benzyl (p-tolyl 5-amino-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulpyranosid)onate

Base Information

• Chemical Name: benzyl (p-tolyl 5-amino-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulpyranosid)onate
• CAS No.: 445022-67-3
• Molecular Formula: C₂₃H₂₉NO₇S
• Molecular Weight: 463.552
• Mol file: 445022-67-3.mol

Synonyms:benzyl (p-tolyl 5-amino-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulpyranosid)onate

Chemical Property of benzyl (p-tolyl 5-amino-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulpyranosid)onate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of benzyl (p-tolyl 5-amino-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulpyranosid)onate

There total 3 articles about benzyl (p-tolyl 5-amino-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulpyranosid)onate 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: 81.0%

benzyl (p-tolyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulpyranosid)onate (445022-65-1) → benzyl (p-tolyl 5-amino-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulpyranosid)onate (445022-67-3)

Guidance literature:

With methanesulfonic acid; In methanol; at 60 ℃; for 24h;

DOI:10.1016/S0008-6215(02)00057-5

Reference yield:

benzyl (5-acetamido-4,7,8,9-tetra-O-acetyl-2-chloro-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulpyranosid)onate (113757-77-0) → benzyl (p-tolyl 5-amino-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulpyranosid)onate (445022-67-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 84 percent / iPr₂EtN / CH₂Cl₂ / 20 °C

2: 81 percent / methanesulfonic acid / methanol / 24 h / 60 °C

With methanesulfonic acid; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane;

DOI:10.1016/S0008-6215(02)00057-5

Reference yield:

(1S,2R)-1-((2R,3R,4S,6R)-3-acetamido-4,6-diacetoxy-6-(benzyloxycarbonyl)tetrahydro-2H-pyran-2-yl)propane-1,2,3-triyl triacetate (113757-76-9) → benzyl (p-tolyl 5-amino-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulpyranosid)onate (445022-67-3)

Guidance literature:

Multi-step reaction with 3 steps

1: HCl; AcCl / 48 h / 20 °C

2: 84 percent / iPr₂EtN / CH₂Cl₂ / 20 °C

3: 81 percent / methanesulfonic acid / methanol / 24 h / 60 °C

With hydrogenchloride; methanesulfonic acid; N-ethyl-N,N-diisopropylamine; acetyl chloride; In methanol; dichloromethane;

DOI:10.1016/S0008-6215(02)00057-5

upstream raw materials:

benzyl (p-tolyl 5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulpyranosid)onate

(1S,2R)-1-((2R,3R,4S,6R)-3-acetamido-4,6-diacetoxy-6-(benzyloxycarbonyl)tetrahydro-2H-pyran-2-yl)propane-1,2,3-triyl triacetate

benzyl (5-acetamido-4,7,8,9-tetra-O-acetyl-2-chloro-3,5-dideoxy-D-glycero-α-D-galacto-non-2-ulpyranosid)onate

Downstream raw materials:

benzyl (p-tolyl 5-azido-4,7,8,9-tetra-O-benzyl-3,5-dideoxy-2-thio-D-glycero-α-D-galacto-non-2-ulpyranosid)onate