Issue 0, 1974

Pyrrolo[1,2-a]quinolines. A re-investigation

Abstract

The reaction between ethyl 2-quinolylacetate and phenacyl bromide has been re-investigated and is now shown to proceed via C-alkylation to yield 2-(1-benzoyl-2-ethoxycarbonylethyl)quinoline. Treatment of this compound with acetic anhydride yielded 2-benzoyl-3-ethoxycarbonyl-1-methylpyrrolo[1,2-a]quinoline and 3-ethoxycarbonyl-1-phenylpyrrolo[1,2-a]quinoline.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1974, 250-252

Pyrrolo[1,2-a]quinolines. A re-investigation

W. J. Irwin and D. G. Wibberley, J. Chem. Soc., Perkin Trans. 1, 1974, 250 DOI: 10.1039/P19740000250

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