Abstract
Several 2-substituted benzotellurazoles have been prepared by the reaction of N-allyl derivatives of o-methyltelluroaniline with POC13 or SOC12 followed by reduction of the σ-telluranes which are formed. The use of the zinc and sodium salts of o-aminotellurophenol and 2-chlorotellurenylazobenzene, in a procedure similar to that used to prepare benzothiazoles and benzoselenazoles, did not lead to the formation of benzotellurazoles.
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For Communication 1, see [1].
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 120–125, January, 1989.
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Sadekov, I.D., Abakarov, G.M., Shneider, A.A. et al. Nitrogen-tellurium heterocycles. Chem Heterocycl Compd 25, 103–108 (1989). https://doi.org/10.1007/BF00472631
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DOI: https://doi.org/10.1007/BF00472631