Brief introduction of 5-Aminopyrazine-2-carbonitrile

The synthetic route of 5-Aminopyrazine-2-carbonitrile has been constantly updated, and we look forward to future research findings.

Synthetic Route of 113305-94-5, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 113305-94-5, name is 5-Aminopyrazine-2-carbonitrile belongs to pyrazines compound, it is a common compound, a new synthetic route is introduced below.

A solution of (R)-tert-butyl 2-((2-chloro-5-(4-methoxyphenyl)pyridin-4- ylamino)methyl)morpholine-4-carboxylate (0.036 g, 0.083 mmol), 2-amino-4- cyanopyrazine (0.014 g, 0.116 mmol), Xantphos (0.008 g, 0.013 mmol), cesium carbonate (0.054 g, 0.166 mmol), tris(dibenzylideneacetone)dipalladium chloroform complex (0.007 g, 0.008 mmol) in dioxane (0.7 ml_) was stirred at room temperature under nitrogen for 10 min, then heated under microwave irradiation for 60 min at 150 0C. The reaction mixture was purified by ion exchange on SCX-II acidic resin (1 g), eluting with methanol / dichloromethane (1 / 1) then 2M ammonia-methanol. The basic fractions were combined and solvent was removed in vacuo. The crude product was purified by preparative thin layer chromatography, eluting with ethyl acetate / hexane (1 / 1), to give the title compound as a yellow solid (0.014 g, 32%).1H NMR (CDCI3, 500 MHz) delta 8.82 (s, 1H), 8.46 (s, 1H), 7.79 (s, 1H), 7.31 (d, 2H, J = 8.7 Hz), 7.06 (s, 1 H), 7.03 (d, 2H, J = 8.7 Hz), 5.01 (t, 1 H, J = 5.3 Hz), 3.85 (s, 3H), 3.86-3.84 (m, 1H), 3.74-3.64 (m, 1H), 3.30-3.50 (m, 1H), 3.26-3.17 (m, 2H), 2.99 (d, 1 H, J = 13.7 Hz), 2. 86 (2H, d, J = 6.9 Hz), 2.73-2.63 (m, 1 H). LCMS (4) Rt = 2.17 min; m/z (ESI+) 518 [MH+].

The synthetic route of 5-Aminopyrazine-2-carbonitrile has been constantly updated, and we look forward to future research findings.