Abstract
Substituted thiazoles, 1,4-benzothiazines, imidazo[2,1-b]thiazoles, and imidazo[1,2-a]pyridines containing acylamide residues as substituents were obtained by reaction of ω-chloro-ω-acylaminoacetophenones with thioamides, o-aminothiophenol, 2-aminothiazole, and 2-aminopyridine. Some of these substances can be used for the synthesis of heterocyclic bases with an unsubstituted amino group.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 928–931, July, 1974.
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Drach, B.S., Dolgushina, I.Y. & Sinitsa, A.D. Some cyclization reactions of ω-chloro-ω-acylamidoacetophenones. Chem Heterocycl Compd 10, 810–812 (1974). https://doi.org/10.1007/BF00471360
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DOI: https://doi.org/10.1007/BF00471360