phenyl 4-O-methyl-2-S-phenyl-2,6-di-deoxy-β-L-glucopyranosyl-(1->4)-2,3-O-isopropylidene-1-thio-α-L-rhamnopyranoside

Base Information

Chemical Name:phenyl 4-O-methyl-2-S-phenyl-2,6-di-deoxy-β-L-glucopyranosyl-(1->4)-2,3-O-isopropylidene-1-thio-α-L-rhamnopyranoside
CAS No.:327603-85-0
Molecular Formula:C₂₈H₃₆O₇S₂
Molecular Weight:548.722
Hs Code.:

Synonyms:phenyl 4-O-methyl-2-S-phenyl-2,6-di-deoxy-β-L-glucopyranosyl-(1->4)-2,3-O-isopropylidene-1-thio-α-L-rhamnopyranoside

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Chemical Property of phenyl 4-O-methyl-2-S-phenyl-2,6-di-deoxy-β-L-glucopyranosyl-(1->4)-2,3-O-isopropylidene-1-thio-α-L-rhamnopyranoside

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Technology Process of phenyl 4-O-methyl-2-S-phenyl-2,6-di-deoxy-β-L-glucopyranosyl-(1->4)-2,3-O-isopropylidene-1-thio-α-L-rhamnopyranoside

There total 3 articles about phenyl 4-O-methyl-2-S-phenyl-2,6-di-deoxy-β-L-glucopyranosyl-(1->4)-2,3-O-isopropylidene-1-thio-α-L-rhamnopyranoside 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: 93.0%

: 327603-72-5
phenyl 3-O-(methylthio)carbonyl-4-O-methyl-2-S-phenyl-2,6-di-deoxy-β-L-glucopyranosyl-(1->4)-2,3-O-isopropylidene-1-thio-α-L-rhamnopyranoside

: 327603-85-0
phenyl 4-O-methyl-2-S-phenyl-2,6-di-deoxy-β-L-glucopyranosyl-(1->4)-2,3-O-isopropylidene-1-thio-α-L-rhamnopyranoside

Guidance literature:: With sodium methylate; In methanol; at 60 ℃; for 72h;
DOI:10.1021/ol006894+

Reference yield:

: 327603-45-2
phenyl 4-O-methyl-1-thio-α-L-rhamnopyranoside

: 327603-85-0
phenyl 4-O-methyl-2-S-phenyl-2,6-di-deoxy-β-L-glucopyranosyl-(1->4)-2,3-O-isopropylidene-1-thio-α-L-rhamnopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 81 percent / tetrahydrofuran / 2 h / Heating

2: 90 percent / 4 Angstroem molecular sieves; 2,6-di-tert-butyl-4-methylpyridine / CH₂Cl₂ / 20 °C

3: 93 percent / NaOMe / methanol / 72 h / 60 °C

With 2,6-di-tert-butyl-4-methylpyridine; 4 A molecular sieve; sodium methylate; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/ol006894+

Reference yield:

: 327603-48-5
phenyl 4-O-methyl-2,3-O-thionocarbonyl-1-thio-α-L-rhamnopyranoside

: 327603-85-0
phenyl 4-O-methyl-2-S-phenyl-2,6-di-deoxy-β-L-glucopyranosyl-(1->4)-2,3-O-isopropylidene-1-thio-α-L-rhamnopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / 4 Angstroem molecular sieves; 2,6-di-tert-butyl-4-methylpyridine / CH₂Cl₂ / 20 °C

2: 93 percent / NaOMe / methanol / 72 h / 60 °C

With 2,6-di-tert-butyl-4-methylpyridine; 4 A molecular sieve; sodium methylate; In methanol; dichloromethane;
DOI:10.1021/ol006894+