A single-step preparation of thiazolo[5,4-b]pyridine- and thiazolo[5,4-c]pyridine derivatives from chloronitropyridines and thioamides, or thioureas
A one‐step synthesis of thiazolo[5,4‐b]pyridines from an appropriately substituted chloronitropyridine and thioamide, or thiourea, is presented. In particular, the reaction was used to prepare a large number of 6‐nitrothiazolo[5,4‐b]pyridine derivatives, bearing hydrogen, alkyl, substituted alkyl, c...
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Veröffentlicht in: | Journal of heterocyclic chemistry 2009-11, Vol.46 (6), p.1125-1131 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | A one‐step synthesis of thiazolo[5,4‐b]pyridines from an appropriately substituted chloronitropyridine and thioamide, or thiourea, is presented. In particular, the reaction was used to prepare a large number of 6‐nitrothiazolo[5,4‐b]pyridine derivatives, bearing hydrogen, alkyl, substituted alkyl, cycloalkyl, aryl, heteroaryl, and amine substituents at the 2‐position. The reaction could also be extended to produce a thiazolo[4,5‐c]pyridine derivative and thiazolo[5,4‐b]pyridines with alternative substituents on the pyridinoid ring. J. Heterocyclic Chem., (2009). |
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ISSN: | 0022-152X 1943-5193 |
DOI: | 10.1002/jhet.185 |