Sources of common compounds: 3-Iodo-2-nitropyridine

Statistics shows that 54231-34-4 is playing an increasingly important role. we look forward to future research findings about 3-Iodo-2-nitropyridine.

Application of 54231-34-4, 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.54231-34-4, name is 3-Iodo-2-nitropyridine, molecular formula is C5H3IN2O2, molecular weight is 249.99, as common compound, the synthetic route is as follows.

A mixture of 3-iodo-2-nitropyridine (2 g, 8 mmol), (4-chlorophenyl)boronic acid (1.5 g, 9.6 mmol), Na2CO3 (1.7 g, 16 mmol) and Pd(PPh3)4(277 mg, 0.24 mmol) in dioxane (20 mL) and water (10 mL) was degassed with nitrogen, heated to 110 C. and stirred for 18 hours under nitrogen atmosphere. The reaction was cooled to r.t, filtered and concentrated in vacuo. The residue was diluted with water, extracted with EA. The combined organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography (Petroleum ether/EtOAc=3:1) to give 3-(4-chlorophenyl)-2-nitropyridine (1.4 g, 75% yield) as a yellow solid. LC/MS (ESI, m/z): [M+1]+=234.6.

Statistics shows that 54231-34-4 is playing an increasingly important role. we look forward to future research findings about 3-Iodo-2-nitropyridine.

Reference:
Patent; Kymera Therapeutics, Inc.; Ji, Nan; Kluge, Arthur F.; Weiss, Matthew M.; Zhang, Yi; (180 pag.)US2020/10468; (2020); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem