p-tolyl N-benzyl-2-amino-2,3-N,O-carbonyl-4,6-O-diacetyl-2-deoxy-1-thio-β-D-glucopyranoside

Base Information

Chemical Name:p-tolyl N-benzyl-2-amino-2,3-N,O-carbonyl-4,6-O-diacetyl-2-deoxy-1-thio-β-D-glucopyranoside
CAS No.:1038395-36-6
Molecular Formula:C₂₅H₂₇NO₇S
Molecular Weight:485.558
Hs Code.:

Synonyms:p-tolyl N-benzyl-2-amino-2,3-N,O-carbonyl-4,6-O-diacetyl-2-deoxy-1-thio-β-D-glucopyranoside

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

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Chemical Property of p-tolyl N-benzyl-2-amino-2,3-N,O-carbonyl-4,6-O-diacetyl-2-deoxy-1-thio-β-D-glucopyranoside

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Technology Process of p-tolyl N-benzyl-2-amino-2,3-N,O-carbonyl-4,6-O-diacetyl-2-deoxy-1-thio-β-D-glucopyranoside

There total 1 articles about p-tolyl N-benzyl-2-amino-2,3-N,O-carbonyl-4,6-O-diacetyl-2-deoxy-1-thio-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: 90.0%

: 956103-68-7
p-tolyl N-benzyl-2-amino-2,3-N,O-carbonyl-2-deoxy-1-thio-β-D-glucopyranoside

: 108-24-7
acetic anhydride

: 1038395-36-6
p-tolyl N-benzyl-2-amino-2,3-N,O-carbonyl-4,6-O-diacetyl-2-deoxy-1-thio-β-D-glucopyranoside

Guidance literature:: With pyridine; at 20 ℃; for 3h;
DOI:10.1016/j.tet.2008.03.103

Reference yield: 70.0%

: 1038395-36-6
p-tolyl N-benzyl-2-amino-2,3-N,O-carbonyl-4,6-O-diacetyl-2-deoxy-1-thio-β-D-glucopyranoside

: 4356-80-3,34212-64-1,40653-32-5,53008-65-4,68027-27-0,73111-53-2,128184-63-4,138794-99-7,55094-38-7,641635-63-4
methyl 2,3,4-tri-O-benzyl-α-D-galactopyranoside

: 1446749-20-7
C₄₆H₅₁NO₁₃

Guidance literature:: With N-iodo-succinimide; silver trifluoromethanesulfonate; In dichloromethane; at 20 ℃; stereoselective reaction; Molecular sieve; Inert atmosphere;
DOI:10.1002/chem.201204550

Reference yield:

: 1038395-36-6
p-tolyl N-benzyl-2-amino-2,3-N,O-carbonyl-4,6-O-diacetyl-2-deoxy-1-thio-β-D-glucopyranoside

: 76375-66-1
methyl 2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside

: 1038395-41-3
methyl (N-benzyl-2-amino-2,3-N,O-carbonyl-4,6-O-diacetyl-2-deoxy-α-D-glucopyranosyl)-(1->3)-2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside

: 1038395-42-4
methyl (N-benzyl-2-amino-2,3-N,O-carbonyl-4,6-O-diacetyl-2-deoxy-β-D-glucopyranosyl)-(1->3)-2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside

Guidance literature:: p-tolyl N-benzyl-2-amino-2,3-N,O-carbonyl-4,6-O-diacetyl-2-deoxy-1-thio-β-D-glucopyranoside; With trifluoromethylsulfonic anhydride; In dichloromethane; at -73 ℃;

methyl 2-O-benzyl-4,6-O-benzylidene-α-D-glucopyranoside; In dichloromethane; at -50 ℃; Further stages.;
DOI:10.1016/j.tet.2008.03.103