Analyzing the synthesis route of 72617-82-4

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,72617-82-4, its application will become more common.

Adding a certain compound to certain chemical reactions, such as: 72617-82-4, 6-(2,2,2-Trifluoroethoxy)pyridin-3-amine, 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, 72617-82-4, blongs to pyridine-derivatives compound. name: 6-(2,2,2-Trifluoroethoxy)pyridin-3-amine

EXAMPLE 3 N-[2-(2,2,2-Trifluoroethoxy)-5-pyridyl]-1,3-dithietan-2-imine 8.8 g (0.048 mol) 2-(2,2,2-Trifluoroethoxy)-5-aminopyridine and 3.50 g (0.046 mol) carbon disulphide were combined. Over 5 minutes, 4.65 g (0.046 mol) triethylamine was added, dropwise. The reaction mixture was then stirred at 70 C. for 1 hour. After this 50 ml diethyl ether was added at room temperature. The resulting crystals were separated and dried. 12.0 g (70.6% of theory) triethylammonium N-[2-(2,2,2-trifluoroethoxy)-5-pyridyl]dithiocarbamate was obtained.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,72617-82-4, its application will become more common.

Reference:
Patent; Schering Aktiengesellschaft; US4897415; (1990); A;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem