Four kinds of naphthyridinones, i.e. l,6-naphthyridin-5-one, l,7-naphthyridin-8-one, 2,6-naphthyridin-2-one, and 2,7-naphthyridin-l-one derivatives, were commonly synthesized by the intramolecular cyclization of pyridinecarboxamides having an ethynyl group or β,β-dimethoxyethyl group adjacent to the carbamoyl group. The syntheses of the starting pyridine derivatives were easily accomplished by cross-coupling of the corresponding halopyridines with acetylenes. © 1985, The Pharmaceutical Society of Japan. All rights reserved.
CITATION STYLE
Sakamoto, T., Kondo, Y., & Yamanaka, H. (1985). Condensed Heteroaromatic Ring Systems. III.1,2) Synthesis of Naphthyridine Derivatives by Cyclization of Ethynylpyridinecarboxamides. Chemical and Pharmaceutical Bulletin, 33(2), 626–633. https://doi.org/10.1248/cpb.33.626
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