p-iodophenyl-2,3,6-tri-O-acetyl-4-O-(2,3-di-O-acetyl-4-S-acetyl-6-O-benzoyl-4-thio-α-D-glucopyranosyl)-α-D-glucopyranosyde

Base Information

Chemical Name:p-iodophenyl-2,3,6-tri-O-acetyl-4-O-(2,3-di-O-acetyl-4-S-acetyl-6-O-benzoyl-4-thio-α-D-glucopyranosyl)-α-D-glucopyranosyde
CAS No.:119803-59-7
Molecular Formula:C₃₇H₄₁IO₁₇S
Molecular Weight:916.693
Hs Code.:

Synonyms:p-iodophenyl-2,3,6-tri-O-acetyl-4-O-(2,3-di-O-acetyl-4-S-acetyl-6-O-benzoyl-4-thio-α-D-glucopyranosyl)-α-D-glucopyranosyde

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Chemical Property of p-iodophenyl-2,3,6-tri-O-acetyl-4-O-(2,3-di-O-acetyl-4-S-acetyl-6-O-benzoyl-4-thio-α-D-glucopyranosyl)-α-D-glucopyranosyde

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Technology Process of p-iodophenyl-2,3,6-tri-O-acetyl-4-O-(2,3-di-O-acetyl-4-S-acetyl-6-O-benzoyl-4-thio-α-D-glucopyranosyl)-α-D-glucopyranosyde

There total 8 articles about p-iodophenyl-2,3,6-tri-O-acetyl-4-O-(2,3-di-O-acetyl-4-S-acetyl-6-O-benzoyl-4-thio-α-D-glucopyranosyl)-α-D-glucopyranosyde 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: 22.0%

: 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

: 10387-40-3
potassium thioacetate

: 119803-60-0
Benzoic acid (2R,3R,4R,5R,6S)-4,5-diacetoxy-3-acetylsulfanyl-6-[(2R,3R,4S,5R,6S)-4,5-diacetoxy-2-acetoxymethyl-6-(4-iodo-phenoxy)-tetrahydro-pyran-3-yloxy]-tetrahydro-pyran-2-ylmethyl ester

: 119803-59-7
p-iodophenyl-2,3,6-tri-O-acetyl-4-O-(2,3-di-O-acetyl-4-S-acetyl-6-O-benzoyl-4-thio-α-D-glucopyranosyl)-α-D-glucopyranosyde

Guidance literature:: In tetrahydrofuran; for 24h; 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

: 119803-59-7
p-iodophenyl-2,3,6-tri-O-acetyl-4-O-(2,3-di-O-acetyl-4-S-acetyl-6-O-benzoyl-4-thio-α-D-glucopyranosyl)-α-D-glucopyranosyde

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: 44 percent / tetrahydrofuran / 24 h / Ambient temperature

With pyridine; tin(IV) chloride; sodium nitrite; In tetrahydrofuran; methanol; 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

: 119803-59-7
p-iodophenyl-2,3,6-tri-O-acetyl-4-O-(2,3-di-O-acetyl-4-S-acetyl-6-O-benzoyl-4-thio-α-D-glucopyranosyl)-α-D-glucopyranosyde

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: 44 percent / tetrahydrofuran / 24 h / Ambient temperature

With pyridine; tin(IV) chloride; triethylamine; sodium nitrite; In tetrahydrofuran; methanol; nitromethane; dichloromethane; chloroform; N,N-dimethyl-formamide;