33266-39-6

Upstream product

• 598-50-5 N-Methylurea 
• 70498-78-1 2-(3,4-dimethoxy-phenyl)-malonaldehyde 

Downstream Products

• 76972-15-1 2-amino-5-(3,4-dimethoxyphenyl)pyrimidine 
• 76972-18-4 5-(3,4-dimethoxyphenyl)-2-hydrazinopyrimidine 
• 76972-16-2 2-cyclopropylamino-5-(3,4-dimethoxyphenyl)pyrimidine 
• 76972-19-5 6-(3,4-dimethoxyphenyl)-s-triazolo<4,3-a>pyrimidine 
• 76972-17-3 2-(3-dimethylaminopropyl)amino-5-(3,4-dimethoxyphenyl)pyrimidine 
• 76972-12-8 5-(3,4-dimethoxyphenyl)-2-(1-piperazinyl)pyrimidine 
• 76972-23-1 (5-(3,4-dimethoxyphenyl)-pyrimidin-2-yloxy)acetic acid 
• 76972-21-9 2-chloro-5-(3,4-dimethoxyphenyl)-1,6-dihydro-6-phenylpyrimidine 
• 76972-20-8 2-(4,5-dihydro-1H-imidazo-2-ylthio)-5-(3,4-dimethoxyphenyl)pyrimidine 
• 76972-22-0 [5-(3,4-Dimethoxy-phenyl)-pyrimidin-2-yloxy]-acetic acid ethyl ester 
• 76972-14-0 5-(3,4-dimethoxyphenyl)-2-<4-(3,4-dimethoxyphenyl)methyl>piperazinylpyrimidine 
• 374633-46-2 1-(3,4-Methylenedioxyphenyl)-2-[5-(3,4-dimethoxyphenyl)pyrimidin-2-yl]-2,3,4,9-tetrahydro-1H-β-carboline 
• 76972-10-6 2-chloro-5-(3,4-dimethoxyphenyl)pyrimidine 

Relevant academic research and scientific papers

Synthesis and biological activities of novel β-carbolines as PDE5 inhibitors

A series of N2-furoyl and N2pyrimidinyl β-carbolines was discovered to possess potent inhibitory activity against PDE5. During the synthesis we developed a tandem resin quenching protocol, which allowed us to synthesize large number