ethyl 6-bromo-4-((3-(trifluoromethyl)phenyl)amino)quinoline-3-carboxylate

Base Information

• Chemical Name: ethyl 6-bromo-4-((3-(trifluoromethyl)phenyl)amino)quinoline-3-carboxylate
• CAS No.: 449197-54-0
• Molecular Formula: C₁₉H₁₄BrF₃N₂O₂
• Molecular Weight: 439.232
• Mol file: 449197-54-0.mol

Synonyms:ethyl 6-bromo-4-((3-(trifluoromethyl)phenyl)amino)quinoline-3-carboxylate

Chemical Property of ethyl 6-bromo-4-((3-(trifluoromethyl)phenyl)amino)quinoline-3-carboxylate

Chemical Property:

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of ethyl 6-bromo-4-((3-(trifluoromethyl)phenyl)amino)quinoline-3-carboxylate

There total 5 articles about ethyl 6-bromo-4-((3-(trifluoromethyl)phenyl)amino)quinoline-3-carboxylate 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: 91.0%

3-trifluoromethylaniline (98-16-8) + 6-bromo-4-chloroquinoline-3-carboxylic acid ethyl ester (206257-39-8) → ethyl 6-bromo-4-((3-(trifluoromethyl)phenyl)amino)quinoline-3-carboxylate (449197-54-0)

Guidance literature:

With sodium acetate; acetic acid; at 20 ℃; for 0.5h;

DOI:10.1016/j.bmc.2015.11.003

Reference yield:

4-bromo-aniline (106-40-1) → ethyl 6-bromo-4-((3-(trifluoromethyl)phenyl)amino)quinoline-3-carboxylate (449197-54-0)

Guidance literature:

Multi-step reaction with 4 steps

1: 2 h / 80 °C

2: diphenylether / 6 h / 250 °C

3: trichlorophosphate; N,N-dimethyl-formamide / 4 h / Reflux

4: sodium acetate; acetic acid / 0.5 h / 20 °C

With sodium acetate; acetic acid; N,N-dimethyl-formamide; trichlorophosphate; In diphenylether;

DOI:10.1016/j.bmc.2015.11.003

Reference yield:

diethyl 2-ethoxymethylenemalonate (87-13-8) → ethyl 6-bromo-4-((3-(trifluoromethyl)phenyl)amino)quinoline-3-carboxylate (449197-54-0)

Guidance literature:

Multi-step reaction with 4 steps

1: 2 h / 80 °C

2: diphenylether / 6 h / 250 °C

3: trichlorophosphate; N,N-dimethyl-formamide / 4 h / Reflux

4: sodium acetate; acetic acid / 0.5 h / 20 °C

With sodium acetate; acetic acid; N,N-dimethyl-formamide; trichlorophosphate; In diphenylether;

DOI:10.1016/j.bmc.2015.11.003

upstream raw materials:

3-trifluoromethylaniline

6-bromo-4-chloroquinoline-3-carboxylic acid ethyl ester

4-bromo-aniline

diethyl 2-ethoxymethylenemalonate

Downstream raw materials:

Torin₂