Journal of Lanzhou University of Technology ›› 2026, Vol. 52 ›› Issue (4): 66-71.doi: 10.13295/j.cnki.issn1673-5196.2026.04.008

• Chemical Industry and Light Industry • Previous Articles     Next Articles

An efficient protocol for the synthesis of furano [3,4-b] pyridine derivatives

YANG Zheng1,2,3, LIU Xue-jun1, GAO Jiang1, XIE Heng-shen2, CONG Xing-shun3   

  1. 1. School of Urban Safety and Operations, Jiangsu Vocational University of Architectural Technology, Xuzhou 221116, China;
    2. Jiangsu Engineering Laboratory of Biomass Resources Comprehensive Utilization, Jiangsu Vocational University of Architectural Technology, Xuzhou221116, China;
    3. College of Chemistry, Chemical Engineering and Materials Science, Zaozhuang University, Zaozhuang 277160, China
  • Received:2024-01-03 Online:2026-08-28 Published:2026-09-03

Abstract: By using 2,3-epoxypropan-1-ones and enaminoketone, a PTSA-promoted in situ ring opening-hydrogen migration/intramolecular cyclization reaction at 100 ℃ was developed in DMF, affording a series of furano [3,4-b] pyridine derivatives in 70%~78% yields. The structures of all products were characterised by IR spectra, 1H NMR and HRMS. In addition, single-crystal X-ray diffraction confirmed the structure of compound 3a.

Key words: 2,3-epoxypropan-1-one, enaminoketone, furano [3,4-b] pyridine derivatives

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