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Arzneimittelforschung ; 49(12): 1006-11, 1999 Dec.
Article in English | MEDLINE | ID: mdl-10635446

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-(alpha-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.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/chemical synthesis , Thiazoles/chemical synthesis , Triazoles/chemical synthesis , Animals , Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Anti-Inflammatory Agents, Non-Steroidal/toxicity , Carrageenan , Edema/chemically induced , Edema/prevention & control , Female , Magnetic Resonance Spectroscopy , Male , Mice , Stomach Ulcer/chemically induced , Stomach Ulcer/pathology , Thiazoles/pharmacology , Thiazoles/toxicity , Triazoles/pharmacology , Triazoles/toxicity
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