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Mild synthesis of N'-aryl-N,N-dimethylformamidinium chloride by Vilsmeier-Haack reagent

Mild synthesis of N'-aryl-N,N-dimethylformamidinium chloride by Vilsmeier-Haack reagent
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摘要 Formamidine derivatives could be used as the building blocks for substituted heterocyclic compounds with various biological activities. N'-Aryl-N,N-dimethylformamidinium chlorides have been synthesized in high yields by reaction of aromatic primary amines with Vilsmeier-Haack reagent at room temperature. The structures of all the new compounds were identified by ESI-MS, IR and NMR spectra. The steric structures of some of these compounds were clarified by X-ray single crystal analysis. Formamidine derivatives could be used as the building blocks for substituted heterocyclic compounds with various biological activities. N'-Aryl-N,N-dimethylformamidinium chlorides have been synthesized in high yields by reaction of aromatic primary amines with Vilsmeier-Haack reagent at room temperature. The structures of all the new compounds were identified by ESI-MS, IR and NMR spectra. The steric structures of some of these compounds were clarified by X-ray single crystal analysis.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2011年第9期1043-1046,共4页 中国化学快报(英文版)
基金 the Chinese Postdoctoral Science Foundation for financial support(No.2004036602)
关键词 Vilsmcier-Haack rcagcnt Formamidinium X-ray singlc crystal Vilsmcier-Haack rcagcnt Formamidinium X-ray singlc crystal
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参考文献13

  • 1J. Quiroga, Y. Diaz, B. insuasty, et al. Tetrahedron Lett. 51 (2010) 2928.
  • 2B. Eftekhari-Sis, M. Zirak, A. Akbari, et al. J. Heterocycl. Chem. 47 (2010) 463.
  • 3L. Jiao, C. Yu, J. Li, et al. J. Org. Chem. 74 (2009) 7525.
  • 4W. Dohle, A. Staubitz, E Knochel, Chem. Eur. J. 9 (2003) 5323.
  • 5D.S. Yoon, Y. Han, T.M. Stark, et al. Org. Lett. 6 (2004) 4775.
  • 6J.A. Heath, M.M. Mehrotra, S. Chi, et al. Bioorg. Med. Chem. Lett. 14 (2004) 4867.
  • 7A. Staubitz, W. Dohle, E Knochel, Synthesis 2 (2003) 233.
  • 8D.M. Lindsay, W. Dohle, A.E. Jensen, et al. Org. Lett. 4(2002) 1819.
  • 9J. Domarkas, F. Dudouit, C. Williams, et al. J. Med. Chem. 49 (2006) 3544.
  • 10A. Wissner, M.B. Floyd, B.D. Johnson, et al. J. Med. Chem. 48 (2005) 7560.

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