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Microwave-mediated reactions of 3-aminomethylpyridines with acetylenedicarboxylates. A novel synthetic route to dihydronaphthyridines and naphthyridine-1-ones
Authors:Vladimir Y. Vvedensky  Yury V. Ivanov  Volodymyr Kysil  Caroline Williams  Sergei Tkachenko  Alexander Kiselyov  Alexander V. Khvat  Alexandre V. Ivachtchenko
Affiliation:ChemDiv Inc., 11558 Sorrento Valley Rd., San Diego, CA 92121, USA
Abstract:Reaction of 3-(1-alkylamino)pyridines with electron deficient acetylenes in the presence of acids yields 1,2-dihydro[2,7]naphthyridine-3,4-dialkyldicarboxylates 4 in 35-72% yield. Compounds 4 unsubstituted in position 1 can be easily oxidized with potassium permanganate into the respective naphthyridine-1-ones derivatives 5 in good yields.
Keywords:[2,7]Naphthyridines   Anabasine   Enamines
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