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Pyrazine

Pyrazine is a heterocyclic aromatic organic compound with the chemical formula C4H4N2. Pyrazine is a heterocyclic aromatic organic compound with the chemical formula C4H4N2. Pyrazine is a symmetrical molecule with point group D2h. Pyrazine is less basic than pyridine, pyridazine and pyrimidine. Derivatives such as phenazine are well known for their antitumor, antibiotic and diuretic activities. Tetramethylpyrazine (also known as ligustrazine) is reported to scavenge superoxide anion and decrease nitric oxide production in human polymorphonuclear leukocytes. Many methods exist for the organic synthesis of pyrazine and its derivatives. Some of these are among the oldest synthesis reactions still in use. In the Staedel–Rugheimer pyrazine synthesis (1876) 2-chloroacetophenone is reacted with ammonia to the amino ketone, then condensed and then oxidized to a pyrazine. A variation is the Gutknecht pyrazine synthesis (1879) also based on this selfcondensation, but differing in the way the alpha-ketoamine is synthesised. The Gastaldi synthesis (1921) is another variation:

[ "Photochemistry", "Derivative (finance)", "Organic chemistry", "Inorganic chemistry", "Stereochemistry", "Alkylpyrazine", "Benzoquinoxaline", "2-chloropyrazine", "Creutz–Taube complex", "Fructosazine" ]
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