Acta Crystallographica Section E (Jan 2009)

3-Amino-5-bromo-2-iodopyridine

  • Kevin D. Bunker,
  • Neal W. Sach,
  • Seiji Nukui,
  • Arnold L. Rheingold,
  • Alex Yanovsky

DOI
https://doi.org/10.1107/S1600536808040452
Journal volume & issue
Vol. 65, no. 1
pp. o28 – o28

Abstract

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The reaction of 3-amino-5-bromopyridine with N-iodosuccinimide in the presence of acetic acid produces the title compound, C5H4BrIN, with an iodo substituent in position 2 of the pyridine ring. The crystal structure features rather weak intermolecular N—H...N hydrogen bonds linking the molecules into chains along the z axis of the crystal.