methyl 2-acetamido-3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4-O-benzyl-2-deoxy-4-O-phenoxythiocarbonyl-β-D-glucopyranoside

Base Information

Chemical Name:methyl 2-acetamido-3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4-O-benzyl-2-deoxy-4-O-phenoxythiocarbonyl-β-D-glucopyranoside
CAS No.:144684-86-6
Molecular Formula:C₅₂H₅₇NO₁₃S
Molecular Weight:936.089
Hs Code.:

Synonyms:methyl 2-acetamido-3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4-O-benzyl-2-deoxy-4-O-phenoxythiocarbonyl-β-D-glucopyranoside

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Chemical Property of methyl 2-acetamido-3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4-O-benzyl-2-deoxy-4-O-phenoxythiocarbonyl-β-D-glucopyranoside

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Technology Process of methyl 2-acetamido-3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4-O-benzyl-2-deoxy-4-O-phenoxythiocarbonyl-β-D-glucopyranoside

There total 1 articles about methyl 2-acetamido-3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4-O-benzyl-2-deoxy-4-O-phenoxythiocarbonyl-β-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:

: 116981-12-5,144732-86-5
methyl 2-acetamido-3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside

: 144684-86-6
methyl 2-acetamido-3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4-O-benzyl-2-deoxy-4-O-phenoxythiocarbonyl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 73 percent / sodium cyanoborohydride

2: 65 percent / 4-dimethylaminopyridine / acetonitrile / 1.) reflux, 20 h, 2.) r.t., 20 h

With dmap; sodium cyanoborohydride; In acetonitrile;

Reference yield: 77.0%

: 144684-86-6
methyl 2-acetamido-3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4-O-benzyl-2-deoxy-4-O-phenoxythiocarbonyl-β-D-glucopyranoside

: 144684-87-7
methyl 2-acetamido-3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4-O-benzyl-2,4-dideoxy-β-D-xylo-hexopyranoside

Guidance literature:: With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In toluene; at 80 ℃; for 2h;

Reference yield:

: 144684-86-6
methyl 2-acetamido-3-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-galactopyranosyl)-4-O-benzyl-2-deoxy-4-O-phenoxythiocarbonyl-β-D-glucopyranoside

: 144684-89-9
methyl 2-acetamido-6-O-benzyl-2,4-dideoxy-3-O-<3,4,6-tri-O-benzyl-2-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-β-D-galactopyranosyl>-β-D-xylo-hexopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 77 percent / 2,2'-azobis(isobutyronitrile), Bu₃SnH / toluene / 2 h / 80 °C

2: 88 percent / methanolic 0.05 N MeONa / Ambient temperature

3: 57 percent / 4 Angstroem molecular sieves, tetraethylammonium bromide / CH₂Cl₂; dimethylformamide / 24 h

With 2,2'-azobis(isobutyronitrile); 4 A molecular sieve; tetraethylammonium bromide; tri-n-butyl-tin hydride; sodium methylate; In dichloromethane; N,N-dimethyl-formamide; toluene;