Introduction of a new synthetic route about 2,6-Dibromo-4-methylpyridine

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,73112-16-0, its application will become more common.

Reference of 73112-16-0, Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps,and cheap raw materials. 73112-16-0, name is 2,6-Dibromo-4-methylpyridine. A new synthetic method of this compound is introduced below.

To a vial were added 2,6-dibromo-4-methylpyridine (121 mg, 0.482 mmol), cw-butyl 4- [l-hydroxy-l-(l,3-thiazol-2-yl)ethyl]cyclohexanecarboxylate (75 mg, 0.241 mmol), potassium carbonate (100 mg, 0.722 mmol), pivalic acid (5.59 mu, 0.048 mmol),tetrakis(triphenylphosphine)palladium(0) (11.1 mg, 9.63 mu?iotaomicronGamma) and N,N-dimethylacetamide (760 mu). The vial was sealed and placed under argon through 3 cycles of evacuation and argon flushing then reacted at 80 C overnight. The resulting mixture was cooled, diluted with ethyl acetate, filtered through a plug of CELITE and concentrated. The residue was purified by column chromatography on silica gel (0-100% ethyl acetate/hexanes) to afford racemic-cw-butyl 4- { 1 -[5-(6-bromo-4-methylpyridin-2-yl)- 1 ,3 -thiazol-2-yl]- 1 -hydroxyethyl } – cyclohexanecarboxylate.Two enantiomers were separated by chiral super critical fluid chromatography (ChiralTechnology IC-H, 2.1 x 25 cm, 5 uM, 70/30 ethanol/C02, Flow Rate: 70 mL/min, 8 min run time, WL: 220 nm). Elution was observed at 5.20 min and 6.08 min. Pooled fractions of each peak were concentrated under reduced pressure.Enantiomer 1 (retention time 5.20 min): MS ESI calc’d. for C22H29BrF3N203S [M + H+] 481 and 483, found 481 and 483.Enantiomer 2 (retention time 6.08 min): MS ESI calc’d. for C22H29BrF3N203S [M + H+] 481 and 483, found 481 and 483.

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,73112-16-0, its application will become more common.

Reference:
Patent; MERCK SHARP & DOHME CORP.; ALTMAN, Michael, D.; DI FRANCESCO, Maria Emilia; HAIDLE, Andrew, M.; OTTE, Ryan, D.; ELLIS, John Michael; CHILDERS, Kaleen Konrad; NORTHRUP, Alan, B.; YANG, Liping; WO2012/154520; (2012); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem