120301-12-4

Upstream product

• 583-55-1 1-Bromo-2-iodobenzene 
• 402-26-6 3-(trifluoromethyl)phenylmagnesium bromide 
• 525-76-8 2-methyl-4-oxo-3,1-benzoxazine 
• 952340-26-0 (E)-3-(2-bromophenyl)acrylamide 
• 401-78-5 3-bromo-1-trifluoromethylbenzene 
• 401-81-0 m-trifluoromethylphenyl iodide 
• 28582-36-7 2'-(m-Trifluoromethyl-benzoyl)-acetanilid 

Downstream Products

• 105189-19-3 2-[4-(2-hydroxyethyl)-1-piperazinyl]-4-(3-trifluoromethylphenyl)quinoline 
• 105189-17-1 2-(4-ethyl-1-piperazinyl)-4-(3-trifluoromethylphenyl)quinoline 
• 105189-01-3 2-(1-piperazinyl)-4-(3-trifluoromethylphenyl)quinoline 
• 120314-06-9 2-chloro-4-(3-trifluoromethylphenyl)quinoline 

Relevant academic research and scientific papers

4-Aryl-2-quinolones through a Pseudo-Domino Heck/Buchwald-Hartwig reaction in a molten tetrabutylammonium acetate/ tetrabutylammonium bromide mixture

4-Aryl-2-quinolones can be prepared from readily available o-bromocinnamamide and aryl iodides using phosphine-free palladium(II) ace-tate as the precatalyst and a molten tetra(n-butyl)-ammonium acetate/tetra(n-butyl) ammonium bro-mide mixture as the reac

2-(1-piperazinyl)-4-substituted phenylquinoline derivatives, processes for the preparation thereof, and pharmaceutical composition containing the same

Compounds of the formula: STR1 wherein R1 represents fluorine atom at the para position, chlorine atom at the para position, methyl group at the para position or trifluoromethyl group at the para or meta position; and R2 represents h