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Mendeleev Communications, 1992, Volume 2, Issue 4, Pages 151–153
DOI: https://doi.org/10.1070/MC1992v002n04ABEH000180
(Mi mendc5451)
 

This article is cited in 10 scientific papers (total in 10 papers)

Reactions of N-Aminoquinolones with Ketones: A New Approach to the Synthesis of Tricyclic 6-Fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic Acids

O. N. Chupakhina, Yu. A. Azevb, S. G. Alexeevc, S. V. Shorshnevb, E. Tsoid, V. N. Charushind

a I. Ya. Postovsky Institute of Organic Synthesis, Urals Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
b Ural Scientific Research Institute of Technology of Medical Preparations, Ekaterinburg, Russian Federation
c Urals State Technical University, Ekaterinburg, Russian Federation
d Department of Organic Chemistry, Urals State Technical University, Ekaterinburg, Russian Federation
Abstract: Reactions of 7-(X)-substituted ethyl 1-amino-4-oxo-1,4-dihydroquinoline-3-carboxylates (1a-c; X = F, Cl and 4-methylpiperazin-1-yl) with mono- and di-ketones have been studied. Treatment of 1a; X = F with cyclopentanone and cyclopentanone in acetic acid resulted in the corresponding azomethynes; α-dicarbonyl compounds such as glyoxal, glyoxylic acid or ethyl pyruvate caused desamination of 1a into ethyl, 6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate, while reactions of 1a-c with acetoacetone resulted in tricyclic 7-fluoro-4-oxopyrazolo[1,5-a]quinoline-4-carboxylic acids
Document Type: Article
Language: English


Citation: O. N. Chupakhin, Yu. A. Azev, S. G. Alexeev, S. V. Shorshnev, E. Tsoi, V. N. Charushin, “Reactions of N-Aminoquinolones with Ketones: A New Approach to the Synthesis of Tricyclic 6-Fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic Acids”, Mendeleev Commun., 2:4 (1992), 151–153
Linking options:
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  • https://www.mathnet.ru/eng/mendc/v2/i4/p151
  • This publication is cited in the following 10 articles:
    1. A. A. Boteva, O. P. Krasnykh, “The methods of synthesis, modification, and biological activity of 4-quinolones (review)”, Chem Heterocycl Comp, 45:7 (2009), 757  crossref
    2. V. N. Charushin, O. N. Chupakhin, “Nucleophilic aromatic substitution of hydrogen and related reactions”, Mendeleev Commun., 17:5 (2007), 249–254  mathnet  crossref
    3. E. V. Nosova, N. N. Mochul'skaya, S. K. Kotovskaya, G. N. Lipunova, V. N. Charushin, “Fluorinated benzazoles and benzazines”, Heteroatom Chemistry, 17:6 (2006), 579  crossref
    4. El-Sayed H El-Ashry, El-Sayed I Ibrahim, Advances in Heterocyclic Chemistry, 84, 2003, 71  crossref
    5. Yu. A. Azev, E. Lork, D. Gabel, T. Duelcks, “New way of the reaction of 1-amino-6,7-difluoro-4-oxoquinolyl-3-ethylcarboxylate with acetoacetone”, Mendeleev Commun., 13:4 (2003), 184–185  mathnet  crossref
    6. E. Tsoi, V. N. Charushin, E. V. Nosova, G. N. Lipunova, A. V. Tkachev, “New approach to [a]-fused fluoroquinolones: the synthesis of 5-oxo-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinolines”, Mendeleev Commun., 11:2 (2001), 53–54  mathnet  crossref
    7. David Barrett, Hiroshi Sasaki, Takayoshi Kinoshita, Akihiko Fujikawa, Kazuo Sakane, “A novel synthesis of the pyrazolo[1,5-a]quinoline ring system. New N1-C2 bridged DNA gyrase inhibitors via a novel tandem 1,4-conjugate addition-Michael [3+2] annulation process”, Tetrahedron, 52:25 (1996), 8471  crossref
    8. Nucleophilic Aromatic Substitution of Hydrogen, 1994, 287  crossref
    9. O. N. CHUPAKHIN, YU. A. AZEV, S. G. ALEXEEV, S. V. SHORSHNEV, E. TSOI, V. N. CHARUSHIN, “ChemInform Abstract: Reactions of N‐Aminoquinolones with Ketones: A New Approach to the Synthesis of Tricyclic 6‐Fluoro‐4‐oxo‐1,4‐dihydroquinoline‐3‐ carboxylic Acids.”, ChemInform, 24:15 (1993)  crossref
    10. Yu. A. Azev, S. V. Shorshnev, S. G. Alexeev, V. N. Charushin, O. N. Chupakhin, “ipso-Substitution of an Acyl group in Reactions of 3-Acyl-substituted Ethyl 7,8-Difluoro-5-oxo-5,9a-dihydropyrazolo[1,5-a]quinoline-4-carboxylates with Electrophilic Reagents”, Mendeleev Commun., 3:3 (1993), 99–100  mathnet  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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