Phenyl-O-(4-amino-4,6-didesoxy-α-D-glucopyranosyl)-(1->4)-O-(α-D-glucopyranosyl)-(1->4)-α-D-glucopyranosid

Base Information

Chemical Name:Phenyl-O-(4-amino-4,6-didesoxy-α-D-glucopyranosyl)-(1->4)-O-(α-D-glucopyranosyl)-(1->4)-α-D-glucopyranosid
CAS No.:88773-03-9
Molecular Formula:C₂₄H₃₇NO₁₄
Molecular Weight:563.556
Hs Code.:

Synonyms:Phenyl-O-(4-amino-4,6-didesoxy-α-D-glucopyranosyl)-(1->4)-O-(α-D-glucopyranosyl)-(1->4)-α-D-glucopyranosid

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Chemical Property of Phenyl-O-(4-amino-4,6-didesoxy-α-D-glucopyranosyl)-(1->4)-O-(α-D-glucopyranosyl)-(1->4)-α-D-glucopyranosid

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Technology Process of Phenyl-O-(4-amino-4,6-didesoxy-α-D-glucopyranosyl)-(1->4)-O-(α-D-glucopyranosyl)-(1->4)-α-D-glucopyranosid

There total 2 articles about Phenyl-O-(4-amino-4,6-didesoxy-α-D-glucopyranosyl)-(1->4)-O-(α-D-glucopyranosyl)-(1->4)-α-D-glucopyranosid 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: 72.0%

: 88772-99-0
Phenyl-O-(4-azido-2,3-di-O-benzyl-4,6-didesoxy-α-D-glucopyranosyl)-(1->4)-O-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranosid

: 88773-03-9
Phenyl-O-(4-amino-4,6-didesoxy-α-D-glucopyranosyl)-(1->4)-O-(α-D-glucopyranosyl)-(1->4)-α-D-glucopyranosid

Guidance literature:: With acetic acid; palladium on activated charcoal; In methanol; ethyl acetate; for 48h;
DOI:10.1002/jlac.198319831106

Reference yield:

: 87591-19-3
Phenyl-O-(2,3,6-tri-O-benzyl-α-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-α-D-glucopyranosid

: 88773-03-9
Phenyl-O-(4-amino-4,6-didesoxy-α-D-glucopyranosyl)-(1->4)-O-(α-D-glucopyranosyl)-(1->4)-α-D-glucopyranosid

Guidance literature:: Multi-step reaction with 2 steps

1: 22 percent / diethyl ether - BF₃ / CH₂Cl₂ / 4.5 h / Ambient temperature

2: 72 percent / acetic acid / Pd/C / methanol; ethyl acetate / 48 h

With boron trifluoride diethyl etherate; acetic acid; palladium on activated charcoal; In methanol; dichloromethane; ethyl acetate;
DOI:10.1002/jlac.198319831106