3-(benzyloxycarbonyl)aminopropyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1→3)-6-O-benzyl-2-deoxy-2-(2′,2′,2′-trichloroethoxycarbonylamin)-β-D-galactopyranosyl-(1→3)-2,4,6-tri-O-benzyl-α-D-mannopyranoside

Base Information

Chemical Name:3-(benzyloxycarbonyl)aminopropyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1→3)-6-O-benzyl-2-deoxy-2-(2′,2′,2′-trichloroethoxycarbonylamin)-β-D-galactopyranosyl-(1→3)-2,4,6-tri-O-benzyl-α-D-mannopyranoside
CAS No.:1262208-57-0
Molecular Formula:C₈₃H₉₁Cl₃N₂O₂₀
Molecular Weight:1543
Hs Code.:

3-(benzyloxycarbonyl)aminopropyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1→3)-6-O-benzyl-2-deoxy-2-(2′,2′,2′-trichloroethoxycarbonylamin)-β-D-galactopyranosyl-(1→3)-2,4,6-tri-O-benzyl-α-D-mannopyranoside

Synonyms:3-(benzyloxycarbonyl)aminopropyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1→3)-6-O-benzyl-2-deoxy-2-(2′,2′,2′-trichloroethoxycarbonylamin)-β-D-galactopyranosyl-(1→3)-2,4,6-tri-O-benzyl-α-D-mannopyranoside

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Chemical Property of 3-(benzyloxycarbonyl)aminopropyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1→3)-6-O-benzyl-2-deoxy-2-(2′,2′,2′-trichloroethoxycarbonylamin)-β-D-galactopyranosyl-(1→3)-2,4,6-tri-O-benzyl-α-D-mannopyranoside

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Technology Process of 3-(benzyloxycarbonyl)aminopropyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1→3)-6-O-benzyl-2-deoxy-2-(2′,2′,2′-trichloroethoxycarbonylamin)-β-D-galactopyranosyl-(1→3)-2,4,6-tri-O-benzyl-α-D-mannopyranoside

There total 2 articles about 3-(benzyloxycarbonyl)aminopropyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1→3)-6-O-benzyl-2-deoxy-2-(2′,2′,2′-trichloroethoxycarbonylamin)-β-D-galactopyranosyl-(1→3)-2,4,6-tri-O-benzyl-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: 80.0%

: 3-(benzyloxycarbonyl)aminopropyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1→3)-4,6-O-benzylidene-2-deoxy-2-(2′,2′,2′-trichloroethoxycarbonylamino)-β-D-galactopyranosyl-(1→3)-2,4,6-tri-O-benzyl-α-D-mannopyranoside

: 1262208-57-0
3-(benzyloxycarbonyl)aminopropyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1→3)-6-O-benzyl-2-deoxy-2-(2′,2′,2′-trichloroethoxycarbonylamin)-β-D-galactopyranosyl-(1→3)-2,4,6-tri-O-benzyl-α-D-mannopyranoside

Guidance literature:: In acetonitrile; at 0 ℃; for 1h; regioselective reaction; Inert atmosphere;

Reference yield: 80.0%

: 1262208-55-8
3-(benzyloxycarbonyl)aminopropyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1->3)-4,6-O-benzylidene-2-deoxy-2-(2',2',2'-trichloroethoxycarbonylamino)-β-D-galactopyranosyl-(1->3)-2,4,6-tri-O-benzyl-α-D-mannopyranoside

: 1262208-57-0
3-(benzyloxycarbonyl)aminopropyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1→3)-6-O-benzyl-2-deoxy-2-(2′,2′,2′-trichloroethoxycarbonylamin)-β-D-galactopyranosyl-(1→3)-2,4,6-tri-O-benzyl-α-D-mannopyranoside

Guidance literature:: With boron trifluoride diethyl etherate; trimethylamine borane; In acetonitrile; at 0 ℃; for 1h; regioselective reaction; Inert atmosphere;
DOI:10.1021/ol1026188

Reference yield: 89.0%

: 1262208-57-0
3-(benzyloxycarbonyl)aminopropyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1→3)-6-O-benzyl-2-deoxy-2-(2′,2′,2′-trichloroethoxycarbonylamin)-β-D-galactopyranosyl-(1→3)-2,4,6-tri-O-benzyl-α-D-mannopyranoside

: 141263-01-6
Ethyl 2,3-di-O-benzyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside

: 3-(benzyloxycarbonyl)aminopropyl 2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl-(1→3)-[6-O-benzyl-2-deoxy-2-(2′,2′,2′-trichloroethoxycarbonylamino)-β-D-galactopyranosyl-(1→3)-2,3-di-O-benzyl-4,6-O-benzylidene-α-D-glucopyranosyl-(1→4)]-2,4,6-tri-O-benzyl-α-D-mannopyranoside

Guidance literature:: With N-iodo-succinimide; trifluorormethanesulfonic acid; at 0 - 20 ℃; for 8h; stereoselective reaction; Inert atmosphere; Molecular sieve;