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Synthesis of substituted diazines, diazoles, and condensed thia- and oxadiazoles

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The corresponding 2-arylhydrazono-3-oxoimidazo[1,2-a]pyridines, 3-arylhydrazono-2-oxoimidazo [1,2-a]benzothiazoles, 2-oxoimidazolidino[3,2-a]benzimidazoles, 2-oxoimidazo[1,2-a]benzoxazoles, and 2-arylhydrazono-3-oxothiazolo[2,3-a]benzimidazoles were obtained by the condensation of arylazochloroacetyl chlorides with 2-aminopyridine, 2-aminobenzothiazole, 2-aminobenzoxazole, 2-aminobenzimidazole, and 2-mercaptobenzimidazole. 5-Arylhydrazono-1,2-diphenylimidazole-4-ones and 5-arylhydrazono-3,4-diaryl-1,2,4-oxidiazine-6-ones were synthesized by the reaction of arylazochloroacetyl chlorides with N-phenylbenzamidine and N-phenylamidoxime.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 930–936, July, 1971.

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Lozinskii, M.O., Shivanyuk, A.F. & Pel'kis, P.S. Synthesis of substituted diazines, diazoles, and condensed thia- and oxadiazoles. Chem Heterocycl Compd 7, 869–874 (1971). https://doi.org/10.1007/BF00475714

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  • DOI: https://doi.org/10.1007/BF00475714

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