10480-25-8

Upstream product

• 99-61-6 3-nitro-benzaldehyde 
• 106-47-8 4-chloro-aniline 
• 619-25-0 3-Nitrobenzyl alcohol 

Downstream Products

• 110200-66-3 2,3-Bis-[(1H-indol-3-yl)-(3-nitro-phenyl)-methyl]-1H-indole 
• 99-61-6 3-nitro-benzaldehyde 
• 1602-00-2 bis-(4-chloro-phenyl)-diazene 
• 10480-24-7 1-(4-chloro-phenyl)-5-(3-nitro-phenyl)-4,5-dihydro-1H-[1,2,3]triazole 
• 1343454-77-2 6-chloro-3,3-dimethyl-2-(3-nitro-phenyl)-1,2,3,4-tetrahydro-quinolin-4-ol 
• 1343454-83-0 2-[3-(6-chloro-3,3-dimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenylamino]-2-methyl-propionic acid methyl ester 
• 1343454-79-4 3-(6-chloro-3,3-dimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenylamine 
• 1343454-78-3 6-chloro-3,3-dimethyl-2-(3-nitro-phenyl)-1,2,3,4-tetrahydro-quinoline 
• 1343454-74-9 2-[3-(6-chloro-3,3-dimethyl-1,2,3,4-tetrahydro-quinolin-2-yl)-phenylamino]-2-methyl-propionic acid 
• 108417-40-9 1-{3-[(4-Chloro-phenylamino)-methyl]-phenyl}-6,6-dimethyl-1,6-dihydro-[1,3,5]triazine-2,4-diamine; hydrochloride 
• 769881-83-6 N-(m-aminobenzyl)-p-chloroaniline 

Relevant academic research and scientific papers

Imino Diels-Alder reactions: Efficient synthesis of 2-aryl-4-(2'- oxopyrrolidinyl-1')-1,2,3,4-tetrahydroquinolines catalyzed by Antimony(III) Sulfate

Antimony(III) sulfate is found to catalyze the imino Diels-Alder reaction of Schiff's bases with N-vinylpyrrolidin-2-one to afford 2-aryl-4-(2'- oxopyrrolidinyl-1')-1,2,3,4-tetrahydroquinolines. One-pot synthesis of 1,2,3,4-tetrahydroquinolines from 3-nit

Ru Nanoparticles-Loaded Covalent Organic Framework for Solvent-Free One-Pot Tandem Reactions in Air

Condensation of benzene-1,3,5-tricarbohydrazide with benzene-1,4-dicarboxaldehyde generated a new covalent organic framework, COF-ASB (1), in which the organic units are held together via hydrazone linkage to form porous frameworks. COF-ASB (1) is highly crystalline and displays good chemical and thermal stability and is permanently porous. In addition, 1 can be an ideal support to load Ru nanoparticles (Ru NPs) to generate Ru@COF-ASB (2). The obtained composite material is able to highly promote one-pot tandem synthesis of imine products from benzyl alcohols and corresponding amines under solvent-free conditions in air.

Synthesis of some novel 2-substituted benzothiazole derivatives containing benzylamine moiety as monoamine oxidase inhibitory agents

In the present work, 12 new 2-(5-substituted-benzothiazol-2-ylsulfanyl)-N-(substitutedbenzyl)-N-(4-substitutedphenyl) acetamide derivatives (4a–l) was designed and synthesized. The structures of the synthesized compounds were clarified using Fourier trans

Mechanochemical milling promoted solvent-free imino Diels-Alder reaction catalyzed by FeCl3: Diastereoselective synthesis of cis-2,4-diphenyl-1,2,3,4-tetrahydroquinolines

Under mechanochemical ball-milling at room temperature, FeCl3 promoted Diels-Alder cycloaddition of styrene with in situ generated N-aryl aldimines in the absence of any solvent afforded exclusively cis-2,4-diphenyltetrahydroquinolines in good to excellent yields within 90 minutes. The isolation work up just involves washing the resulting reaction mixture with water and recrystallization from EtOH-H2O. The advantages of high diastereoselectivity, short reaction time, free use of organic solvent, low cost, employment of cheap, easily available and nontoxic catalyst, and simple work-up procedure make this protocol a very efficient and green alternative to traditional methods for constructing these kinds of heterocyclic skeletons.

NOVEL 3,3-DIMETHYL TETRAHYDROQUINOLINE DERIVATIVES

A compound of formula (I) as well as pharmaceutically acceptable salt thereof, wherein R1 to R5 have the significance given in claim 1, can be used as a medicament.

NOVEL 3,3-DIMETHYL TETRAHYDROQUINOLINE DERIVATIVES

A compound of formula (I) as well as pharmaceutically acceptable salt thereof, wherein R1 to R5 have the significance given in claim 1, can be used as a medicament.

AMINOHALOBORANE IN ORGANIC SYNTHESIS. VIII. A ONE-STEP SYNTHESIS OF 2-AMINOBENZHYDROLS FROM ANILINES

2-Aminobenzhydrols were obtained regiospecifically from anilines and benzaldehydes with the aid of phenyldichloroborane and triethylamine via N-anilinophenylchloroborane.