Gemini basic ionic liquid as bi-functional catalyst for the synthesis of 2,3-dihydroquinazolin-4(1H)-ones at room temperature
[Display omitted] •Bi-functional nature of the ionic liquid as catalyst cum solvent.•Another benefit of the present strategy is avoiding conventional organic solvents.•First room temperature protocol from 2-aminobenzonitriles and carbonyls.•Some challenging aromatic ketones were utilized as substrat...
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Veröffentlicht in: | Tetrahedron letters 2020-03, Vol.61 (10), p.151587, Article 151587 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | [Display omitted]
•Bi-functional nature of the ionic liquid as catalyst cum solvent.•Another benefit of the present strategy is avoiding conventional organic solvents.•First room temperature protocol from 2-aminobenzonitriles and carbonyls.•Some challenging aromatic ketones were utilized as substrates for the first time.
A cascade synthesis of 2,3-dihydroquinazolin-4(1H)-ones has been developed from 2-aminobenzonitriles and carbonyl analogues using Gemini basic ionic liquid as green catalyst cum solvent at room temperature. Both aldehydes and ketones were condensed with 2-aminobenzonitriles affording good to excellent yields of products. Moreover, the ionic liquids can be reused up to 5th cycle without significant loss of catalytic activity. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/j.tetlet.2019.151587 |