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Orthoamide und Iminiumsalze, CIX. Umsetzungen von Orthoamiden der Alkincarbonsäuren mit Diolen, Ethandithiol und CH-aciden Nitroverbindungen

  • Willi Kantlehner EMAIL logo , Kai Edelmann , Markus Vettel , Hansjörg Lehmann , Jochen Mezger and Wolfgang Frey
Published/Copyright: March 8, 2023
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Abstract

Orthoamides of alkyne carboxylic acids 17 react with 1,2- and 1,3-dioles to give vinylogous cyclic urea acetals. Analogous reactions with ethandithiol deliver vinylogous thioureas. The condensation of orthoamides 17 with 3,5-dimethyl-4-nitroisoxazol affords 1,1-diamino-butadiene derivatives. From nitro acetaldehyde diethylacetal and orthoamides 17 can be prepared reactive vinylogous urea acetals, which condense with cyano-acetic acid ester under formation of 7,7-diamino-2,4,6-hexatrienecarboxylic acid esters. 5,5-Bis(dimethylamino)-2-nitro-2,4-butadienecarboxylic acid esters, which are accessible from the orthoamides 17 and nitro acetic ester, cyclize to give 5-dimethylamino-pyrrole-2-carboxylic acid esters on treatment with zinc/acetic acid.


Herrn Professor Dr. Gerhard Müller zum 70. Geburtstag gewidmet.



Corresponding author: Willi Kantlehner, Abteilung Technische Organische Synthesechemie und Katalyseforschung, Institut für Angewandte Forschung, Hochschule Aalen, Beethovenstraße 1, 73430 Aalen, Germany; und Institut für Organische Chemie, Universität Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart, Germany, E-mail:

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  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: None declared.

  3. Conflict of interest statement: The authors declare no conflicts of interest regarding this article.

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Erhalten: 2022-12-06
Angenommen: 2023-01-25
Online erschienen: 2023-03-08
Erschienen im Druck: 2023-03-28

© 2023 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

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