Synthesis of novel N-, S-substituted-polyhalo-1, 3-butadienes and crystal structure of dibutadienyl homopiperazine

Deniz N. G., Ibis C.

JOURNAL OF CHEMICAL SCIENCES, cilt.125, sa.4, ss.755-764, 2013 (SCI-Expanded, Scopus) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 125 Sayı: 4
  • Basım Tarihi: 2013
  • Dergi Adı: JOURNAL OF CHEMICAL SCIENCES
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.755-764
  • Anahtar Kelimeler: Piperazine, homopiperazine, thiomorpholine, 1, 3-butadiene, E-isomers, X-ray structure, ARYLPIPERAZINE DERIVATIVES, MORPHOLINE, THIOMORPHOLINE, IDENTIFICATION, 2-NITRODIENES, NITRODIENES, PIPERAZINE, RECEPTORS, LIGANDS, DIENES
  • İstanbul Üniversitesi-Cerrahpaşa Adresli: Hayır

Özet

Polyhalogenated-2-nitro-1, 3-butadienes are important synthetic precursors for a variety of poly-functionalized bioactive heterocycles. Herein, we report the reactions of 1, 1, 3, 4, 4-pentachloro-2-nitro-1, 3-butadiene 1 and 4-bromo-1, 1, 3, 4-tetrachloro-2-nitro-1, 3-butadiene 2 with amino and thiol containing nucleophiles to obtain highly functionalized (E)-polyhalodiene-2-nitro-1, 3-butadiene derivatives. Most of these reactions were found to be highly selective resulting in good to high yields of the products. All new compounds have been characterized by nuclear magnetic resonance spectroscopy (NMR), mass spectrometry (MS) and Fourier transform infrared spectroscopy (FT-IR) spectroscopic data. Single crystal X-ray structure analysis of compound 8c is reported.