A convenient synthesis of pyridine and 2,2′-bipyridine derivatives

Marta Altuna-Urquijo, Alexander Gehre, Stephen Stanforth, Brian Tarbit

Research output: Contribution to journalArticlepeer-review

28 Citations (Scopus)

Abstract

α-Chloro-α-acetoxy-β-keto-esters 9 were readily prepared from β-keto-esters 6 in good overall yields. These compounds reacted as α,β-diketo-ester equivalents 2 with amidrazones 1 yielding triazines 3, generally in good yields. Picolinates 10 provided an alternative source of α,β-diketo-ester equivalents 2 when treated with copper(II) acetate. A ‘one-pot’ reaction of the α,β-diketo-ester equivalents 2 with amidrazones 1 in the presence of 2,5-norbornadiene 5 in boiling ethanol yielded the pyridines 4 and 2,2′-bipyridines 4 (R1=2-pyridyl) directly without the need to isolate the corresponding triazines 3. Triazine 3c reacted with the aza-dienophiles 13 and 17 affording the products 16 and 18, respectively, in good yields.
Original languageEnglish
Pages (from-to)975-984
JournalTetrahedron
Volume65
Issue number5
DOIs
Publication statusPublished - Jan 2009

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