name: 2,3-Dichloro-6,7-dimethylquinoxaline, New research progress on 63810-80-0 in 2021. Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. 63810-80-0, Name is 2,3-Dichloro-6,7-dimethylquinoxaline, molecular formula is C10H8Cl2N2. In a Article，once mentioned of 63810-80-0
A trifluoroacetic acid promoted step-economical one-pot approach to the synthesis of furo-fused quinoxalines/pyrazines by the reaction of 2,3-dichloroquinoxalines/pyrazines with alkynes is described. The reaction involves a selective in-situ Sonogashira coupling step and a hydroxylation followed by a metal-free 5-endo-dig cyclization. Preliminary experiments show that trifluoroacetic acid acts as a source of oxygen for the oxyarylation step, and isotopic labeling studies support the proposal that the mechanistic pathway involves activation of the alkyne by the acidic medium. Various kinds of substituents are tolerated, which should prove valuable for structural and biological investigations.
We’ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 63810-80-0, and how the biochemistry of the body works.name: 2,3-Dichloro-6,7-dimethylquinoxaline
Reference：
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1831 | ChemSpider