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Mendeleev Communications, 2025, Volume 35, Issue 5, Pages 530–532
DOI: https://doi.org/10.71267/mencom.7748
(Mi mendc7281)
 

Communications

One-pot synthesis of acetyl(iso)quinolines/pyridines employing the sodium-promoted Claisen condensation of the corresponding carboxylates

X. Hea, T. Yuana, J. Suib, Sh. Donga, Z. Wanga, D. Liua, Y. Zouc

a School of Chemical and Pharmaceutical Engineering, Changzhou Vocational Institute of Engineering, 213164 Changzhou, P. R. China
b Nanjing Customs Testing Center for Dangerous Goods and Packaging, 213100 Changzhou, P. R. China
c Department of Medicinal Chemistry, China Pharmaceutical University, 210009 Nanjing, P. R. China
References:
Abstract: A convenient one-pot synthesis of acetylated quinolines/isoquinolines/pyridines involves the sodium-promoted Claisen condensation of the corresponding ethyl hetarenecarboxylates with ethyl acetate as the reactant and the solvent. The thus formed intermediate ethyl 3-hetaryl-3-oxopropanoates can be decarboxylated in the same reactor by refluxing with 25% H2SO4 to afford the title products in good to excellent yields.
Keywords: acetylquinolines, acetylisoquinolines, acetylpyridines, acetylation, Claisen condensation, one-pot synthesis, solvent-free process.
Funding agency Grant number
Research Fund of Changzhou Vocational Institute of Engineering
Received: 17.02.2025
Accepted: 14.03.2025
Published: 17.07.2025
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (3.7 Mb)


Citation: X. He, T. Yuan, J. Sui, Sh. Dong, Z. Wang, D. Liu, Y. Zou, “One-pot synthesis of acetyl(iso)quinolines/pyridines employing the sodium-promoted Claisen condensation of the corresponding carboxylates”, Mendeleev Commun., 35:5 (2025), 530–532
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