420106-07-6Relevant academic research and scientific papers
Solvent free microwave accelerated synthesis of heterocyclic thiazolidin-4-ones as antimicrobial and antifungal agents
Sekhar, Kondapalli Venkata Gowri Chandra,Rao, Vajja Sambasiva,Reddy, Aravalli Satish,Sunandini, Ravada,Kumar Satuluri
, p. 1219 - 1222 (2010)
A simple and efficient method has been developed for conversion of arenecarbaldehyde-3-methylquinoxalin-2-ylhydrazones to 3-(2-methylquinoxalin-3- yl)-2-(substitutedphenyl)thiazolidin-4-ones in good yields using microwave irradiation technique on silica a
Synthesis of some new 4-styryltetrazolo[1,5-a]quinoxaline and 1-substituted-4-styryl[1,2,4]triazolo[4,3-a]quinoxaline derivatives as potent anticonvulsants
Wagle, Shivananda,Adhikari, Airody Vasudeva,Kumari, Nalilu Suchetha
experimental part, p. 1135 - 1143 (2009/09/27)
4-Methyltetrazolo[1,5-a]quinoxaline (3) was prepared by the azide cyclocondensation of 2-chloro-3-methylquinoxaline (2). The reaction of 3 with aromatic aldehydes furnished 4-styryltetrazolo[1,5-a]quinoxalines (4a-f). Compound 2, on treatment with hydrazi
Hypervalent iodine-mediated synthesis of 1-aryl-4-methyl-1,2,4-triazolo[4, 3-a]quinoxalines by oxidative cyclization of arene carbaldehyde-3- methylquinoxalin-2-yl hydrazones
Aggarwal, Ranjana,Sumran, Garima
, p. 1873 - 1878 (2007/10/03)
Arene carbaldehyde-3-methylquinoxalin-2-yl hydrazones (2) obtained by the condensation of 2-hydrazino-3-methylquinoxaline (1) with various aromatic aldehydes, on treatment with iodobenzene diacetate (IBD) in dichloromethane, undergo oxidative cyclization
Synthesis and antimicrobial activity of 2-substituted benzyl hydrazino-3-methyl quinoxalines
Vyas,Chauhan,Parikh
, p. 972 - 974 (2007/10/03)
Reduction of 3-methyl-2-(arylidcne hydrazino)quinoxalines 5a-1 with NaBH4 in controlled experimental conditions to give the 2-substituted benzyl hydrazine-3-methyl quinoxalines 6a-l have been described. The structure of compounds 6a-l have been confirmed from elemental analysis, IR, 1H NMR and mass spectral data. All the compounds have been screened for their antimicrobial activity against several microbes.
