Journal of Heterocyclic Chemistry · 1978 · 42 citations · 17 references
Natural SciencesChemistryMedicinal ChemistryGreen ChemistryOrganic ChemistrySynthetic Medicinal ChemistryCoordination ChemistryHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsMacrocycle SynthesisHeterocyclic LigandsMacrocycle Library SynthesisMacrocyclic CompoundsMacrocyclic Library SynthesisMacrocyclic LigandsPolycyclic HeterocyclesPyridine ChemistryPyridine Synthesis
Abstract Two new series of macrocyclic polyether‐diester ligands ( 4‐15 ) containing a pyridine subcyclic unit have been prepared by treating various oligoethylene glycols and sulfur‐containing oligo‐ethylene glycols with 2,6‐ and 3,5‐pyridine dicarbonyl chlorides. The compounds prepared from 2,6‐pyridine dicarbonyl chloride were: 3,6,9,12‐tetraoxa‐18‐azabicyclo[12.3.1 ]oetadeca‐1(18), 14,16‐triene‐2,13‐dione ( 4 ); 3,6,9,12,15‐pentaoxa‐21‐azabieyclo[15.3.1]heneicosa‐1(21),17,19‐triene‐2,16‐dione ( 5 ); 3,6,12,15‐tetraoxa‐9‐thia‐21‐azabicyclo[15.3.1 ]heneicosa‐1(21),17,19‐tri‐ene‐2,16‐dione( 6 ); 3,9,15‐trioxa‐6,12‐dithia‐21‐azabicyclo[15.3.1]heneicosa‐1(21),17,19‐triene‐2,16‐dione ( 7 ); 3,6,9,12,15,18‐hexaoxa‐24‐azabicyclo[18.3.1 ]tetracosa‐1(24),20,22‐triene‐2,19‐dione ( 8 ); 3,6,9,12,15,18,21‐heptaoxa‐27‐azabicyclo[21.3.1]heptacosa‐1(27),23,25‐triene‐2,22‐dione ( 9 ); and the corresponding analogues from 3,5‐pyridine dicarbonyl chloride ( 10‐15 ). The solid potassium thiocyanate complex of compound 5 was also prepared.
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