{[1-(2-amino-ethylcarbamoyl)-2-(4-nitro-phenyl)-ethylcarbamoyl]-methyl}-carbamic acid tert-butyl ester

Base Information

• Chemical Name: {[1-(2-amino-ethylcarbamoyl)-2-(4-nitro-phenyl)-ethylcarbamoyl]-methyl}-carbamic acid tert-butyl ester
• CAS No.: 929217-81-2
• Molecular Formula: C₁₈H₂₇N₅O₆
• Molecular Weight: 409.442
• Mol file: 929217-81-2.mol

Synonyms:{[1-(2-amino-ethylcarbamoyl)-2-(4-nitro-phenyl)-ethylcarbamoyl]-methyl}-carbamic acid tert-butyl ester

Chemical Property of {[1-(2-amino-ethylcarbamoyl)-2-(4-nitro-phenyl)-ethylcarbamoyl]-methyl}-carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of {[1-(2-amino-ethylcarbamoyl)-2-(4-nitro-phenyl)-ethylcarbamoyl]-methyl}-carbamic acid tert-butyl ester

There total 6 articles about {[1-(2-amino-ethylcarbamoyl)-2-(4-nitro-phenyl)-ethylcarbamoyl]-methyl}-carbamic 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: 99.0%

2-(2-tert-butoxycarbonylamino-acetylamino)-3-(4-nitro-phenyl)-propionic acid methyl ester (929217-80-1) + ethylenediamine (107-15-3,85404-18-8) → {[1-(2-amino-ethylcarbamoyl)-2-(4-nitro-phenyl)-ethylcarbamoyl]-methyl}-carbamic acid tert-butyl ester (929217-81-2)

Guidance literature:

In methanol; at 20 ℃; for 3h;

DOI:10.1002/jlcr.1031

Reference yield:

4-nitrophenylalanine (1991-83-9,2922-40-9,56613-61-7,949-99-5) → {[1-(2-amino-ethylcarbamoyl)-2-(4-nitro-phenyl)-ethylcarbamoyl]-methyl}-carbamic acid tert-butyl ester (929217-81-2)

Guidance literature:

Multi-step reaction with 4 steps

1: 91 percent / HCl / 18 h / 20 °C

2: Et₃N / methanol; diethyl ether / 4 h / 0 °C

3: tetrahydrofuran / 1 h / 20 °C

4: 99 percent / methanol / 3 h / 20 °C

With hydrogenchloride; triethylamine; In tetrahydrofuran; methanol; diethyl ether;

DOI:10.1002/jlcr.1031

Reference yield:

(+)-Methyl 2-amino-3-(4-nitrophenyl)propionate hydrochloride (17193-40-7,67877-95-6,105359-55-5,108450-75-5) → {[1-(2-amino-ethylcarbamoyl)-2-(4-nitro-phenyl)-ethylcarbamoyl]-methyl}-carbamic acid tert-butyl ester (929217-81-2)

Guidance literature:

Multi-step reaction with 3 steps

1: Et₃N / methanol; diethyl ether / 4 h / 0 °C

2: tetrahydrofuran / 1 h / 20 °C

3: 99 percent / methanol / 3 h / 20 °C

With triethylamine; In tetrahydrofuran; methanol; diethyl ether;

DOI:10.1002/jlcr.1031

upstream raw materials:

2-(2-tert-butoxycarbonylamino-acetylamino)-3-(4-nitro-phenyl)-propionic acid methyl ester

ethylenediamine

BOC-glycine

4-nitrophenylalanine

Downstream raw materials:

N-(2-aminoethyl)-glycyl 4-nitriphenylalaninamide

3-(4-nitrobenzyl)triethylenetetraamine