Abstract
The reactivity of 3-cinnamoylindole, 3-cinnamoylantipyrine and 1-(3-methyl-1-phenyl-5-pyrazolon-4-yl)-4- antipyrin-4-yl)-prop-2-ene-1 one(la-c) towards 2- aminobenzimidazole, 3-amino-1,2,4-triazole, 5-aminotetrazole monohydrate, 5-amino-3-phenylpyrazole and 3-amino-1-phenyl-2- pyrazolin-5-one to give the fused heterocycles 2a-c, 4a,b, 5a,b, 8a,b, and 10a-c has been investigated. Structures of the synthesized compounds were confirmed by both the analytical and the spectral data (IR, UV and 1H NMR).
| Original language | English |
|---|---|
| Pages (from-to) | 232-235 |
| Number of pages | 4 |
| Journal | Bollettino Chimico Farmaceutico |
| Volume | 135 |
| Issue number | 4 |
| State | Published - Apr 1996 |
| Externally published | Yes |
Keywords
- aminoazoles
- heterocycles
- pyr imidines
- pyrazolo-pyridines
- pyrimidobenzimidazoles
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