A new synthetic route of 6-Ethylpyridin-3-amine

Statistics shows that 126553-00-2 is playing an increasingly important role. we look forward to future research findings about 6-Ethylpyridin-3-amine.

Electric Literature of 126553-00-2, With the rapid development and complex challenges of chemical substances, the synthesis of new drugs is usually one of the most effective ways to increase yield.126553-00-2, name is 6-Ethylpyridin-3-amine, molecular formula is C7H10N2, molecular weight is 122.17, as common compound, the synthetic route is as follows.

3-Amino-2-chloro-6-ethylpyridine 2 g (16.4 mmol) of 5-amino-2-ethylpyridine (for the preparation see G. H. Cooper and R. L. Rickard, J. Chem. Soc. C, 3257-60 (1971) are dissolved in 17.7 ml of concentrated HCl, and 2.2 ml (21.4 mol) of 30% strength H2 O2 solution are then carefully added. An exothermic reaction starts. The temperature is kept at about 50 C. by cooling with an ice-bath, and when the reaction has subsided the mixture is subsequently stirred at this temperature for a further 15 minutes. For working up, the mixture is poured onto 200 ml of water, the pH is brought to 10 with 40% strength sodium hydroxidde solution and the mixture is extracted twice with 100 ml of methylene chloride each time. After drying with Na2 SO4, the mixture is evaporated and the residue is stirred with petroleum ether and filtered off with suction. Yield: 1.6 g (62.3% of theory) Melting point: 104 C.

Statistics shows that 126553-00-2 is playing an increasingly important role. we look forward to future research findings about 6-Ethylpyridin-3-amine.

Reference:
Patent; Bayer Aktiengesellschaft; US4988694; (1991); A;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem