8-(tert-Butyldimethylsilanyloxy)-5-[4-(1-phenyl-1H-benzimidazol-2-yl)phenyl]quinoline

Base Information

Chemical Name:8-(tert-Butyldimethylsilanyloxy)-5-[4-(1-phenyl-1H-benzimidazol-2-yl)phenyl]quinoline
CAS No.:1321844-69-2
Molecular Formula:C₃₄H₃₃N₃OSi
Molecular Weight:527.741
Hs Code.:

Synonyms:8-(tert-Butyldimethylsilanyloxy)-5-[4-(1-phenyl-1H-benzimidazol-2-yl)phenyl]quinoline

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Chemical Property of 8-(tert-Butyldimethylsilanyloxy)-5-[4-(1-phenyl-1H-benzimidazol-2-yl)phenyl]quinoline

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Technology Process of 8-(tert-Butyldimethylsilanyloxy)-5-[4-(1-phenyl-1H-benzimidazol-2-yl)phenyl]quinoline

There total 6 articles about 8-(tert-Butyldimethylsilanyloxy)-5-[4-(1-phenyl-1H-benzimidazol-2-yl)phenyl]quinoline 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: 80.0%

: 892878-80-7
8-(tert-butyldimethylsilyloxy)-5-iodoquinoline

: 1146340-38-6
1-phenyl-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-phenyl]-1H-benzo[d]imidazole

: 1321844-69-2
8-(tert-Butyldimethylsilanyloxy)-5-[4-(1-phenyl-1H-benzimidazol-2-yl)phenyl]quinoline

Guidance literature:: 8-(tert-butyldimethylsilyloxy)-5-iodoquinoline; 1-phenyl-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-phenyl]-1H-benzo[d]imidazole; In 1,4-dioxane; toluene; for 0.5h;

With tris-(o-tolyl)phosphine; palladium diacetate; In 1,4-dioxane; toluene; at 80 ℃; for 8h;

Reference yield:

: 534-85-0
N-phenyl-1,2-benzenediamine

: 1321844-69-2
8-(tert-Butyldimethylsilanyloxy)-5-[4-(1-phenyl-1H-benzimidazol-2-yl)phenyl]quinoline

Guidance literature:: Multi-step reaction with 3 steps

1.1: Oxone / N,N-dimethyl-formamide / 20 - 40 °C / Inert atmosphere

2.1: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane / 6 h / Reflux

3.1: toluene; 1,4-dioxane / 0.5 h

3.2: 8 h / 80 °C

With Oxone; potassium acetate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,4-dioxane; N,N-dimethyl-formamide; toluene; 3.1: Suzuki Coupling;

Reference yield:

: 1122-91-4
4-bromo-benzaldehyde

: 1321844-69-2
8-(tert-Butyldimethylsilanyloxy)-5-[4-(1-phenyl-1H-benzimidazol-2-yl)phenyl]quinoline

Guidance literature:: Multi-step reaction with 3 steps

1.1: Oxone / N,N-dimethyl-formamide / 20 - 40 °C / Inert atmosphere

2.1: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane / 6 h / Reflux

3.1: toluene; 1,4-dioxane / 0.5 h

3.2: 8 h / 80 °C

With Oxone; potassium acetate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,4-dioxane; N,N-dimethyl-formamide; toluene; 3.1: Suzuki Coupling;