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Journal of the Chilean Chemical Society
versión On-line ISSN 0717-9707
Resumen
SHAMSUZZAMAN; SHAHEEN KHAN, MOHD y ALAM, MAHBOOB. SYNTHESIS, CHARACTERIZATION AND ANTI-MICROBIAL ACTIVITY OF NEW STEROIDAL CHOLEST-5-EN-7-ONE DERIVATIVES FUSED WITH SUBSTITUTED PYRAZOLINE RING. J. Chil. Chem. Soc. [online]. 2009, vol.54, n.4, pp. 372-374. ISSN 0717-9707. http://dx.doi.org/10.4067/S0717-97072009000400010.
The reaction of cholest-5-en-7-one (1), its 3β-acetoxy (2) and 3β-chloro (3) analogues with thiosemicarbazide in sodium ethoxide affords 2'-thiocarbamoyl-cholest [5,7-cd] pyrazoline (4), 2'-thiocarbamoyl-3β-acetoxycholest [5,7-cd] pyrazoline (5), and 2'-thiocarbamoyl-3β-chloro cholest [5,7-cd] pyrazoline (6), respectively. The structures of the newly synthesized compounds have been established on the basis of physical, analytical and spectral data. Their antibacterial activities were tested in vitro by disk diffusion assay against Gram-positive and Gram-negative bacterial strains of bacteria.
Palabras llave : thiosemicarbazide; pyrazolines; cholest-5-en-7-one; thiocarbamoyl; anti-bacterial activity.











