SYNTHESIS OF 1H-PYRROLO[2,3-<i>b</i>]РНЕNОХАТHIIN-2,3-DIОNЕ

Authors

  • G. Loloiu Faculty of Сhemistry, Org. Chem. Dept., University of Bucharest, 90-92 Panduri Road, 76233
  • T. Loloiu Faculty of Сhemistry, Org. Chem. Dept., University of Bucharest, 90-92 Panduri Road, 76233
  • О. Maior Faculty of Pharmacy, Org. Chem. Dept., University of Medicine and Pharmacy "Carol Davila", 6 Traian Vuia street, Bucharest

Abstract

The title compound was obtained using Sandmeyer reaction starting from 2-amino-phenoxathiine. A new synthesis of N-methylpyrrolo[2,3-b]рhenoxathiin-2,3-dione was also presented. Chemical and spectral data, supporting the structure of the newly synthesized compounds were given. The isatin analog, 1-methylpyrrolo[2,3-b]phenoxathiin-2,3-dione 10,10-dioxide, could not be obtained.

How to Cite
Loloiu, G.; Loloiu, T.; Maior, O. Chem. Heterocycl. Compd. 1998, 34, 363. [Khim. Geterotsikl. Soedin. 1998, 34, 396.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02290733

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Published

1998-03-25

Issue

No. 3 (1998)

Section

Original Papers