Synthesis of thio- and furan-fused heterocycles: furopyranone, furopyrrolone, and thienopyrrolone derivatives

Ergun M., DENGİZ Ç., Ozer M. S., ŞAHİN E., Balci M.

TETRAHEDRON, cilt.70, sa.35, ss.5993-5998, 2014 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 70 Sayı: 35
  • Basım Tarihi: 2014
  • Doi Numarası: 10.1016/j.tet.2014.05.071
  • Dergi Adı: TETRAHEDRON
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.5993-5998
  • Anahtar Kelimeler: Acyl azide, Furopyranone, Furopyrrolone, Thienopyrrolone, Curtius rearrangement, IN-VITRO, CONSTRUCTION, THIOPHENE
  • Atatürk Üniversitesi Adresli: Evet

Özet

We report herein the synthesis of a novel class of compounds, ethyl 4-oxo-4H-furo[3,2-c]pyran-6-yl carbonate, (7E)-7-[(dimethylamino)methylene]-4H-furo[3,2-c]pyran-4,6(7H)-dione, 5-oxo-N-phenyl-2,5-dihydro-4H-furo[3,2-b]pyrrole-4-carboxamide,and 5-oxo-N-phenyl-5,6-dihydro-4H-thieno[3,2-b] pyrrole-4-carboxamide starting from the corresponding acid derivatives. Intramolecular cyclization in the presence of thionyl chloride formed the target fused ring systems. Additional transformation was seen in the cyclization of furan-fused heterocycle. A mechanism was proposed based on experimental and computational findings. (C) 2014 Elsevier Ltd. All rights reserved.