N-(4-{2-[(2S,3R,4S,5R,6R)-3,5-Bis-benzyloxy-4-((2S,3R,4R,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-6-hydroxymethyl-tetrahydro-pyran-2-yloxy]-ethyl}-phenyl)-4-methyl-benzenesulfonamide

Base Information

Chemical Name:N-(4-{2-[(2S,3R,4S,5R,6R)-3,5-Bis-benzyloxy-4-((2S,3R,4R,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-6-hydroxymethyl-tetrahydro-pyran-2-yloxy]-ethyl}-phenyl)-4-methyl-benzenesulfonamide
CAS No.:81823-10-1
Molecular Formula:C₆₂H₆₇NO₁₃S
Molecular Weight:1066.28
Hs Code.:

N-(4-{2-[(2S,3R,4S,5R,6R)-3,5-Bis-benzyloxy-4-((2S,3R,4R,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-6-hydroxymethyl-tetrahydro-pyran-2-yloxy]-ethyl}-phenyl)-4-methyl-benzenesulfonamide

Synonyms:N-(4-{2-[(2S,3R,4S,5R,6R)-3,5-Bis-benzyloxy-4-((2S,3R,4R,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-6-hydroxymethyl-tetrahydro-pyran-2-yloxy]-ethyl}-phenyl)-4-methyl-benzenesulfonamide

Suppliers and Price of N-(4-{2-[(2S,3R,4S,5R,6R)-3,5-Bis-benzyloxy-4-((2S,3R,4R,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-6-hydroxymethyl-tetrahydro-pyran-2-yloxy]-ethyl}-phenyl)-4-methyl-benzenesulfonamide

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Chemical Property of N-(4-{2-[(2S,3R,4S,5R,6R)-3,5-Bis-benzyloxy-4-((2S,3R,4R,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-6-hydroxymethyl-tetrahydro-pyran-2-yloxy]-ethyl}-phenyl)-4-methyl-benzenesulfonamide

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Technology Process of N-(4-{2-[(2S,3R,4S,5R,6R)-3,5-Bis-benzyloxy-4-((2S,3R,4R,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-6-hydroxymethyl-tetrahydro-pyran-2-yloxy]-ethyl}-phenyl)-4-methyl-benzenesulfonamide

There total 7 articles about N-(4-{2-[(2S,3R,4S,5R,6R)-3,5-Bis-benzyloxy-4-((2S,3R,4R,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-6-hydroxymethyl-tetrahydro-pyran-2-yloxy]-ethyl}-phenyl)-4-methyl-benzenesulfonamide 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: 73.0%

: 81823-08-7
4-Nitro-benzoic acid (2S,3R,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-((2R,3R,4S,5R,6S)-3,5-bis-benzyloxy-2-phenylcarbamoyloxymethyl-6-{2-[4-(toluene-4-sulfonylamino)-phenyl]-ethoxy}-tetrahydro-pyran-4-yloxy)-tetrahydro-pyran-3-yl ester

: 81823-10-1
N-(4-{2-[(2S,3R,4S,5R,6R)-3,5-Bis-benzyloxy-4-((2S,3R,4R,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-6-hydroxymethyl-tetrahydro-pyran-2-yloxy]-ethyl}-phenyl)-4-methyl-benzenesulfonamide

Guidance literature:: With sodium ethanolate; In ethanol; Ambient temperature;
DOI:10.1016/S0008-6215(00)88056-8

Reference yield:

: 20672-66-6,40246-26-2,84926-76-1,114179-79-2,115184-49-1
3,4,6-tri-O-benzyl-D-glucopyranose

: 81823-10-1
N-(4-{2-[(2S,3R,4S,5R,6R)-3,5-Bis-benzyloxy-4-((2S,3R,4R,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-6-hydroxymethyl-tetrahydro-pyran-2-yloxy]-ethyl}-phenyl)-4-methyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: 90 percent / pyridine / Ambient temperature

2: hydrogen chloride / diethyl ether / 24 h / Ambient temperature

3: acetonitrile / 0.25 h / Ambient temperature

4: 68 percent / acetonitrile / 24 h / Ambient temperature; in the dark

5: 73 percent / sodium ethoxide / ethanol / Ambient temperature

With pyridine; hydrogenchloride; sodium ethanolate; In diethyl ether; ethanol; acetonitrile;
DOI:10.1016/S0008-6215(00)88056-8

Reference yield:

: 81823-02-1
3,4,6-tri-O-benzyl-2-O-p-nitrobenzoyl-α-D-glucopyranosyl chloride

: 81823-10-1
N-(4-{2-[(2S,3R,4S,5R,6R)-3,5-Bis-benzyloxy-4-((2S,3R,4R,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-hydroxy-tetrahydro-pyran-2-yloxy)-6-hydroxymethyl-tetrahydro-pyran-2-yloxy]-ethyl}-phenyl)-4-methyl-benzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: acetonitrile / 0.25 h / Ambient temperature

2: 68 percent / acetonitrile / 24 h / Ambient temperature; in the dark

3: 73 percent / sodium ethoxide / ethanol / Ambient temperature

With sodium ethanolate; In ethanol; acetonitrile;
DOI:10.1016/S0008-6215(00)88056-8