methyl (2,3,4-tri-O-acetyl-6-O-benzyl-β-D-galactopyranosyl)-(1->4)-3-O-benzoyl-6-O-benzyl-2-deoxy-2-tetrachlorophthalimido-β-D-glucopyranoside

Base Information

Chemical Name:methyl (2,3,4-tri-O-acetyl-6-O-benzyl-β-D-galactopyranosyl)-(1->4)-3-O-benzoyl-6-O-benzyl-2-deoxy-2-tetrachlorophthalimido-β-D-glucopyranoside
CAS No.:403832-93-9
Molecular Formula:C₄₈H₄₅Cl₄NO₁₆
Molecular Weight:1033.69
Hs Code.:

Synonyms:methyl (2,3,4-tri-O-acetyl-6-O-benzyl-β-D-galactopyranosyl)-(1->4)-3-O-benzoyl-6-O-benzyl-2-deoxy-2-tetrachlorophthalimido-β-D-glucopyranoside

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Chemical Property of methyl (2,3,4-tri-O-acetyl-6-O-benzyl-β-D-galactopyranosyl)-(1->4)-3-O-benzoyl-6-O-benzyl-2-deoxy-2-tetrachlorophthalimido-β-D-glucopyranoside

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Technology Process of methyl (2,3,4-tri-O-acetyl-6-O-benzyl-β-D-galactopyranosyl)-(1->4)-3-O-benzoyl-6-O-benzyl-2-deoxy-2-tetrachlorophthalimido-β-D-glucopyranoside

There total 7 articles about methyl (2,3,4-tri-O-acetyl-6-O-benzyl-β-D-galactopyranosyl)-(1->4)-3-O-benzoyl-6-O-benzyl-2-deoxy-2-tetrachlorophthalimido-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: 93.0%

: 67-56-1
methanol

: 403832-87-1
pent-4-enyl (2,3,4-tri-O-acetyl-6-O-benzyl-β-D-galactopyranosyl)-(1->4)-3-O-benzoyl-6-O-benzyl-2-deoxy-2-tetrachlorophthalimido-β-D-glucopyranoside

: 403832-93-9
methyl (2,3,4-tri-O-acetyl-6-O-benzyl-β-D-galactopyranosyl)-(1->4)-3-O-benzoyl-6-O-benzyl-2-deoxy-2-tetrachlorophthalimido-β-D-glucopyranoside

Guidance literature:: With N-iodo-succinimide; triethylsilyl trifluoromethyl sulfonate; In dichloromethane; for 0.5h;
DOI:10.1081/CAR-100108275

Reference yield:

: 100-39-0
benzyl bromide

: 403832-93-9
methyl (2,3,4-tri-O-acetyl-6-O-benzyl-β-D-galactopyranosyl)-(1->4)-3-O-benzoyl-6-O-benzyl-2-deoxy-2-tetrachlorophthalimido-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1.1: (Bu₃Sn)2O / methanol / 2 h / 75 °C

1.2: 69 percent / tetrabutylammonium bromide / 20 h / 90 °C

2.1: 87 percent / AgOTf; molecular sieves 3 Angstroem / CH₂Cl₂ / 1 h / -60 °C

3.1: 88 percent / pyridine / CH₂Cl₂ / 20 °C

4.1: 93 percent / NIS; triethylsilyl triflate / CH₂Cl₂ / 0.5 h

With pyridine; N-iodo-succinimide; 3 A molecular sieve; triethylsilyl trifluoromethyl sulfonate; silver trifluoromethanesulfonate; bis(tri-n-butyltin)oxide; In methanol; dichloromethane;
DOI:10.1081/CAR-100108275

Reference yield:

: 107855-14-1
ethyl 2,3,4-tri-O-acetyl-6-O-benzyl-1-thio-β-D-galactopyranoside

: 403832-93-9
methyl (2,3,4-tri-O-acetyl-6-O-benzyl-β-D-galactopyranosyl)-(1->4)-3-O-benzoyl-6-O-benzyl-2-deoxy-2-tetrachlorophthalimido-β-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: Br₂ / CH₂Cl₂ / 0.5 h / 20 °C

2: 87 percent / AgOTf; molecular sieves 3 Angstroem / CH₂Cl₂ / 1 h / -60 °C

3: 88 percent / pyridine / CH₂Cl₂ / 20 °C

4: 93 percent / NIS; triethylsilyl triflate / CH₂Cl₂ / 0.5 h

With pyridine; N-iodo-succinimide; 3 A molecular sieve; bromine; triethylsilyl trifluoromethyl sulfonate; silver trifluoromethanesulfonate; In dichloromethane;
DOI:10.1081/CAR-100108275