2-acetamido-4,6-O-benzylidene-1,5-(benzyloxycarbonyl)imino-1,2,5-trideoxy-3-O-[(1R)-1-(4-nitrophenoxy)carbonyl]ethyl-D-glucitol

Base Information

Chemical Name:2-acetamido-4,6-O-benzylidene-1,5-(benzyloxycarbonyl)imino-1,2,5-trideoxy-3-O-[(1R)-1-(4-nitrophenoxy)carbonyl]ethyl-D-glucitol
CAS No.:1356848-64-0
Molecular Formula:C₃₂H₃₃N₃O₁₀
Molecular Weight:619.628
Hs Code.:

Synonyms:2-acetamido-4,6-O-benzylidene-1,5-(benzyloxycarbonyl)imino-1,2,5-trideoxy-3-O-[(1R)-1-(4-nitrophenoxy)carbonyl]ethyl-D-glucitol

Suppliers and Price of 2-acetamido-4,6-O-benzylidene-1,5-(benzyloxycarbonyl)imino-1,2,5-trideoxy-3-O-[(1R)-1-(4-nitrophenoxy)carbonyl]ethyl-D-glucitol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-acetamido-4,6-O-benzylidene-1,5-(benzyloxycarbonyl)imino-1,2,5-trideoxy-3-O-[(1R)-1-(4-nitrophenoxy)carbonyl]ethyl-D-glucitol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-acetamido-4,6-O-benzylidene-1,5-(benzyloxycarbonyl)imino-1,2,5-trideoxy-3-O-[(1R)-1-(4-nitrophenoxy)carbonyl]ethyl-D-glucitol

There total 6 articles about 2-acetamido-4,6-O-benzylidene-1,5-(benzyloxycarbonyl)imino-1,2,5-trideoxy-3-O-[(1R)-1-(4-nitrophenoxy)carbonyl]ethyl-D-glucitol 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: 72.0%

: 1356848-62-8
2-acetamido-4,6-O-benzylidene-1,5-(benzyloxycarbonyl)imino-3-O-[(1R)-1-carboxy]ethyl-1,2,5-trideoxy-D-glucitol

: 658-78-6
1-nitro-4-trifluoroacetoxy-benzene

: 1356848-64-0
2-acetamido-4,6-O-benzylidene-1,5-(benzyloxycarbonyl)imino-1,2,5-trideoxy-3-O-[(1R)-1-(4-nitrophenoxy)carbonyl]ethyl-D-glucitol

Guidance literature:: With pyridine; triethylamine; In dichloromethane; for 23h; Inert atmosphere;
DOI:10.1021/ml2002746

Reference yield:

: C₂₁H₃₂N₂O₆Si

: 1356848-64-0
2-acetamido-4,6-O-benzylidene-1,5-(benzyloxycarbonyl)imino-1,2,5-trideoxy-3-O-[(1R)-1-(4-nitrophenoxy)carbonyl]ethyl-D-glucitol

Guidance literature:: Multi-step reaction with 5 steps

1.1: dimethyl sulfide borane / tetrahydrofuran; dichloromethane / 18 h / 0 - 20 °C / Inert atmosphere

2.1: pyridine / dichloromethane / 1 h / 20 °C / Inert atmosphere

3.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 24 h / 20 °C / Inert atmosphere

4.1: sodium hydride / tetrahydrofuran; oil / 0.5 h / 60 °C / Inert atmosphere

4.2: 21 h / 20 - 60 °C

5.1: pyridine; triethylamine / dichloromethane / 23 h / Inert atmosphere

With pyridine; tetrabutyl ammonium fluoride; dimethyl sulfide borane; sodium hydride; triethylamine; In tetrahydrofuran; dichloromethane; oil;
DOI:10.1021/ml2002746

Reference yield:

: C₂₁H₃₄N₂O₄Si

: 1356848-64-0
2-acetamido-4,6-O-benzylidene-1,5-(benzyloxycarbonyl)imino-1,2,5-trideoxy-3-O-[(1R)-1-(4-nitrophenoxy)carbonyl]ethyl-D-glucitol

Guidance literature:: Multi-step reaction with 4 steps

1.1: pyridine / dichloromethane / 1 h / 20 °C / Inert atmosphere

2.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 24 h / 20 °C / Inert atmosphere

3.1: sodium hydride / tetrahydrofuran; oil / 0.5 h / 60 °C / Inert atmosphere

3.2: 21 h / 20 - 60 °C

4.1: pyridine; triethylamine / dichloromethane / 23 h / Inert atmosphere

With pyridine; tetrabutyl ammonium fluoride; sodium hydride; triethylamine; In tetrahydrofuran; dichloromethane; oil;
DOI:10.1021/ml2002746