Reactions of Triacetonamine Part II, Synthesis of Novel Pyrazolo(4,3-c)pyridine Derivatives, and 2-(Piperidin-4-ylidene)hydrazinecarbothioamide Derivatives Derived From 2,2,6,6-Tetramethyl-piperidin-4-one for In vitro Anticancer Evaluation

Mahmoud NM Yousif; Ahmed A Fayed; Nabil M Yousif

Abstract

Reactions of Triacetonamine Part II, Synthesis of Novel Pyrazolo(4,3-c)pyridine Derivatives, and 2-(Piperidin-4-ylidene)hydrazinecarbothioamide Derivatives Derived From 2,2,6,6-Tetramethyl-piperidin-4-one for In vitro Anticancer Evaluation

Author(s): Mahmoud NM Yousif, Ahmed A Fayed, Nabil M Yousif

2,2,6,6-Tetramethylpiperidin-4-one reacts with 2 moles of aromatic aldehydes and thiosemicarbazide or semicarbazide hydrochloride in different conditions to afford piperidine derivatives 1a-f and pyrazolo(4,3-c)pyridine derivatives 2a-f. Pyrazolo[4,3-c]pyridine-2-carbothioamide derivative 2b reacts with benzophenone, 4-cholorobenzophenone, and 4-bromobenzophenone to give 5-(pyrazolo[4,3-c]pyridine-2-yl) thiazole derivatives 3a-c. Piperidine derivative 1b reacts with acetic anhydride to afford compounds 4a-b. Pyrazolo(4,3-c)pyridine derivative 2c reacts with acetic anhydride to afford compounds 5a-b. Hydrazinecarbothioamide derivative 1a reacts with benzoin and benzoin oxime to give compounds 6, and 7 respectively. Anticancer evaluation of some of synthesized compounds is reported.

Full-Text PDF

Select your language of interest to view the total content in your interested language