Adding a certain compound to certain chemical reactions, such as: 59207-23-7, 2-Methylthieno[3,2-c]pyridin-4(5H)-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, 59207-23-7, blongs to pyridine-derivatives compound. Application In Synthesis of 2-Methylthieno[3,2-c]pyridin-4(5H)-one
7-bromo-2-methyIthieno [3,2-cl pyridin-4(5//)-one; To a solution of 2-methylthieno [3,2- c]pyridin-4(5H)-one (4.84 g, 28.9 mmol) in acetic acid (84.0 mL) is added bromine drop wise (1.64 mL, 31.8 mmol). The reaction mixture is heated to reflux for one hour. After one hour, the solution is cooled to rt, and water is added until a solid is formed. The remaining solid is filtered, rinsed with water, and dried under vacuum to afford the title compound (6.01 g, 85% yield). 1H NMR delta 11.7 (br s, IH), 7.47 (s, IH), 7.30 (s, IH), 3.38 (s, 3H). LCMS (ES, M+H=245).
These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,59207-23-7, its application will become more common.
Reference:
Patent; ASTRAZENECA AB; ASTRAZENECA UK LIMITED; WO2006/106326; (2006); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem