67718-18-7

Upstream product

• 67718-11-0 6-phenyl-furo[2,3-b]pyrazine 4-oxide 
• 66479-90-1 2-Phenylfuro<2,3-b>pyrazine 
• 1011736-18-7 1-(4-methoxybenzyl)-5-chloro-3-(2-phenylethynyl)pyrazin-2(1H)-one 
• 1034194-61-0 2-chloro-7-iodo-6-phenyl-furo[2,3-b]pyrazine 
• 536-74-3 phenylacetylene 

Downstream Products

• 1011736-57-4 2-morpholin-4-yl-6-phenylfuro[2,3-b]pyrazine 
• 1011736-51-8 C₁₉H₁₄N₂O 
• 67718-27-8 2-chloro-6-phenyl-furo[2,3-b]pyrazine 4-oxide 
• 67718-25-6 2,7-dichloro-6-phenyl-furo[2,3-b]pyrazine 

Relevant academic research and scientific papers

Synthesis of functionalized furopyrazines as restricted dipeptidomimetics

Herein, an efficient synthetic approach to a furopyrazine scaffold with four points of diversity, starting from 2(1H)-pyrazinones, with dipeptomimetic properties, is presented. R-groups corresponding to amino acid side chains were introduced during the 2(

Ag+-mediated synthesis of substituted furo[2,3-b]pyrazines

A highly efficient method for the preparation of trisubstituted furo[2,3-b]pyrazines has been developed. Sonogashira coupling reaction with the readily available 1-(4-methoxybenzyl)-3,5-dichloropyrazin-2(1H)-ones was followed by silver-catalyzed heteroann