Conclusions
A method of synthesis is given for monoarylhydrazones of benzoylglyoxal, of 1-aryl-1,2-propandione, and of 1-aryl-1,2-butandiones. Cyclization of monoarylhydrazones of 1-aryl-1,2-butandiones under conditions of the Fischer reaction yielded a series of derivatives of 2-aroylindole, which on reaction with dimethyl sulfate in an alkaline medium were converted to the corresponding N-methyl derivatives of 2-aroylindole.
Similar content being viewed by others
Literature cited
M. D. Mashkovskaya, Medicinal Substances [in Russian], Moscow (1967).
R. J. Sundberg, J. Org. Chem.,16, 3604 (1965).
L. Bellamy, Infrared Spectra of Complex Molecules [in Russian], Moscow (1963).
V. I. Shvedov, L. B. Altukhova, and A. N. Grinev, Zh. Organ. Khim.,2, 1608 (1966).
V. I. Shvedov, L. B. Altukhova, and A. N. Grinev, Khimiya Geterotsiklich. Soedinenii, No. 3, 365 (1965).
Author information
Authors and Affiliations
Additional information
Translated from Khimiko-Farmatsevticheskii Zhurnal, No. 8, pp. 8–13, August, 1958.
Rights and permissions
About this article
Cite this article
Shvedov, V.I., Alekseev, V.V. & Grinev, A.N. Synthesis of 2-aroylindole derivatives. Pharm Chem J 2, 418–422 (1968). https://doi.org/10.1007/BF00759390
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00759390