156496-75-2

Upstream product

• 126-81-8 dimedone 
• 62-53-3 aniline 
• 104-88-1 4-chlorobenzaldehyde 
• 109-77-3 malononitrile 
• 18940-21-1 5,5-dimethyl-3-(phenylamino)cyclohex-2-en-1-one 
• 1867-38-5 4-chlorobenzylidenemalonodinitrile 

Relevant academic research and scientific papers

A clean synthesis of 1,4-diarylquinoline derivatives catalyzed by TEBAC in aqueous media

A series of 1,4-diarylquinoline derivatives were synthesized by the reaction of arylmethylidene-malononitriles or 2-cyano-3-aryl-1-acrylate and 3-arylamino-5,5-dimethylcyclohex-2-enone in aqueous media at 100 °C catalyzed by TEBAC. Meanwhile, the water me

Synthesis of N -Aryl-4-arylhexahydroquinoline Derivatives by Reaction of Cyclic Enaminones with Arylidenemalononitriles in DMSO

The reaction of cyclic enaminones with arylidenemalono nitriles was carried out in the presence of 13X molecular sieves in dimethyl sulfoxide. Under these mild reaction conditions, various bioactive N -aryl-4-arylhexahydroquinoline derivatives were obtain

One-pot synthesis of 1,4-dihydropyridines and N-arylquinolines in the presence of copper complex stabilized on MnFe2O4 (MFO) as a novel organic–inorganic hybrid material and magnetically retrievable catalyst

In this work, the design and synthesis of a heterogeneous catalyst based on functionalization of manganese ferrite nanoparticles encapsulated in a silica layer with Schiff base and subsequent incorporation of copper is presented. The fabricated hybrid mat

Eco-friendly and ingenious multicomponent synthesis of N-arylquinolines using DABCO/TEAB in water

An easy, improved, and environmentally benign synthesis of N-arylquinolines is reported via one-pot multicomponent reaction of aromatic aldehydes, active methylene compounds and 3-arylamino-5,5-dimethylcyclohex-2-enone utilizing catalytic amount of combin

DBU-catalyzed expeditious and facile multicomponent synthesis of N-arylquinolines under microwave irradiation

N-Arylquinoline derivatives are obtained in excellent yields by a rapid, easy, and efficient one-pot multicomponent reaction of aromatic aldehydes, 3-arylamino-5,5-dimethylcyclohex-2-enone, and active methylene compounds utilizing 1,8-diazabicyclo[5.4.0]u

Fluoride ion catalyzed multicomponent reactions for efficient synthesis of 4H-chromene and N-arylquinoline derivatives in aqueous media

4H-Chromene and N-arylquinoline derivatives are obtained in good to excellent yields by proceeding through a simple, mild, and efficient procedure utilizing tetrabutylammonium fluoride (TBAF) as catalyst.

Heteroannulation of cyclic enaminone and dimedone

Enaminone (1) undergo cyclization with benzylidenes (2a-c) to give quinolines (3a-c) which are converted into quinolinopyrimidines (5a-c) by treatment with benzoylisothiocyanate. Cyclocondensation of 1 with benzolisothiocyanate furnishes quinazolone (7).