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Structure of Products of Reaction between Benzoylacetylene and 1,5-Diphenyldithiobiuret

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Reaction of benzoylacetylene with 1,5-diphenyldithiobiuret in glacial AcOH in the presence of equimolar amounts of HClO4 leads exclusively to 2-benzoylmethyl-4,6-di(phenylimino)-1,3,5-dithiazinium perchlorate. In MeOH, benzene, and MeCN medium, the reaction proceeds nonselectively and a mixture is formed that includes 2-benzoylmethyl-4,6-di(phenylimino)-1,3,5-dithiazine, 2-benzoylmethyl-4-benzoylvinylthio-3-phenyl-6-phenylimino-1,3,5-thiadiazine, 2-benzoylmethyl-4,6-di-(thiocarbonyl)-1,3-diphenyl-1,3,5-triazine, and N-benzoylvinyl-N'-phenylthiourea.

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Glotova, T.E., Nakhmanovich, A.S., Albanov, A.I. et al. Structure of Products of Reaction between Benzoylacetylene and 1,5-Diphenyldithiobiuret. Chemistry of Heterocyclic Compounds 38, 74–78 (2002). https://doi.org/10.1023/A:1014859410679

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  • DOI: https://doi.org/10.1023/A:1014859410679

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