6-Bromo-2-methylpyridine-3-carboxaldehyde

39919-65-8

68-12-2

926293-55-2

General procedure for the synthesis of 6-bromo-2-methylnicotinic aldehyde from 2,5-dibromo-6-methylpyridine and N,N-dimethylformamide: To a solution of 3,6-dibromo-2-methylpyridine (60 g, 239 mmol) in tetrahydrofuran (THF, 600 mL) under nitrogen protection was slowly added at -78°C n-butyllithium (n-BuLi, 100 mL. 251 mmol). The reaction mixture was stirred continuously at -78 °C for 1 hour. Subsequently, N,N-dimethylformamide (DMF, 20.4 mL, 263 mmol) was added dropwise and stirring was continued at -78 °C for 1 hour. The reaction mixture was slowly warmed to 25 °C and the reaction was quenched by the addition of 1 M aqueous hydrochloric acid (300 mL). This reaction mixture was combined and processed with five other parallel reactions (30 g, 120 mmol and 4 x 50 g, 199 mmol of 3,6-dibromo-2-methylpyridine, respectively, maintaining the same reagent and solvent ratios). The combined reaction mixtures were extracted with ethyl acetate (EtOAc, 800 mL × 4), and the combined organic layers were washed with deionized water (H2O, 300 mL × 3), dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure to afford the target product, 6-bromo-2-methylnicotinic aldehyde (260 g, 492 mmol, 42.5% combined yield), as a red oil The product was analyzed by NMR hydrogen spectroscopy. The product was confirmed by nuclear magnetic resonance hydrogen spectroscopy (1H NMR, 400 MHz, chloroform-d): δ10.28 (s, 1H), 7.92 (d, J=7.9 Hz, 1H), 7.64 (s, 1H), 2.88-2.83 (m, 3H). Liquid chromatography-mass spectrometry (LCMS) analysis showed [M+H]+ peaks at m/z = 200.1 and 202.1.