Month: November 2021

Driowya, M; Guillot, R; Bonnet, P; Guillaumet, G in [Driowya, Mohsine; Bonnet, Pascal; Guillaumet, Gerald] Univ Orleans, Inst Chim Organ & Analyt, UMR CNRS 7311, Orleans, France; [Guillot, Regis] Univ Paris Saclay, Univ Paris Sud, Inst Chim Mol & Mat Orsay, UMR CNRS 8182, Orsay, France published Development of Novel and Efficient Processes for the Synthesis of 5-Amino and 5-Iminoimidazo[1,2-a] imidazoles via Three-Component Reaction Catalyzed by Zirconium(IV) Chloride in 2019.0, Cited 48.0. Application In Synthesis of 3-Pyridinecarboxaldehyde. The Name is 3-Pyridinecarboxaldehyde. Through research, I have a further understanding and discovery of 500-22-1.

General and efficient approaches for the synthesis of new 5-amino and 5-iminoimidazo[1,2-a] imidazoles were developed through a three-component reaction of 1-unsubstituted 2-aminoimidazoles with various aldehydes and isocyanides mediated by zirconium(IV) chloride. The protocols were established considering the reactivity of the starting substrate, which varies depending on the presence of a substituent on the 2-aminoimidazole moiety. A library of new N-fused ring systems with wide structural diversification, novel synthetic, and potential pharmacological interest was obtained in moderate to good yields.

Application In Synthesis of 3-Pyridinecarboxaldehyde. About 3-Pyridinecarboxaldehyde, If you have any questions, you can contact Driowya, M; Guillot, R; Bonnet, P; Guillaumet, G or concate me.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

Formula: C6H5NO. I found the field of Chemistry very interesting. Saw the article Design and synthesis of novel sugar-based nitrogen-containing heterocycles as potential anticancer agents under microwave in water published in 2019.0, Reprint Addresses Du, K (corresponding author), Shaoxing Univ, Sch Chem & Chem Engn, Shaoxing 312000, Peoples R China.; Zheng, H (corresponding author), Hangzhou Normal Univ, Coll Mat Chem & Chem Engn, Hangzhou 310016, Zhejiang, Peoples R China.. The CAS is 500-22-1. Through research, I have a further understanding and discovery of 3-Pyridinecarboxaldehyde.

A series of novel glycosyl nitrogen-containing heterocycles derivatives were designed and synthesized. With the help of microwave, the reaction was carried out in water rapidly and afforded the target compounds in good yields. The acid catalysts that were essential for this kind of reaction under traditional heating method were avoided through this strategy. Preliminary biological evaluation showed that most of the compounds could inhibit the growth of A549 cells, but the inhibition of HepG-2 cells was relatively poor. Notably, compound 2i displayed the best potency with an IC50 value of 3.42 mu M against A549 cell lines, which is comparable with the common anticarcinogen paclitaxel (5.12 mu M). Molecular modeling studies suggested that 2i may bind to the ATP-binding site of epidermal growth factor receptor (EGFR), indicating a rational design strategy. These results provide a starting point for designing glycosyl nitrogen-containing heterocycles as the potential drugs in lung cancer therapy.

Formula: C6H5NO. About 3-Pyridinecarboxaldehyde, If you have any questions, you can contact Liu, J; Wu, CL; Jin, HM; Du, K; Zheng, H or concate me.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem