D-galactopyranosyl)-(1→6)-(2,3,4-tri-O-benzoyl-β-D-glucopyranosyl)-(1→3)-4-O-acetyl-6-O-benzyl-2-deoxy-2-N-phthalimido-β-D-galactopyranoside

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Technology Process of p-methoxyphenyl (2,6-di-O-benzyl-α-D-galactopyranosyl)-(1→6)-(2,3,4-tri-O-benzoyl-β-D-glucopyranosyl)-(1→3)-4-O-acetyl-6-O-benzyl-2-deoxy-2-N-phthalimido-β-D-galactopyranoside

There total 1 articles about p-methoxyphenyl (2,6-di-O-benzyl-α-D-galactopyranosyl)-(1→6)-(2,3,4-tri-O-benzoyl-β-D-glucopyranosyl)-(1→3)-4-O-acetyl-6-O-benzyl-2-deoxy-2-N-phthalimido-β-D-galactopyranoside 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:

C80H77NO22 → p-methoxyphenyl (2,6-di-O-benzyl-α-D-galactopyranosyl)-(1→6)-(2,3,4-tri-O-benzoyl-β-D-glucopyranosyl)-(1→3)-4-O-acetyl-6-O-benzyl-2-deoxy-2-N-phthalimido-β-D-galactopyranoside (1453085-87-4)

Guidance literature:

With acetic acid; In water; at 80 ℃; for 1.5h;

DOI:10.1016/j.tetasy.2013.06.005

Reference yield: 74.0%

p-methoxyphenyl (2,6-di-O-benzyl-α-D-galactopyranosyl)-(1→6)-(2,3,4-tri-O-benzoyl-β-D-glucopyranosyl)-(1→3)-4-O-acetyl-6-O-benzyl-2-deoxy-2-N-phthalimido-β-D-galactopyranoside (1453085-87-4) + ethyl (2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-(1→4)-3-O-acetyl-6-O-benzoyl-2-deoxy-2-N-phthalimido-1-thio-β-D-galactopyranoside (1453085-88-5) → p-methoxyphenyl (2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-(1→4)-(3-O-acetyl-6-O-benzoyl-2-deoxy-2-N-phthalimido-β-D-galactopyranosyl)-(1→3)-(2,6-di-O-benzyl-α-D-galactopyranosyl)-(1→6)-(2,3,4-tri-O-benzoyl-β-D-glucopyranosyl)-(1→3)-4-O-acetyl-6-O-benzyl-2-deoxy-2-N-phthalimido-β-D-galactopyranoside

Guidance literature:

p-methoxyphenyl (2,6-di-O-benzyl-α-D-galactopyranosyl)-(1→6)-(2,3,4-tri-O-benzoyl-β-D-glucopyranosyl)-(1→3)-4-O-acetyl-6-O-benzyl-2-deoxy-2-N-phthalimido-β-D-galactopyranoside; ethyl (2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-(1→4)-3-O-acetyl-6-O-benzoyl-2-deoxy-2-N-phthalimido-1-thio-β-D-galactopyranoside; In dichloromethane; at -30 ℃; for 0.5h; Molecular sieve; Inert atmosphere;

With N-iodo-succinimide; trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at -30 ℃; for 0.75h; stereoselective reaction; Inert atmosphere;

DOI:10.1016/j.tetasy.2013.06.005

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