Synthesis of 1,2,4-Triazolo[4,3-d][1,2,4]Triazepines By 1,3-Dipolar Cycloaddition
β Scribed by M. El Messaoudi; A. Hasnaoui; M. El Mouhtadi; J.-P. Lavergne
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2010
- Weight
- 330 KB
- Volume
- 101
- Category
- Article
- ISSN
- 0037-9646
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β¦ Synopsis
Abstract
The reaction of NβarylβCβethoxycarbonyl nitrilimines with [1,2,4]triazepinβ3,5βdithione leads to title compounds. The 1,3βdipolar cycloaddition is completely peri and regioselective. The preferred orientation of addition is predicted correctly by AM~1~ calculation.
π SIMILAR VOLUMES
In some foregoing communications"'. we reported the synthesis and anorectic activity of some thiazolo-and thiazinoperimidine derivatives. As an extension of our study in this series, we wish now to describe the method of fusing a 1,2,4-triazole component onto the perimidine nucleus. Theoretically, t