A convenient synthesis of quinolines by reactions of o-isocyano-β-methoxystyrenes with nucleophiles |
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Authors: | Kazuhiro Kobayashi Keiichi Yoneda Kazuna Miyamoto Osamu Morikawa Hisatoshi Konishi |
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Affiliation: | Department of Materials Science, Faculty of Engineering, Tottori University, Koyama-minami, Tottori 680-8552, Japan |
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Abstract: | 2,4-Disubstituted quinolines have been synthesized by reactions of o-isocyano-β-methoxystyrenes, which can be easily prepared from commercially available o-aminophenyl ketones in three steps, with alkyl(or aryl)lithiums in generally good yields. Subsequently, o-isocyano-β-methoxystyrenes have also proved to react efficiently with lithium dialkylamides to afford the corresponding 4-substituted N,N-dialkylquinolin-2-amines in satisfactory yields. |
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Keywords: | Isocyanide Lithium amide Organolithium Quinoline Styrene |
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