Adding a certain compound to certain chemical reactions, such as: 36953-37-4, 4-Bromopyridin-2(1H)-one, 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, 36953-37-4, blongs to pyridine-derivatives compound. Recommanded Product: 4-Bromopyridin-2(1H)-one
Compound 41.2. 7-Bromo-[l ,2,4]triazolo[4,3-]pyridine. 4-Bromo-2- hydrazinylpyridine (compound 41.1) was suspended in formic acid (3 mL). The mixture was heated at 100 C for one hour, then upon complete reaction, the mixture cooled to room temperature. The volatile organics were removed under reduced pressure, then water (50 mL) was added to the residue. The solids that formed were filtered, washed with water and dried under reduced pressure at 50 C to give 1.68 g (90%) of the title compound as an off-white solid, m/z (ES+) 198, 200 (M+H)+.
These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,36953-37-4, its application will become more common.
Reference:
Patent; 3-V BIOSCIENCES, INC.; OSLOB, Johan D.; MCDOWELL, Robert S.; JOHNSON, Russell; YANG, Hanbiao; EVANCHIK, Marc; ZAHARIA, Cristiana A.; CAI, Haiying; HU, Lily W.; WO2014/8197; (2014); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem