4-[3-({[(S)-2-Benzyloxycarbonyl-1-((S)-1-benzyloxycarbonyl-2-cyclooctyl-ethylcarbamoyl)-ethylcarbamoyl]-methyl}-ethyl-carbamoyl)-propyl]-piperidine-1-carboxylic acid tert-butyl ester

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Chemical Name:4-[3-({[(S)-2-Benzyloxycarbonyl-1-((S)-1-benzyloxycarbonyl-2-cyclooctyl-ethylcarbamoyl)-ethylcarbamoyl]-methyl}-ethyl-carbamoyl)-propyl]-piperidine-1-carboxylic acid tert-butyl ester
CAS No.:1025970-90-4
Molecular Formula:C₄₇H₆₈N₄O₉
Molecular Weight:833.078
Hs Code.:

4-[3-({[(S)-2-Benzyloxycarbonyl-1-((S)-1-benzyloxycarbonyl-2-cyclooctyl-ethylcarbamoyl)-ethylcarbamoyl]-methyl}-ethyl-carbamoyl)-propyl]-piperidine-1-carboxylic acid tert-butyl ester

Synonyms:4-[3-({[(S)-2-Benzyloxycarbonyl-1-((S)-1-benzyloxycarbonyl-2-cyclooctyl-ethylcarbamoyl)-ethylcarbamoyl]-methyl}-ethyl-carbamoyl)-propyl]-piperidine-1-carboxylic acid tert-butyl ester

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Chemical Property of 4-[3-({[(S)-2-Benzyloxycarbonyl-1-((S)-1-benzyloxycarbonyl-2-cyclooctyl-ethylcarbamoyl)-ethylcarbamoyl]-methyl}-ethyl-carbamoyl)-propyl]-piperidine-1-carboxylic acid tert-butyl ester

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Technology Process of 4-[3-({[(S)-2-Benzyloxycarbonyl-1-((S)-1-benzyloxycarbonyl-2-cyclooctyl-ethylcarbamoyl)-ethylcarbamoyl]-methyl}-ethyl-carbamoyl)-propyl]-piperidine-1-carboxylic acid tert-butyl ester

There total 12 articles about 4-[3-({[(S)-2-Benzyloxycarbonyl-1-((S)-1-benzyloxycarbonyl-2-cyclooctyl-ethylcarbamoyl)-ethylcarbamoyl]-methyl}-ethyl-carbamoyl)-propyl]-piperidine-1-carboxylic acid tert-butyl 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:

: 100-43-6,329041-72-7
4-vinylpyridine

: 1025970-90-4
4-[3-({[(S)-2-Benzyloxycarbonyl-1-((S)-1-benzyloxycarbonyl-2-cyclooctyl-ethylcarbamoyl)-ethylcarbamoyl]-methyl}-ethyl-carbamoyl)-propyl]-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) NaH / 1.) EtOH, 80 deg C, 30 min, 2.) EtOH, 80 deg C, 3 h

2: 20percent aq. HCl / 16 h / Heating

3: H₂, AcOH / PtO₂ / methanol / 16 h / 2585.7 Torr

4: 1 N aq. NaOH / tetrahydrofuran / 16 h / Ambient temperature

5: Et₃N / CH₂Cl₂ / 0.5 h / 0 °C

6: Et₃N / CH₂Cl₂ / 16 h / Ambient temperature

With hydrogenchloride; sodium hydroxide; hydrogen; sodium hydride; acetic acid; triethylamine; platinum(IV) oxide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jm9801096

Reference yield:

: 92501-98-9
ethyl 2-ethoxycarbonyl-4-(pyrid-4-yl)-butanoate

: 1025970-90-4
4-[3-({[(S)-2-Benzyloxycarbonyl-1-((S)-1-benzyloxycarbonyl-2-cyclooctyl-ethylcarbamoyl)-ethylcarbamoyl]-methyl}-ethyl-carbamoyl)-propyl]-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 20percent aq. HCl / 16 h / Heating

2: H₂, AcOH / PtO₂ / methanol / 16 h / 2585.7 Torr

3: 1 N aq. NaOH / tetrahydrofuran / 16 h / Ambient temperature

4: Et₃N / CH₂Cl₂ / 0.5 h / 0 °C

5: Et₃N / CH₂Cl₂ / 16 h / Ambient temperature

With hydrogenchloride; sodium hydroxide; hydrogen; acetic acid; triethylamine; platinum(IV) oxide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jm9801096

Reference yield:

: 102878-73-9
γ-(pyridin-4-yl)butyric acid

: 1025970-90-4
4-[3-({[(S)-2-Benzyloxycarbonyl-1-((S)-1-benzyloxycarbonyl-2-cyclooctyl-ethylcarbamoyl)-ethylcarbamoyl]-methyl}-ethyl-carbamoyl)-propyl]-piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: H₂, AcOH / PtO₂ / methanol / 16 h / 2585.7 Torr

2: 1 N aq. NaOH / tetrahydrofuran / 16 h / Ambient temperature

3: Et₃N / CH₂Cl₂ / 0.5 h / 0 °C

4: Et₃N / CH₂Cl₂ / 16 h / Ambient temperature

With sodium hydroxide; hydrogen; acetic acid; triethylamine; platinum(IV) oxide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jm9801096