phenyl 3,4-di-O-benzoyl-2-deoxy-1-thio-2-trifluoroacetylamino-6-O-triisopropylsilyl-β-D-glucopyranoside

Base Information

• Chemical Name: phenyl 3,4-di-O-benzoyl-2-deoxy-1-thio-2-trifluoroacetylamino-6-O-triisopropylsilyl-β-D-glucopyranoside
• CAS No.: 1447811-15-5
• Molecular Formula: C₃₇H₄₄F₃NO₇SSi
• Molecular Weight: 731.906
• Mol file: 1447811-15-5.mol

Synonyms:phenyl 3,4-di-O-benzoyl-2-deoxy-1-thio-2-trifluoroacetylamino-6-O-triisopropylsilyl-β-D-glucopyranoside

Chemical Property of phenyl 3,4-di-O-benzoyl-2-deoxy-1-thio-2-trifluoroacetylamino-6-O-triisopropylsilyl-β-D-glucopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of phenyl 3,4-di-O-benzoyl-2-deoxy-1-thio-2-trifluoroacetylamino-6-O-triisopropylsilyl-β-D-glucopyranoside

There total 2 articles about phenyl 3,4-di-O-benzoyl-2-deoxy-1-thio-2-trifluoroacetylamino-6-O-triisopropylsilyl-β-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: 83.0%

phenyl 2-deoxy-1-thio-2-trifluoroacetylamino-6-O-triisopropylsilyl-β-D-glucopyranoside (1447811-14-4) + benzoyl chloride (98-88-4) → phenyl 3,4-di-O-benzoyl-2-deoxy-1-thio-2-trifluoroacetylamino-6-O-triisopropylsilyl-β-D-glucopyranoside (1447811-15-5)

Guidance literature:

With pyridine; at 20 ℃; for 20h; Inert atmosphere;

DOI:10.1016/j.bmcl.2013.05.036

Reference yield:

phenyl 2-amino-2-deoxy-1-thio-6-O-(triisopropylsilyl)-β-D-glucopyranoside (1447811-13-3) → phenyl 3,4-di-O-benzoyl-2-deoxy-1-thio-2-trifluoroacetylamino-6-O-triisopropylsilyl-β-D-glucopyranoside (1447811-15-5)

Guidance literature:

Multi-step reaction with 2 steps

1: pyridine / 0 - 20 °C / Inert atmosphere

2: pyridine / 20 h / 20 °C / Inert atmosphere

With pyridine;

DOI:10.1016/j.bmcl.2013.05.036

Reference yield: 78.0%

2-Benzyloxyethanol (622-08-2,1201808-31-2) + phenyl 3,4-di-O-benzoyl-2-deoxy-1-thio-2-trifluoroacetylamino-6-O-triisopropylsilyl-β-D-glucopyranoside (1447811-15-5) → 1-O-(2-benzyloxyethyl)-2-deoxy-3,4-di-O-benzoyl-2-trifluoroacetylamino-6-O-triisopropylsilyl-β-D-glucopyranoside (1447811-16-6)

Guidance literature:

With N-iodo-succinimide; trifluorormethanesulfonic acid; In dichloromethane; at 20 ℃; Molecular sieve; Inert atmosphere;

DOI:10.1016/j.bmcl.2013.05.036

upstream raw materials:

phenyl 2-amino-2-deoxy-1-thio-6-O-(triisopropylsilyl)-β-D-glucopyranoside

phenyl 2-deoxy-1-thio-2-trifluoroacetylamino-6-O-triisopropylsilyl-β-D-glucopyranoside

benzoyl chloride

Downstream raw materials:

3,4-di-O-benzoyl-2-deoxy-1-O-(2-hydroxyethyl)-2-trifluoroacetylamino-6-O-triisopropylsilyl-β-D-glucopyranoside

3,4-di-O-benzoyl-2-deoxy-1-O-[2-(4,4'-dimethoxytrityloxy)ethyl]-2-trifluoroacetylamino-6-O-triisopropylsilyl-β-D-glucopyranoside

3,4-di-O-benzoyl-2-deoxy-1-O-[2-(4,4'-dimethoxytrityloxy)ethyl]-2-trifluoroacetylamino-β-D-glucopyranoside

C₄₉H₄₆F₃NO₁₄