3-azido-2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-mannopyranosyl 2-O-benzoyl-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

Base Information

Chemical Name:3-azido-2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-mannopyranosyl 2-O-benzoyl-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside
CAS No.:102561-92-2
Molecular Formula:C₄₇H₄₅N₃O₁₁
Molecular Weight:827.888
Hs Code.:

Synonyms:3-azido-2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-mannopyranosyl 2-O-benzoyl-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

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Chemical Property of 3-azido-2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-mannopyranosyl 2-O-benzoyl-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

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Technology Process of 3-azido-2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-mannopyranosyl 2-O-benzoyl-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

There total 3 articles about 3-azido-2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-mannopyranosyl 2-O-benzoyl-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 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: 68.0%

: 532-32-1
sodium benzoate

: 3-azido-2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-mannopyranosyl 3-O-benzyl-4,6-O-benzylidene-2-O-trifluoromethylsulfonyl-α-D-glucopyranoside

: 102561-92-2
3-azido-2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-mannopyranosyl 2-O-benzoyl-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

Guidance literature:: In N,N-dimethyl-formamide; for 21h; Heating;
DOI:10.1016/0008-6215(85)85008-4

Reference yield:

: 90593-19-4,127128-53-4
C₄₀H₄₂O₁₁

: 102561-92-2
3-azido-2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-mannopyranosyl 2-O-benzoyl-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 90.3 percent / CH₂Cl₂; pyridine / 1.) 0 deg C, 2.) 0 deg C - room temperature

2: 55.1 percent / NaN₃, tetrabutylammonium hydrogensulfate / toluene; H₂O / 168 h / Heating

3: 68 percent / dimethylformamide / 21 h / Heating

With sodium azide; tetra(n-butyl)ammonium hydrogensulfate; In pyridine; dichloromethane; water; N,N-dimethyl-formamide; toluene;
DOI:10.1016/0008-6215(85)85008-4

Reference yield:

: 102561-88-6
2-O-benzyl-4,6-O-benzylidene-3-O-trifluoromethylsulfonyl-α-D-altropyranosyl 3-O-benzyl-4,6-O-benzylidene-2-O-trifluoromethylsulfonyl-α-D-glucopyranoside

: 102561-92-2
3-azido-2-O-benzyl-4,6-O-benzylidene-3-deoxy-α-D-mannopyranosyl 2-O-benzoyl-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 55.1 percent / NaN₃, tetrabutylammonium hydrogensulfate / toluene; H₂O / 168 h / Heating

2: 68 percent / dimethylformamide / 21 h / Heating

With sodium azide; tetra(n-butyl)ammonium hydrogensulfate; In water; N,N-dimethyl-formamide; toluene;
DOI:10.1016/0008-6215(85)85008-4