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Synthesis of substituted thiazoles and oxazoles from 2-amino-1-(p-nitrophenyl)ethanol

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

New thiourea derivatives have been synthesized by the condensation of 2-amino-1-(p-nitrophenyl)ethanol with aryl and alkyl isothiocyanates. Their cyclization with ω-bromoacetophenone and methyl monochloroacetate and also their desulfurization with yellow lead oxide have been studied.

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Authors and Affiliations

  1. Institute of Organic Chemistry, AS UKrSSR, Kiev

    M. O. Lozinskii, T. N. Soroka, D. F. Yavorskii, S. S. Kirienko, V. Ya. Yakovleva & P. S. Pel'kis

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  1. M. O. Lozinskii
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  2. T. N. Soroka
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  3. D. F. Yavorskii
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  4. S. S. Kirienko
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  5. V. Ya. Yakovleva
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  6. P. S. Pel'kis
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Lozinskii, M.O., Soroka, T.N., Yavorskii, D.F. et al. Synthesis of substituted thiazoles and oxazoles from 2-amino-1-(p-nitrophenyl)ethanol. Chem Heterocycl Compd 5, 374–375 (1969). https://doi.org/10.1007/BF00471148

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  • DOI: https://doi.org/10.1007/BF00471148

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