benzyl 2-amino-4-O-(2-amino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl)-2-deoxy-6-O-trityl-β-D-glucopyranoside

Base Information

Chemical Name:benzyl 2-amino-4-O-(2-amino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl)-2-deoxy-6-O-trityl-β-D-glucopyranoside
CAS No.:183659-11-2
Molecular Formula:C₄₅H₄₈N₂O₉
Molecular Weight:760.884
Hs Code.:

Synonyms:benzyl 2-amino-4-O-(2-amino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl)-2-deoxy-6-O-trityl-β-D-glucopyranoside

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Chemical Property of benzyl 2-amino-4-O-(2-amino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl)-2-deoxy-6-O-trityl-β-D-glucopyranoside

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Technology Process of benzyl 2-amino-4-O-(2-amino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl)-2-deoxy-6-O-trityl-β-D-glucopyranoside

There total 5 articles about benzyl 2-amino-4-O-(2-amino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl)-2-deoxy-6-O-trityl-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: 73.0%

: 183659-12-3
benzyl 2-acetylamino-4-O-(2-acetylamino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl)-2-deoxy-6-O-trityl-β-D-glucopyranoside

: 183659-11-2
benzyl 2-amino-4-O-(2-amino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl)-2-deoxy-6-O-trityl-β-D-glucopyranoside

Guidance literature:: With potassium hydroxide; In ethanol; at 110 - 120 ℃; for 12h;
DOI:10.1248/cpb.44.1958

Reference yield:

: 19272-52-7
benzyl 2-acetylamino-4-O-(2-acetylamino-2-deoxy-β-D-glucopyranosyl)-2-deoxy-β-D-glucopyranoside

: 183659-11-2
benzyl 2-amino-4-O-(2-amino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl)-2-deoxy-6-O-trityl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / p-TsOH monohydrate / dimethylformamide / 17 h / 40 - 50 °C

2: 49 percent / DMAP / dimethylformamide; pyridine / 144 h / 50 - 60 °C

3: 73 percent / KOH / ethanol / 12 h / 110 - 120 °C

With dmap; potassium hydroxide; toluene-4-sulfonic acid; In pyridine; ethanol; N,N-dimethyl-formamide;
DOI:10.1248/cpb.44.1958

Reference yield:

: 129579-88-0
benzyl 2-acetamido-4-O-(2'-acetamido-4',6'-O-benzylidene-2'-deoxy-β-D-glucopyranosyl)-2-deoxy-β-D-glucopyranoside

: 183659-11-2
benzyl 2-amino-4-O-(2-amino-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl)-2-deoxy-6-O-trityl-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 49 percent / DMAP / dimethylformamide; pyridine / 144 h / 50 - 60 °C

2: 73 percent / KOH / ethanol / 12 h / 110 - 120 °C

With dmap; potassium hydroxide; In pyridine; ethanol; N,N-dimethyl-formamide;
DOI:10.1248/cpb.44.1958