102252-89-1

Upstream product

• 4023-80-7 1-(4-methoxyphenyl)butan-1,3-dione 
• 631-61-8 ammonium acetate 

Downstream Products

• 23263-96-9 3-(4-methoxyphenyl)-5-methyl-1H-pyrazole 
• 61428-21-5 3-(4-methoxy-phenyl)-5-methylisoxazole 
• 4211-85-2 5-(4-methoxyphenyl)-3-methylisoxazole 
• 90276-22-5 5-(4-methoxy-phenyl)-3-methyl-1-phenyl-1H-pyrazole 
• 21129-51-1 3-(4-methoxyphenyl)-5-methyl-1H-pyrrole-2-carboxylic acid ethyl ester 
• 102252-90-4 5-(4-Methoxybenzoyl)-6-methyl-2(1H)pyridinone 
• 254734-22-0 methyl 4,5-dihydro-5-hydroxy-5-(4-methoxyphenyl)-3-methylpyrazole-1-carboxylate 
• 254734-48-0 5-(4-methoxyphenyl)-3-methylpyrazole-1-carboxamide 
• 102252-75-5 5-(4-methoxyphenyl)-1,6-naphthyridin-2(1H)-one 
• 102252-99-3 6-((E)-2-Dimethylamino-vinyl)-5-(4-methoxy-benzoyl)-1H-pyridin-2-one 
• 948350-57-0 6-ethyl-3-(4-methoxy-benzoyl)-2-methyl-1H-pyridin-4-one 

Relevant academic research and scientific papers

Design, Synthesis, and Crystallization-Induced Emission of Boron Difluorides β-Ketoiminates

A series of new nitrogen-containing analogues of boron difluoride benzoylacetonates with hydrogen and methyl substituents at the nitrogen atom have been synthesized. A comparative study of boron difluoride β-ketoiminates and their oxygen-containing analogues by means of luminescence and IR spectroscopic methods as well as quantum chemistry simulations was also performed.

Metal-Free Cascade Annulation Approach for Modular Assembly of Alkynyl/Benzoyl Functionalized Quinolines

A concise and efficient synthetic method for alkynyl quinolines through TfOH-promoted cascade 1,4-conjugate addition/intramolecular annulation/aromatization process is established. By virtue of reactive aza-o-AQM (in situ generated from modular propargylamine), this reaction proceeds smoothly to afford a variety of alkynyl quinolines in good to excellent yields. This transition-metal-free process features halogen groups tolerance, such as the ?Cl, ?Br, and ?I groups; thus, this protocol circumvents the inherent shortcomings of the existing Sonogashira coupling of halogenated quinolines.

Copper-Catalyzed Reductive Ring-Cleavage of Isoxazoles: Synthesis of Fluoroalkylated Enaminones and Application for the Preparation of Celecoxib, Deracoxib, and Mavacoxib

We have identified a new reactivity of copper/diamine catalysis for the reductive ring-cleavage of isoxazoles to yield fluoroalkylated enaminones. This protocol has the advantage of using commercially available reagents, ease of setting up, broad tolerance of functionality, and is regiospecific and free of defluorination and reduction of reducible functional groups. The utility was demonstrated by a one-step, regioselective synthesis of fluoroalkylated pyrazole-based drugs such as celecoxib, deracoxib, and mavacoxib.

Solid-state synthesis of β-enamino ketones from solid 1,3-dicarbonyl compounds and ammonium salts or amines

A facile amination of solid 1,3-dicarbonyl compounds with ammonium salts or amines in solid state has been achieved by mechanochemical grinding in the presence of KHSO4 and SiO2. Most of the reactions proceed smoothly at room temperature under solid-state conditions and give their corresponding β-imino derivatives in high yields. The method has the advantage of simple manipulation and mild conditions. Georg Thieme Verlag Stuttgart.

NOVEL DUAL ACTION RECEPTORS ANTAGONISTS (DARA) AT THE AT1 AND ETA RECEPTORS

The present invention relates to new compounds of the formula [Chemical formula should be inserted here. Please see paper copy] wherein R1, R2, R3, and R31 are as specified herein. The invention also relates to a method for preparation thereof, as well as combinations of the new compounds with previously known agents. The invention also relates to the use of the above-mentioned compounds and combinations for the preparation of a medicament for treating hypertension of different kinds, alleviating organ damage of different kinds, treating or preventing diabetic nephropathy, treating endothelin and angiotensin mediated disorders, and treating prostate cancer.

The use of K-10/ultrasound in the selective synthesis of unsymmetrical β-enamino ketones

p-Phenyl substituted β-enamino ketones 2a-p and cyclic β-enamino ketones 4, 6a-f have been prepared by a selective method by dispersing 1,3- diketones and amines on montmorillonite K-10 under sonication.

A Facile and Novel Synthesis of 1,6-Naphthyridin-2(1H)-ones

A new and convenient procedure for the synthesis of 1,6-naphthyridin-2(1H)-ones and their derivatives is described.In the first scheme 5-acetyl-6--1,2-dihydro-2-oxo-3-pyridinecarbonitrile (4) obtained by the reaction of N,N-dimet