1395085-48-9

Upstream product

• 104-87-0 4-methyl-benzaldehyde 
• 1395085-50-3 C₁₆H₁₈N₄O₂ 
• 141-97-9 ethyl acetoacetate 
• 299949-24-9 ethyl 6-methyl-2-oxo-4-p-tolyl-1,2,3,4-tetrahydropyrimidine-5-carboxylate 
• 1245716-49-7 ethyl 4-methyl-6-p-tolyl-2-(tosyloxy)pyrimidine-5-carboxylate 

Relevant academic research and scientific papers

Heterogenized hybrid catalyst of 1-sulfonic acid-3-methyl imidazolium ferric chloride over NaY zeolite for one-pot synthesis of 2-amino-4-arylpyrimidine derivatives: A viable approach

A new hybrid material of NaY zeolite supported 1-sulfonic acid-3-methyl imidazolium ferric chloride [Msim][FeCl4] has been developed by modifying the zeolite surface with six different w/w ratios through wet impregnation method. These composite

Direct amination of pyrimidin-2-yl tosylates with aqueous ammonia under metal-free and mild conditions

Abstract A metal-free synthesis of pyrimidine functionalized primary amines via direct amination of pyrimidin-2-yl tosylate with aqueous ammonia has been developed under mild conditions. The desired products pyrimidin-2-amines can be generated in excellen

One-pot synthesis of 4-aryl-2-cyanoimino-3,4-dihydro-1h-pyrimidines and their reactions

A series of 4-aryl-2-cyanoimino-3,4-dihydro-1H-pyrimidines was obtained as a result of a multicomponent Biginelli reaction using 1,3-dicarbonyl compounds, aromatic aldehydes, and cyanamide. Alkylation of the obtained compounds with benzyl chloride takes place at the two nitrogen atoms of the tetrahydropyrimidine ring, while oxidation with manganese dioxide leads to the corresponding 1-(pyrimidin-2-yl)carbamides or pyrimidine-2-amines, depending on the conditions.