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Synthesis of Hetarylquinolines from 2-{[(4-Methylquinolin-2-yl)sulfanyl]acetyl}-N-phenylhydrazine-1-carbothioamides

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Abstract

Intramolecular cyclization of 2-{[(4-methyl(or 4,6- and 4,8-dimethyl)quinolin-2-yl)sulfanyl]-acetyl}-N-phenylhydrazine-1-carbothioamides in alkaline and acidic media afforded {[(4-methyl(or 4,6- and 4,8-dimethyl)quinolin-2-yl)sulfanyl]acetyl}-substituted 1,2,4-triazoles and 1,3,4-thiadiazoles. The reaction of these compounds with ethyl bromoacetate gave thiazolidinone derivatives.

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Authors and Affiliations

  1. Yerevan State University, ul. Aleka Manukyana 1, Yerevan, 0025, Armenia

    I. L. Aleksanyan & L. P. Hambardzumyan

Authors
  1. I. L. Aleksanyan
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  2. L. P. Hambardzumyan
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Correspondence to I. L. Aleksanyan.

Additional information

Original Russian Text © I.L. Aleksanyan, L.P. Ambartsumyan, 2018, published in Zhurnal Organicheskoi Khimii, 2018, Vol. 54, No. 9, pp. 1386–1389.

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Aleksanyan, I.L., Hambardzumyan, L.P. Synthesis of Hetarylquinolines from 2-{[(4-Methylquinolin-2-yl)sulfanyl]acetyl}-N-phenylhydrazine-1-carbothioamides. Russ J Org Chem 54, 1402–1405 (2018). https://doi.org/10.1134/S1070428018090221

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  • DOI: https://doi.org/10.1134/S1070428018090221

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