Utilization of thiazolylacetonitriles in the synthesis of thiophene, thiazole, pyrazolo[1,5-a]pyrimidine and pyrazolo [5,1-c]triazine derivatives
โ Scribed by Abdou O. Abdelhamid; Hussein F. Zohdi; Gaber S. Mohamed
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 291 KB
- Volume
- 10
- Category
- Article
- ISSN
- 1042-7163
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โฆ Synopsis
Thiazolylcyanothioacetanilides react with โฃ-haloketones and haloesters to give the corresponding thiophene or thiazole derivatives according to the reaction conditions. Pyrazolo [1,5-a]pyrimidines and pyrazolo [5,1-c]triazines were synthesized by reaction of 3-amino-4-(4ะ-arylthiazol-2ะ-yl)-5-phenylaminopyrazole with different reagents. Structures of the new compounds were confirmed by elemental analyses, spectral data, and alternative methods of synthesis whenever possible.
๐ SIMILAR VOLUMES
## 2-Acetylbenzothiazole (1) reacts with dimethylformamide dimethylacetal (DMF-DMA) to afford the enaminone 2. Compound 2 reacts regioselectively with some nitrilimines 5a-d and nitrile oxides 6b-d to afford the novel pyrazole and isoxazole derivatives 11a-d and 12b-d, respectively, which react wi