Abstract
5H-Pyridazo[4,5-b]indol-1-ones were obtained by heating 2-acetylindole-3- or 2-aroylindole-3-carboxylic acids with hydrazine hydrate in ethylene glycol or alcohol. 1-Chloro-5H-pyridazo[4,5-b]indoles are formed by treatment of 5H-pyridazo[4,5-b]indol-1-ones with phosphorus oxychloride.
Similar content being viewed by others
Literature cited
N. N. Suvorov, Zh. D. Ovchinnikova, and Yu. N. Sheinker, Zh. Obshch. Khim., 31, 2333 (1961).
R. S. Pandit and S. Seshadri, Indian J. Chem., 12, 943 (1974).
P. Nantka-Namirski and Z. Ozdowska, Acta, Pol. Pharm., 32, 273 (1975).
H. King and E. Stiller, J. Chem. Soc., No. 2, 466 (1937).
N. A. Kogan and M. I. Vlasova, Khim. Geterotsikl. Soedin., No. 12, 1654 (1973).
V. A. Monge, V. Huarte, J. A. Palop, M. T. Martinez, and A. E. Fernandez, An. Quim., 73 (2), 278 (1977); Chem. Abstr., 87, 152107 (1977).
R. Staunton and A. Topham, J. Chem. Soc., No. 6, 1889 (1953).
M. I. Vlasova and N. A. Kogan, Khim. Geterosikl. Soedin., No. 6, 754 (1974).
M. A. Rekhter, V. I. Gorgos, L. M. Zorin, and G. I. Zhungietu, USSR Inventor's Certificate No. 696016; Byull. Izobret., No. 41, 91 (1979).
G. I. Zhungietu, V. I. Gorgos, M. A. Rekhter, and A. I., Korpan', Izv. Akad. Nauk Moldavsk. SSR, Ser. Biol. Khim. Nauk, No. 3, 61 (1980).
G. I. Zhungietu, L. M. Zorin, and M. A., Rekhter, Izv. Akad. Nauk Moldavsk. SSR, Ser. Biol. Khim. Nauk, No. 2, 57 (1981).
A. N. Kost, M. A. Yurovskaya, and Nguyen Minh Thao, Khim. Geterotsikl. Soedin., No. 5, 659 (1975).
Author information
Authors and Affiliations
Additional information
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1064–1066, August, 1982.
Rights and permissions
About this article
Cite this article
Zhungietu, G.I., Zorin, L.M., Gorgos, V.I. et al. Synthesis of 5H-pyridazo[4,5-b]indoles by condensation of 2-acylindole-3-carboxylic acids with hydrazine. Chem Heterocycl Compd 18, 811–813 (1982). https://doi.org/10.1007/BF00506584
Received:
Revised:
Issue Date:
DOI: https://doi.org/10.1007/BF00506584