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Di-4(3H)-quinazolinon-2-yl Derivatives from the Diacid Chlorides of Pinic and sym-Homopinic Acids

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Abstract

The corresponding diamides have been synthesized by the interaction of the diacid chlorides of cis-2,2-dimethyl-3-carboxycyclobutaneacetic acid (pinic acid) and cis-2,2-dimethylcyclobutane-1,3-diacetic acid (sym-homopinic acid) with two equivalents of anthranilic acid. Treatment of the diamides with formamide gave 2,2-dimethyl-1-[4(3H)-quinazolinon-2-yl]methyl-3-[4(3H)-quinazolinon-2-yl]cyclobutane and 2,2-dimethyl-1,3-di[4(3H)-quinazolinon-2-ylmethyl]cyclobutane respectively.

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Authors and Affiliations

  1. Riga Technical University, Riga, LV-1658, Latvia

    F. M. Avotin'sh, M. V. Petrova & A. Ya. Strakov

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  1. F. M. Avotin'sh
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  2. M. V. Petrova
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  3. A. Ya. Strakov
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Avotin'sh, F.M., Petrova, M.V. & Strakov, A.Y. Di-4(3H)-quinazolinon-2-yl Derivatives from the Diacid Chlorides of Pinic and sym-Homopinic Acids. Chemistry of Heterocyclic Compounds 37, 1241–1243 (2001). https://doi.org/10.1023/A:1013801711372

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  • DOI: https://doi.org/10.1023/A:1013801711372

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