1-(2-chloro-4-((2-morpholinoethyl)amino)phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one

Base Information

Chemical Name:1-(2-chloro-4-((2-morpholinoethyl)amino)phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one
CAS No.:1256700-74-9
Molecular Formula:C₁₈H₁₉ClF₃N₃O₂
Molecular Weight:401.816
Hs Code.:

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

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

Chemical Property:

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

There total 6 articles about 1-(2-chloro-4-((2-morpholinoethyl)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:

: 110-91-8,99108-56-2
morpholine

: 1256700-79-4
1-(2-chloro-4-((2-chloroethyl)amino)-phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one

: 1256700-74-9
1-(2-chloro-4-((2-morpholinoethyl)amino)phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one

Guidance literature:: With sodium iodide; In acetonitrile; for 24h; Reflux;

Reference yield:

: 33252-63-0,79894-13-6
5-(trifluoromethyl)-2(1H)-pyridone

: 1256700-74-9
1-(2-chloro-4-((2-morpholinoethyl)amino)phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate; sodium iodide / dimethyl sulfoxide / 4 h / 130 °C

2.1: hydrogenchloride; iron / ethanol / 5 h / Reflux

2.2: pH 10

3.1: potassium carbonate / N,N-dimethyl-formamide / 12 h / 130 °C

4.1: thionyl chloride; triethylamine / dichloromethane / 28 h / 20 °C

5.1: sodium iodide / acetonitrile / 24 h / Reflux

With hydrogenchloride; thionyl chloride; iron; potassium carbonate; triethylamine; sodium iodide; In ethanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1256700-68-1
5-trifluoromethyl-(1-(2-chloro-4-(2-hydroxylethyl)amino)phenyl)pyridine-2(1H)-one

: 1256700-74-9
1-(2-chloro-4-((2-morpholinoethyl)amino)phenyl)-5-(trifluoromethyl)pyridin-2(1H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride; triethylamine / dichloromethane / 28 h / 20 °C

2: sodium iodide / acetonitrile / 24 h / Reflux

With thionyl chloride; triethylamine; sodium iodide; In dichloromethane; acetonitrile;