95222-73-4

Upstream product

• 2960-55-6 (E)-3-(4-nitrophenyl)-1-phenylprop-2-en-1-one 
• 15723-90-7 4-nitrobenzamidine hydrochloride 
• 555-16-8 4-nitrobenzaldehdye 
• 20517-71-9 1-(2-oxo-2-phenylethyl)pyridin-1-ium chloride 
• 1222-98-6 4-nitrochalcone 
• 4187-87-5 1-Phenyl-2-propyn-1-ol 
• 636-98-6 p-nitrobenzene iodide 

Downstream Products

• 302928-07-0 C₂₆H₂₂N₄O₂ 

Relevant academic research and scientific papers

A novel three-component one-pot pyrimidine synthesis based upon a coupling-isomerization sequence

(Equation presented) 246-Tri(hetero)aryl-substituted pyrimidines can be readily synthesized in a three-component one-pot process based upon a coupling-isomerization sequence of an electron-poor (hetero)aryl halide and a terminal propargyl alcohol subseque

Synthesis of isomeric bis(aminophenyl)pyrimidines from nitrochalcones

A series of isomeric bis(nitrophenyl)pyrimidines containing a phenyl substituent in the heteroring were synthesized from nitrochalcones and benzamidines. The corresponding isomeric bis(aminophenyl)-pyrimidines were prepared by reductive acetylation follow

Facile synthesis of triarylpyrimidines with microwave-irradiated reactions of N-phenacylpyridinium chloride

In a system of ammonium acetate and acetic acid under microwave irradiation, N-phenacylpyridinium chloride 1 reacted with 2 mol of aromatic aldehydes 2a-h to give 2,4,6-triarylpyrimidine 3a-h, reacted with pyridinecarboxaldehyde 4a-c and acetophenone 5 to yield bipyridine derivatives 6a-c. The structure of the products was characterized with 1H NMR, 13C NMR, IR, and mass spectroscopy. Copyright Taylor & Francis Group, LLC.