Abstract
Thiazolo[3,2-b]-1,2,4-triazole-5(6H)-ones (4-10) were obtained in a one step synthesis by heating 3-aryl-5-mercapto-1,2,4-triazoles (3a-d) with chloroacetic acid and appropriate aromatic aldehyde in acetic acid and acetic anhydride in the presence of anhydrous NaOAc. Michael type addition of cyclic secondary amines (N-methylpiperazine, piperidine) to 4-10 gave 2-phenyl-6- (α-aminoarylmethyl)thiazolo[3,2-b]-1,2,4-triazole-5-ols (4a-10b). The structures of the compounds were confirmed by spectral and elementary analysis. The compounds synthesized in previous and present studies were investigated for their anti-inflammatory activities.
| Original language | English |
|---|---|
| Pages (from-to) | 1006-1011 |
| Number of pages | 6 |
| Journal | Arzneimittel-Forschung/Drug Research |
| Volume | 49 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 1999 |
Keywords
- 6-(α-Aminoarylmethyl)thiazolo[3,2,b]-1,2,4-triazole-5-ols
- Thiazolo[3,2- b]-1,2,4-triazole-5(6H)-ones, anti-inflammatory activity, synthesis
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