17965-72-9Relevant academic research and scientific papers
Synthetic method of 7-bromo-1,5-naphthyridine-3-methanoic acid
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Paragraph 0057; 0058; 0059, (2018/11/03)
The invention provides a synthetic method of 7-bromo-1,5-naphthyridine-3-methanoic acid. The synthetic method of the 2-bromo-1,5-naphthyridine-3-methanoic acid comprises the steps of taking 1,5-naphthyridine as a raw material and reacting to generate 7-bromo-1,5-naphthyridine-3-methyl pyrazinecarboxylate; and finally hydrolyzing the 7-bromo-1,5-naphthyridine-3-methyl pyrazinecarboxylate under thealkaline condition to generate the 7-bromo-1,5-naphthyridine-3-methanoic acid. According to the synthetic method of the 7-bromo-1,5-naphthyridine-3-methanoic acid, a synthetic route which takes 1,5-naphthyridine as a raw material is provided. The synthetic method of the 7-bromo-1,5-naphthyridine-3-methanoic acid has the advantages that the synthetic route is simple, the raw materials are low in cost, are simple and are easily obtained, aftertreatment is facilitated, the success rate is high, the synthetic route is easy to enlarge and the like.
SUBSTITUTED NAPHTHYRIDINE AND QUINOLINE COMPOUNDS AS MAO INHIBITORS
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Paragraph 0370; 0371, (2014/09/30)
The invention provides a chemical entity of Formula (I) wherein R1, R2, R3, Y, and n have any of the values described herein and compositions comprising such chemical entities; methods of making them; and their use in a wi
Synthesis and SAR comparison of regioisomeric aryl naphthyridines as potent mGlu5 receptor antagonists
Galatsis, Paul,Yamagata, Koji,Wendt, John A.,Connolly, Cleo J.,Mickelson, John W.,Milbank, Jared B.J.,Bove, Susan E.,Knauer, Christopher S.,Brooker, Rachel M.,Augelli-Szafran, Corinne E.,Schwarz, Roy D.,Kinsora, Jack J.,Kilgore, Kenneth S.
, p. 6525 - 6528 (2008/03/18)
We describe three novel regioisomeric series of aryl naphthyridine analogs, which are potent antagonists of the Class III GPCR mGlu5 receptor. The synthesis and in vitro and in vivo pharmacological activities of these analogs are discussed.
