Acetic acid (2R,3S,4R,5R,6S)-5-benzenesulfonylamino-6-((2R,3S,4R,5R,6S)-5-benzenesulfonylamino-4-benzyloxy-2-benzyloxymethyl-6-hydroxy-tetrahydro-pyran-3-yloxy)-4-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yl ester

Base Information

Chemical Name:Acetic acid (2R,3S,4R,5R,6S)-5-benzenesulfonylamino-6-((2R,3S,4R,5R,6S)-5-benzenesulfonylamino-4-benzyloxy-2-benzyloxymethyl-6-hydroxy-tetrahydro-pyran-3-yloxy)-4-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yl ester
CAS No.:539836-13-0
Molecular Formula:C₅₄H₅₈N₂O₁₄S₂
Molecular Weight:1023.19
Hs Code.:

Acetic acid (2R,3S,4R,5R,6S)-5-benzenesulfonylamino-6-((2R,3S,4R,5R,6S)-5-benzenesulfonylamino-4-benzyloxy-2-benzyloxymethyl-6-hydroxy-tetrahydro-pyran-3-yloxy)-4-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yl ester

Synonyms:Acetic acid (2R,3S,4R,5R,6S)-5-benzenesulfonylamino-6-((2R,3S,4R,5R,6S)-5-benzenesulfonylamino-4-benzyloxy-2-benzyloxymethyl-6-hydroxy-tetrahydro-pyran-3-yloxy)-4-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yl ester

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Chemical Property of Acetic acid (2R,3S,4R,5R,6S)-5-benzenesulfonylamino-6-((2R,3S,4R,5R,6S)-5-benzenesulfonylamino-4-benzyloxy-2-benzyloxymethyl-6-hydroxy-tetrahydro-pyran-3-yloxy)-4-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yl ester

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Technology Process of Acetic acid (2R,3S,4R,5R,6S)-5-benzenesulfonylamino-6-((2R,3S,4R,5R,6S)-5-benzenesulfonylamino-4-benzyloxy-2-benzyloxymethyl-6-hydroxy-tetrahydro-pyran-3-yloxy)-4-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yl ester

There total 1 articles about Acetic acid (2R,3S,4R,5R,6S)-5-benzenesulfonylamino-6-((2R,3S,4R,5R,6S)-5-benzenesulfonylamino-4-benzyloxy-2-benzyloxymethyl-6-hydroxy-tetrahydro-pyran-3-yloxy)-4-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yl ester 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:

: 98-10-2
benzenesulfonamide

: 187879-68-1
Acetic acid (2R,3S,4R,5R,6S)-5-benzenesulfonylamino-4-benzyloxy-6-((2R,3S,4R)-4-benzyloxy-2-benzyloxymethyl-3,4-dihydro-2H-pyran-3-yloxy)-2-benzyloxymethyl-tetrahydro-pyran-3-yl ester

: 539836-13-0
Acetic acid (2R,3S,4R,5R,6S)-5-benzenesulfonylamino-6-((2R,3S,4R,5R,6S)-5-benzenesulfonylamino-4-benzyloxy-2-benzyloxymethyl-6-hydroxy-tetrahydro-pyran-3-yloxy)-4-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yl ester

Guidance literature:: benzenesulfonamide; Acetic acid (2R,3S,4R,5R,6S)-5-benzenesulfonylamino-4-benzyloxy-6-((2R,3S,4R)-4-benzyloxy-2-benzyloxymethyl-3,4-dihydro-2H-pyran-3-yloxy)-2-benzyloxymethyl-tetrahydro-pyran-3-yl ester; With iodonium(di-γ-collidine) perchlorate;

With triethylamine; In tetrahydrofuran; water;
DOI:10.1016/S0040-4039(03)00101-1

Reference yield:

: 69739-34-0
t-butyldimethylsiyl triflate

: 539836-13-0
Acetic acid (2R,3S,4R,5R,6S)-5-benzenesulfonylamino-6-((2R,3S,4R,5R,6S)-5-benzenesulfonylamino-4-benzyloxy-2-benzyloxymethyl-6-hydroxy-tetrahydro-pyran-3-yloxy)-4-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yl ester

: 539836-14-1
Acetic acid (2R,3S,4R,5R,6S)-5-benzenesulfonylamino-6-[(2R,3S,4R,5R,6R)-5-benzenesulfonylamino-4-benzyloxy-2-benzyloxymethyl-6-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-pyran-3-yloxy]-4-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yl ester

Guidance literature:: With 2,6-dimethylpyridine; In dichloromethane;
DOI:10.1016/S0040-4039(03)00101-1

Reference yield:

: 539836-13-0
Acetic acid (2R,3S,4R,5R,6S)-5-benzenesulfonylamino-6-((2R,3S,4R,5R,6S)-5-benzenesulfonylamino-4-benzyloxy-2-benzyloxymethyl-6-hydroxy-tetrahydro-pyran-3-yloxy)-4-benzyloxy-2-benzyloxymethyl-tetrahydro-pyran-3-yl ester

: 539836-15-2
C₅₈H₇₀N₂O₁₃S₂Si

Guidance literature:: Multi-step reaction with 2 steps

1: 2,6-lutidine / CH₂Cl₂

2: NaOMe / methanol

With 2,6-dimethylpyridine; sodium methylate; In methanol; dichloromethane; 2: Zemplen deacetylation;
DOI:10.1016/S0040-4039(03)00101-1