Abstract
2-Aminothiazolo[5,4-b]pyridines and 2-aminobenzoxazoles havebeen synthesized from 2-hydroxy-3-thioureidopyridine and 2-hydroxy-3-thioureidobenzene respectively via acid catalyzed cyclization, which were prepared by the reaction of isothiocyanates with 2-hydroxy-3-aminopyridine or 2-aminophenol. The hydroxyl group of N-(2-hydroxy-5-phenyl)-N′-phenyl thiourea reacted as nucleophile to thioureido carbon to give 2-aminobenzoxazoles, whereas that of N-(2-hydroxypyridino)-N′-phenylthiourea was reacted as leaving group upon nuclephillic sulfur of thiourea group in the presence of trifluoroacetic acid or phosphoric acid.
Original language | English |
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Pages (from-to) | 2729-2740 |
Number of pages | 12 |
Journal | Heterocycles |
Volume | 65 |
Issue number | 11 |
DOIs | |
Publication status | Published - 2005 Nov 1 |
All Science Journal Classification (ASJC) codes
- Analytical Chemistry
- Pharmacology
- Organic Chemistry