2-bromo-N-(3,4-dichlorobenzyl)-N-[2-(4-nitro-1H-imidazol-1-yl)ethyl]ethanamine

Base Information

• Chemical Name: 2-bromo-N-(3,4-dichlorobenzyl)-N-[2-(4-nitro-1H-imidazol-1-yl)ethyl]ethanamine
• CAS No.: 1383981-65-4
• Molecular Formula: C₁₄H₁₅BrCl₂N₄O₂
• Molecular Weight: 422.109
• Mol file: 1383981-65-4.mol

Synonyms:2-bromo-N-(3,4-dichlorobenzyl)-N-[2-(4-nitro-1H-imidazol-1-yl)ethyl]ethanamine

Chemical Property of 2-bromo-N-(3,4-dichlorobenzyl)-N-[2-(4-nitro-1H-imidazol-1-yl)ethyl]ethanamine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-bromo-N-(3,4-dichlorobenzyl)-N-[2-(4-nitro-1H-imidazol-1-yl)ethyl]ethanamine

There total 3 articles about 2-bromo-N-(3,4-dichlorobenzyl)-N-[2-(4-nitro-1H-imidazol-1-yl)ethyl]ethanamine 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: 55.4%

2-bromo-N-(2-bromoethyl)-N-(3,4-dichlorobenzyl)ethanamine (1096706-57-8) + 1H-4(5)-nitroimidazole (3034-38-6) → 2-bromo-N-(3,4-dichlorobenzyl)-N-[2-(4-nitro-1H-imidazol-1-yl)ethyl]ethanamine (1383981-65-4) + 2-bromo-N-(3,4-dichlorobenzyl)-N-[2-(5-nitro-1H-imidazol-1-yl)ethyl]ethanamine (1383981-66-5)

Guidance literature:

1H-4⁽⁵⁾-nitroimidazole; With potassium carbonate; In acetonitrile; at 60 ℃; for 1h;

2-bromo-N-(2-bromoethyl)-N-(3,4-dichlorobenzyl)ethanamine; In acetonitrile; at 60 ℃; for 2h;

DOI:10.1016/j.bmc.2013.05.007

Reference yield:

3,4-Dichlorophenylmethyl chloride (102-47-6) → 2-bromo-N-(3,4-dichlorobenzyl)-N-[2-(4-nitro-1H-imidazol-1-yl)ethyl]ethanamine (1383981-65-4)

Guidance literature:

Multi-step reaction with 3 steps

1.1: acetonitrile / 50 °C

2.1: phosphorus tribromide / chloroform / 2 h / Reflux

3.1: potassium carbonate / acetonitrile / 1 h / 60 °C

3.2: 2 h / 60 °C

With phosphorus tribromide; potassium carbonate; In chloroform; acetonitrile;

DOI:10.1016/j.bmc.2013.05.007

Reference yield:

2-[(2-Hydroxy-ethyl)-(3,4-dichloro-benzyl)-amino]-ethanol (60876-94-0) → 2-bromo-N-(3,4-dichlorobenzyl)-N-[2-(4-nitro-1H-imidazol-1-yl)ethyl]ethanamine (1383981-65-4)

Guidance literature:

Multi-step reaction with 2 steps

1.1: phosphorus tribromide / chloroform / 2 h / Reflux

2.1: potassium carbonate / acetonitrile / 1 h / 60 °C

2.2: 2 h / 60 °C

With phosphorus tribromide; potassium carbonate; In chloroform; acetonitrile;

DOI:10.1016/j.bmc.2013.05.007

upstream raw materials:

3,4-Dichlorophenylmethyl chloride

2-[(2-Hydroxy-ethyl)-(3,4-dichloro-benzyl)-amino]-ethanol

2-bromo-N-(2-bromoethyl)-N-(3,4-dichlorobenzyl)ethanamine

1H-4⁽⁵⁾-nitroimidazole

Downstream raw materials:

N-(3,4-dichlorobenzyl)-N-(2-(4-nitro-1H-imidazol-1-yl)ethyl)-2-(2-berberinoxyethoxy)ethanamine