Synthesis of substituted imidazo[1,2-b]-1,2,4-triazolo[4,3-d]-1,2,4-triazepine and 4H-imidazo[1,2-b]-1,2,4-triazino[4,3-d]-1,2,4-triazepin-7-one
β Scribed by V. P. Kruglenko; M. V. Povstyanoi; N. A. Klyuev; V. A. Idzikovskii
- Publisher
- Springer US
- Year
- 1997
- Tongue
- English
- Weight
- 75 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0009-3122
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π SIMILAR VOLUMES
Substituted 5H-imidazo[l,2-b]-l,2,4-triazepin-4-ones react with alkyl (alkenyl) halides, 2-chloroethanol, glycerin dichlorohydrin, haloacetic acids, the methyl ester and amide of menochloroacetic acid in a methanol-sodium methylate system to form N(s)-alkylation products, and with hydroxylamino-O-su
## 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.