methyl 4-O-acetyl-2-azido-3-O-(2-azido-3-O-benzyl-2-deoxy-β-D-mannopyranosyl)-6-O-tert-butyldiphenylsilyl-2-deoxy-β-L-galactopyranoside

Base Information

• Chemical Name: methyl 4-O-acetyl-2-azido-3-O-(2-azido-3-O-benzyl-2-deoxy-β-D-mannopyranosyl)-6-O-tert-butyldiphenylsilyl-2-deoxy-β-L-galactopyranoside
• CAS No.: 849222-06-6
• Molecular Formula: C₃₈H₄₈N₆O₁₀Si
• Molecular Weight: 776.919
• Mol file: 849222-06-6.mol

Synonyms:methyl 4-O-acetyl-2-azido-3-O-(2-azido-3-O-benzyl-2-deoxy-β-D-mannopyranosyl)-6-O-tert-butyldiphenylsilyl-2-deoxy-β-L-galactopyranoside

Chemical Property of methyl 4-O-acetyl-2-azido-3-O-(2-azido-3-O-benzyl-2-deoxy-β-D-mannopyranosyl)-6-O-tert-butyldiphenylsilyl-2-deoxy-β-L-galactopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of methyl 4-O-acetyl-2-azido-3-O-(2-azido-3-O-benzyl-2-deoxy-β-D-mannopyranosyl)-6-O-tert-butyldiphenylsilyl-2-deoxy-β-L-galactopyranoside

There total 10 articles about methyl 4-O-acetyl-2-azido-3-O-(2-azido-3-O-benzyl-2-deoxy-β-D-mannopyranosyl)-6-O-tert-butyldiphenylsilyl-2-deoxy-β-L-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: 62.0%

methyl 4-O-acetyl-2-azido-3-O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl)-6-O-tert-butyldiphenylsilyl-2-deoxy-β-L-galactopyranoside (849222-05-5) → methyl 4-O-acetyl-2-azido-3-O-(2-azido-3-O-benzyl-2-deoxy-β-D-mannopyranosyl)-6-O-tert-butyldiphenylsilyl-2-deoxy-β-L-galactopyranoside (849222-06-6)

Guidance literature:

With camphor-10-sulfonic acid; In tetrahydrofuran; methanol; for 18h;

DOI:10.1002/chem.200400862

Reference yield:

(2S,3S,4S,5S,6S)-5-Azido-2-hydroxymethyl-6-methoxy-tetrahydro-pyran-3,4-diol → methyl 4-O-acetyl-2-azido-3-O-(2-azido-3-O-benzyl-2-deoxy-β-D-mannopyranosyl)-6-O-tert-butyldiphenylsilyl-2-deoxy-β-L-galactopyranoside (849222-06-6)

Guidance literature:

Multi-step reaction with 5 steps

1: 1.00 g / pyridine / 4 h

2: CSA / dimethylformamide / 1 h

3: 943 mg / aq. AcOH / 0.25 h

4: 53 percent / 1-benzenesulfinyl piperidine; tri-tert-butylpyrimidine; Tf₂O / 3 Angstroem molecular sieves / CH₂Cl₂ / -60 - 20 °C

5: 62 percent / CSA / tetrahydrofuran; methanol / 18 h

With pyridine; 1-benzenesulfinyl piperidine; trifluoromethylsulfonic anhydride; 2,4,5-tri-tert-butylpyrimidine; camphor-10-sulfonic acid; acetic acid; 3 A molecular sieve; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1002/chem.200400862

Reference yield:

methyl 3,4,6-tri-O-acetyl-2-azido-2-deoxy-β-L-galactopyranoside (849222-01-1) → methyl 4-O-acetyl-2-azido-3-O-(2-azido-3-O-benzyl-2-deoxy-β-D-mannopyranosyl)-6-O-tert-butyldiphenylsilyl-2-deoxy-β-L-galactopyranoside (849222-06-6)

Guidance literature:

Multi-step reaction with 6 steps

1: t-BuOK / methanol / 1 h

2: 1.00 g / pyridine / 4 h

3: CSA / dimethylformamide / 1 h

4: 943 mg / aq. AcOH / 0.25 h

5: 53 percent / 1-benzenesulfinyl piperidine; tri-tert-butylpyrimidine; Tf₂O / 3 Angstroem molecular sieves / CH₂Cl₂ / -60 - 20 °C

6: 62 percent / CSA / tetrahydrofuran; methanol / 18 h

With pyridine; 1-benzenesulfinyl piperidine; trifluoromethylsulfonic anhydride; 2,4,5-tri-tert-butylpyrimidine; camphor-10-sulfonic acid; potassium tert-butylate; acetic acid; 3 A molecular sieve; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1002/chem.200400862

upstream raw materials:

methyl 4-O-acetyl-2-azido-3-O-(2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-β-D-mannopyranosyl)-6-O-tert-butyldiphenylsilyl-2-deoxy-β-L-galactopyranoside

methyl 3,4,6-tri-O-acetyl-2-azido-2-deoxy-β-L-galactopyranoside

Acetic acid (2S,3R,4R,5S)-3,5-diacetoxy-2-acetoxymethyl-6-bromo-tetrahydro-pyran-4-yl ester

phenyl 3,4,6-tri-O-acetyl-2-azido-2-deoxy-1-seleno-α-L-galactopyranoside

Downstream raw materials:

methyl 4-O-acetyl-2-azido-3-O-{2-azido-3-O-benzyl-4-O-(3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-6-O-tert-butyldimethylsilyl-2-deoxy-β-D-mannopyranosyl}-6-O-tert-butyldiphenylsilyl-2-deoxy-β-L-galactopyranoside

methyl 2-acetamido-4-O-acetyl-3-O-{2-acetamido-3-O-benzyl-4-O-(2-acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl)-6-O-tert-butyldimethylsilyl-2-deoxy-β-D-mannopyranosyl}-6-O-tert-butyldiphenylsilyl-2-deoxy-β-L-galactopyranoside

methyl 4-O-acetyl-2-azido-3-O-{2-azido-3-O-benzyl-4-O-(2-acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl)-6-O-tert-butyldimethylsilyl-2-deoxy-β-D-mannopyranosyl}-6-O-tert-butyldiphenylsilyl-2-deoxy-β-L-galactopyranoside

C₄₈H₅₇N₃O₁₉