153254-91-2

Upstream product

• 82736-91-2 4-(dimethoxymethyl)pyridine 
• 352-11-4 1-chloromethyl-4-fluorobenzene 

Downstream Products

• 1075195-80-0 4-[3-(4-fluorophenyl)-1H-pyrrolo[3,2-b]pyridin-2-yl]pyridine-2-carboxylic acid amide 
• 1075195-62-8 2-(2-chloropyridin-4-yl)-3-(4-fluorophenyl)-1H-pyrrolo[3,2-b]pyridine 
• 1075194-91-0 {4-[1-(2-fluoroethyl)-3-(4-fluorophenyl)-1H-pyrrolo[3,2-b]pyridin-2-yl]pyridin-2-yl}-(3-fluorophenyl)amine 
• 1075194-88-5 2-(2-chloropyridin-4-yl)-1-(2-fluoroethyl)-3-(4-fluorophenyl)-1H-pyrrolo[3,2-b]pyridine 
• 1075195-69-5 N-{4-[3-(4-fluorophenyl)-6-methyl-1H-pyrrolo[3,2-b]pyridin-2-yl]pyridin-2-yl}malonamic acid methyl ester 
• 1075195-51-5 4-[3-(4-fluorophenyl)-6-methyl-1H-pyrrolo[3,2-b]pyridin-2-yl]pyridin-2-ylamine 
• 1075195-15-1 benzyl-{4-[3-(4-fluorophenyl)-6-methyl-1H-pyrrolo[3,2-b]pyridin-2-yl]pyridin-2-yl}-amine 
• 1075197-89-5 2-(2-chloropyridin-4-yl)-6-methyl-3-(4-fluorophenyl)-1H-pyrrolo[3,2-b]pyridine 
• 1075197-88-4 3-(4-fluorophenyl)-6-methyl-2-(1-oxy-pyridin-4-yl)-1H-pyrrolo[3,2-b]pyridine 
• 1075194-86-3 1-allyl-2-(2-chloropyridin-4-yl)-3-(4-fluorophenyl)-1H-pyrrolo[3,2-b]pyridine 
• 1075197-86-2 (2-chloropyridin-3-yl)-[2-(4-fluorophenyl)-1-(1-oxy-pyridin-4-yl)ethylidene]amine 
• 610270-92-3 2-(2-chloropyridin-4-yl)-3-(4-fluorophenyl)-1H-pyrrolo[3,2-b]pyridine 
• 610270-86-5 4-[2-(4-fluorophenyl)-1,1-dimethoxyethyl]pyridin-1-ol 
• 115858-98-5 1-(4-fluorophenyl)-2-(pyridin-4-yl)-2-ethanone 

Relevant academic research and scientific papers

4-AZA INDOLE DERIVATIVES AND THEIR USE AS FUNGICIDES

The present invention relates to a method of preventing and/or controlling fungal infection in plants and/or plant propagation material comprising applying to the plant or plant propagation material a fungicidally effective amount of a compound of formula

Design and Synthesis of 4-Azaindoles as Inhibitors of p38 MAP Kinase

Inhibition of the biosynthesis of proinflammatory cytokines such as tumor necrosis factor and interleukin-1 via p38 has been an approach toward the development of a disease modifying agent for the treatment of chronic inflammation and autoimmune diseases.

The anion of 4-dimethoxymethylpyridine. A convenient synthesis of some 4-pyridyl ketones

n-Butyllithium at -78°C abstracts the methine proton from 4-dimethoxymethylpyridine. The anion reacts efficiently with electrophiles. Simple ketal products can be readily hydrolysed to 4-pyridyl ketones.