(S)-4-(3-{(2S,3R)-3-Hydroxymethyl-7-[3-(2-hydroxymethyl-oxazol-5-yl)-1-methoxymethyl-1H-indol-4-yl]-2-methoxycarbonyl-2,3-dihydro-benzofuran-3-yl}-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

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Chemical Name:(S)-4-(3-{(2S,3R)-3-Hydroxymethyl-7-[3-(2-hydroxymethyl-oxazol-5-yl)-1-methoxymethyl-1H-indol-4-yl]-2-methoxycarbonyl-2,3-dihydro-benzofuran-3-yl}-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester
CAS No.:760980-28-7
Molecular Formula:C₄₆H₄₇N₃O₁₁
Molecular Weight:817.893
Hs Code.:

(S)-4-(3-{(2S,3R)-3-Hydroxymethyl-7-[3-(2-hydroxymethyl-oxazol-5-yl)-1-methoxymethyl-1H-indol-4-yl]-2-methoxycarbonyl-2,3-dihydro-benzofuran-3-yl}-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

Synonyms:(S)-4-(3-{(2S,3R)-3-Hydroxymethyl-7-[3-(2-hydroxymethyl-oxazol-5-yl)-1-methoxymethyl-1H-indol-4-yl]-2-methoxycarbonyl-2,3-dihydro-benzofuran-3-yl}-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

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Chemical Property of (S)-4-(3-{(2S,3R)-3-Hydroxymethyl-7-[3-(2-hydroxymethyl-oxazol-5-yl)-1-methoxymethyl-1H-indol-4-yl]-2-methoxycarbonyl-2,3-dihydro-benzofuran-3-yl}-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

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Technology Process of (S)-4-(3-{(2S,3R)-3-Hydroxymethyl-7-[3-(2-hydroxymethyl-oxazol-5-yl)-1-methoxymethyl-1H-indol-4-yl]-2-methoxycarbonyl-2,3-dihydro-benzofuran-3-yl}-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

There total 11 articles about (S)-4-(3-{(2S,3R)-3-Hydroxymethyl-7-[3-(2-hydroxymethyl-oxazol-5-yl)-1-methoxymethyl-1H-indol-4-yl]-2-methoxycarbonyl-2,3-dihydro-benzofuran-3-yl}-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl 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: 93.0%

: 760980-02-7
C₅₈H₇₅N₃O₁₁Si₂

: 760980-28-7
(S)-4-(3-{(2S,3R)-3-Hydroxymethyl-7-[3-(2-hydroxymethyl-oxazol-5-yl)-1-methoxymethyl-1H-indol-4-yl]-2-methoxycarbonyl-2,3-dihydro-benzofuran-3-yl}-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 25 ℃; for 0.333333h;
DOI:10.1021/ja040091q

Reference yield:

: 405519-78-0
4-bromo-3-[2-(tert-butyl-diphenyl-silanyloxymethyl)-oxazol-5-yl]-1-methoxymethyl-1H-indole

: 760980-28-7
(S)-4-(3-{(2S,3R)-3-Hydroxymethyl-7-[3-(2-hydroxymethyl-oxazol-5-yl)-1-methoxymethyl-1H-indol-4-yl]-2-methoxycarbonyl-2,3-dihydro-benzofuran-3-yl}-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 92 percent / tetra-n-butylammonium fluoride / tetrahydrofuran / 0.17 h / 0 °C

2: 93 percent / Et₃N / CH₂Cl₂ / 0.33 h / 0 °C

3: 83 percent / Pd(diphenylphosphinoferrocene)Cl₂*CH₂Cl₂; K₂CO₃ / 1,2-dimethoxy-ethane / 12 h / Heating

4: 93 percent / tetra-n-butylammonium fluoride / tetrahydrofuran / 0.33 h / 25 °C

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; tetrabutyl ammonium fluoride; potassium carbonate; triethylamine; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; 3: Suzuki coupling;
DOI:10.1021/ja040091q

Reference yield:

: 760979-81-5
[5-(4-bromo-1-methoxymethyl-1H-indol-3-yl)-oxazol-2-yl]-methanol

: 760980-28-7
(S)-4-(3-{(2S,3R)-3-Hydroxymethyl-7-[3-(2-hydroxymethyl-oxazol-5-yl)-1-methoxymethyl-1H-indol-4-yl]-2-methoxycarbonyl-2,3-dihydro-benzofuran-3-yl}-4-methoxy-benzyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 93 percent / Et₃N / CH₂Cl₂ / 0.33 h / 0 °C

2: 83 percent / Pd(diphenylphosphinoferrocene)Cl₂*CH₂Cl₂; K₂CO₃ / 1,2-dimethoxy-ethane / 12 h / Heating

3: 93 percent / tetra-n-butylammonium fluoride / tetrahydrofuran / 0.33 h / 25 °C

With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; tetrabutyl ammonium fluoride; potassium carbonate; triethylamine; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; 2: Suzuki coupling;
DOI:10.1021/ja040091q