benzyl 2-acetamido-3-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2,6-dideoxy-6-fluoro-α-D-galactopyranoside

Base Information

Chemical Name:benzyl 2-acetamido-3-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2,6-dideoxy-6-fluoro-α-D-galactopyranoside
CAS No.:114669-42-0
Molecular Formula:C₂₃H₃₃FN₂O₁₀
Molecular Weight:516.521
Hs Code.:

Synonyms:benzyl 2-acetamido-3-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2,6-dideoxy-6-fluoro-α-D-galactopyranoside

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Chemical Property of benzyl 2-acetamido-3-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2,6-dideoxy-6-fluoro-α-D-galactopyranoside

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Technology Process of benzyl 2-acetamido-3-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2,6-dideoxy-6-fluoro-α-D-galactopyranoside

There total 2 articles about benzyl 2-acetamido-3-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2,6-dideoxy-6-fluoro-α-D-galactopyranoside 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: 75.0%

: 114669-41-9
Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-((2S,3R,4R,5R,6S)-3-acetylamino-2-benzyloxy-6-fluoromethyl-5-hydroxy-tetrahydro-pyran-4-yloxy)-tetrahydro-pyran-4-yl ester

: 114669-42-0
benzyl 2-acetamido-3-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2,6-dideoxy-6-fluoro-α-D-galactopyranoside

Guidance literature:: With sodium methylate; In methanol;
DOI:10.1016/0008-6215(87)80111-8

Reference yield:

: 85230-49-5
benzyl 2-acetamido-3-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-2-deoxy-α-D-galactopyranoside

: 114669-42-0
benzyl 2-acetamido-3-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2,6-dideoxy-6-fluoro-α-D-galactopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 36 percent / Et₂NSF₃

2: 75 percent / NaOMe / methanol

With diethylamino-sulfur trifluoride; sodium methylate; In methanol;
DOI:10.1016/0008-6215(87)80111-8