Hydrazone

About: Hydrazone is a research topic. Over the lifetime, 4853 publications have been published within this topic receiving 65160 citations. The topic is also known as: hydrazone.

Divergent Synthesis of 1H-Indazoles and 1H-Pyrazoles from Hydrazones via Iodine-Mediated Intramolecular Aryl and sp3 C–H Amination

Abstract: A divergent intramolecular C−H amination of hydrazones has been developed employing molecular iodine (I2) as the sole oxidant. The required hydrazone substrates were readily obtained by condensation of hydrazines with the corresponding ketones. In the presence of potassium iodide, I2-mediated oxidative cyclization of diaryl and tert-butyl aryl ketone hydrazones produced 1H-indazoles via direct aryl C−H amination. Under similar reaction conditions, primary and secondary alkyl ketone hydrazones were transformed into 1H-pyrazole products in a reaction involving sp3 C−H amination. This synthetic methodology does not involve transition metals, and is operationally simple, providing facile access to indazole and pyrazole derivatives in an efficient and scalable fashion.

Detection of hydrazine compounds in gaseous samples by their conversion to nitric oxide-yielding derivatives

Abstract: Disclosed is a method and apparatus for detecting hydrazine, monomethylhydrazine (MMH), and unsymmetrical dimethylhydrazine (UDMH) in a gaseous sample. The hydrazine compound detector includes a sample converter wherein vapors of an aldehyde such as acetaldehyde or a ketone such as acetone are mixed with a sample in gaseous form, and the mixture is allowed to react to form azine and hydrazone derivatives of the aldehyde or ketone. The derivatives may be transported long distances and then analyzed, as by heating in the presence of an oxidant in a pyrolyzer containing a nickel surface to produce nitric oxide (NO), followed by measurement of the NO in a NO detector such as a chemiluminescent analyzer.

Identification of bisindolylmethane–hydrazone hybrids as novel inhibitors of β-glucuronidase, DFT, and in silico SAR intimations

Abstract: The present study involves the synthesis of bisindolylmethane–hydrazone hybrids, 1–30, in a three-step reaction sequence, followed by evaluation against β-glucuronidase enzyme. The IC50 values for the potent compounds were in the range from 0.10 to 83.50 μM. Compound, a trihydroxy analog was found to be the most potent derivative, having an IC50 value of 0.10 ± 0.001 μM. Molecular docking revealed that the active compounds could fit perfectly into the binding groove of β-D-glucuronidase. The presence of hydroxyl groups on the aromatic side chain proved to be the single most important factor that contributed toward the inhibitory potential of these compounds. On the other hand, the imino group of the hydrazone linkage displayed interactions with the side chain carboxyl oxygen (Oe2) of Asp207. The high inhibitory potential of these compounds could be associated with these strong hydrogen bonds. Structures of all the synthesized compounds were confirmed using modern spectroscopic methods.