Synthesis of New 2,3 Disubstituted Quinoxalines from 2'-Hydroxy-4'- Methyl-5'-Chloro-4-Substituted Chalcones
C. K. Patil and A. G. Doshi
Department of Chemistry, Vidya Bharati Mahavidyalaya, Camp, Amravati- 444 602 (India)
2'-Hydroxy-4'-methyl-5'-chloro-4-methoxy chalcone (Ia), 2'-hydroxy-4'-methyl-5'-chloro chalcone (Ib), 2'-hydroxy-4'-methyl-5'-chloro-4 chloro chalcone (Ic) and 2'-hydroxy-4'-methyl-5-chloro-4-dimethyl amino chalcone (Id) reacts with bromine n acetic acid gives chalcone dibromides (II a-d). The chalcone dibromide (II a-d) condenses with Benzene 1,2-diamine (BDA) in presence of few drops of concentrated H2SO4 in methanol medium affords 2-(2'-hydroxy-4'-methyl-5'-chloro) benzyl-3-(4-substituted phenyl)-quinoxaline (III a-d). The structure of these compounds were confirmed by analytical and spectral data."
KEYWORDS:Substituted quinoxalines; Chalcones
Download this article as:Copy the following to cite this article: Patil C. K, Doshi A. G. Synthesis of New 2,3 Disubstituted Quinoxalines from 2'-Hydroxy-4'- Methyl-5'-Chloro-4-Substituted Chalcones. Orient J Chem 2003;19(1). |
Copy the following to cite this URL: Patil C. K, Doshi A. G. Synthesis of New 2,3 Disubstituted Quinoxalines from 2'-Hydroxy-4'- Methyl-5'-Chloro-4-Substituted Chalcones. Orient J Chem 2003;19(1). Available from: http://www.orientjchem.org/?p=17626 |
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