4-[12-(4-nitrobenzyloxycarbonylamino)dodecanoyl]piperazine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:4-[12-(4-nitrobenzyloxycarbonylamino)dodecanoyl]piperazine-1-carboxylic acid tert-butyl ester
CAS No.:933046-47-0
Molecular Formula:C₂₉H₄₆N₄O₇
Molecular Weight:562.707
Hs Code.:

Synonyms:4-[12-(4-nitrobenzyloxycarbonylamino)dodecanoyl]piperazine-1-carboxylic acid tert-butyl ester

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Chemical Property of 4-[12-(4-nitrobenzyloxycarbonylamino)dodecanoyl]piperazine-1-carboxylic acid tert-butyl ester

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Technology Process of 4-[12-(4-nitrobenzyloxycarbonylamino)dodecanoyl]piperazine-1-carboxylic acid tert-butyl ester

There total 3 articles about 4-[12-(4-nitrobenzyloxycarbonylamino)dodecanoyl]piperazine-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: 70.0%

: 873584-07-7
12-(4-nitrobenzyloxycarbonylamino)dodecanoic acid

: 57260-71-6
1-t-Butoxycarbonylpiperazine

: 933046-47-0
4-[12-(4-nitrobenzyloxycarbonylamino)dodecanoyl]piperazine-1-carboxylic acid tert-butyl ester

Guidance literature:: 12-(4-nitrobenzyloxycarbonylamino)dodecanoic acid; With triethylamine; isobutyl chloroformate; In tetrahydrofuran; at -25 - -20 ℃; for 0.25h;

1-t-Butoxycarbonylpiperazine; In tetrahydrofuran; at 20 ℃; for 2h;
DOI:10.1016/j.ejmech.2006.07.010

Reference yield:

: 693-57-2
12-Aminododecanoic acid

: 933046-47-0
4-[12-(4-nitrobenzyloxycarbonylamino)dodecanoyl]piperazine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: 75 percent / aq. NaOH / tetrahydrofuran / 2.17 h / 0 - 20 °C

2.1: isobutyl chloroformate; triethylamine / tetrahydrofuran / 0.25 h / -25 - -20 °C

2.2: 70 percent / tetrahydrofuran / 2 h / 20 °C

With sodium hydroxide; triethylamine; isobutyl chloroformate; In tetrahydrofuran;
DOI:10.1016/j.ejmech.2006.07.010

Reference yield:

: 4457-32-3
4-nitrobenzyl chloroformate

: 933046-47-0
4-[12-(4-nitrobenzyloxycarbonylamino)dodecanoyl]piperazine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: 75 percent / aq. NaOH / tetrahydrofuran / 2.17 h / 0 - 20 °C

2.1: isobutyl chloroformate; triethylamine / tetrahydrofuran / 0.25 h / -25 - -20 °C

2.2: 70 percent / tetrahydrofuran / 2 h / 20 °C

With sodium hydroxide; triethylamine; isobutyl chloroformate; In tetrahydrofuran;
DOI:10.1016/j.ejmech.2006.07.010