23813-24-3Relevant articles and documents
Studies on pyrazine derivatives. XLIX. Synthesis and antibacterial activity of 6-methoxypyrazine-2-carboxylic acid hydrazide derivatives
Gobis, Katarzyna,Foks, Henryk,Zuralska, Aleksandra,Kedzia, Anna
, p. 2615 - 2626 (2006)
The new 6-methoxy-pyrazine derivatives have been synthesized. 6-Methoxy-pyrazine-2-carboxylic acid hydrazide was used as an initial material to obtain mono- and dithioester of hydrazinecarbodithioic acid (2 and 3). Compound (2) in reaction with ethanolamine gave triazole derivative (8) with β-hydoxyethyl substituent in 4-position and hydroxyl group in 6-position of pyrazine ring. Dithioester (3) in a reaction with morpholine cyclized to 1,3,4-oxadiazole (11). The same substrate with alkyldiamines gave the few following derivatives: 1,3-diazacycloalkane derivatives (9 and 10), S-methyl-1,3,4-oxadiazole derivative (12) and 1,2,4-triazoletetrahydropyrimidine (13). The compounds obtained were tested in vitro for their activity towards pathogenic strains of anaerobic and aerobic bacteria. Derivative (9) was the most active against both types of tested strains.{A figure is presented}. 6-Methoxypyrazine-2-carboxylic Acid Hydrazide Hydrazinecarbodithioic Acid Ester Acid Ester 1,3,4-Oxadiazolethiol 1,2,4-Triazolethione.