845960-43-2

Upstream product

• 946494-15-1 4-(4-ethoxy-phenyl)-1-phenyl-3H-pyridine-2,6-dione 
• 542-05-2 acetonedicarboxylic acid 
• 67141-88-2 β-(4-ethoxyphenyl)glutaconic acid 
• 62-53-3 aniline 
• 103-73-1 Phenetole 

Downstream Products

• 845960-45-4 4'-(4-ethoxy-phenyl)-1'-phenyl-3,4,5,6-tetrahydro-2H,1'H-[1,2']bipyridinyl-6'-one 
• 845960-44-3 4-(4-ethoxyphenyl)-6-(morpholin-1-yl)-1-phenylpyridin-2(1H)-one 
• 1255142-34-7 4-(4-ethoxyphenyl)-6-(4-methylpiperazinyl)-1-phenyl-2(1H)-pyridinone 
• 1255142-35-8 4-(4-ethoxyphenyl)-6-(4-ethylpiperazinyl)-1-phenyl-2(1H)-pyridinone 
• 1255142-40-5 4-(4-ethoxyphenyl)-3-(2-methylphenylazo)-6-(4-methylpiperazinyl)-1-phenyl-2(1H)-pyridinone 
• 1255142-51-8 4-(4-ethoxyphenyl)-5-(2-methylphenylazo)-6-(4-methylpiperazinyl)-1-phenyl-2(1H)-pyridinone 
• 1255142-41-6 4-(4-ethoxyphenyl)-3-(3-methylphenylazo)-6-(4-methylpiperazinyl)-1-phenyl-2(1H)-pyridinone 
• 1255142-52-9 4-(4-ethoxyphenyl)-5-(3-methylphenylazo)-6-(4-methylpiperazinyl)-1-phenyl-2(1H)-pyridinone 
• 1255142-42-7 4-(4-ethoxyphenyl)-3-(4-methylphenylazo)-6-(4-methylpiperazinyl)-1-phenyl-2(1H)-pyridinone 
• 1255142-53-0 4-(4-ethoxyphenyl)-5-(4-methylphenylazo)-6-(4-methylpiperazinyl)-1-phenyl-2(1H)-pyridinone 
• 1255142-54-1 4-(4-ethoxyphenyl)-6-(4-methylpiperazinyl)-5-(2-nitrophenylazo)-1-phenyl-2(1H)-pyridinone 
• 1255142-43-8 4-(4-ethoxyphenyl)-6-(4-methylpiperazinyl)-3-(2-nitrophenylazo)-1-phenyl-2(1H)-pyridinone 
• 1255142-55-2 4-(4-ethoxyphenyl)-6-(4-methylpiperazinyl)-5-(3-nitrophenylazo)-1-phenyl-2(1H)-pyridinone 
• 1255142-44-9 4-(4-ethoxyphenyl)-6-(4-methylpiperazinyl)-3-(3-nitrophenylazo)-1-phenyl-2(1H)-pyridinone 

Relevant academic research and scientific papers

Synthesis of novel 6-(substituted amino)-4-(4-ethoxyphenyl)-1-phenyl-2(1H)- pyridinones via azo coupling

6-(Substituted amino)-4-(4-ethoxyphenyl)-1-phenyl-2(1H)-pyridinones were prepared from β-aryl glutaconic acid, which, on fusion with aniline, results in 4-(4-ethoxyphenyl)-1-phenylpyridine-2,6(1H,5H)-dione. This, on further treatment with phosphorus oxych

Synthesis of novel 6-substituted-aminopyridin-2(H)-ones

6-Substituted-amino-4-(4-ethoxyphenyl)-1-phenylpyridin-2(H)-ones 4,5 have been prepared from citric acid. It is treated with conc. H2SO 4 and then with phenetole to give β-arylglutaconic acid which on fusion with arylamine results in 4-(4-ethoxyphenyl)-1-aryl-5-H-pyridine-2,6- diones 2. When 2 (Ar=phenyl) is reacted with phosphorous oxychloride it gives 6-chloro-4-(4-ethoxyphenyl)-1-phenylpyridin-2(H)-one 3, which on treatment with secondary amines yields 6-substituted-amino-4-(4-ethoxyphenyl)-1-phenylpyridin- 2(H)-ones 4 and 5. When 4 and 5 are subjected to azo coupling with different aryldiazonium chlorides furnish two isomers 6-substituted-amino-4-(4- ethoxyphenyl)-1-phenyl-3-(arylazo)pyridin-2(H)-ones 6a-j and 7a-j and 6-substituted-amino-4-(4-ethoxyphenyl)-1-phenyl-5-(arylazo)pyridin-2(H)-ones 6k-t and 7k-t. However, the Mannich reaction on 4 and 5 gives only single product identified as 6-substituted-amino-4-(4-ethoxyphenyl)-1-phenyl-3- (aminomethyl)pyridin-2(H)-ones 8a-b and 9a-b. All the compounds have been characterized by elemental analysis, IR and NMR spectral data.