117358-61-9

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 134-32-7 1-amino-naphthalene 
• 126-81-8 dimedone 
• 135569-53-8 N-(4-chlorobenzylidene)naphthalene-1-amine 
• 90-15-3 α-naphthol 
• 555-16-8 4-nitrobenzaldehdye 

Downstream Products

• 117358-70-0 7-(p-chlorophenyl)-10,10-dimethyl-8,9,10,11-tetrahydrobenz[c]acridin-8-one 
• 932748-12-4 C₂₅H₂₂ClNS 

Relevant academic research and scientific papers

Synthesis of benzo[h]quinolone and benzo[c]acridinone derivatives by Fe3O4@PS-Arginine[HSO4] as an efficient magnetic nanocatalyst

Fe3O4 magnetic nanoparticles were synthesized and functionalized by propylsilan and after that arginine. The synthesized Fe3O4@PS-Arginine magnetic nanoparticles were modified to obtain Fe3O4/su

γ-Fe2O3@Si-(CH2)3@mel@(CH2)4SO3H as a magnetically bifunctional and retrievable nanocatalyst for green synthesis of benzo[c]acridine-8(9H)-ones and 2-amino-4H-chromenes

The present work describes the synthesis and characterization of melamine functionalized with sulfonic acid supported on the magnetic nanoparticle, γ-Fe2O3@Si-(CH2)3@melamine@butyl sulfonic acid nanoparticle as

Iron(III) phosphate-catalyzed synthesis of 7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-ones

One-pot FePO4-catalyzed three-component reaction of 1-naphthylamine, aldehydes, and cyclic 1,3-dicarbonyl compounds affords 7,10,11,12-tetrahydrobenzo[c]acridines in high yields.

TiO2 nanoparticles as an efficient catalyst for the one-pot preparation of Tetrahydrobenzo[c]acridines in aqueous media

A series of tetrahydrobenzo[c]acridinone derivatives have been prepared by a one-pot fourcomponent reaction of 1-naphthol, aromatic aldehydes, dimedone, and ammonium acetate in aqueous media using a catalytic amount of titanium dioxide nanoparticles (TiO2 NPs). The advantages of this novel protocol include the excellent yields, operational simplicity, short reaction time, easy work-up, reusability of the catalyst and an environmentally friendly procedure.

L-Proline-catalysed one-pot synthesis of tetrahydrobenzo[c]acridin-8(7H)- ones at room temperature

Only 10 mol% of l-Proline in ethanol proved to be a very efficient catalyst for the one-pot synthesis of a wide variety of highly substituted tetrahydrobenzo[c]acridin-8(7H)-ones at room temperature. The key advantages of this process are high yields, cos

NH2SO3H and H6P2W 18O6218H2O-catalyzed, three-component, one-pot synthesis of benzo[ c[acridine derivatives

We report here two simple methods for the synthesis of benzo[c]acridine derivatives from three-component, one-pot condensation of 1-naphthylamine, dimedone, and a variety of substituted aldehydes in the presence of a catalytic amount of NH2SOs

Ultrasound-promoted one-pot synthesis of 7-aryl-7,10,11,12- tetrahydrobenzo[c]acridin-8(9H)-one derivatives

A series of 7-aryl-7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-one derivatives were synthesized via the three-component coupling from aromatic aldehydes, 1-naphthylamine, and 5,5-dimethylcyclohexane-1,3-dione catalyzed by stannous chloride dihydrate (SnCl

An efficient ultrasound-promoted method for the one-pot synthesis of 7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-one derivatives

A new, efficient and general method for preparation of 7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-one derivatives using ultrasound irradiation is reported. Under ultrasound, the reaction time is short, the yields are high and the reaction conditions are m

Microwave-induced synthesis and anti-microbial activities of 7,10,11,12-tetrahydrobenzo[c]acridin-8(9H)-one derivatives

Some new substituted tetrahydroacridin-8-ones and diverse derivatives were synthesized by uncatalysed multi-component reaction of dimedone or cyclohexan-1,3-dione, α-naphthylamine and various (o,p,m)-substituted benzaldehydes. The in vitro anti-microbial

An efficient one-pot synthesis of polyhydrobenzoacridine-1-one derivatives under microwave irradiation without catalyst

A series of 3,3-dimethyl-9-substituted-1,2,3,4,9,10-hexahydrobenzo[c] acridine-1-ones and 3,3-dimethyl-9-substituted-1,2,3,4,9,10-hexahydrobenzo[a] acridine-1-ones were synthesized by the reaction of an aldehyde, α-naphthylamine or β-naphthylamine and dim