96110-83-7

Upstream product

• 22261-94-5 N-(1-methyl-4-piperidinyl)aniline 
• 100-47-0 benzonitrile 

Downstream Products

• 96110-99-5 ethyl 2-[[[2-(1-methyl-4-piperidinyl)aminophenyl](phenyl)methylen]amino]acetate 
• 93591-97-0 1,3-dihydro-1-(4-piperidinyl)-5-phenyl-2H-1,4-benzodiazepin-2-one 
• 93592-17-7 1,3-dihydro-1-(1-ethoxycarbonyl-4-piperidinyl)-5-phenyl-2H-1,4-benzodiazepin-2-one 
• 93592-71-3 1-(1-methyl-4-piperidinyl)-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepin-2-one 

Relevant academic research and scientific papers

Ortho-mono-substituted amino)phenylimines

Novel ortho-(mono-substituted amino)phenylimines being intermediates to psychotropic drugs and other drugs are economically and industrially prepared by reacting anilines with nitriles in the presence of a boron trifluoride ether adduct and a halide-type

Process for preparing 1-substituted-1,4-benzodiazepine derivatives

Improvement in the production of psychotropic 1-substituted-1,3-dihydro-1,4-benzodiazepin-2-ones starting from 2-(1-substituted)amino-benzophenonimines through novel intermediates of the formula: STR1 (wherein R is hydrogen, methyl or benzyl, R1/sup

Aminohaloborane in Organic Synthesis. IX. Exclusive ortho Acylation Reaction of N-Monoaminoalkylanilines

The exclusive ortho acylation reaction of aniline derivatives using boron trichloride made possible the one-step synthesis of 2-acyl-N-monoaminoalkylanilines (1) and the corresponding imines (2) from N-monoaminoalkylanilines, even in the case of compounds with a bulky substituent at the nitrogen atom.Conventional methods only give 1 via elaborate procedures.Keywords: regioselective reaction; 2-acylaniline derivative; 2-acylaniline-imine derivative; boron trichloride