1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(3-(pyridin-3-yl)quinoxaline-6-carbonyl)phenyl)urea

Base Information

Chemical Name:1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(3-(pyridin-3-yl)quinoxaline-6-carbonyl)phenyl)urea
CAS No.:1427632-30-1
Molecular Formula:C₂₈H₁₇ClF₃N₅O₂
Molecular Weight:547.923
Hs Code.:

Synonyms:1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(3-(pyridin-3-yl)quinoxaline-6-carbonyl)phenyl)urea

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Chemical Property of 1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(3-(pyridin-3-yl)quinoxaline-6-carbonyl)phenyl)urea

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Technology Process of 1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(3-(pyridin-3-yl)quinoxaline-6-carbonyl)phenyl)urea

There total 8 articles about 1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(3-(pyridin-3-yl)quinoxaline-6-carbonyl)phenyl)urea 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: 29.3%

: 1427632-32-3
(3-aminophenyl)(3-(pyridin-3-yl)quinoxalin-6-yl)methanone

: 327-78-6
4-chloro-3-(trifluoromethyl)phenyl isocyanate

: 1427632-30-1
1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(3-(pyridin-3-yl)quinoxaline-6-carbonyl)phenyl)urea

Guidance literature:: With triethylamine; In dichloromethane;

Reference yield:

: 6925-00-4
quinoxaline-6-carboxylic acid

: 1427632-30-1
1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(3-(pyridin-3-yl)quinoxaline-6-carbonyl)phenyl)urea

Guidance literature:: Multi-step reaction with 7 steps

1.1: thionyl chloride; N,N-dimethyl-formamide / Reflux

1.2: 0 - 20 °C

2.1: diisobutylaluminium hydride / tetrahydrofuran / 0.5 h / -78 °C

3.1: sec.-butyllithium / tetrahydrofuran / 0.5 h / -78 °C

3.2: 1 h / -78 °C

4.1: manganese(IV) oxide / dichloromethane

5.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium carbonate / 1,4-dioxane; water / 100 °C / Inert atmosphere

6.1: hydrogenchloride; acetic acid / water / 4 h / 110 °C

7.1: triethylamine / dichloromethane

With hydrogenchloride; manganese(IV) oxide; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; thionyl chloride; sec.-butyllithium; diisobutylaluminium hydride; sodium carbonate; acetic acid; triethylamine; N,N-dimethyl-formamide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water;

Reference yield:

: 1425486-34-5
3-chloro-N-methoxy-N-methylquinoxaline-6-carboxamide

: 1427632-30-1
1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(3-(pyridin-3-yl)quinoxaline-6-carbonyl)phenyl)urea

Guidance literature:: Multi-step reaction with 6 steps

1.1: diisobutylaluminium hydride / tetrahydrofuran / 0.5 h / -78 °C

2.1: sec.-butyllithium / tetrahydrofuran / 0.5 h / -78 °C

2.2: 1 h / -78 °C

3.1: manganese(IV) oxide / dichloromethane

4.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium carbonate / 1,4-dioxane; water / 100 °C / Inert atmosphere

5.1: hydrogenchloride; acetic acid / water / 4 h / 110 °C

6.1: triethylamine / dichloromethane

With hydrogenchloride; manganese(IV) oxide; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sec.-butyllithium; diisobutylaluminium hydride; sodium carbonate; acetic acid; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water;