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[摘要]:A synthesis of quinoline derivatives is described via reaction between etyl bromopyruvate (=ethyl 3-bromo-2-oxopropanoate), acetylenedicarboxylate, and isatin (=1H-indole-2,3-dione) in the presence of NaH as a base. Also, these reactions were performed without ethyl bromopyruvate. The reaction in the presence of ethyl bromopyruvate provides regioselectively a quinoline with the ethyl ester group in 4-position. In the absence of ethyl bromopyruvate, the reaction leads to functionalized quinolines with the same ester groups in 2-,3-, and 4-positions. |
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