17064-83-4Relevant academic research and scientific papers
Synthesis, antiprotozoal activity, and cheminformatic analysis of 2-phenyl-2h-indazole derivatives
Aguilera-Perdomo, Jacobo David,Cortés-Benítez, Francisco,Cortés-Gines, Miguel,Del Angel, Kevin Samael Olascoaga,Pérez-Villanueva, Jaime,Palacios-Espinosa, Juan Francisco,Quintana-Salazar, Edgar A.,Rodríguez-Villar, Karen,Soria-Arteche, Olivia,Yépez-Mulia, Lilián
, (2021/05/28)
Indazole is an important scaffold in medicinal chemistry. At present, the progress on synthetic methodologies has allowed the preparation of several new indazole derivatives with interesting pharmacological properties. Particularly, the antiprotozoal activity of indazole derivatives have been recently reported. Herein, a series of 22 indazole derivatives was synthesized and studied as antiprotozoals. The 2-phenyl-2H-indazole scaffold was accessed by a one-pot procedure, which includes a combination of ultrasound synthesis under neat conditions as well as Cadogan’s cyclization. Moreover, some compounds were derivatized to have an appropriate set to provide structure-activity relationships (SAR) information. Whereas the antiprotozoal activity of six of these compounds against E. histolytica, G. intestinalis, and T. vaginalis had been previously reported, the activity of the additional 16 compounds was evaluated against these same protozoa. The biological assays revealed structural features that favor the antiprotozoal activity against the three protozoans tested, e.g., electron withdrawing groups at the 2-phenyl ring. It is important to mention that the indazole derivatives possess strong antiprotozoal activity and are also characterized by a continuous SAR.
Exceptional effect of nitro substituent on the phosphonation of imines: The first report on phosphonation of imines to α-iminophosphonates and α-(N-phosphorylamino)phosphonates
Motevalli, Somayeh,Iranpoor, Nasser,Etemadi-Davan, Elham,Moghadam, Khashayar Rajabi
, p. 100070 - 100076 (2015/12/04)
A novel and chemoselective method is reported for the simple phosphonation of imines. By change of the electronic effects of the substituents, this method offers the selective synthesis of either α-iminophosphonates or α-(N-phosphorylamino)phosphonates. The mild reaction condition makes this protocol very attractive for synthesis of these two classes of phosphorous compounds.
Regioselective synthesis of 2 H-indazoles using a mild, one-pot condensation-cadogan reductive cyclization
Genung, Nathan E.,Wei, Liuqing,Aspnes, Gary E.
supporting information, p. 3114 - 3117 (2014/06/23)
An operationally simple and efficient one-pot synthesis of 2H-indazoles from commercially available reagents is reported. Ortho-imino-nitrobenzene substrates, generated via condensation, undergo reductive cyclization promoted by tri-n-butylphosophine to afford substituted 2H-indazoles under mild reaction conditions. A variety of electronically diverse ortho-nitrobenzaldehydes and anilines were examined. To further extend the scope of the transformation, aliphatic amines were also employed to form N2-alkyl indazoles selectively under the optimized reaction conditions.
