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Synthesis and Crystal Structure of Ethyl 2,7,7-Trimethyl-4-(4'-methylphenyl)- 5-oxo-1,4,5,6,7,8-hexahydroquinoline-3- carboxylate in Aqueous Medium

Synthesis and Crystal Structure of Ethyl 2,7,7-Trimethyl-4-(4'-methylphenyl)- 5-oxo-1,4,5,6,7,8-hexahydroquinoline-3- carboxylate in Aqueous Medium
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摘要 The title compound (C22H27NO3) was obtained by the reaction of 4-methylbenzal- dehyde, dimedone, ethyl acetoacetate and ammonium acetate in water in the presence of triethyl- benzylammonium chloride (TEBA). The crystal is of orthorhombic, space group Pbcn with a = 18.242(2), b = 15.651(1), c = 14.207(2) ?, V = 4056.15(64) ?3, Mr = 353.45, Z = 8, Dc = 1.158 g/cm3, μ = 0.076, λ(MoKα) = 0.71073 ? and F(000) = 1520. The final R = 0.0453 and wR = 0.0436 for 1156 observed reflections with I > 2σ(I). X-ray analysis revealed that the pyridine ring is of boat conformation and the six-member ring fused with it adopts half-chair conformation. The title compound (C22H27NO3) was obtained by the reaction of 4-methylbenzal- dehyde, dimedone, ethyl acetoacetate and ammonium acetate in water in the presence of triethyl- benzylammonium chloride (TEBA). The crystal is of orthorhombic, space group Pbcn with a = 18.242(2), b = 15.651(1), c = 14.207(2) ?, V = 4056.15(64) ?3, Mr = 353.45, Z = 8, Dc = 1.158 g/cm3, μ = 0.076, λ(MoKα) = 0.71073 ? and F(000) = 1520. The final R = 0.0453 and wR = 0.0436 for 1156 observed reflections with I > 2σ(I). X-ray analysis revealed that the pyridine ring is of boat conformation and the six-member ring fused with it adopts half-chair conformation.
出处 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2005年第6期696-700,共5页 结构化学(英文)
基金 This work was supported by the foundation of "Innovation Project" of Xuzhou Normal University
关键词 hexahydroquinoline crystal structure green synthesis hexahydroquinoline, crystal structure, green synthesis
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  • 1Janis, R. A.; Silver. E J.; Triggle, D. J. Adv. Drug Res. 1987, 16, 309.
  • 2Bossert, E; Meyer, H.; Wehinger, E. Angew. Chem., Int. Ed. Engl. 1981, 20, 762.
  • 3Nakayama, H.; Kasoaka, Y. Heterocycles 1996, 42,901.
  • 4Godfraid, T.; Miller, R.; Wibo, M. Pharmocol. Rev. 1986, 38, 321.
  • 5Sausins, A.; Dubcrrs, G. Heterocycles 1988.27, 269.
  • 6Mager, P. P.; Coburn, R. A., Solo, A. J.; Triggte, D. J.; Rothe, H. Drug Design Discovery 1992, 8, 273.
  • 7Mannhold, R., Jablonka, B., Voigdt, W.; Schoenafinger, K., Schravan, K. Eur. J. Med. Chem. 1992, 27, 229.
  • 8Hantzsch, A. Ann. Chem. 1882, 1, 215.
  • 9Breslow, R.; Bovy, P.; Hersh, C. L. J. Am. Chem. Soc. 1980, 102, 2115.
  • 10Breslow, R. Acc. Chem. Res. 1991, 24,317.

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