Analyzing the synthesis route of 72093-07-3

Statistics shows that 72093-07-3 is playing an increasingly important role. we look forward to future research findings about 5-Chloro-2-methylpyridine.

Reference of 72093-07-3, 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.72093-07-3, name is 5-Chloro-2-methylpyridine, molecular formula is C6H6ClN, molecular weight is 127.57, as common compound, the synthetic route is as follows.

To a solution of 5-chloro-2-methylpyridine (Step A, 1.1 g, 8.7 mmol) in 15 mL anhydrous ether was added phenyl lithium (1.8 M in cyclohexane/ether, 7.2 mL, 13 mmol) at 0C, and the reaction was stirred at room temperature for 30 min. The resulting mixture was cooled back to 0C, and was added (LR, 2R)-1-phenylpropylene oxide (2.3 g, 17 mmol), and the reaction was allowed to warm to room temperature overnight. The reaction mixture was partitioned between EtOAc (100 mL) and water (100 mL). The organic layer was separated and the aqueous layer extracted with EtOAc (2 x 100 mL). The combined organic extracts were dried over anhydrous MGS04, filtered, and concentrated to dryness, and the residue was purified by flash column chromatography on silica gel eluted with 10 to 40% EtOAc in hexane to afford the title compound. 1H NMR (500 MHz, CD30D) : 8 8.28 (d, 1H), 7.59 (dd, 1H), 7.25-7. 12 (m, 5H), 7.05 (d, 1H), 4.03 (m, 1H), 3.29 (dd, 1H), 3.19 (dd, 1H), 3.12 (m, 1H), 1.12 (d, 3H).

Statistics shows that 72093-07-3 is playing an increasingly important role. we look forward to future research findings about 5-Chloro-2-methylpyridine.

Reference:
Patent; MERCK & CO., INC.; WO2004/48317; (2004); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem