allyl 2-acetamido-6-O-benzyl-2-deoxy-3,4-O-dibenzoyl-α-D-glucopyranoside

Base Information

Chemical Name:allyl 2-acetamido-6-O-benzyl-2-deoxy-3,4-O-dibenzoyl-α-D-glucopyranoside
CAS No.:191925-22-1
Molecular Formula:C₃₂H₃₃NO₈
Molecular Weight:559.616
Hs Code.:

Synonyms:allyl 2-acetamido-6-O-benzyl-2-deoxy-3,4-O-dibenzoyl-α-D-glucopyranoside

Suppliers and Price of allyl 2-acetamido-6-O-benzyl-2-deoxy-3,4-O-dibenzoyl-α-D-glucopyranoside

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of allyl 2-acetamido-6-O-benzyl-2-deoxy-3,4-O-dibenzoyl-α-D-glucopyranoside

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of allyl 2-acetamido-6-O-benzyl-2-deoxy-3,4-O-dibenzoyl-α-D-glucopyranoside

There total 5 articles about allyl 2-acetamido-6-O-benzyl-2-deoxy-3,4-O-dibenzoyl-α-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:

: 7512-17-6,72-87-7,1136-42-1,1136-44-3,6082-29-7,6730-06-9,7772-94-3,10036-64-3,14131-60-3,14131-64-7,14131-68-1,14215-68-0,62057-49-2,62057-50-5,62057-51-6,62057-52-7,62057-53-8,62057-54-9,62057-55-0,62057-56-1,62075-50-7,62137-54-6,134451-97-1,134522-12-6,148347-16-4
N-Acetyl-D-glucosamine

: 191925-22-1
allyl 2-acetamido-6-O-benzyl-2-deoxy-3,4-O-dibenzoyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1: boron trifluoride etherate / 5 h / 95 °C

2: 47 g / tosic acid / dimethylformamide / 2 h / 60 - 80 °C

3: 53 percent / Et₃N / CHCl₃ / 2 h / Heating

4: 3 A molecular sieves; sodium cyanoborohydride / tetrahydrofuran / 0 °C

5: 7 g / pyridine / CH₂Cl₂ / 2 h

With pyridine; 3 A molecular sieve; boron trifluoride diethyl etherate; sodium cyanoborohydride; toluene-4-sulfonic acid; triethylamine; In tetrahydrofuran; dichloromethane; chloroform; N,N-dimethyl-formamide; 1: glycosylation / 2: transacetalation / 3: benzoylation / 4: Ring cleavage / 5: benzoylation;
DOI:10.1016/S0008-6215(97)00039-6

Reference yield:

: 88903-97-3
N-((3R,4R,5S,6R)-2-(allyloxy)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2Hpyran-3-yl)acetamide

: 191925-22-1
allyl 2-acetamido-6-O-benzyl-2-deoxy-3,4-O-dibenzoyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 47 g / tosic acid / dimethylformamide / 2 h / 60 - 80 °C

2: 53 percent / Et₃N / CHCl₃ / 2 h / Heating

3: 3 A molecular sieves; sodium cyanoborohydride / tetrahydrofuran / 0 °C

4: 7 g / pyridine / CH₂Cl₂ / 2 h

With pyridine; 3 A molecular sieve; sodium cyanoborohydride; toluene-4-sulfonic acid; triethylamine; In tetrahydrofuran; dichloromethane; chloroform; N,N-dimethyl-formamide; 1: transacetalation / 2: benzoylation / 3: Ring cleavage / 4: benzoylation;
DOI:10.1016/S0008-6215(97)00039-6

Reference yield:

: 74984-84-2
prop-2-en-1-yl 2-(acetylamino)-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside

: 191925-22-1
allyl 2-acetamido-6-O-benzyl-2-deoxy-3,4-O-dibenzoyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 53 percent / Et₃N / CHCl₃ / 2 h / Heating

2: 3 A molecular sieves; sodium cyanoborohydride / tetrahydrofuran / 0 °C

3: 7 g / pyridine / CH₂Cl₂ / 2 h

With pyridine; 3 A molecular sieve; sodium cyanoborohydride; triethylamine; In tetrahydrofuran; dichloromethane; chloroform; 1: benzoylation / 2: Ring cleavage / 3: benzoylation;
DOI:10.1016/S0008-6215(97)00039-6