benzyl [3,6-di-O-benzyl-2,4-di-O-(2,5-difluorobenzoyl)-α-D-mannopyranosyl-(1→3)]-2,4-di-O-benzyl-β-D-mannopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Base Information

• Chemical Name: benzyl [3,6-di-O-benzyl-2,4-di-O-(2,5-difluorobenzoyl)-α-D-mannopyranosyl-(1→3)]-2,4-di-O-benzyl-β-D-mannopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
• CAS No.: 1400810-15-2
• Molecular Formula: C₁₁₇H₁₀₆F₄N₂O₂₅
• Molecular Weight: 2016.12
• Mol file: 1400810-15-2.mol

Synonyms:benzyl [3,6-di-O-benzyl-2,4-di-O-(2,5-difluorobenzoyl)-α-D-mannopyranosyl-(1→3)]-2,4-di-O-benzyl-β-D-mannopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Chemical Property of benzyl [3,6-di-O-benzyl-2,4-di-O-(2,5-difluorobenzoyl)-α-D-mannopyranosyl-(1→3)]-2,4-di-O-benzyl-β-D-mannopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Chemical Property:

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MSDS Files:

Useful:

Technology Process of benzyl [3,6-di-O-benzyl-2,4-di-O-(2,5-difluorobenzoyl)-α-D-mannopyranosyl-(1→3)]-2,4-di-O-benzyl-β-D-mannopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

There total 1 articles about benzyl [3,6-di-O-benzyl-2,4-di-O-(2,5-difluorobenzoyl)-α-D-mannopyranosyl-(1→3)]-2,4-di-O-benzyl-β-D-mannopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-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: 88.0%

benzyl [3,6-di-O-benzyl-2,4-O-(2,5-difluorobenzoyl)-α-D-mannopyranosyl-(1→3)]-2-O-benzyl-4,6-O-(R)-benzylidene-β-D-mannopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-Dglucopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside (1400810-14-1) → benzyl [3,6-di-O-benzyl-2,4-di-O-(2,5-difluorobenzoyl)-α-D-mannopyranosyl-(1→3)]-2,4-di-O-benzyl-β-D-mannopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside (1400810-15-2)

Guidance literature:

With borane-THF; di-n-butylboron triflate; In tetrahydrofuran; dichloromethane; toluene; at 0 ℃; for 4h; Inert atmosphere;

DOI:10.1021/ja307628w

Reference yield: 90.0%

benzyl [3,6-di-O-benzyl-2,4-di-O-(2,5-difluorobenzoyl)-α-D-mannopyranosyl-(1→3)]-2,4-di-O-benzyl-β-D-mannopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside (1400810-15-2) + thioethyl 3,4,6-tri-O-benzyl-2-O-(2,5-difluorobenzoyl)-α-D-mannopyranoside (1400810-16-3) → benzyl [3,6-di-O-benzyl-2,4-di-O-(2,5-difluorobenzoyl)-α-D-mannopyranosyl-(1→3)]-[3,4,6-tri-Obenzyl-2-O-(2,5-difluorobenzoyl)-α-D-mannopyranosyl-(1→6)]-2,4-di-O-benzyl-β-D-mannopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside

Guidance literature:

benzyl [3,6-di-O-benzyl-2,4-di-O-(2,5-difluorobenzoyl)-α-D-mannopyranosyl-(1→3)]-2,4-di-O-benzyl-β-D-mannopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside; thioethyl 3,4,6-tri-O-benzyl-2-O-(2,5-difluorobenzoyl)-α-D-mannopyranoside; In dichloromethane; toluene; at 20 ℃; for 2h; Inert atmosphere; Molecular sieve;

With N-iodo-succinimide; silver trifluoromethanesulfonate; In dichloromethane; toluene; at -50 - -20 ℃; for 12h; Inert atmosphere;

DOI:10.1021/ja307628w

upstream raw materials:

benzyl [3,6-di-O-benzyl-2,4-O-(2,5-difluorobenzoyl)-α-D-mannopyranosyl-(1→3)]-2-O-benzyl-4,6-O-(R)-benzylidene-β-D-mannopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-Dglucopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside