Abstract
3-(N-morpholino)-3-cyanoquinuclidine has been shown to form only 1-methyl-3-(N-morpholino)-3-cyanoquinuclidinium iodide or 1-benzyl-3-(N-morpholino)-3-cyanoquinuclidinium chloride when treated with iodomethane (1∶1 or 1∶2.3) or benzene chloride (1∶1), respectively. The direction of quarternization is determined using1H NMR spectroscopy.
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References
E. E. Mikhlina, V. Ya. Vorob'eva, and N. V. Rubtsov,Khim. Geterocycl. Soedin., No. 1. 74 - 77 (1970).
L. N. Yachontov,Heterocycles,7, 1033 - 1090 (1977).
H. C. Brown and N. R. Eldred,J. Am. Chem. Soc. 71, 445 - 450 (1949).
C. G. Swain and N. D. Hershey,J. Am. Chem. Soc.,94, 1901 - 1905 (1972).
B. Armarzogi, A. V. George, and N. S. Isaacs,Tetrahedron,42, 601 - 607 (1986).
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Alekseeva, N.N., Koikov, L.N. Quarternization of 3-(N-morpholino)-3-cyanoquinuclidine. Pharm Chem J 29, 146–147 (1995). https://doi.org/10.1007/BF02226531
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DOI: https://doi.org/10.1007/BF02226531