5-(methoxycarbonyl)pentyl 2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside

Base Information

Chemical Name:5-(methoxycarbonyl)pentyl 2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside
CAS No.:848828-28-4
Molecular Formula:C₃₅H₄₆N₆O₁₀
Molecular Weight:710.784
Hs Code.:

Synonyms:5-(methoxycarbonyl)pentyl 2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside

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Chemical Property of 5-(methoxycarbonyl)pentyl 2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside

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Technology Process of 5-(methoxycarbonyl)pentyl 2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside

There total 9 articles about 5-(methoxycarbonyl)pentyl 2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-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: 95.0%

: 848828-27-3
5-(methoxycarbonyl)pentyl 4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside

: 115234-11-2
ethyl 2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-1-thio-α-D-mannopyranoside

: 848828-28-4
5-(methoxycarbonyl)pentyl 2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside

Guidance literature:: With N-iodo-succinimide; 4 A molecular sieve; silver trifluoromethanesulfonate; In dichloromethane; toluene; at 0 - 20 ℃;
DOI:10.1016/j.tetasy.2004.11.021

Reference yield: 53.0%

: 4547-43-7
methyl 6-hydroxycaproate

: 1447757-41-6
2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl (1→2) 4-azido-3-O-benzyl-4,6-dideoxy-D-mannopyranosyl N-phenyltrifluoroacetimidate

: 848828-28-4
5-(methoxycarbonyl)pentyl 2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In toluene; at 100 ℃; for 1h; Molecular sieve;
DOI:10.1002/anie.201302303

Reference yield:

: 4547-43-7
methyl 6-hydroxycaproate

: 848828-28-4
5-(methoxycarbonyl)pentyl 2-O-acetyl-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranosyl-(1->2)-4-azido-3-O-benzyl-4,6-dideoxy-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / BF₃*Et₂O / CH₂Cl₂ / 24 h / 20 °C

2: 95 percent / N-iodosuccinimide; silver(I) trifluoromethanesulfonate; molecular sieves 4 Angstroem / CH₂Cl₂; toluene / 0 - 20 °C

With N-iodo-succinimide; 4 A molecular sieve; boron trifluoride diethyl etherate; silver trifluoromethanesulfonate; In dichloromethane; toluene; 2: Zemplen deacetylation;
DOI:10.1016/j.tetasy.2004.11.021