p-aminophenyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6)-2-acetamido-2-deoxy-α-D-galactopyranoside

Base Information

Chemical Name:p-aminophenyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6)-2-acetamido-2-deoxy-α-D-galactopyranoside
CAS No.:1316822-87-3
Molecular Formula:C₂₂H₃₃N₃O₁₁
Molecular Weight:515.518
Hs Code.:

Synonyms:p-aminophenyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6)-2-acetamido-2-deoxy-α-D-galactopyranoside

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Chemical Property of p-aminophenyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6)-2-acetamido-2-deoxy-α-D-galactopyranoside

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Technology Process of p-aminophenyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6)-2-acetamido-2-deoxy-α-D-galactopyranoside

There total 13 articles about p-aminophenyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6)-2-acetamido-2-deoxy-α-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: 81.0%

: 235752-73-5
p-nitrophenyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6)-2-acetamido-2-deoxy-α-D-galactopyranoside

: 1316822-87-3
p-aminophenyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6)-2-acetamido-2-deoxy-α-D-galactopyranoside

Guidance literature:: With 10% palladium on activated charcoal; hydrogen; In water; for 1h;
DOI:10.1016/j.carres.2011.03.036

Reference yield:

: 501088-85-3
ethyl 2-amino-2,3-N,O-carbonyl-2-deoxy-1-thio-β-D-glucopyranoside

: 1316822-87-3
p-aminophenyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6)-2-acetamido-2-deoxy-α-D-galactopyranoside

Guidance literature:: Multi-step reaction with 6 steps

1.1: pyridine / 1 h / 0 °C / Cooling with ice

2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 1.5 h / 0 °C / Cooling with ice

3.1: 2,6-di-tert-butyl-4-methylpyridine / dichloromethane / 0.33 h / 20 °C / Inert atmosphere; Molecular sieve

3.2: 1 h / 0 - 20 °C / Inert atmosphere; Molecular sieve

4.1: pyridine / 20 °C

5.1: methanol; dichloromethane / 0.5 h

5.2: Dowex H+

6.1: 10% palladium on activated charcoal; hydrogen / water / 1 h

With 2,6-di-tert-butyl-4-methylpyridine; 10% palladium on activated charcoal; hydrogen; N-ethyl-N,N-diisopropylamine; In pyridine; methanol; dichloromethane; water;
DOI:10.1016/j.carres.2011.03.036

Reference yield:

: 1316823-00-3
p-nitrophenyl 2-azido-3-O-benzoyl-2-deoxy-4,6-O-p-methoxybenzylidene-α-D-galactopyranoside

: 1316822-87-3
p-aminophenyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->6)-2-acetamido-2-deoxy-α-D-galactopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1.1: water; acetic acid / dichloromethane / 50 h / 20 - 50 °C

2.1: 2,6-di-tert-butyl-4-methylpyridine / dichloromethane / 0.33 h / 20 °C / Inert atmosphere; Molecular sieve

2.2: 1 h / 0 - 20 °C / Inert atmosphere; Molecular sieve

3.1: pyridine / 20 °C

4.1: methanol; dichloromethane / 0.5 h

4.2: Dowex H+

5.1: 10% palladium on activated charcoal; hydrogen / water / 1 h

With 2,6-di-tert-butyl-4-methylpyridine; 10% palladium on activated charcoal; water; hydrogen; acetic acid; In pyridine; methanol; dichloromethane; water;
DOI:10.1016/j.carres.2011.03.036