N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-(4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-β-D-glucopyranoside

Base Information

Chemical Name:N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-(4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-β-D-glucopyranoside
CAS No.:250330-64-4
Molecular Formula:C₅₈H₈₃NO₃₃
Molecular Weight:1322.28
Hs Code.:

N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-(4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-β-D-glucopyranoside

Synonyms:N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-(4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-β-D-glucopyranoside

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Chemical Property of N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-(4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-β-D-glucopyranoside

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Technology Process of N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-(4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-β-D-glucopyranoside

There total 8 articles about N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-(4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-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: 56.0%

: 250330-63-3
4-O-(4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetylα-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α/β-D-glucopyranosyl trichloroacetimidate

: 250330-58-6
benzyl N-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethyl]carbamate

: 250330-64-4
N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-(4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-β-D-glucopyranoside

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; In dichloromethane; at -20 ℃; for 0.5h;
DOI:10.1016/S0968-0896(99)00139-X

Reference yield:

: 37860-51-8
tetraethylene glycol di(p-toluenesulfonate)

: 250330-64-4
N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-(4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1.1: NaH / dimethylformamide / 2 h / 50 °C

2.1: 1.34 g / AcOH / tetrahydrofuran; H₂O / 4 h / 20 °C

3.1: PPh₃ / pyridine / 2 h / 20 °C

3.2: conc. NH₄OH / pyridine / 2 h / 20 °C

4.1: 1.53 g / iPr₂NEt / dimethylformamide; H₂O / 0.5 h / 20 °C

5.1: 56 percent / TMSOTf; molecular sieves 4 Angstroem / CH₂Cl₂ / 0.5 h / -20 °C

With trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; sodium hydride; acetic acid; N-ethyl-N,N-diisopropylamine; triphenylphosphine; In tetrahydrofuran; pyridine; dichloromethane; water; N,N-dimethyl-formamide; 1.1: Substitution / 2.1: Hydrolysis / 3.1: Addition / 3.2: Hydrolysis / 4.1: Acylation / 5.1: Substitution;
DOI:10.1016/S0968-0896(99)00139-X

Reference yield:

: 76821-26-6
maltotriose peracetate

: 250330-64-4
N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-(4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / hydrazine acetate / dimethylformamide / 1 h / 20 °C

2: 71 percent / Cs₂CO₃ / CH₂Cl₂ / 2 h / 20 °C

3: 56 percent / TMSOTf; molecular sieves 4 Angstroem / CH₂Cl₂ / 0.5 h / -20 °C

With trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; hydrazinium monoacetate; caesium carbonate; In dichloromethane; N,N-dimethyl-formamide; 1: Deacetylation / 2: Substitution / 3: Substitution;
DOI:10.1016/S0968-0896(99)00139-X