N-(3-(1-(6-aminopyrimidin-4-yl)-1H-indol-6-yl)phenyl)-4-chloro-3-(trifluoromethyl)benzamide

Base Information

Chemical Name:N-(3-(1-(6-aminopyrimidin-4-yl)-1H-indol-6-yl)phenyl)-4-chloro-3-(trifluoromethyl)benzamide
CAS No.:1298083-99-4
Molecular Formula:C₂₆H₁₇ClF₃N₅O
Molecular Weight:507.902
Hs Code.:

Synonyms:N-(3-(1-(6-aminopyrimidin-4-yl)-1H-indol-6-yl)phenyl)-4-chloro-3-(trifluoromethyl)benzamide

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Chemical Property of N-(3-(1-(6-aminopyrimidin-4-yl)-1H-indol-6-yl)phenyl)-4-chloro-3-(trifluoromethyl)benzamide

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Technology Process of N-(3-(1-(6-aminopyrimidin-4-yl)-1H-indol-6-yl)phenyl)-4-chloro-3-(trifluoromethyl)benzamide

There total 6 articles about N-(3-(1-(6-aminopyrimidin-4-yl)-1H-indol-6-yl)phenyl)-4-chloro-3-(trifluoromethyl)benzamide 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:

: 1737-36-6
4-chloro-3-(trifluoromethyl)benzoic acid

: 1298084-33-9
6-(6-(3-aminophenyl)-1H-indol-1-yl)pyrimidin-4-amine

: 1298083-99-4
N-(3-(1-(6-aminopyrimidin-4-yl)-1H-indol-6-yl)phenyl)-4-chloro-3-(trifluoromethyl)benzamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; at 20 ℃; for 15h;

Reference yield:

: 52415-29-9
6-bromo-1H-indole

: 1298083-99-4
N-(3-(1-(6-aminopyrimidin-4-yl)-1H-indol-6-yl)phenyl)-4-chloro-3-(trifluoromethyl)benzamide

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / N,N-dimethyl-formamide; water / 2 h / 20 °C

2: sodium hydride / N,N-dimethyl-formamide; mineral oil / 13 h / 0 - 20 °C

3: ammonia / isopropyl alcohol; DMSOI (dimethylsulfoxide) / 15 h / 100 °C / In a sealed reactor

4: hydrogen / Raney nickel / 1,4-dioxane; methanol / 1.5 h / 760.05 Torr

5: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / tetrahydrofuran / 15 h / 20 °C

With ammonia; hydrogen; sodium hydride; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; 1,4-dioxane; methanol; DMSOI (dimethylsulfoxide); water; N,N-dimethyl-formamide; isopropyl alcohol; mineral oil;

Reference yield:

: 1266726-40-2
6-(3-nitrophenyl)-1H-indole

: 1298083-99-4
N-(3-(1-(6-aminopyrimidin-4-yl)-1H-indol-6-yl)phenyl)-4-chloro-3-(trifluoromethyl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 13 h / 0 - 20 °C

2: ammonia / isopropyl alcohol; DMSOI (dimethylsulfoxide) / 15 h / 100 °C / In a sealed reactor

3: hydrogen / Raney nickel / 1,4-dioxane; methanol / 1.5 h / 760.05 Torr

4: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / tetrahydrofuran / 15 h / 20 °C

With ammonia; hydrogen; sodium hydride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; Raney nickel; In tetrahydrofuran; 1,4-dioxane; methanol; DMSOI (dimethylsulfoxide); N,N-dimethyl-formamide; isopropyl alcohol; mineral oil;