Extended knowledge of 2-Bromo-3,5-dimethylpyridine

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 92992-85-3, 2-Bromo-3,5-dimethylpyridine.

Application of 92992-85-3, The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 92992-85-3, name is 2-Bromo-3,5-dimethylpyridine. This compound has unique chemical properties. The synthetic route is as follows.

Example 166 2-[2-(3,5-dimethylpyridin-2-yl)-5,8-dioxo-6-(propan-2-yl)-5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a]pyrrolo[3,4-d]pyrimidin-4-yl]-N-(5-fluoropyridin-2-yl)acetamide . A mixture of 2-bromo-3,5-dimethylpyridine (64 mg, 345 muetaetaomicronIota) and hexamethylditin (72 muIota, 350 muetaetaomicronIota) in 1,4-dioxane (3 ml) was degassed with a stream of nitrogen, then tetrakis(triphenylphosphine)palladium(0) (12 mg, 10.8 muetaetaomicronIota) was added. The reaction was subjected to microwave irradiation at 1 10 C for 2h. 2-[2-Bromo-5,8-dioxo-6-(propan-2-yl)-5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a]pyrrolo[3,4-d]pyrimidin-4-yl]-N-(5-fluoropyridin-2-yl)acetamide (100 mg, 216 muetaetaomicronIota) (example 75) was added, and the reaction irradiated at 1 10C for a further 2h. KF and celite (1 :1 mixture, 250 mg) were added, and the solution stirred for one hour, before being filtered, washing with ethyl acetate/methanol, and concentrated under reduced pressure. The crude mixture was taken up in toluene (3 ml), and degassed with a stream of N2 for 5mins. Tetrakis(triphenylphosphine)palladium(0) (12 mg, 10.8 muetaetaomicronIota) was added, and the reaction irradiated to 120C in the microwave for 1 h, the irradiation was then repeated until conversion was complete. KF and celite (1 :1 mixture, 250 mg) were added, and the solution stirred for one hour, before being filtered, washing with ethyl acetate/methanol, and concentrated under reduced pressure. The crude material was purified by preparative HPLC, then further purified by trituration from MeCN to afford 27.7 mg (26% yield) of the title compound as an off-white powder. 1H NMR (500 MHz, Chloroform-d) delta [ppm] 1.34 (d, 6H), 2.35 (s, 3H), 2.75 (s, 3H), 4.39 (s, 2H), 4.51 – 4.64 (m, 1H), 5.46 (s, 2H), 6.95 (s, 1H), 7.37 – 7.44 (m, 2H), 8.09 – 8.17 (m, 2H), 8.33 (s, 1H), 8.91 (s, 1H). LC-MS (Analytical Method F) Rt = 2.30 min; MS (ESIpos): m/z = 490 [M+H]+.

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 92992-85-3, 2-Bromo-3,5-dimethylpyridine.

Reference:
Patent; BAYER AKTIENGESELLSCHAFT; BAYER PHARMA AKTIENGESELLSCHAFT; KOPPITZ, Marcus; SIEBENEICHER, Holger; BRAeUER, Nico; POOK, Elisabeth; ROTGERI, Andrea; NEUHAUS, Roland; FISCHER, Oliver, Martin; NAGEL, Jens; DAVENPORT, Adam, James; CARR, James, Lindsay; TOWNSEND, Robert, James; CONNELLY URSINYOVA, Nina; PARROTT, Shelley, Anne; (471 pag.)WO2019/81343; (2019); A1;,
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