6-[N-(benzyloxycarbonylamino)hexyl]-2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-[3,4-O-isopropylidene-2-O-(3,4-O-isopropylidene-α-L-fucopyranosyl)-α-L-fucopyranosyl]-β-D-glucopyranoside

Base Information

Chemical Name:6-[N-(benzyloxycarbonylamino)hexyl]-2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-[3,4-O-isopropylidene-2-O-(3,4-O-isopropylidene-α-L-fucopyranosyl)-α-L-fucopyranosyl]-β-D-glucopyranoside
CAS No.:852311-82-1
Molecular Formula:C₄₇H₆₆N₂O₁₆
Molecular Weight:915.045
Hs Code.:

6-[N-(benzyloxycarbonylamino)hexyl]-2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-[3,4-O-isopropylidene-2-O-(3,4-O-isopropylidene-α-L-fucopyranosyl)-α-L-fucopyranosyl]-β-D-glucopyranoside

Synonyms:6-[N-(benzyloxycarbonylamino)hexyl]-2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-[3,4-O-isopropylidene-2-O-(3,4-O-isopropylidene-α-L-fucopyranosyl)-α-L-fucopyranosyl]-β-D-glucopyranoside

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Chemical Property of 6-[N-(benzyloxycarbonylamino)hexyl]-2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-[3,4-O-isopropylidene-2-O-(3,4-O-isopropylidene-α-L-fucopyranosyl)-α-L-fucopyranosyl]-β-D-glucopyranoside

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Technology Process of 6-[N-(benzyloxycarbonylamino)hexyl]-2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-[3,4-O-isopropylidene-2-O-(3,4-O-isopropylidene-α-L-fucopyranosyl)-α-L-fucopyranosyl]-β-D-glucopyranoside

There total 9 articles about 6-[N-(benzyloxycarbonylamino)hexyl]-2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-[3,4-O-isopropylidene-2-O-(3,4-O-isopropylidene-α-L-fucopyranosyl)-α-L-fucopyranosyl]-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:

: 852311-78-5
ethyl 2-O-tert-butyldimethylsilyl-3,4-O-isopropylidene-1-thio-β-L-fucopyranoside

: 852311-82-1
6-[N-(benzyloxycarbonylamino)hexyl]-2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-[3,4-O-isopropylidene-2-O-(3,4-O-isopropylidene-α-L-fucopyranosyl)-α-L-fucopyranosyl]-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 291 mg / tetrabutylammonium bromide; copper(II) bromide; molecular sieves 4 Angstroem / CH₂Cl₂; dimethylformamide / 96 h / 20 °C

2: 94 percent / tetrabutylammonium fluoride / tetrahydrofuran / 6 h / 20 °C

With 4 A molecular sieve; tetrabutyl ammonium fluoride; tetrabutylammomium bromide; copper(ll) bromide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2005.02.009

Reference yield:

: 138343-54-1
ethyl 3,4-di-O-isopropylidene-1-thio-β-L-fucopyranoside

: 852311-82-1
6-[N-(benzyloxycarbonylamino)hexyl]-2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-[3,4-O-isopropylidene-2-O-(3,4-O-isopropylidene-α-L-fucopyranosyl)-α-L-fucopyranosyl]-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / imidazole / dimethylformamide / 16 h / 20 °C

2: 291 mg / tetrabutylammonium bromide; copper(II) bromide; molecular sieves 4 Angstroem / CH₂Cl₂; dimethylformamide / 96 h / 20 °C

3: 94 percent / tetrabutylammonium fluoride / tetrahydrofuran / 6 h / 20 °C

With 1H-imidazole; 4 A molecular sieve; tetrabutyl ammonium fluoride; tetrabutylammomium bromide; copper(ll) bromide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2005.02.009

Reference yield:

: 852311-80-9
6-[N-(benzyloxycarbonylamino)hexyl]-2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-(3,4-O-isopropylidene-α-L-fucopyranosyl)-β-D-glucopyranoside

: 852311-82-1
6-[N-(benzyloxycarbonylamino)hexyl]-2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-[3,4-O-isopropylidene-2-O-(3,4-O-isopropylidene-α-L-fucopyranosyl)-α-L-fucopyranosyl]-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 291 mg / tetrabutylammonium bromide; copper(II) bromide; molecular sieves 4 Angstroem / CH₂Cl₂; dimethylformamide / 96 h / 20 °C

2: 94 percent / tetrabutylammonium fluoride / tetrahydrofuran / 6 h / 20 °C

With 4 A molecular sieve; tetrabutyl ammonium fluoride; tetrabutylammomium bromide; copper(ll) bromide; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2005.02.009