Issue 5, 1989

Quinoline alkaloids. Part 26. Pseudobases from the reaction of furoquinolinones with methyl iodide. A new route to 3-(3-methyl-2-oxobutyl)quinolin-2(1H)-ones

Abstract

Reaction of 2-isopropyl-9-methylfuro[2,3-b]quinolin-4(9H)-ones (5) with methyl iodide gave salts believed to be pseudobase hydriodides (7), which were converted with base into 4-methoxy-1-methyl-3-(3-methyl-2-oxobutyl)quinolin-2(1H)-ones (6); the analogous pseudobase derivative (12) from the furoquinoline alkaloid skimmianine gives the furoquinolin-4-one isoskimmianine on further reaction with methyl iodide. The mechanisms of these reactions and of the acid-catalysed rearrangement of furoquinolinones (5) are discussed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1989, 905-908

Quinoline alkaloids. Part 26. Pseudobases from the reaction of furoquinolinones with methyl iodide. A new route to 3-(3-methyl-2-oxobutyl)quinolin-2(1H)-ones

J. L. Gaston and M. F. Grundon, J. Chem. Soc., Perkin Trans. 1, 1989, 905 DOI: 10.1039/P19890000905

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