benzyl 6-O-acetyl-3-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-4-O-(methyl 2-O-acetyl-3-O-benzyl-4-O-levulinoyl-α-L-idopyranosyluronate)-α-D-glucopyranoside

Base Information

• Chemical Name: benzyl 6-O-acetyl-3-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-4-O-(methyl 2-O-acetyl-3-O-benzyl-4-O-levulinoyl-α-L-idopyranosyluronate)-α-D-glucopyranoside
• CAS No.: 126684-08-0
• Molecular Formula: C₅₁H₅₇NO₁₇
• Molecular Weight: 956.01
• Mol file: 126684-08-0.mol

Synonyms:benzyl 6-O-acetyl-3-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-4-O-(methyl 2-O-acetyl-3-O-benzyl-4-O-levulinoyl-α-L-idopyranosyluronate)-α-D-glucopyranoside

Chemical Property of benzyl 6-O-acetyl-3-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-4-O-(methyl 2-O-acetyl-3-O-benzyl-4-O-levulinoyl-α-L-idopyranosyluronate)-α-D-glucopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of benzyl 6-O-acetyl-3-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-4-O-(methyl 2-O-acetyl-3-O-benzyl-4-O-levulinoyl-α-L-idopyranosyluronate)-α-D-glucopyranoside

There total 3 articles about benzyl 6-O-acetyl-3-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-4-O-(methyl 2-O-acetyl-3-O-benzyl-4-O-levulinoyl-α-L-idopyranosyluronate)-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: 46.0%

benzyl 6-O-acetyl-3-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-α-D-glucopyranoside (87907-06-0) + (methyl 3-O-benzyl-4-O-levulinoyl-β-L-idopyranuronate) 1,2-(tert-butyl orthoacetate) (126684-03-5) → benzyl 6-O-acetyl-3-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-4-O-(methyl 2-O-acetyl-3-O-benzyl-4-O-levulinoyl-α-L-idopyranosyluronate)-α-D-glucopyranoside (126684-08-0)

Guidance literature:

With 2,6-lutidinium perchlorate; In 1,2-dichloro-ethane; chlorobenzene; for 1.5h; Heating;

DOI:10.1002/hlca.19890720613

Reference yield:

levulinic anhydride (40608-06-8) → benzyl 6-O-acetyl-3-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-4-O-(methyl 2-O-acetyl-3-O-benzyl-4-O-levulinoyl-α-L-idopyranosyluronate)-α-D-glucopyranoside (126684-08-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 4-(dimethylamino)pyridine / pyridine / 17 h / 0 °C

2: 46 percent / 2,6-dimethylpyridinium perchlorate / 1,2-dichloro-ethane; chlorobenzene / 1.5 h / Heating

With dmap; 2,6-lutidinium perchlorate; In pyridine; 1,2-dichloro-ethane; chlorobenzene;

DOI:10.1002/hlca.19890720613

Reference yield:

methyl 3-O-benzyl-β-L-idopyranuronate 1,2-(tert-butyl orthoacetate) (87326-83-8) → benzyl 6-O-acetyl-3-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-4-O-(methyl 2-O-acetyl-3-O-benzyl-4-O-levulinoyl-α-L-idopyranosyluronate)-α-D-glucopyranoside (126684-08-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 4-(dimethylamino)pyridine / pyridine / 17 h / 0 °C

2: 46 percent / 2,6-dimethylpyridinium perchlorate / 1,2-dichloro-ethane; chlorobenzene / 1.5 h / Heating

With dmap; 2,6-lutidinium perchlorate; In pyridine; 1,2-dichloro-ethane; chlorobenzene;

DOI:10.1002/hlca.19890720613

upstream raw materials:

benzyl 6-O-acetyl-3-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-α-D-glucopyranoside

(methyl 3-O-benzyl-4-O-levulinoyl-β-L-idopyranuronate) 1,2-(tert-butyl orthoacetate)

levulinic anhydride

methyl 3-O-benzyl-β-L-idopyranuronate 1,2-(tert-butyl orthoacetate)

Downstream raw materials:

benzyl 6-O-acetyl-3-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-4-O-(methyl 2-O-acetyl-3-O-benzyl-α-L-idopyranosyluronate)-α-D-glucopyranoside