Abstract
The corresponding carboxymethylthiothiadiazoles are formed by the action of formic acid on 3-aminorhodanine and 3-(3-phenylthioureido)rhodanine, and the action of rhodanineaniline on 3-(3-phenylthioureido)rhodanine leads to 2-anilino-5-carboxy-methylthiothiadiazole anilide, whereas similar treatment of 3-ureidorhodanine leads to a semicarbazide derivative.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 51–53, January, 1981.
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Mikitenko, E.K., Romanov, N.N. Synthesis and reactions of 3-aminothiazolidine-2-thion-4-one derivatives. 1. Conversion of 3-aminothiazolidine-2-thion-4-one derivatives to substituted mercapto-1,3,4-thiadiazoles. Chem Heterocycl Compd 17, 40–42 (1981). https://doi.org/10.1007/BF00507088
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DOI: https://doi.org/10.1007/BF00507088