313822-60-5

Upstream product

• 175847-14-0 N-<1-(2-fluorophenyl)ethylidene>-2-(trifluopromethyl)aniline 
• 110802-10-3 2-(2-fluorophenyl)quinolin-4(1H)-one 

Downstream Products

• 924621-07-8 N-(4-hydroxybutyl)-2-(2-fluorophenyl)quinolin-4-amine 
• 1099705-50-6 N,N-diethyl-2-(2-fluorophenyl)quinolin-4-amine 
• 422565-93-3 2-(2-fluorophenyl)quinolin-4-amine 
• 1099705-48-2 2-(2-fluorophenyl)-N,N-dimethylquinolin-4-amine 
• 924621-10-3 N-(4-chlorobutyl)-2-(2-fluorophenyl)quinolin-4-amine 
• 918970-00-0 N-[3-(dimethylamino)propyl]-2-(2-fluorophenyl)quinolin-4-amine 
• 924621-14-7 2-(2-fluorophenyl)-4-(N-methylpiperazino)quinoline 

Relevant academic research and scientific papers

4-aminoquinoline compound, and preparation method and application thereof

The invention discloses a 4-aminoquinoline compound, and a preparation method and application thereof. The second site of the 4-aminoquinoline compound is replaced by cyclic R-base, the 4-aminoquinoline compound is obtained by 4-step reaction of anthranil

Investigation of amination in 4-chloro-2-phenylquinoline derivatives with amide solvents

Novel 4-amino-2-phenylquinoline derivatives were synthesized by reacting various 4-chloro-2-arylquinoline compounds having activated chloro group with the corresponding amide solvents at reflux for overnight. The activity of amination by the amide solvent

Synthesis of 2-phenylquinolin-4-amines substituted with diverse amino and aminoalkyl groups

Facile synthetic approaches to 2-phenylquinolin-4-amines containing an aminoalkyl group at N4 of the quinolin-4-amine and amino or aminoalkyl groups at the phenyl moiety are presented.