1-(2-chloro-4-((2-(piperidin-1-yl)ethyl)amino)phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one

Base Information

• Chemical Name: 1-(2-chloro-4-((2-(piperidin-1-yl)ethyl)amino)phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one
• CAS No.: 1256700-73-8
• Molecular Formula: C₁₉H₂₁ClF₃N₃O
• Molecular Weight: 399.843
• Mol file: 1256700-73-8.mol

Synonyms:1-(2-chloro-4-((2-(piperidin-1-yl)ethyl)amino)phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one

Chemical Property of 1-(2-chloro-4-((2-(piperidin-1-yl)ethyl)amino)phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-(2-chloro-4-((2-(piperidin-1-yl)ethyl)amino)phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one

There total 6 articles about 1-(2-chloro-4-((2-(piperidin-1-yl)ethyl)amino)phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one 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:

piperidine (110-89-4) + 1-(2-chloro-4-((2-chloroethyl)amino)-phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one (1256700-79-4) → 1-(2-chloro-4-((2-(piperidin-1-yl)ethyl)amino)phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one (1256700-73-8)

Guidance literature:

With potassium iodide; In acetonitrile; for 4h; Reflux;

DOI:10.1016/j.bmcl.2017.07.001

Reference yield:

3-chloro-4-fluoronitrobenzene (350-30-1) → 1-(2-chloro-4-((2-(piperidin-1-yl)ethyl)amino)phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one (1256700-73-8)

Guidance literature:

Multi-step reaction with 5 steps

1: potassium carbonate / dimethyl sulfoxide / 4 h / 130 °C

2: iron; hydrogenchloride / water; ethanol / Reflux

3: potassium carbonate / butan-1-ol / 20 h / 95 - 100 °C

4: triethylamine; thionyl chloride / dichloromethane / 4 h / Reflux

5: potassium iodide / acetonitrile / 4 h / Reflux

With hydrogenchloride; thionyl chloride; iron; potassium carbonate; triethylamine; potassium iodide; In ethanol; dichloromethane; water; dimethyl sulfoxide; acetonitrile; butan-1-ol;

DOI:10.1016/j.bmcl.2017.07.001

Reference yield:

5-(trifluoromethyl)-2(1H)-pyridone (33252-63-0,79894-13-6) → 1-(2-chloro-4-((2-(piperidin-1-yl)ethyl)amino)phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one (1256700-73-8)

Guidance literature:

Multi-step reaction with 5 steps

1: potassium carbonate / dimethyl sulfoxide / 4 h / 130 °C

2: iron; hydrogenchloride / water; ethanol / Reflux

3: potassium carbonate / butan-1-ol / 20 h / 95 - 100 °C

4: triethylamine; thionyl chloride / dichloromethane / 4 h / Reflux

5: potassium iodide / acetonitrile / 4 h / Reflux

With hydrogenchloride; thionyl chloride; iron; potassium carbonate; triethylamine; potassium iodide; In ethanol; dichloromethane; water; dimethyl sulfoxide; acetonitrile; butan-1-ol;

DOI:10.1016/j.bmcl.2017.07.001

upstream raw materials:

3-chloro-4-fluoronitrobenzene

5-(trifluoromethyl)-2(1H)-pyridone

5-trifluoromethyl-(1-(2-chloro-4-(2-hydroxylethyl)amino)phenyl)pyridine-2(1H)-one

1-(2-chloro-4-nitrophenyl)-5-(trifluoromethyl)pyridin-2(1H)-one