(S)-4-Benzyl-3-[(2S,3R,4R,6S,7R,8S,10R)-3-hydroxy-6,8-dimethoxy-4,10-dimethyl-2-(2,2,2-trichloro-ethoxy)-7-triethylsilanyloxy-11-triisopropylsilanyloxy-undecanoyl]-oxazolidin-2-one

Base Information

Chemical Name:(S)-4-Benzyl-3-[(2S,3R,4R,6S,7R,8S,10R)-3-hydroxy-6,8-dimethoxy-4,10-dimethyl-2-(2,2,2-trichloro-ethoxy)-7-triethylsilanyloxy-11-triisopropylsilanyloxy-undecanoyl]-oxazolidin-2-one
CAS No.:126789-15-9
Molecular Formula:C₄₂H₇₄Cl₃NO₉Si₂
Molecular Weight:899.581
Hs Code.:

(S)-4-Benzyl-3-[(2S,3R,4R,6S,7R,8S,10R)-3-hydroxy-6,8-dimethoxy-4,10-dimethyl-2-(2,2,2-trichloro-ethoxy)-7-triethylsilanyloxy-11-triisopropylsilanyloxy-undecanoyl]-oxazolidin-2-one

Synonyms:(S)-4-Benzyl-3-[(2S,3R,4R,6S,7R,8S,10R)-3-hydroxy-6,8-dimethoxy-4,10-dimethyl-2-(2,2,2-trichloro-ethoxy)-7-triethylsilanyloxy-11-triisopropylsilanyloxy-undecanoyl]-oxazolidin-2-one

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Chemical Property of (S)-4-Benzyl-3-[(2S,3R,4R,6S,7R,8S,10R)-3-hydroxy-6,8-dimethoxy-4,10-dimethyl-2-(2,2,2-trichloro-ethoxy)-7-triethylsilanyloxy-11-triisopropylsilanyloxy-undecanoyl]-oxazolidin-2-one

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Technology Process of (S)-4-Benzyl-3-[(2S,3R,4R,6S,7R,8S,10R)-3-hydroxy-6,8-dimethoxy-4,10-dimethyl-2-(2,2,2-trichloro-ethoxy)-7-triethylsilanyloxy-11-triisopropylsilanyloxy-undecanoyl]-oxazolidin-2-one

There total 4 articles about (S)-4-Benzyl-3-[(2S,3R,4R,6S,7R,8S,10R)-3-hydroxy-6,8-dimethoxy-4,10-dimethyl-2-(2,2,2-trichloro-ethoxy)-7-triethylsilanyloxy-11-triisopropylsilanyloxy-undecanoyl]-oxazolidin-2-one 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:

: 80522-42-5
triisopropylsilyl trifluoromethanesulfonate

: 126789-15-9
(S)-4-Benzyl-3-[(2S,3R,4R,6S,7R,8S,10R)-3-hydroxy-6,8-dimethoxy-4,10-dimethyl-2-(2,2,2-trichloro-ethoxy)-7-triethylsilanyloxy-11-triisopropylsilanyloxy-undecanoyl]-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 2,6-lutidine / CH₂Cl₂ / 0 °C

2: 1.) AgNO₃, NCS, 2,6-lutidine, 2.) glyoxylic acid hydrate, HOAc / 1.) CH₃OH, THF, 20 deg C, 2.) CH₂Cl₂, 40 deg C

3: 1.) Et₃N, n-Bu₂BOTf / 1.) 0 deg C

With 2,6-dimethylpyridine; N-chloro-succinimide; di-n-butylboryl trifluoromethanesulfonate; silver nitrate; acetic acid; triethylamine; Glyoxilic acid; In dichloromethane;
DOI:10.1021/ja00164a023

Reference yield:

: 126789-11-5
(2R,4S,5R,6S,8R)-8-[1,3]Dithian-2-yl-4,6-dimethoxy-2-methyl-5-triethylsilanyloxy-nonan-1-ol

: 126789-15-9
(S)-4-Benzyl-3-[(2S,3R,4R,6S,7R,8S,10R)-3-hydroxy-6,8-dimethoxy-4,10-dimethyl-2-(2,2,2-trichloro-ethoxy)-7-triethylsilanyloxy-11-triisopropylsilanyloxy-undecanoyl]-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 2,6-lutidine / CH₂Cl₂ / 0 °C

2: 1.) AgNO₃, NCS, 2,6-lutidine, 2.) glyoxylic acid hydrate, HOAc / 1.) CH₃OH, THF, 20 deg C, 2.) CH₂Cl₂, 40 deg C

3: 1.) Et₃N, n-Bu₂BOTf / 1.) 0 deg C

With 2,6-dimethylpyridine; N-chloro-succinimide; di-n-butylboryl trifluoromethanesulfonate; silver nitrate; acetic acid; triethylamine; Glyoxilic acid; In dichloromethane;
DOI:10.1021/ja00164a023

Reference yield:

: 2-((1R,3S,4R,5S,7R)-3,5-Dimethoxy-1,7-dimethyl-4-triethylsilanyloxy-8-triisopropylsilanyloxy-octyl)-[1,3]dithiane

: 126789-15-9
(S)-4-Benzyl-3-[(2S,3R,4R,6S,7R,8S,10R)-3-hydroxy-6,8-dimethoxy-4,10-dimethyl-2-(2,2,2-trichloro-ethoxy)-7-triethylsilanyloxy-11-triisopropylsilanyloxy-undecanoyl]-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) AgNO₃, NCS, 2,6-lutidine, 2.) glyoxylic acid hydrate, HOAc / 1.) CH₃OH, THF, 20 deg C, 2.) CH₂Cl₂, 40 deg C

2: 1.) Et₃N, n-Bu₂BOTf / 1.) 0 deg C

With 2,6-dimethylpyridine; N-chloro-succinimide; di-n-butylboryl trifluoromethanesulfonate; silver nitrate; acetic acid; triethylamine; Glyoxilic acid;
DOI:10.1021/ja00164a023