Adding a certain compound to certain chemical reactions, such as: 15513-48-1, 4-Chloro-2,6-dimethyl-3-nitropyridine, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound, Product Details of 15513-48-1, blongs to pyridine-derivatives compound. Product Details of 15513-48-1
(c) 4-(4-Cyanophenyl)amino-2,6-dimethyl-3-nitropyridine A solution of 4-chloro-2,6-dimethyl-3-nitropyridine (9.80 g, 52.5 mmol) and 4-aminobenzonitrile (6.20 g, 52.5 mmol) in ethanol (160 ml) was stirred at room temperature for 16 hours. The solvent was removed under reduced pressure and the residue was dissolved in dichloromethane (200 ml), and washed with saturated aqueous sodium bicarbonate (100 ml). The organic phase was dried (MgSO4) and concentrated under reduced pressure to give a gum which was crystallized by adding ether (100 ml) and sonicating for 5 minutes.
The synthetic route of 15513-48-1 has been constantly updated, and we look forward to future research findings.
Reference:
Patent; Pfizer Inc.; US4935430; (1990); A;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem