4-(1-adamantyl)-N-((5-((R)-3-((S)-4-benzyl-2-oxo-oxazolidin-3-yl)-2-(cyclohexylmethyl)-3-oxopropyl)-2-propoxyphenyl)methyl)benzamide

Base Information

Chemical Name:4-(1-adamantyl)-N-((5-((R)-3-((S)-4-benzyl-2-oxo-oxazolidin-3-yl)-2-(cyclohexylmethyl)-3-oxopropyl)-2-propoxyphenyl)methyl)benzamide
CAS No.:1401791-65-8
Molecular Formula:C₄₈H₅₄N₂O₅
Molecular Weight:738.967
Hs Code.:

Synonyms:4-(1-adamantyl)-N-((5-((R)-3-((S)-4-benzyl-2-oxo-oxazolidin-3-yl)-2-(cyclohexylmethyl)-3-oxopropyl)-2-propoxyphenyl)methyl)benzamide

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Chemical Property of 4-(1-adamantyl)-N-((5-((R)-3-((S)-4-benzyl-2-oxo-oxazolidin-3-yl)-2-(cyclohexylmethyl)-3-oxopropyl)-2-propoxyphenyl)methyl)benzamide

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Technology Process of 4-(1-adamantyl)-N-((5-((R)-3-((S)-4-benzyl-2-oxo-oxazolidin-3-yl)-2-(cyclohexylmethyl)-3-oxopropyl)-2-propoxyphenyl)methyl)benzamide

There total 9 articles about 4-(1-adamantyl)-N-((5-((R)-3-((S)-4-benzyl-2-oxo-oxazolidin-3-yl)-2-(cyclohexylmethyl)-3-oxopropyl)-2-propoxyphenyl)methyl)benzamide 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:

: 1401791-64-7
5-((R)-3-((S)-4-benzyl-2-oxo-oxazolidin-3-yl)-2-(cyclohexylmethyl)-3-oxopropyl)-2-propoxybenzaldehyde

: 117101-74-3
4-(1-adamantyl)benzamide

: 1401791-65-8
4-(1-adamantyl)-N-((5-((R)-3-((S)-4-benzyl-2-oxo-oxazolidin-3-yl)-2-(cyclohexylmethyl)-3-oxopropyl)-2-propoxyphenyl)methyl)benzamide

Guidance literature:: With triethylsilane; trifluoroacetic acid; In toluene; for 48h; Reflux; Inert atmosphere;
DOI:10.1016/j.bmc.2012.08.061

Reference yield:

: 1259391-04-2
benzyl 2-propoxy-5-formylsalicylate

: 1401791-65-8
4-(1-adamantyl)-N-((5-((R)-3-((S)-4-benzyl-2-oxo-oxazolidin-3-yl)-2-(cyclohexylmethyl)-3-oxopropyl)-2-propoxyphenyl)methyl)benzamide

Guidance literature:: Multi-step reaction with 7 steps

1: sodium tetrahydroborate / ethanol / 0 - 20 °C

2: phosphorus tribromide / diethyl ether / 2 h / 0 °C

3: sodium hexamethyldisilazane / tetrahydrofuran / -50 - -15 °C / Inert atmosphere

4: 10% Pd/C; hydrogen / ethyl acetate / 1500.15 - 2250.23 Torr

5: borane-THF / 0 - 20 °C

6: pyridinium dichromate / dichloromethane / 12 h / 20 °C

7: triethylsilane; trifluoroacetic acid / toluene / 48 h / Reflux; Inert atmosphere

With triethylsilane; sodium tetrahydroborate; borane-THF; 10% Pd/C; pyridinium dichromate; hydrogen; sodium hexamethyldisilazane; phosphorus tribromide; trifluoroacetic acid; In tetrahydrofuran; diethyl ether; ethanol; dichloromethane; ethyl acetate; toluene;
DOI:10.1016/j.bmc.2012.08.061

Reference yield:

: 1259391-05-3
benzyl 5-hydroxymethyl-2-propoxybenzoate

: 1401791-65-8
4-(1-adamantyl)-N-((5-((R)-3-((S)-4-benzyl-2-oxo-oxazolidin-3-yl)-2-(cyclohexylmethyl)-3-oxopropyl)-2-propoxyphenyl)methyl)benzamide

Guidance literature:: Multi-step reaction with 6 steps

1: phosphorus tribromide / diethyl ether / 2 h / 0 °C

2: sodium hexamethyldisilazane / tetrahydrofuran / -50 - -15 °C / Inert atmosphere

3: 10% Pd/C; hydrogen / ethyl acetate / 1500.15 - 2250.23 Torr

4: borane-THF / 0 - 20 °C

5: pyridinium dichromate / dichloromethane / 12 h / 20 °C

6: triethylsilane; trifluoroacetic acid / toluene / 48 h / Reflux; Inert atmosphere

With triethylsilane; borane-THF; 10% Pd/C; pyridinium dichromate; hydrogen; sodium hexamethyldisilazane; phosphorus tribromide; trifluoroacetic acid; In tetrahydrofuran; diethyl ether; dichloromethane; ethyl acetate; toluene;
DOI:10.1016/j.bmc.2012.08.061