82376-73-6

Upstream product

• 82363-24-4 (3,4-dimethoxybenzylidene)-(4-methoxyphenyl)amine 
• 104-94-9 4-methoxy-aniline 
• 130632-09-6 (E)-1-(3,4-dimethoxyphenyl)-N-(4-methoxyphenyl)methanimine 
• 93-03-8 (3,4-dimethoxyphenyl)methanol 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 140934-50-5 2-{2-[(3,4-Dimethoxy-benzyl)-(4-methoxy-phenyl)-amino]-acetylamino}-benzoic acid 
• 929564-36-3 C₂₄H₂₇NO₅ 
• 929564-42-1 1'-(3,4-dimethoxybenzyl)-6'-methoxy-4,4-dimethyl-1',4'-dihydro-2H,2'H,6H-spiro[cyclohexane-1,3'-quinoline]-2,6-dione 
• 1295581-90-6 N-benzyl-N-(3,4-dimethoxybenzyl)-4-methoxyaniline 
• 1295581-91-7 N-(3,4-dimethoxybenzyl)-4-methoxy-N-phenethylaniline 

Relevant academic research and scientific papers

Metal-Free Ring Opening Cyclization of Cyclopropane Carbaldehydes and N-Benzyl Anilines: An Eco-Friendly Access to Functionalized Benzo[b]azepine Derivatives

Herein, we report a p-toluenesulfonic acid (PTSA) initiated mild and user-friendly ring opening/domino ring opening cyclization reaction (depends on substituent present in N-benzyl aniline) of cyclopropane carbaldehyde and N-benzyl aniline towards the formation of substituted 4-amino butanal/2,3-dihydro-1H-benzo[b]azepine. The product dihydro-1H-benzo[b]azepine was also converted into the corresponding tetrahydro-1H-benzo[b]azepine. (Figure presented.).

Method for preparing secondary amine compound through imine hydrogenation reduction

The invention belongs to the technical field of medical and natural compound chemical intermediates and related chemistry, and provides a method for preparing secondary amine compounds through imine hydrogenation reduction. According to the method, the im

Novel N-Alkylbenzimidazole-Ruthenium (II) complexes: Synthesis and catalytic activity of N-alkylating reaction under solvent-free medium

In this article, direct N-alkylation reactions of amines with alcohols derivatives have been investigated. For this purpose, a new series ruthenium (II) complexes bearing N-coordinated benzimidazole complexes with have been synthesized and fully characterized by elemental analysis, FT-IR, 1H NMR and, 13C NMR spectroscopies. Additionally, the structures of the complexes 2b and 2c have been confirmed by X-ray crystallography. Although the N-alkylating reaction is usually performed in toluene, the catalytic study of complexes 2a-d has carried out no additional solvent and alcohol acted both as solvent and reactant of alkylating by using a little excess of alcohols. Surprisingly, conversion and selectivity of amine product for alkylation reaction have been seen high in medium solvent-free relative to in toluene.

Application of a catalyst-free Domino Mannich/Friedel-Crafts alkylation reaction for the synthesis of novel tetrahydroquinolines of potential antitumor activity

A useful and efficient method to construct diversely substituted 1,2,3,4-tetrahydroquinolines in good to excellent yields has been developed through a catalyst-free Domino Mannich and intramolecular Friedel-Crafts alkylation reactions of N-arylamines with

Parallel solution synthesis of lavendustin analogs as antileishmanial agents

A concise parallel synthesis of 12 lavendustin analogs is described. Starting with differently substituted benzaldehydes, a two-step sequence involving reductive amination and N-benzylation accelerated by microwaves was performed to provide the compounds