Russian Chemical Bulletin

, Volume 43, Issue 12, pp 2083–2086 | Cite as

Synthesis and amination of 5- and 8-amino derivatives of 2-phenylnaphtho[2,3-d]-1,3-thiazole-4,9-dione

  • R. P. Shishkina
  • N. V. Sergienko
Organic Chemistry


5- and 8-Amino-2-phenylnaphtho[2,3-d]-1,3-thiazole-4,9-diones were obtained by treatment of 3,5-diamino-2-chloro- and 2,5-diamino-3-chloro-1,4-naphthoquinones with sodium sulfide followed by condensation with benzaldehyde. Thermal and photochemical butylamination and CoCl{in2}-promoted arylamination of 5-amino-2-phenylnaphthothiazole-4,9-dione in position 8 was carried out.

Key words

1,4-naphthoquinone 5- and 8-amino-2-phenyl-naphtho[2,3-d]-1,3-thiazole-4,9-dione heteroannelation direct amination photoamination 


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Copyright information

© Plenum Publishing Corporation 1995

Authors and Affiliations

  • R. P. Shishkina
    • 1
  • N. V. Sergienko
    • 1
  1. 1.Novosibirsk Institute of Organic ChemistrySiberian Branch of the Russian Academy of SciencesNovosibirskRussian Federation

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