isopropyl O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranosyl)-(1→4)-O-(3-O-benzyl-α-L-idopyranosyluronic acid)-(1→4)-2-acetamido-3-O-benzyl-2-deoxy-α-D-glucopyranoside

Base Information

Chemical Name:isopropyl O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranosyl)-(1→4)-O-(3-O-benzyl-α-L-idopyranosyluronic acid)-(1→4)-2-acetamido-3-O-benzyl-2-deoxy-α-D-glucopyranoside
CAS No.:1420235-89-7
Molecular Formula:C₅₁H₆₀N₄O₁₆
Molecular Weight:985.055
Hs Code.:

isopropyl O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranosyl)-(1→4)-O-(3-O-benzyl-α-L-idopyranosyluronic acid)-(1→4)-2-acetamido-3-O-benzyl-2-deoxy-α-D-glucopyranoside

Synonyms:isopropyl O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranosyl)-(1→4)-O-(3-O-benzyl-α-L-idopyranosyluronic acid)-(1→4)-2-acetamido-3-O-benzyl-2-deoxy-α-D-glucopyranoside

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Chemical Property of isopropyl O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranosyl)-(1→4)-O-(3-O-benzyl-α-L-idopyranosyluronic acid)-(1→4)-2-acetamido-3-O-benzyl-2-deoxy-α-D-glucopyranoside

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Technology Process of isopropyl O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranosyl)-(1→4)-O-(3-O-benzyl-α-L-idopyranosyluronic acid)-(1→4)-2-acetamido-3-O-benzyl-2-deoxy-α-D-glucopyranoside

There total 1 articles about isopropyl O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranosyl)-(1→4)-O-(3-O-benzyl-α-L-idopyranosyluronic acid)-(1→4)-2-acetamido-3-O-benzyl-2-deoxy-α-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: 89.0%

: 857895-90-0
isopropyl O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranosyl)-(1→4)-O-(methyl-3-O-benzyl-2-O-pivaloyl-α-L-idopyranosyluronate)-(1→4)-2-acetamido-6-O-benzoyl-3-O-benzyl-2-deoxy-α-D-glucopyranoside

: 1420235-89-7
isopropyl O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranosyl)-(1→4)-O-(3-O-benzyl-α-L-idopyranosyluronic acid)-(1→4)-2-acetamido-3-O-benzyl-2-deoxy-α-D-glucopyranoside

Guidance literature:: isopropyl O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranosyl)-(1→4)-O-(methyl-3-O-benzyl-2-O-pivaloyl-α-L-idopyranosyluronate)-(1→4)-2-acetamido-6-O-benzoyl-3-O-benzyl-2-deoxy-α-D-glucopyranoside; With dihydrogen peroxide; lithium hydroxide; In tetrahydrofuran; water; at 0 - 20 ℃; for 24h;

With potassium hydroxide; In tetrahydrofuran; water; at 0 - 20 ℃; for 24h;
DOI:10.1002/chem.201202770

Reference yield: 82.0%

: 1420235-89-7
isopropyl O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranosyl)-(1→4)-O-(3-O-benzyl-α-L-idopyranosyluronic acid)-(1→4)-2-acetamido-3-O-benzyl-2-deoxy-α-D-glucopyranoside

: 121-44-8
triethylamine

: isopropyl O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranosyl)-(1→4)-O-(3-O-benzyl-2-O-sulfo-α-L-idopyranosyluronic acid)-(1→4)-2-acetamido-3-O-benzyl-2-deoxy-6-O-sulfo-α-D-glucopyranoside triethylammonium salt

Guidance literature:: isopropyl O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranosyl)-(1→4)-O-(3-O-benzyl-α-L-idopyranosyluronic acid)-(1→4)-2-acetamido-3-O-benzyl-2-deoxy-α-D-glucopyranoside; With sulfur trioxide trimethylamine complex; In N,N-dimethyl-formamide; at 50 ℃; for 48h; Inert atmosphere;

triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 0.0833333h; Inert atmosphere;
DOI:10.1002/chem.201202770

Reference yield:

: 1420235-89-7
isopropyl O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-glucopyranosyl)-(1→4)-O-(3-O-benzyl-α-L-idopyranosyluronic acid)-(1→4)-2-acetamido-3-O-benzyl-2-deoxy-α-D-glucopyranoside

: 1431693-96-7
C₅₁H₆₂N₂O₂₂S₂

Guidance literature:: Multi-step reaction with 2 steps

1.1: sulfur trioxide trimethylamine complex / N,N-dimethyl-formamide / 48 h / 50 °C / Inert atmosphere

1.2: 0.08 h / 20 °C / Inert atmosphere

2.1: sodium hydroxide; trimethylphosphane / water; tetrahydrofuran / 3 h / 0 - 20 °C

With sulfur trioxide trimethylamine complex; sodium hydroxide; trimethylphosphane; In tetrahydrofuran; water; N,N-dimethyl-formamide;
DOI:10.1002/chem.201202770