S-Methyl-(-N-aryl and -N-alkyl)isothioureas derived from 2-aminobenzothiazole

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Abstract

S-Methylisothioureas, 2-N-H, -N-alkyl and -N-aryl are synthesized from the reaction of ammonia or the corresponding aromatic amines with benzothiazole dithiomethylcarboimidate. The reaction with pyrrolidine and piperazine are reported. Compounds were characterized by 1H and 13C NMR spectroscopy and the X-ray molecular structure of S-methy-N- benzothiazolelisothiourea derivative is reported.

Original languageEnglish
Pages (from-to)200-209
Number of pages10
JournalArkivoc
Volume2008
Issue number5
DOIs
StatePublished - 2008

Keywords

  • 2-Aminobenzothiazole
  • Carbon disulfide
  • Guanidines
  • Isothioureas
  • Piperazine
  • Pyrrolidine
  • S-methyl group

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