Regioselective synthesis of some novel pyrazoles, isoxazoles, pyrazolo[3,4-d]pyridazines and isoxazolo[3,4-d]pyridazines pendant to benzimidazole
β Scribed by Mohamed R. Shaaban; Ahmad M. Farag; Tamer S. Saleh; Fayez H. Osman
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2007
- Tongue
- English
- Weight
- 383 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
β¦ Synopsis
The latter compound reacts regioselectively with some nitrilimines and nitrile oxides to afford the corresponding pyrazole and isoxazole derivatives, respectively. These reaction products react with hydrazine hydrate to give the novel pyrazolo [3,4-d]pyridazine and isoxazolo [3,4-d]pyridazine derivatives, respectively.
π SIMILAR VOLUMES
## Abstract Reactions of the pyridazine derivatives **1aβc** with phenyl isothiocyanate followed by heterocyclization with ethyl chloroacetate gave the thiazolidinone derivatives **6aβc**. The reactivity of **6a** towards some chemical reagents was studied. Β© 2002 Wiley Periodicals, Inc. Heteroatom
## Abstract magnified image 4βAcetylβ5βmethylβ1βphenylβ1__H__βpyrazole reacts with dimethylformamide dimethylacetal (DMFβDMA) to afford the corresponding (__E__)1β(5βmethylβ1βphenylβ1__H__βpyrazolβ4βyl)β3β(__N,N__βdimethylamino)β2βpropenβ1βone. The latter product undergoes regioselective 1,3βdipol