Reaction of pyridinium and quinolinium salts having the leaving group at the 2- or 4-position with active methylene compounds

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Abstract

The reactions of 2- or 4-cyanopyridinium salts with active methylene compounds such as dimethyl malonate, malononitrile, and cyclohexane-1,3-dione affording 2- or 4-(substituted methylene) pyridines are described. Similar reactions of 4-cyano-2-methylthiopyridinium and 4-cyano-2-methylthioquinolinium salts, both of which have two leaving groups, were readily prepared from 4-cyano-1-methyl-2(1H)-pyridone and 4-cyano-1-methyl-2(1H)-quinolone via 4-cyano-1-methyl-2(1H)-thiopyridone and 4-cyano-1-methyl-2(1H-thioquinolone in two steps, proceeding at the 2-and/or 4-positions on the pyridine or quinoline rings. © 2006 The Pharmaceutical Society of Japan.

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APA

Fujita, R., Hoshino, M., Tojyo, Y., Kimura, A., & Hongo, H. (2006). Reaction of pyridinium and quinolinium salts having the leaving group at the 2- or 4-position with active methylene compounds. Yakugaku Zasshi, 126(2), 99–108. https://doi.org/10.1248/yakushi.126.99

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