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

Base Information

Chemical Name:p-iodophenyl 2,3,6-tri-O-benzoyl-4-S-<4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl>-4-thio-α-D-glucopyranoside
CAS No.:119803-72-4
Molecular Formula:C₅₉H₆₁IO₂₅S
Molecular Weight:1329.09
Hs Code.:

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

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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

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

There total 7 articles about p-iodophenyl 2,3,6-tri-O-benzoyl-4-S-<4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl>-4-thio-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: 73.0%

: 119803-70-2
C₃₄H₂₆F₃IO₁₁S

: 119803-71-3
(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-acetyl-1-S-acetyl-1-thio-α-D-glucopyranose

: 119803-72-4
p-iodophenyl 2,3,6-tri-O-benzoyl-4-S-<4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl>-4-thio-α-D-glucopyranoside

Guidance literature:: With 1,4-dithio-erythritol; Cysteamine; In N,N,N,N,N,N-hexamethylphosphoric triamide; for 3h; Ambient temperature;

Reference yield:

: 52571-61-6
O-(4-iodophenyl)-(2,3,4,6-O-tetraacetyl)-α-D-galactopyranose

: 119803-72-4
p-iodophenyl 2,3,6-tri-O-benzoyl-4-S-<4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl>-4-thio-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) 1M-sodium methoxide, 2.) Amberlite / methanol / 12 h

2: triethylamine / CH₂Cl₂ / 48 h / Ambient temperature

3: pyridine / CH₂Cl₂

4: 73 percent / 1,4-dithioerythritol, cysteamine / hexamethylphosphoric acid triamide / 3 h / Ambient temperature

With pyridine; 1,4-dithio-erythritol; Amberlite; sodium methylate; triethylamine; Cysteamine; In methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane;

Reference yield:

: 52571-68-3
p-iodophenyl-α-D-galactopyranoside

: 119803-72-4
p-iodophenyl 2,3,6-tri-O-benzoyl-4-S-<4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl>-4-thio-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / CH₂Cl₂ / 48 h / Ambient temperature

2: pyridine / CH₂Cl₂

3: 73 percent / 1,4-dithioerythritol, cysteamine / hexamethylphosphoric acid triamide / 3 h / Ambient temperature

With pyridine; 1,4-dithio-erythritol; triethylamine; Cysteamine; In N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane;