benzyl O-(2-azido-4-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-O-(methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-3-O-benzyl-2-(benzyloxycarbonyl)amino-2-deoxy-α-D-glucopyranoside

Base Information

Chemical Name:benzyl O-(2-azido-4-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-O-(methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-3-O-benzyl-2-(benzyloxycarbonyl)amino-2-deoxy-α-D-glucopyranoside
CAS No.:87907-40-2
Molecular Formula:C₅₅H₆₂N₄O₁₇
Molecular Weight:1051.11
Hs Code.:

benzyl O-(2-azido-4-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-O-(methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-3-O-benzyl-2-(benzyloxycarbonyl)amino-2-deoxy-α-D-glucopyranoside

Synonyms:benzyl O-(2-azido-4-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-O-(methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-3-O-benzyl-2-(benzyloxycarbonyl)amino-2-deoxy-α-D-glucopyranoside

Suppliers and Price of benzyl O-(2-azido-4-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-O-(methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-3-O-benzyl-2-(benzyloxycarbonyl)amino-2-deoxy-α-D-glucopyranoside

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 benzyl O-(2-azido-4-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-O-(methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-3-O-benzyl-2-(benzyloxycarbonyl)amino-2-deoxy-α-D-glucopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of benzyl O-(2-azido-4-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-O-(methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-3-O-benzyl-2-(benzyloxycarbonyl)amino-2-deoxy-α-D-glucopyranoside

There total 8 articles about benzyl O-(2-azido-4-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-O-(methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-3-O-benzyl-2-(benzyloxycarbonyl)amino-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:

: 87327-03-5
methyl (2,4-di-O-acetyl-3-O-benzyl-α-L-idopyranosyl bromide)uronate

: 87907-40-2
benzyl O-(2-azido-4-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-O-(methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-3-O-benzyl-2-(benzyloxycarbonyl)amino-2-deoxy-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 6 steps

1: 73 percent / 2,4,6-trimethylpyridine / CH₂Cl₂ / 15 h / Ambient temperature

2: 1.) methanol, K₂CO₃, 2.) pyridine / 1.) -20 deg C, 5 h, 2.) dichloromethane, -20 deg C, 30 min

3: 35 percent / 0.2 M 2,6-dimethylpyridinium perchlorate / chlorobenzene / 1.5 h / Heating

4: 86 percent / thiourea, ethanol / pyridine / 0.5 h / 100 °C

5: 88 percent / 4 A molecular sieve, 2,4,6-trimethylpyridine, silver triflate / CH₂Cl₂ / 2 h / -20 °C / in the dark

6: 1.) M NaOH, methanol / 1.) 1,2-dimethoxyethane, 0 deg C, 6 h, 2.) methanol/ether, 30 min

With pyridine; 2,4,6-trimethyl-pyridine; methanol; sodium hydroxide; ethanol; 4 A molecular sieve; silver trifluoromethanesulfonate; 2,6-lutidinium perchlorate; potassium carbonate; thiourea; In pyridine; dichloromethane; chlorobenzene;
DOI:10.1016/0008-6215(84)85281-7

Reference yield:

: 87326-82-7
methyl 4-O-acetyl-3-O-benzyl-β-L-idopyranuronate 1,2-(tert-butyl orthoacetate)

: 87907-40-2
benzyl O-(2-azido-4-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-O-(methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-3-O-benzyl-2-(benzyloxycarbonyl)amino-2-deoxy-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) methanol, K₂CO₃, 2.) pyridine / 1.) -20 deg C, 5 h, 2.) dichloromethane, -20 deg C, 30 min

2: 35 percent / 0.2 M 2,6-dimethylpyridinium perchlorate / chlorobenzene / 1.5 h / Heating

3: 86 percent / thiourea, ethanol / pyridine / 0.5 h / 100 °C

4: 88 percent / 4 A molecular sieve, 2,4,6-trimethylpyridine, silver triflate / CH₂Cl₂ / 2 h / -20 °C / in the dark

5: 1.) M NaOH, methanol / 1.) 1,2-dimethoxyethane, 0 deg C, 6 h, 2.) methanol/ether, 30 min

With pyridine; 2,4,6-trimethyl-pyridine; methanol; sodium hydroxide; ethanol; 4 A molecular sieve; silver trifluoromethanesulfonate; 2,6-lutidinium perchlorate; potassium carbonate; thiourea; In pyridine; dichloromethane; chlorobenzene;
DOI:10.1016/0008-6215(84)85281-7

Reference yield:

: 87907-09-3
methyl 3-O-benzyl-4-O-monochloroacetyl-β-L-idopyranuronate 1,2-(tert-butyl orthoacetate)

: 87907-40-2
benzyl O-(2-azido-4-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->4)-O-(methyl 3-O-benzyl-α-L-idopyranosyluronate)-(1->4)-3-O-benzyl-2-(benzyloxycarbonyl)amino-2-deoxy-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 35 percent / 0.2 M 2,6-dimethylpyridinium perchlorate / chlorobenzene / 1.5 h / Heating

2: 86 percent / thiourea, ethanol / pyridine / 0.5 h / 100 °C

3: 88 percent / 4 A molecular sieve, 2,4,6-trimethylpyridine, silver triflate / CH₂Cl₂ / 2 h / -20 °C / in the dark

4: 1.) M NaOH, methanol / 1.) 1,2-dimethoxyethane, 0 deg C, 6 h, 2.) methanol/ether, 30 min

With 2,4,6-trimethyl-pyridine; methanol; sodium hydroxide; ethanol; 4 A molecular sieve; silver trifluoromethanesulfonate; 2,6-lutidinium perchlorate; thiourea; In pyridine; dichloromethane; chlorobenzene;
DOI:10.1016/0008-6215(84)85281-7