Some tips on 2-Iodopyrazine

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 2-Iodopyrazine, other downstream synthetic routes, hurry up and to see.

Reference of 32111-21-0, 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. 32111-21-0, name is 2-Iodopyrazine belongs to pyrazines compound, it is a common compound, a new synthetic route is introduced below.

4.4 ml of tetrabutylammonium fluoride (1M solution in THF) are added to a solution of 450 mg (2.18 mmol) of iodopyrazine, 647 mg (3.28 mmol) of 5-chloro-3-methoxy-2-(prop-2-ynyloxy)-pyridine (Example P7), 83 mg (0.44 mmol) of copper(l) iodide and 153 mg (0.22 mmol) of bis(triphenylphosphine)palladium dichloride (Pd(PPh3)2CI2) in 14 ml of dioxane. The reaction mixture is stirred for 3 hours at 50C under an argon atmosphere and is then allowed to cool to 20C. The solvent is removed under reduced pressure and the crude product obtained is purified by means of flash chromatography (eluant: ethyl acetate/petroleum ether 1/2). The desired title compound is obtained as a brown solid having a melting point of 142C in a yield of 510 mg (84 % of theory). Rf = 0.50 in ethyl acetate/petroleum ether 1/1;1H NMR (CDCI3): delta(ppm)= 3.89 (s, 3H); 5.29 (s, 2H); 7.08 (d, J=2.2 Hz, 1H); 7.71 (d, J=2.2 Hz, 1H); 8.48 (d, J=2.5 Hz, 1H); 8.52 (dxd, J=1.3 and 2.5 Hz, 1H); 8.66 (d, J=1.3 Hz, 1H).

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 2-Iodopyrazine, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; SYNGENTA PARTICIPATIONS AG; WO2003/104206; (2003); A2;,
Pyrazine – Wikipedia,
Pyrazine | C4H4N2 – PubChem