(2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranosylidene)amino 4-methylbenzene-1-sulfonate

Base Information

Chemical Name:(2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranosylidene)amino 4-methylbenzene-1-sulfonate
CAS No.:154125-84-5
Molecular Formula:C₃₆H₃₈N₂O₈S
Molecular Weight:658.772
Hs Code.:

Synonyms:(2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranosylidene)amino 4-methylbenzene-1-sulfonate

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Chemical Property of (2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranosylidene)amino 4-methylbenzene-1-sulfonate

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Technology Process of (2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranosylidene)amino 4-methylbenzene-1-sulfonate

There total 3 articles about (2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranosylidene)amino 4-methylbenzene-1-sulfonate 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: 100.0%

: 98-59-9
p-toluenesulfonyl chloride

: 154125-83-4
2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-D-gluconhydroximo-1,5-lactone

: 154125-84-5
(2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranosylidene)amino 4-methylbenzene-1-sulfonate

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 3h;
DOI:10.1002/hlca.19930760811

Reference yield:

: 4171-79-3,121123-45-3,4171-72-6
N-((3R,4R,5S,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)-2-hydroxy-tetrahydro-2H-pyran-3-yl)acetamide

: 154125-84-5
(2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranosylidene)amino 4-methylbenzene-1-sulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) NH₂OH*HCl, Na; 2.) NaIO₄, NaOAc / 1.) MeOH, EtOH, 60 deg C, 33 h; 2.) H₂O, EtOH, 17.75 h

2: 100 percent / Et₃N / CH₂Cl₂ / 3 h / 0 °C

With sodium periodate; hydroxylamine hydrochloride; sodium acetate; sodium; triethylamine; In dichloromethane;
DOI:10.1002/hlca.19930760811

Reference yield:

: 154172-26-6
allyl 2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranoside

: 154125-84-5
(2-acetamido-3,4,6-tri-O-benzyl-2-deoxy-D-glucopyranosylidene)amino 4-methylbenzene-1-sulfonate

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) KO(t-Bu); 2.) I₂ / 1.) DMSO, 50 deg C, 15 min; 2.) THF, H₂O, 26 deg C, 15 min

2: 1.) NH₂OH*HCl, Na; 2.) NaIO₄, NaOAc / 1.) MeOH, EtOH, 60 deg C, 33 h; 2.) H₂O, EtOH, 17.75 h

3: 100 percent / Et₃N / CH₂Cl₂ / 3 h / 0 °C

With sodium periodate; hydroxylamine hydrochloride; potassium tert-butylate; iodine; sodium acetate; sodium; triethylamine; In dichloromethane;
DOI:10.1002/hlca.19930760811