Category: 15862-33-6

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.15862-33-6, name is 3-Bromo-2-hydroxy-5-nitropyridine, molecular formula is C5H3BrN2O3, molecular weight is 218.99, as common compound, the synthetic route is as follows.SDS of cas: 15862-33-6

Under ice-cooling, to a solid mixture of 3-bromo-5-nitro-2-ol (21.4 mmol) and quinoline (10.7Mmol) was slowly added dropwise phosphorus oxychloride (27.8 mmol). The mixture was stirred at 120 C for 3.5 hours, cooled to to 100 C, was added 10 ml of water. The reaction was stirred vigorously in an ice water bath for 1 hour. The precipitate was collected by filtration, washed with water, and dried to give 4.15 g of the title compound. 1H-NMR (CD30D) S9.09 (lH, d, J = 2.4Hz), 8.40 (lH, d, J = 2.4Etazeta).

At the same time, in my other blogs, there are other synthetic methods of this type of compound,15862-33-6, 3-Bromo-2-hydroxy-5-nitropyridine, and friends who are interested can also refer to it.

Reference:
Patent; CHIA TAI TIANQING PHARMACEUTICALGROUP CO LTD; Beijing Centaurus Biopharma Technology Co., Ltd.; XIAO, DENGMING; LIANG, ZHI; HU, YUANDONG; HU, QUAN; ZHANG, QINGHUI; HAN, YONGXIN; WANG, HUAN; PENG, YONG; KONG, FANSHENG; LUO, HONG; (60 pag.)CN103130792; (2016); B;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 15862-33-6, name is 3-Bromo-2-hydroxy-5-nitropyridine. This compound has unique chemical properties. The synthetic route is as follows. Recommanded Product: 15862-33-6

Into a 1000 ml 3-necked round bottom flask, was placed 3-bromo-5-nitropyridin-2-ol (30 g, 137.61 mmol, 1.00 equiv). To this was added POBr3 (50 g). To the mixture was added 1,4-dioxane (500 ml). The resulting solution was allowed to react, with stirring, for 2 hours while the temperature was maintained at 110 degrees C. The reaction progress was monitored by TLC (EtOAc/PE=1:10). The crude was worked up and used for next step.

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it, 15862-33-6, 3-Bromo-2-hydroxy-5-nitropyridine.

Reference:
Patent; Synta Pharmaceuticals Corp.; Chen, Shoujun; Bohnert, Gary; Jiang, Jun; Xia, Zhiqiang; (151 pag.)US9604978; (2017); B2;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Adding a certain compound to certain chemical reactions, such as: 15862-33-6, 3-Bromo-2-hydroxy-5-nitropyridine, 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, category: pyridine-derivatives, blongs to pyridine-derivatives compound. category: pyridine-derivatives

Step 2: To a cooled (0-5 C.) mixture of 3-bromo-2-hydroxy-5-nitropyridine (47 g, 0.214 mol) and quinoline (13.7 g, 0.107 mol) was added POCl3 (26 mL, 0.278 mol) dropwise over ~10 min (the mixture was difficult to stir initially but became less viscous as the reaction progressed and the mixture warmed). After stirring at 120 C. for 3.5 h, the mixture was cooled to 100 C. and water (90 mL) was added. The resulting mixture was stirred vigorously while cooling to 0-5 C. The product was collected by filtration, washed with water and dried in vacuo at 45 C. to give 42 g of 3-bromo-2-chloro-5-nitropyridine (82% yield). 1H NMR (CD3OD) delta 9.19 (d, J=2.4 Hz, 1H), 8.93 (d, J=2.4 Hz, 1H).

At the same time, in my other blogs, there are other synthetic methods of this type of compound,15862-33-6, 3-Bromo-2-hydroxy-5-nitropyridine, and friends who are interested can also refer to it.

Reference:
Patent; H. Lundbeck A/S; US2006/79524; (2006); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem