Solvent-free synthesis of new 2,4,6-triarylpyridines catalyzed by a Brønsted acidic ionic liquid as a green and reusable catalyst
✍ Scribed by Hossein Behmadi; Shima Naderipour; Seyed Mahdi Saadati; Mohammad Barghamadi; Mohammad Shaker; Niloofar Tavakoli-Hoseini
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2011
- Tongue
- English
- Weight
- 123 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.697
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✦ Synopsis
Abstract
Some new 4‐(aryl)‐2,6‐di‐2‐naphthylpyridines and 4‐(aryl)‐2,6‐di‐2‐thienylpyridines have been prepared through three‐component condensation of 2‐acetylnaphthalene or 2‐acetylthiophene, aromatic aldehydes, and ammonium acetate in presence of 1‐(4‐sulfonylbutyl) pyridinium hydrogensulfate [(CH~2~)~4~SO~3~HPy][HSO~4~], a Brønsted acidic ionic liquid as a green and reusable catalyst in solvent‐free conditions. Also some new 4,4'‐(1,4‐phenylene)‐bis‐(2,6‐di‐aryl pyridine) was prepared. J. Heterocyclic Chem., (2011).
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A convenient and efficient method for the synthesis of pyrazolo [3,4-d]pyrimidin-4-ones via heterocyclization reaction of 5-amino-1H-pyrazole-4-carboxamides with triethyl orthoesters using two Brønsted-acidic ionic liquids, as efficient homogeneous catalysts under solvent-free conditions is describ
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