[1-(3',4',5',7'-tetra-O-benzoyl-β-D-gluco-hept-2-ulopyranosyl)-4-phenyl-1,2,3-triazole]onamide

Base Information

Chemical Name:[1-(3',4',5',7'-tetra-O-benzoyl-β-D-gluco-hept-2-ulopyranosyl)-4-phenyl-1,2,3-triazole]onamide
CAS No.:1219686-53-9
Molecular Formula:C₄₃H₃₄N₄O₁₀
Molecular Weight:766.764
Hs Code.:

Synonyms:[1-(3',4',5',7'-tetra-O-benzoyl-β-D-gluco-hept-2-ulopyranosyl)-4-phenyl-1,2,3-triazole]onamide

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Chemical Property of [1-(3',4',5',7'-tetra-O-benzoyl-β-D-gluco-hept-2-ulopyranosyl)-4-phenyl-1,2,3-triazole]onamide

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Technology Process of [1-(3',4',5',7'-tetra-O-benzoyl-β-D-gluco-hept-2-ulopyranosyl)-4-phenyl-1,2,3-triazole]onamide

There total 1 articles about [1-(3',4',5',7'-tetra-O-benzoyl-β-D-gluco-hept-2-ulopyranosyl)-4-phenyl-1,2,3-triazole]onamide 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: 92.0%

: 868960-46-7
C-(1-azido-2,3,4,6-tetra-O-benzoyl-1-deoxy-α-D-glucopyranosyl)formamide

: 536-74-3
phenylacetylene

: 1219686-53-9
[1-(3',4',5',7'-tetra-O-benzoyl-β-D-gluco-hept-2-ulopyranosyl)-4-phenyl-1,2,3-triazole]onamide

Guidance literature:: With bis-triphenylphosphano-copper(I)-butyrate; In dichloromethane; at 20 ℃; for 4h; regioselective reaction;
DOI:10.1016/j.carres.2012.01.004

Reference yield: 92.0%

: 1219686-53-9
[1-(3',4',5',7'-tetra-O-benzoyl-β-D-gluco-hept-2-ulopyranosyl)-4-phenyl-1,2,3-triazole]onamide

: 1219686-57-3
[1-(β-D-gluco-hept-2-ulopyranosyl)-4-phenyl-1,2,3-triazole]onamide

Guidance literature:: [1-(3',4',5',7'-tetra-O-benzoyl-β-D-gluco-hept-2-ulopyranosyl)-4-phenyl-1,2,3-triazole]onamide; With methanol; sodium methylate; at 20 ℃;

In methanol;
DOI:10.1016/j.bmc.2009.12.043