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Synthesis of N-(2-chloroethyl)isatins and their β-ethyleneacetals and β-thiosemicarbazones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The nitrogen atoms of isatin, its 5-bromoderivative, and their β-ethyleneacetals are alkylated by 1,2-dichloroethane in K2CO3−DMF and LiH(NaH)-DMF.

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References

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Authors
  1. M. A. Rekhter
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  2. O. M. Radul
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  3. S. M. Bukhanyuk
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Additional information

Institute of Biological Protection of Plants and Institute of Chemistry of the Moldovan Academy of Sciences, Kishinev 2058. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 907–909, July, 1999.

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Rekhter, M.A., Radul, O.M. & Bukhanyuk, S.M. Synthesis of N-(2-chloroethyl)isatins and their β-ethyleneacetals and β-thiosemicarbazones. Chem Heterocycl Compd 35, 792–794 (1999). https://doi.org/10.1007/BF02252101

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  • DOI: https://doi.org/10.1007/BF02252101

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