phenyl 2-azido-2-deoxy-3-O-benzoyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside

Base Information

Chemical Name:phenyl 2-azido-2-deoxy-3-O-benzoyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside
CAS No.:1301693-40-2
Molecular Formula:C₃₅H₃₇N₃O₅SSi
Molecular Weight:639.847
Hs Code.:

Synonyms:phenyl 2-azido-2-deoxy-3-O-benzoyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside

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Chemical Property of phenyl 2-azido-2-deoxy-3-O-benzoyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside

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Technology Process of phenyl 2-azido-2-deoxy-3-O-benzoyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside

There total 13 articles about phenyl 2-azido-2-deoxy-3-O-benzoyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-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:

: C₃₇H₃₆F₆O₁₀S₃Si

: 1301693-40-2
phenyl 2-azido-2-deoxy-3-O-benzoyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside

Guidance literature:: C₃₇H₃₆F₆O₁₀S₃Si; With tetrabutylammoniun azide; In acetonitrile; at -30 ℃; Inert atmosphere;

With tetrabutylammonium nitrite; In acetonitrile; at 20 ℃; Inert atmosphere;
DOI:10.1039/c3ob40935j

Reference yield:

: C₃₆H₃₆F₃N₃O₇S₂Si

: 1301693-40-2
phenyl 2-azido-2-deoxy-3-O-benzoyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside

Guidance literature:: With tetrabutylammonium nitrite; In acetonitrile; at 20 ℃; for 1h; Inert atmosphere;
DOI:10.1021/jo200342v

Reference yield:

: 77481-63-1
phenyl-1-thio-β-D-mannopyranoside

: 1301693-40-2
phenyl 2-azido-2-deoxy-3-O-benzoyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside

Guidance literature:: Multi-step reaction with 8 steps

1.1: dimethyltin dichloride; N-ethyl-N,N-diisopropylamine / tetrahydrofuran; water / 0.08 h / Inert atmosphere

1.2: 2.5 h / 20 °C / Inert atmosphere

2.1: camphor-10-sulfonic acid / acetonitrile / 0.17 h / 20 °C / Inert atmosphere

3.1: pyridine / dichloromethane / 0.17 h / 0 °C / Inert atmosphere

4.1: sodium azide / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere

5.1: water; acetic acid / 1.5 h / 85 °C / Inert atmosphere

6.1: 1H-imidazole / acetonitrile / 0.25 h / 20 °C / Inert atmosphere

7.1: pyridine / dichloromethane / 0.17 h / 0 °C / Inert atmosphere

8.1: tetrabutylammonium nitrite / acetonitrile / 1 h / 20 °C / Inert atmosphere

With pyridine; 1H-imidazole; sodium azide; camphor-10-sulfonic acid; water; dimethyltin dichloride; acetic acid; N-ethyl-N,N-diisopropylamine; tetrabutylammonium nitrite; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jo200342v