phenyl 2,3-di-O-benzyl-6-deoxy-4-O-(3,4-di-O-benzyl-6-deoxy-2-O-(methylthio)thiocarbonyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside

Base Information

Chemical Name:phenyl 2,3-di-O-benzyl-6-deoxy-4-O-(3,4-di-O-benzyl-6-deoxy-2-O-(methylthio)thiocarbonyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside
CAS No.:125209-26-9
Molecular Formula:C₄₈H₅₂O₈S₃
Molecular Weight:853.134
Hs Code.:

Synonyms:phenyl 2,3-di-O-benzyl-6-deoxy-4-O-(3,4-di-O-benzyl-6-deoxy-2-O-(methylthio)thiocarbonyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside

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Chemical Property of phenyl 2,3-di-O-benzyl-6-deoxy-4-O-(3,4-di-O-benzyl-6-deoxy-2-O-(methylthio)thiocarbonyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside

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Technology Process of phenyl 2,3-di-O-benzyl-6-deoxy-4-O-(3,4-di-O-benzyl-6-deoxy-2-O-(methylthio)thiocarbonyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside

There total 5 articles about phenyl 2,3-di-O-benzyl-6-deoxy-4-O-(3,4-di-O-benzyl-6-deoxy-2-O-(methylthio)thiocarbonyl-β-D-glucopyranosyl)-1-thio-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:

: 125085-03-2
phenyl 2,3-di-O-benzyl-6-deoxy-1-thio-β-D-glucopyranoside

: 125209-26-9
phenyl 2,3-di-O-benzyl-6-deoxy-4-O-(3,4-di-O-benzyl-6-deoxy-2-O-(methylthio)thiocarbonyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) molecular sieves 4A, 2.) trimethylsilyl triflate, / 1.) CH₂Cl₂, RT; 1 h, 2.) CH₂Cl₂, -20 deg C, 20 min,

2: 100 percent / Na, / methanol; dioxane / Ambient temperature

3: 1.) NaH, imidazole, / 1.) oil, THF, RT; 1 h, 2.) THF, oil, RT; 20 min,

With 1H-imidazole; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; sodium; sodium hydride; In 1,4-dioxane; methanol;
DOI:10.1016/0008-6215(89)85044-X

Reference yield:

: 125135-31-1
1,2-di-O-acetyl-3,4-di-O-benzyl-6-deoxy-β-D-glucopyranose

: 125209-26-9
phenyl 2,3-di-O-benzyl-6-deoxy-4-O-(3,4-di-O-benzyl-6-deoxy-2-O-(methylthio)thiocarbonyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) molecular sieves 4A, 2.) trimethylsilyl triflate, / 1.) CH₂Cl₂, RT; 1 h, 2.) CH₂Cl₂, -20 deg C, 20 min,

2: 100 percent / Na, / methanol; dioxane / Ambient temperature

3: 1.) NaH, imidazole, / 1.) oil, THF, RT; 1 h, 2.) THF, oil, RT; 20 min,

With 1H-imidazole; trimethylsilyl trifluoromethanesulfonate; 4 A molecular sieve; sodium; sodium hydride; In 1,4-dioxane; methanol;
DOI:10.1016/0008-6215(89)85044-X

Reference yield:

: 125085-11-2
phenyl 4-O-(2-O-acetyl-3,4-di-O-benzyl-6-deoxy-β-D-glucopyranosyl)-2,3-di-O-benzyl-6-deoxy-1-thio-β-D-glucopyranoside

: 125209-26-9
phenyl 2,3-di-O-benzyl-6-deoxy-4-O-(3,4-di-O-benzyl-6-deoxy-2-O-(methylthio)thiocarbonyl-β-D-glucopyranosyl)-1-thio-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / Na, / methanol; dioxane / Ambient temperature

2: 1.) NaH, imidazole, / 1.) oil, THF, RT; 1 h, 2.) THF, oil, RT; 20 min,

With 1H-imidazole; sodium; sodium hydride; In 1,4-dioxane; methanol;
DOI:10.1016/0008-6215(89)85044-X