The title compound 3 was obtained during the rearrangement of isoxazol-5-yl hydrazine 1 to 1 -aminopyrazolone 2 at \(115^{\circ}\). X-ray analysis of the corresponding benzylidene derivative allowed us to achieve the structure assignment.
Hypothermic and antipyretic effects of 3-methyl- and 3-phenyl-5-hydroxy-5-trichloromethyl-4,5-dihydro-1H-pyrazole-1-carboxyamides in mice
✍ Scribed by Fabiane R Souza; Vanessa T Souza; Viviane Ratzlaff; Lysandro P Borges; Marlı́ R Oliveira; Helio G Bonacorso; Nilo Zanatta; Marcos A.P Martins; Carlos F Mello
- Book ID
- 114015023
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- English
- Weight
- 159 KB
- Volume
- 451
- Category
- Article
- ISSN
- 0014-2999
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📜 SIMILAR VOLUMES
## Abstract A convenient method for the synthesis of a novel series of 11, specifically substituted, noncondensed 5,5‐bicycles 2‐[3‐phenyl‐5‐hydroxy‐5‐trichloromethyl‐4,5‐dihydro‐1H‐pyrazol‐1‐yl]‐4‐aryl‐5‐alkylthiazoles (**3a–k**; 65–94% yield) from the reactions of 3‐phenyl‐5‐hydroxy‐5‐trichlorome
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v