Abstract
2-Amino-3-cyano quinoline (1) and bis (methylthio) methylene malononitrile (2) were refluxed in N,N-dimethyl formamide (DMF) in presence of catalytic amount of anhydrous potassium carbonate to afforded 3, 11-dicyano-4-imino-2- methylthio -4H-pyrimido [1, 2-a] quinoline (3). The latter were further reacted with different substituted aniline, phenol, hetryl amine and compound containing active methyl group. Afforded to 3, 11-dicyano-4-imino -4H-pyrimido [1, 2-a] quinoline and their 2-substuited derivatives (4a-7c). All these newly synthesized compounds were characterized by elemental analysis and spectral data, and screened for their antimicrobial activities. © IOP Publishing Ltd 2013.
Cite
CITATION STYLE
Jadhav, A. G., & Halikar, N. K. (2013). Synthesis and biological activity of pyrimido [1, 2-a] quinoline moiety and its 2-substituted derivatives. In Journal of Physics: Conference Series (Vol. 423). Institute of Physics Publishing. https://doi.org/10.1088/1742-6596/423/1/012007
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.