Synthesis and biological activity of pyrimido [1, 2-a] quinoline moiety and its 2-substituted derivatives
Autor: | A G Jadhav, N K Halikar |
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Rok vydání: | 2013 |
Předmět: | |
Zdroj: | Journal of Physics: Conference Series. 423:012007 |
ISSN: | 1742-6596 1742-6588 |
DOI: | 10.1088/1742-6596/423/1/012007 |
Popis: | 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. |
Databáze: | OpenAIRE |
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