425615-33-4

Upstream product

• 107-20-0 2-chloroethanal 
• 3435-28-7 6-methylpyrimidin-4-ylamine 

Downstream Products

• 1179358-02-1 7-methyl-3-[(4-phenylpiperazin-1-yl)methyl]imidazo[1,2-c]pyrimidine 
• 1179358-03-2 3-{[4-(4-chlorophenyl)piperazin-1-yl]methyl}-7-methylimidazo[1,2-c]pyrimidine 
• 1179358-06-5 3-{[4-(4-methoxyphenyl)piperazin-1-yl]methyl}-7-methylimidazo[1,2-c]pyrimidine 
• 1179358-05-4 3-{[4-(2-methoxyphenyl)piperazin-1-yl]methyl}-7-methylimidazo[1,2-c]pyrimidine 
• 1179358-04-3 3-{[4-(3,4-dichlorophenyl)piperazin-1-yl]methyl}-7-methylimidazo[1,2-c]pyrimidine 

Relevant academic research and scientific papers

Design, synthesis and dopamine D4 receptor binding activities of new N-heteroaromatic 5/6-ring Mannich bases

A series of phenylpiperazine-methyl-substituted 1H-pyrrolo[2,3-c]pyridine, imidazo[1,2-c]-, pyrrolo[2,3-d]- and pyrrolo[3,2-d]pyrimidines were prepared as selective dopamine D4-ligands. The pyrrolo[2,3-d]pyrimidine derivatives 12d (Ki = 1,9 nM)