Electric Literature of 82454-61-3 ,Some common heterocyclic compound, 82454-61-3, molecular formula is C7H6N2, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc., below Introduce a new synthetic route.
Copper (I) iodide (4.22 mg, 0.022 mmol) was added to a stirred mixture of 1-6 (1 g, 2.22 mmol), 5-ethynyl-2-pyridinamine (523.68 mg, 4.43 mmol), TEA (924.23 jiL, 6.65 mmol), PdC12(PPh3)2 (31.11 mg, 0.044 mmol) and PPh3 (11.63 mg, 0.044 mmol) in DMF (10 mL). The mixture was purged with N2 for 5 mm and then it was stirred at 90°C for 5 h. The residue was diluted with water and extracted with EtOAc. The organic layer was separated, dried (Na2SO4), filtered and concentrated in vacuo. The crude product was purified by flash column chromatography (silica; MeOH/DCM 0/100 to 05/95). The desired fractions were collected and concentrated in vacuo to yield P-3 (923 mg, 92percent).
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. 82454-61-3, 5-Ethynylpyridin-2-amine, other downstream synthetic routes, hurry up and to see.
Reference:
Patent; JANSSEN PHARMACEUTICA NV; ANDRES-GIL, Jose, Ignacio; VAN GOOL, Michiel, Luc, Maria; BORMANS, Guy, Maurits, R; VERBEEK, Joost; (42 pag.)WO2017/103182; (2017); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem