p-iodophenyl-2,3,6-tri-O-acetyl-4-O-<2,3-di-O-acetyl-6-O-benzoyl-4-S-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-4-thio-β-D-glucopyranosyl>-α-D-glucopyranoside

Base Information

Chemical Name:p-iodophenyl-2,3,6-tri-O-acetyl-4-O-<2,3-di-O-acetyl-6-O-benzoyl-4-S-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-4-thio-β-D-glucopyranosyl>-α-D-glucopyranoside
CAS No.:119803-57-5
Molecular Formula:C₄₉H₅₇IO₂₅S
Molecular Weight:1204.95
Hs Code.:

p-iodophenyl-2,3,6-tri-O-acetyl-4-O-<2,3-di-O-acetyl-6-O-benzoyl-4-S-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-4-thio-β-D-glucopyranosyl>-α-D-glucopyranoside

Synonyms:p-iodophenyl-2,3,6-tri-O-acetyl-4-O-<2,3-di-O-acetyl-6-O-benzoyl-4-S-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-4-thio-β-D-glucopyranosyl>-α-D-glucopyranoside

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Chemical Property of p-iodophenyl-2,3,6-tri-O-acetyl-4-O-<2,3-di-O-acetyl-6-O-benzoyl-4-S-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-4-thio-β-D-glucopyranosyl>-α-D-glucopyranoside

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Technology Process of p-iodophenyl-2,3,6-tri-O-acetyl-4-O-<2,3-di-O-acetyl-6-O-benzoyl-4-S-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-4-thio-β-D-glucopyranosyl>-α-D-glucopyranoside

There total 8 articles about p-iodophenyl-2,3,6-tri-O-acetyl-4-O-<2,3-di-O-acetyl-6-O-benzoyl-4-S-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-4-thio-β-D-glucopyranosyl>-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: 19.0%

: 119803-56-4,119803-76-8
Benzoic acid (2R,3S,4R,5R,6R)-4,5-diacetoxy-6-[(2R,3R,4S,5R)-4,5-diacetoxy-2-acetoxymethyl-6-(4-iodo-phenoxy)-tetrahydro-pyran-3-yloxy]-3-trifluoromethanesulfonyloxy-tetrahydro-pyran-2-ylmethyl ester

: 62860-10-0
2,3,4,6-tetra-O-acetyl-1-S-acetyl-1-thio-α-D-glucopyranoside

: 119803-58-6
C₄₉H₅₇IO₂₅S

: 119803-57-5
p-iodophenyl-2,3,6-tri-O-acetyl-4-O-<2,3-di-O-acetyl-6-O-benzoyl-4-S-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-4-thio-β-D-glucopyranosyl>-α-D-glucopyranoside

Guidance literature:: With 1,4-dithio-erythritol; Cysteamine; In N,N,N,N,N,N-hexamethylphosphoric triamide; for 2h; Ambient temperature;

Reference yield:

: 119803-50-8
1,2,3,6-tetra-O-acetyl-4-O-(2,3-di-O-acetyl-6-O-benzoyl-α-D-glucopyranosyl)-β-D-glucopyranose

: 119803-57-5
p-iodophenyl-2,3,6-tri-O-acetyl-4-O-<2,3-di-O-acetyl-6-O-benzoyl-4-S-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-4-thio-β-D-glucopyranosyl>-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 7 steps

1: pyridine / CH₂Cl₂ / 0.5 h / 0 °C

2: 51 percent / sodium nitrite / dimethylformamide / 3 h / Ambient temperature

3: 97 percent / pyridine / CH₂Cl₂ / 0 deg C, , 30 min, RT, 3 h

4: tin tetrachloride / CHCl₃; nitromethane / 1.5 h / Ambient temperature

5: pyridine / methanol; CH₂Cl₂ / 24 h / Ambient temperature

6: pyridine / CH₂Cl₂

7: 45 percent / 1,4-dithioerythritol, cysteamine / hexamethylphosphoric acid triamide / 2 h / Ambient temperature

With pyridine; 1,4-dithio-erythritol; tin(IV) chloride; Cysteamine; sodium nitrite; In methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; nitromethane; dichloromethane; chloroform; N,N-dimethyl-formamide;

Reference yield:

: 72718-62-8,81661-67-8,102281-77-6,120852-02-0,93417-43-7
1,2,3,6-tetra-O-acetyl-4-O-(2',3'-di-O-acetyl-α-D-glucopyranosyl)-β-D-glucopyranoside

: 119803-57-5
p-iodophenyl-2,3,6-tri-O-acetyl-4-O-<2,3-di-O-acetyl-6-O-benzoyl-4-S-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-4-thio-β-D-glucopyranosyl>-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 8 steps

1: 73 percent / triethylamine / CH₂Cl₂ / 24 h / Ambient temperature

2: pyridine / CH₂Cl₂ / 0.5 h / 0 °C

3: 51 percent / sodium nitrite / dimethylformamide / 3 h / Ambient temperature

4: 97 percent / pyridine / CH₂Cl₂ / 0 deg C, , 30 min, RT, 3 h

5: tin tetrachloride / CHCl₃; nitromethane / 1.5 h / Ambient temperature

6: pyridine / methanol; CH₂Cl₂ / 24 h / Ambient temperature

7: pyridine / CH₂Cl₂

8: 45 percent / 1,4-dithioerythritol, cysteamine / hexamethylphosphoric acid triamide / 2 h / Ambient temperature

With pyridine; 1,4-dithio-erythritol; tin(IV) chloride; triethylamine; Cysteamine; sodium nitrite; In methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; nitromethane; dichloromethane; chloroform; N,N-dimethyl-formamide;