Sources of common compounds: 67625-36-9

At the same time, in my other blogs, there are other synthetic methods of this type of compound,67625-36-9, Ethyl 5-chloroimidazo[1,2-a]pyridine-2-carboxylate, and friends who are interested can also refer to it.

Adding a certain compound to certain chemical reactions, such as: 67625-36-9, Ethyl 5-chloroimidazo[1,2-a]pyridine-2-carboxylate, 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, Recommanded Product: Ethyl 5-chloroimidazo[1,2-a]pyridine-2-carboxylate, blongs to pyridine-derivatives compound. Recommanded Product: Ethyl 5-chloroimidazo[1,2-a]pyridine-2-carboxylate

Step 2. 5-Chloro-imidazo[1 ,2-a]pyridine-2-carboxylic acid ethyl ester (11.2 g) in concentrated hydrochloric acid (50 mL) and dioxane (50 ml_) was stirred under reflux overnight. The resulting solution was condensed under vacuum, washed with acetone and dried to obtain a solid, delta-chloro-imidazo?^-ajpyridine^-carboxylic acid (6.7 g). LCMS (m/z): 197.2.

At the same time, in my other blogs, there are other synthetic methods of this type of compound,67625-36-9, Ethyl 5-chloroimidazo[1,2-a]pyridine-2-carboxylate, and friends who are interested can also refer to it.

Reference:
Patent; HIGH POINT PHARMACEUTICALS, LLC; MJALLI, Adnan, M.M.; HARI, Anitha; GADDAM, Bapu; GOHIMUKKULA, Devi, Reddy; POLISETTI, Dharma, R.; EL ABDELLAOUI, Hassan; RAO, Mohan; ANDREWS, Robert, C.; XIE, Rongyuan; REN, Tan; WO2010/126745; (2010); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem