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4-(5-Methoxy-2-oxazolyl)naphthalic anhydride and products of its condensation with aromatic amines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

4-(5-Methyl-2-oxoazolyl)naphthalic anhydride was synthesized by condensation of 4-chloroformylnaphthalic anhydride with aminoacetone and subsequent cyclization of the resulting amide. Luminescing methyl-substituted N-phenylnaphthalimide and 1,8-naphthoylene-1′,2′-benzimidazple were obtained by condensation of this product with aniline and o-phenylenediamine, respectively. The relationship between the structures of the products and their electronic absorption and luminescence spectra was investigated.

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Literature cited

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Authors and Affiliations

  1. All-Union Scientific-Research Institute of Single Crystals, Khar'kov

    B. M. Krasovitskii & V. M. Shershukov

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  1. B. M. Krasovitskii
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  2. V. M. Shershukov
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 883–885, July, 1976.

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Krasovitskii, B.M., Shershukov, V.M. 4-(5-Methoxy-2-oxazolyl)naphthalic anhydride and products of its condensation with aromatic amines. Chem Heterocycl Compd 12, 736–738 (1976). https://doi.org/10.1007/BF00476999

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  • DOI: https://doi.org/10.1007/BF00476999

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