[3-methoxy-4-(4-methylimidazol-1-yl)phenyl]-[3-methyl-2-(2-trifluoromethylphenyl)imidazo[1,2-a]pyridin-8-yl]amine

Base Information

Chemical Name:[3-methoxy-4-(4-methylimidazol-1-yl)phenyl]-[3-methyl-2-(2-trifluoromethylphenyl)imidazo[1,2-a]pyridin-8-yl]amine
CAS No.:1232395-02-6
Molecular Formula:C₂₆H₂₂F₃N₅O
Molecular Weight:477.489
Hs Code.:

Synonyms:[3-methoxy-4-(4-methylimidazol-1-yl)phenyl]-[3-methyl-2-(2-trifluoromethylphenyl)imidazo[1,2-a]pyridin-8-yl]amine

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Chemical Property of [3-methoxy-4-(4-methylimidazol-1-yl)phenyl]-[3-methyl-2-(2-trifluoromethylphenyl)imidazo[1,2-a]pyridin-8-yl]amine

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Technology Process of [3-methoxy-4-(4-methylimidazol-1-yl)phenyl]-[3-methyl-2-(2-trifluoromethylphenyl)imidazo[1,2-a]pyridin-8-yl]amine

There total 4 articles about [3-methoxy-4-(4-methylimidazol-1-yl)phenyl]-[3-methyl-2-(2-trifluoromethylphenyl)imidazo[1,2-a]pyridin-8-yl]amine 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: 69.0%

: 958245-18-6
3-methoxy-4-(4-methyl-1H-imidazol-1-yl)aniline

: 1381869-22-2
8-bromo-3-methyl-2-(2-trifluoromethylphenyl)imidazo[1,2-a]pyridine

: 1232395-02-6
[3-methoxy-4-(4-methylimidazol-1-yl)phenyl]-[3-methyl-2-(2-trifluoromethylphenyl)imidazo[1,2-a]pyridin-8-yl]amine

Guidance literature:: With palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; In toluene; at 100 ℃; Inert atmosphere;
DOI:10.1021/jm201710f

Reference yield:

: 1009-36-5
2-chloro-5-nitroanisole

: 1232395-02-6
[3-methoxy-4-(4-methylimidazol-1-yl)phenyl]-[3-methyl-2-(2-trifluoromethylphenyl)imidazo[1,2-a]pyridin-8-yl]amine

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / dimethyl sulfoxide / 6 h / 150 °C / Autoclave; Inert atmosphere

2: 10% Pd/C; hydrogen / methanol / 12 h / 50 °C / 760.05 Torr

3: palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate / toluene / 100 °C / Inert atmosphere

With 10% Pd/C; hydrogen; palladium diacetate; potassium carbonate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; In methanol; dimethyl sulfoxide; toluene;
DOI:10.1021/jm201710f

Reference yield:

: 958245-17-5
1-(2-methoxy-4-nitrophenyl)-4-methyl-1H-imidazole

: 1232395-02-6
[3-methoxy-4-(4-methylimidazol-1-yl)phenyl]-[3-methyl-2-(2-trifluoromethylphenyl)imidazo[1,2-a]pyridin-8-yl]amine

Guidance literature:: Multi-step reaction with 2 steps

1: 10% Pd/C; hydrogen / methanol / 12 h / 50 °C / 760.05 Torr

2: palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate / toluene / 100 °C / Inert atmosphere

With 10% Pd/C; hydrogen; palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; In methanol; toluene;
DOI:10.1021/jm201710f