8H-Isoquino[2,1-b] [2,7]naphthyridin-8-ones: Synthesis of the Alangium alkaloids, alangimaridine and alangimarine

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Abstract

It is shown that 3,4-dihydroisoquinolines are activated toward nucleophilic attack by reaction with trimethylsilyl trifluoromethanesulfonate. The complex so formed reacts readily with the lithio derivative of 3-cyano-4-methyl-5-vinylpyridine, affording in a single step a tetracyclic amidine from which a lacta'm is obtained by hydrolysis. These reactions have been applied to the synthesis of the Alangium alkaloids, (±)-alangimaridine and alangimarine.

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Jahangir, Brook, M. A., Maclean, D. B., & Holland, H. L. (1987). 8H-Isoquino[2,1-b] [2,7]naphthyridin-8-ones: Synthesis of the Alangium alkaloids, alangimaridine and alangimarine. Canadian Journal of Chemistry, 65(10), 2362–2368. https://doi.org/10.1139/v87-394

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