Abstract
By condensation of bridged, aromatic diamines, derivatives of o-aminophenol or o-aminothiophenol, with the diacyl chloride of 2,6-pyridinedicarboxylic acid under high dilution, 15–18-membered macrocyclic diamides containing a pyridine nucleus have been synthesized. The synthesized compounds were characterized by IR and PMR spectroscopy.
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See [1] for Communication 3 in this series.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1559–1562, November, 1989.
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Mikhura, I.V., Formanovskii, A.A. Synthesis of macroheterocycles — Analogs of dibenzo-crown compounds. 4. 15–18-Membered pyridine-containing crown compounds. Chem Heterocycl Compd 25, 1307–1310 (1989). https://doi.org/10.1007/BF00481531
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DOI: https://doi.org/10.1007/BF00481531