Abstract
1-Benzyl-6-hydroxy-7-cyano-5-azaindoline, which was converted to 6-chloro-5-azaindoline through 6-hydroxy-5-azaindoline, was synthesized from O-methylbutyrolactim through 1-benzyl-2-pyrrolidone, 1-benzyl-2-cyano (carbamoylmethylene)-pyrrolidine, and the product of its condensation with dimethylformamide diethylacetal.
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A. A. Prokopov and L. N. Yakhontov, Khim. Geterotsikl. Soedin., No. 11, 1531 (1977).
V. G. Granik, N. B. Marchenko, T. F. Vlasova, and R. G. Glushkov, Khim. Geterotsikl. Soedin., No. 11, 1509 (1976).
L. N. Yakhontov and E. I. Lapan, Khim. Geterotsikl. Soedin., No. 1, 27 (1970).
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See [1] for communication LII.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 355–358, March, 1978.
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Azimov, V.A., Granik, V.G., Glushkov, R.G. et al. Azaindole derivatives. Chem Heterocycl Compd 14, 289–293 (1978). https://doi.org/10.1007/BF00470561
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DOI: https://doi.org/10.1007/BF00470561