ethyl 6-chloro-4-((3-(trifluoromethyl)phenyl)amino)-1,5-naphthyridine-3-carboxylate

Base Information

• Chemical Name: ethyl 6-chloro-4-((3-(trifluoromethyl)phenyl)amino)-1,5-naphthyridine-3-carboxylate
• CAS No.: 1416000-52-6
• Molecular Formula: C₁₈H₁₃ClF₃N₃O₂
• Molecular Weight: 395.768
• Mol file: 1416000-52-6.mol

Synonyms:ethyl 6-chloro-4-((3-(trifluoromethyl)phenyl)amino)-1,5-naphthyridine-3-carboxylate

Chemical Property of ethyl 6-chloro-4-((3-(trifluoromethyl)phenyl)amino)-1,5-naphthyridine-3-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of ethyl 6-chloro-4-((3-(trifluoromethyl)phenyl)amino)-1,5-naphthyridine-3-carboxylate

There total 6 articles about ethyl 6-chloro-4-((3-(trifluoromethyl)phenyl)amino)-1,5-naphthyridine-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: 93.5%

4,6-dichloro-(1,5)-naphthyridine-3-carboxylic acid ethyl ester (127094-57-9) + 3-trifluoromethylaniline (98-16-8) → ethyl 6-chloro-4-((3-(trifluoromethyl)phenyl)amino)-1,5-naphthyridine-3-carboxylate (1416000-52-6)

Guidance literature:

With potassium carbonate; In tert-butyl alcohol; for 3h; Reflux;

Reference yield:

ethyl 6-bromo-4-hydroxy-1,5-naphthyridine-3-carboxylate (1184919-05-8) → ethyl 6-chloro-4-((3-(trifluoromethyl)phenyl)amino)-1,5-naphthyridine-3-carboxylate (1416000-52-6)

Guidance literature:

Multi-step reaction with 2 steps

2: tert-butyl alcohol

In tert-butyl alcohol;

Reference yield:

6-bromopyridine-3-amine (13534-97-9) → ethyl 6-chloro-4-((3-(trifluoromethyl)phenyl)amino)-1,5-naphthyridine-3-carboxylate (1416000-52-6)

Guidance literature:

Multi-step reaction with 4 steps

1: ethanol / 5 h / Reflux

2: diphenylether / 0.75 h / Reflux

3: dimethyl amine; trichlorophosphate / 3 h / Reflux

4: potassium carbonate / tert-butyl alcohol / 3 h / Reflux

With potassium carbonate; dimethyl amine; trichlorophosphate; In diphenylether; ethanol; tert-butyl alcohol;

upstream raw materials:

ethyl 6-bromo-4-hydroxy-1,5-naphthyridine-3-carboxylate

4,6-dichloro-(1,5)-naphthyridine-3-carboxylic acid ethyl ester

3-trifluoromethylaniline

2-bromo-5-nitropyridine