2-(trimethylsilyl)ethyl (2S)-2-(3-((2-aminoethoxy)(3-chlorophenyl)methyl)benzamido)-3-cyclohexylpropyl(methyl)carbamate

Base Information

Chemical Name:2-(trimethylsilyl)ethyl (2S)-2-(3-((2-aminoethoxy)(3-chlorophenyl)methyl)benzamido)-3-cyclohexylpropyl(methyl)carbamate
CAS No.:1093865-43-0
Molecular Formula:C₃₂H₄₈ClN₃O₄Si
Molecular Weight:602.289
Hs Code.:

Synonyms:2-(trimethylsilyl)ethyl (2S)-2-(3-((2-aminoethoxy)(3-chlorophenyl)methyl)benzamido)-3-cyclohexylpropyl(methyl)carbamate

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Chemical Property of 2-(trimethylsilyl)ethyl (2S)-2-(3-((2-aminoethoxy)(3-chlorophenyl)methyl)benzamido)-3-cyclohexylpropyl(methyl)carbamate

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Technology Process of 2-(trimethylsilyl)ethyl (2S)-2-(3-((2-aminoethoxy)(3-chlorophenyl)methyl)benzamido)-3-cyclohexylpropyl(methyl)carbamate

There total 5 articles about 2-(trimethylsilyl)ethyl (2S)-2-(3-((2-aminoethoxy)(3-chlorophenyl)methyl)benzamido)-3-cyclohexylpropyl(methyl)carbamate 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:

: 884511-14-2
(S)-2-(trimethylsilyl)ethyl 2-amino-3-cyclohexylpropyl(methyl)carbamate

: 1093865-43-0
2-(trimethylsilyl)ethyl (2S)-2-(3-((2-aminoethoxy)(3-chlorophenyl)methyl)benzamido)-3-cyclohexylpropyl(methyl)carbamate

Guidance literature:: Multi-step reaction with 5 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 20 h / 20 °C

2: tetrahydrofuran / 7 h / 0 °C

3: toluene-4-sulfonic acid / 4.5 h / 140 °C

4: potassium carbonate / dichloromethane; water / 16 h / 20 °C

5: lithium hydroxide; water / tetrahydrofuran / 5 h / 20 °C

With lithium hydroxide; water; potassium carbonate; toluene-4-sulfonic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; water;

Reference yield:

: 1093865-39-4
(S)-2-(trimethylsilyl)ethyl 3-cyclohexyl-2-(3-formylbenzamido)-propyl(methyl)carbamate

: 1093865-43-0
2-(trimethylsilyl)ethyl (2S)-2-(3-((2-aminoethoxy)(3-chlorophenyl)methyl)benzamido)-3-cyclohexylpropyl(methyl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1: tetrahydrofuran / 7 h / 0 °C

2: toluene-4-sulfonic acid / 4.5 h / 140 °C

3: potassium carbonate / dichloromethane; water / 16 h / 20 °C

4: lithium hydroxide; water / tetrahydrofuran / 5 h / 20 °C

With lithium hydroxide; water; potassium carbonate; toluene-4-sulfonic acid; In tetrahydrofuran; dichloromethane; water;

Reference yield:

: 619-21-6
m-formylphenyl benzoic acid

: 1093865-43-0
2-(trimethylsilyl)ethyl (2S)-2-(3-((2-aminoethoxy)(3-chlorophenyl)methyl)benzamido)-3-cyclohexylpropyl(methyl)carbamate

Guidance literature:: Multi-step reaction with 5 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 20 h / 20 °C

2: tetrahydrofuran / 7 h / 0 °C

3: toluene-4-sulfonic acid / 4.5 h / 140 °C

4: potassium carbonate / dichloromethane; water / 16 h / 20 °C

5: lithium hydroxide; water / tetrahydrofuran / 5 h / 20 °C

With lithium hydroxide; water; potassium carbonate; toluene-4-sulfonic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; water;