Research on new synthetic routes about 22047-25-2

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Adding a certain compound to certain chemical reactions, such as: 22047-25-2, name is Acetylpyrazine, belongs to Pyrazines compound, 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 22047-25-2, Formula: C6H6N2O

General procedure: A 100 mL round-bottom flask charged with 2-acetylpyrazine (1.47 g, 2 mmol) was added MeOH (30 mL), KOH pellets (0.675 g,2 mmol) and water (2 mL). The resulting mixture was stirred for10 min and then added corresponding n,n?-dimethoxybenzaldehydes (1.0 g, 1 mmol) and ammonium solution (6 mL) was added slowly stirring at room temperature for 4 h, a white precipitate obtained was filtered, washed with MeOH and diethyl ether. The crude products on recrystallization in a mixture of CHCl3:MeOH (1:1) gave white crystals of desired compounds, 1-4. 2,2?-[4-(2,3-dimethyoxyphenyl)pyridine-2,6-diyl]dipyrazine(1): Yield: 65%; M.P.: 212 C; 1H NMR (400 MHz, CDCl3, delta ppm): 3.737 (s, 3H, OCH3), 3.945 (s, 3H, OCH3), 7.041e7.045 (d, 1H, ArHC4),7.114e7.119 (d, 1H, ArHC6), 7.134e7.165 (t, 1H, ArHC5), 8.635-8.650(t, 4H, pz, HAA’5,6), 8.683 (s, 2H, pz, HAA’3), 9.869-9.871 (s, 2H, py,HB3,5); 13C{1H} NMR (100 MHz, CDCl3, delta ppm): 153.84 (C2,6 of py),151.02 (C4 of py), 148.73 (C3,30 of pz), 144.58 (C6,60 of pz), 143.57(C5,50 of pz), 133.59 (C6 of ph), 122.11 (C1 of ph), 122.04 (C3,5 of py),110.77 (C5 of ph), 101.31 (C3 of ph), 61.06 (OCH3), 55.08 (OCH3); FTIR (KBr disc, nu cm-1): 2965 (w), 1739 (s), 1588 (m), 1465 (s), 1415(m), 1365 (s), 1270 (s), 1220 (m), 1109 (s), 1053 (s), 1003 (s), 852 (s),786 (s).

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Reference:
Article; Golla, Ramesh; Kumar, P. Raghavendra; Suchethan; Foro, Sabine; Nagaraju; Journal of Molecular Structure; vol. 1201; (2020);,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem