N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-bromo-3-nitrobenzamide

Base Information

• Chemical Name: N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-bromo-3-nitrobenzamide
• CAS No.: 1447017-96-0
• Molecular Formula: C₂₉H₂₂Br₂N₄O₅S
• Molecular Weight: 698.391
• Mol file: 1447017-96-0.mol

Synonyms:N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-bromo-3-nitrobenzamide

Chemical Property of N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-bromo-3-nitrobenzamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-bromo-3-nitrobenzamide

There total 4 articles about N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-bromo-3-nitrobenzamide 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: 69.0%

2-bromo-3-nitrobenzoic acid chloride (6286-36-8) + 2-amino-N-(3-(benzylthio)-2-(methylcarbamoyl)phenyl)-6-bromobenzamide (1447017-93-7) → N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-bromo-3-nitrobenzamide (1447017-96-0)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; Cooling with ice;

DOI:10.1016/j.cclet.2013.04.047

Reference yield:

2-bromo-3-nitro-benzoic acid (573-54-6) → N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-bromo-3-nitrobenzamide (1447017-96-0)

Guidance literature:

Multi-step reaction with 2 steps

1: thionyl chloride / 2 h / Reflux

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Cooling with ice

With thionyl chloride; N-ethyl-N,N-diisopropylamine; In dichloromethane;

DOI:10.1016/j.cclet.2013.04.047

Reference yield:

2-amino-6-bromo-N-(3-bromo-2-(methylcarbamoyl)phenyl)benzamide (1447017-92-6) → N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-bromo-3-nitrobenzamide (1447017-96-0)

Guidance literature:

Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 12 h / 20 °C

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Cooling with ice

With potassium carbonate; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.cclet.2013.04.047

upstream raw materials:

2-bromo-3-nitrobenzoic acid chloride

2-amino-N-(3-(benzylthio)-2-(methylcarbamoyl)phenyl)-6-bromobenzamide

2-bromo-3-nitro-benzoic acid

2-amino-6-bromo-N-(3-bromo-2-(methylcarbamoyl)phenyl)benzamide