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Utilization of thiazolylacetonitriles in the synthesis of thiophene, thiazole, pyrazolo[1,5-a]pyrimidine and pyrazolo [5,1-c]triazine derivatives

โœ 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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โœฆ Synopsis


Thiazolylcyanothioacetanilides react with โฃ-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-(4ะˆ-arylthiazol-2ะˆ-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.


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Heterocyclic synthesis via enaminones: R
โœ Kamal M. Dawood; Zaghloul E. Kandeel; Ahmad M. Farag ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 164 KB ๐Ÿ‘ 2 views

## 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