117358-64-2

Upstream product

• 134-32-7 1-amino-naphthalene 
• 123-11-5 4-methoxy-benzaldehyde 
• 126-81-8 dimedone 
• 33417-05-9 1-(4-methoxyphenyl)-N-(naphthalen-1-yl)methanimine 
• 90-15-3 α-naphthol 

Downstream Products

• 932748-14-6 C₂₆H₂₅NOS 
• 117358-73-3 7-(p-methoxiphenyl)-10,10-dimethyl-8,9,10,11-tetrahydrobenz[c]acridin-8-one 

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

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

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

A simple and clean procedure for the synthesis of polyhydroacridine and quinoline derivatives: Reaction of Schiff base with 1,3-dicarbonyl compounds in aqueous medium

A clean and simple synthesis of benzo[c]acridine, benzo[a]acridine, pyrido[2,3-c]acridine and benzo[f]quinoline derivatives was accomplished in good to excellent yields via the reaction of Schiff base with 1,3-dicarbonyl compounds in aqueous medium catalyzed by TEBA. The structures were characterized by 1H NMR, IR and elemental analysis, and confirmed by X-ray diffraction study.

Synthesis and Spectra of 7-(o- and p-R-Phenyl)-10,10-dimethyl-8,9,10,11-tetrahydrobenzacridin-8-ones. Structure Correction of 1,2,3,4-Tetrahydro-2,2-dimethyl-5-aryl-6-aza-7,8-benzophenanthren-4-ones

It has been reported that dimedone added to α-arylidennaphthylamines in ethanol with formation of 1,4-addition products derivatives of 5-aryl-5,6,7,8,9,10-hexahydrobenzophenanthridin-7-ones, III, which are easily oxidized by chromic anhydride to the co