Abstract
Reaction of 2,3,3-trimethyl-3H-indole chloride with cinnamic and 4-dimethylaminocinnamic aldehydes led to salts of 8-phenyl and 8-(4-dimethylaminophenyl)-10, 10-dimethyl-10H-pyrido[1,2-a]indole.
Similar content being viewed by others
Literature Cited
D. D. Chapman, J. K. Elwood, D. W. Heseltine, H. M. Hess, and D. W. Kurtz, J. Chem. Soc., Chem. Commun., No. 16, 647 (1974).
D. D. Chapman, Res. Disci., No. 128, 35 (1974); Chem. Abstr., 83, 81014 (1975).
D. D. Chapman, J. K. Elwood, D. W. Heseltine, H. M. Hess, and D. W. Kurtz, J. Org. Chem., 42, 2474 (1977).
T. Kurahashi, Sh. Maeda, and H. Yamaga, Jap. Patent 79 127 433, Chem. Abstr., 92, 112256 (1980).
T. Kurahashi, Sh. Maeda, and H. Yamaga, Jap. Patent 79 111 526; Chem. Abstr., 92, 43277 (1980).
Z. Liu, Z. Nan, Z. Zhang, and Y. Huang, Youji Huazue, No. 5, 369 (1984); Chem. Abstr., 102, 78699 (1985).
Sh. Maeda, T. Kurahashi, and H. Yamaga, Jap. Patent 7 908 626; Chem. Abstr., 90, 205784 (1979).
I. B. Lazarenko, N. M. Przhiyalgovskaya, M. A. Gal'bershtam, O. R. Khrolova, and N. N. Suvorov, Khim. Geterotsikl. Soedin., No. 9, 1221 (1978).
H. Psaar, Ger. Patent 2 510 238; Chem. Abstr., 85, 194096 (1976).
H. Ono, S. Watarai, and H. Katsuyaman, Ger. Patent 2 054 253; Chem. Abstr., 75, 110706 (1971).
L. K. Mushkalo, M. Khabubi, N. N. Mushkalo, and L. V. Fedorova, Ukr. Khim. Zh., No. 9, 957 (1974).
B. I. Ionin, B. A. Ershov, and A. I. Kol'tsov, NMR Spectroscopy in Organic Chemistry [in Russian], Khimiya, Leningrad (1983), p. 166.
Author information
Authors and Affiliations
Additional information
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 481–483, April, 1987.
Rights and permissions
About this article
Cite this article
Shachkus, A.A., Degutis, Y.A. Synthesis of 8-phenyl-10H-pyrido[1,2-a]indole salts from 2,3,3-trimethyl-3H-indole chlorides with cinnamaldehyde. Chem Heterocycl Compd 23, 401–403 (1987). https://doi.org/10.1007/BF00546734
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00546734