Acetic acid (2S,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-((2R,3S,4R,5R,6R)-5-acetylamino-2-benzyloxymethyl-4-cyanomethoxy-6-octyloxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yl ester

Base Information

• Chemical Name: Acetic acid (2S,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-((2R,3S,4R,5R,6R)-5-acetylamino-2-benzyloxymethyl-4-cyanomethoxy-6-octyloxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yl ester
• CAS No.: 196876-50-3
• Molecular Formula: C₃₉H₅₆N₂O₁₅
• Molecular Weight: 792.878

Synonyms:Acetic acid (2S,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-((2R,3S,4R,5R,6R)-5-acetylamino-2-benzyloxymethyl-4-cyanomethoxy-6-octyloxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yl ester

Chemical Property of Acetic acid (2S,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-((2R,3S,4R,5R,6R)-5-acetylamino-2-benzyloxymethyl-4-cyanomethoxy-6-octyloxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of Acetic acid (2S,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-((2R,3S,4R,5R,6R)-5-acetylamino-2-benzyloxymethyl-4-cyanomethoxy-6-octyloxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yl ester

There total 5 articles about Acetic acid (2S,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-((2R,3S,4R,5R,6R)-5-acetylamino-2-benzyloxymethyl-4-cyanomethoxy-6-octyloxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yl ester 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: 46.0%

N-((2R,3R,4R,5S,6R)-6-Benzyloxymethyl-4-cyanomethoxy-5-hydroxy-2-octyloxy-tetrahydro-pyran-3-yl)-acetamide (196876-41-2) + 1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside (3068-32-4) → Acetic acid (2R,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-((2R,3S,4R,5R,6R)-5-acetylamino-2-benzyloxymethyl-4-cyanomethoxy-6-octyloxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yl ester + Acetic acid (2S,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-((2R,3S,4R,5R,6R)-5-acetylamino-2-benzyloxymethyl-4-cyanomethoxy-6-octyloxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yl ester (196876-50-3)

Guidance literature:

With 4 A molecular sieve; silver trifluoromethanesulfonate; In dichloromethane; at 0 ℃; for 3h; Yields of byproduct given;

DOI:10.1016/S0008-6215(97)00142-0

Reference yield:

benzaldehyde dimethyl acetal (1125-88-8) → Acetic acid (2S,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-((2R,3S,4R,5R,6R)-5-acetylamino-2-benzyloxymethyl-4-cyanomethoxy-6-octyloxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yl ester (196876-50-3)

Guidance literature:

Multi-step reaction with 4 steps

1: 93 percent / p-TsOH*H₂O / acetonitrile / Ambient temperature

2: 1.) NaH / 1.) CH₃CN, room temperature, 2 h, 2.) from -20 deg C to -15 deg C, 5 h.

3: 84 percent / NaCNBH₃, HCl, molecular sieves 4 Angstroem / tetrahydrofuran; diethyl ether / 1.) -5 deg C, 2 h, 2.) room temperature, overnight.lp

4: 46 percent / AgOTf, molecular sieves 4 Angstroem / CH₂Cl₂ / 3 h / 0 °C

With hydrogenchloride; 4 A molecular sieve; silver trifluoromethanesulfonate; sodium hydride; sodium cyanoborohydride; toluene-4-sulfonic acid; In tetrahydrofuran; diethyl ether; dichloromethane; acetonitrile;

DOI:10.1016/S0008-6215(97)00142-0

Reference yield:

octyl 2-(acetylamino)-2-deoxy-β-D-glucopyranoside (147126-58-7,383417-49-0) → Acetic acid (2S,3R,4S,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-2-((2R,3S,4R,5R,6R)-5-acetylamino-2-benzyloxymethyl-4-cyanomethoxy-6-octyloxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-3-yl ester (196876-50-3)

Guidance literature:

Multi-step reaction with 4 steps

1: 93 percent / p-TsOH*H₂O / acetonitrile / Ambient temperature

2: 1.) NaH / 1.) CH₃CN, room temperature, 2 h, 2.) from -20 deg C to -15 deg C, 5 h.

3: 84 percent / NaCNBH₃, HCl, molecular sieves 4 Angstroem / tetrahydrofuran; diethyl ether / 1.) -5 deg C, 2 h, 2.) room temperature, overnight.lp

4: 46 percent / AgOTf, molecular sieves 4 Angstroem / CH₂Cl₂ / 3 h / 0 °C

With hydrogenchloride; 4 A molecular sieve; silver trifluoromethanesulfonate; sodium hydride; sodium cyanoborohydride; toluene-4-sulfonic acid; In tetrahydrofuran; diethyl ether; dichloromethane; acetonitrile;

DOI:10.1016/S0008-6215(97)00142-0

upstream raw materials:

N-((2R,3R,4R,5S,6R)-6-Benzyloxymethyl-4-cyanomethoxy-5-hydroxy-2-octyloxy-tetrahydro-pyran-3-yl)-acetamide

1-bromo-1-deoxy-2,3,4,6-tetra-O-acetyl-a-D-galactopyranoside

benzaldehyde dimethyl acetal

octyl 2-(acetylamino)-2-deoxy-β-D-glucopyranoside

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