(2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->6)-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-allyl-D-myo-inositol

Base Information

Chemical Name:(2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->6)-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-allyl-D-myo-inositol
CAS No.:1234177-46-8
Molecular Formula:C₅₈H₆₃N₃O₁₁
Molecular Weight:978.152
Hs Code.:

Synonyms:(2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->6)-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-allyl-D-myo-inositol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->6)-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-allyl-D-myo-inositol

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Technology Process of (2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->6)-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-allyl-D-myo-inositol

There total 1 articles about (2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->6)-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-allyl-D-myo-inositol 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: 94.0%

: 1234177-45-7
(2-azido-3-O-benzyl-4,6-di-O-benzylidene-2-deoxy-α-D-glucopyranosyl)-(1/6)-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-allyl-D-myo-inositol

: 1234177-46-8
(2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->6)-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-allyl-D-myo-inositol

Guidance literature:: With hydrogenchloride; sodium cyanoborohydride; In tetrahydrofuran; diethyl ether; water; at 0 ℃; pH=1; regioselective reaction; Inert atmosphere; Molecular sieve;
DOI:10.1016/j.tet.2010.04.014

Reference yield: 53.0%

: 847980-97-6
(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-(1->2)-(4,6-di-O-acetyl-3-O-benzyl-α-D-mannopyranosyl)-(1->2)-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->6)-(2,3,4-tri-O-benzyl-α-D-mannopyranosyl) trichloroacetimidate

: 1234177-46-8
(2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->6)-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-allyl-D-myo-inositol

: C₁₆₃H₁₇₃N₃O₃₃

: (2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-(1->2)-(4,6-di-O-acetyl-3-O-benzyl-α-D-mannopyranosyl)-(1->2)-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1->6)-(2,3,4-tri-O-benzyl-α-D-mannopyranosyl)-(1->4)-(2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranosyl)-(1->6)-3,4,5-tri-O-benzyl-1-O-(4-methoxybenzyl)-2-O-allyl-D-myo-inositol

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In diethyl ether; at 0 ℃; for 0.5h; optical yield given as %de; Inert atmosphere; Molecular sieve;
DOI:10.1016/j.tet.2010.04.014