m-Chloroperbenzoic acid → 5-Bromo-2-chloro-3-(methylsulfonyl)pyridine

Using an analogous method to that described by Ponticello et al, J. Org. Chem., Vol. 44, No. 17, 1979, for the preparation of 2-chloro-3-methylsulfonylpyridine, a solution of 3-chloroperbenzoic acid (75% pure; 5 g, 22 mmol) in chloroform (50 mL) was added to a stirred solution of 5-bromo-2-chloro-3-methylthiopyridine (2.6 g, 10.9 mmol) in chloroform (50 mL) and the mixture was stirred at room temperature for 20 hours. The resultant solution was poured into a saturated aqueous sodium hydrogen carbonate solution. The organic phase was separated, washed twice with saturated aqueous sodium hydrogen carbonate solution and dried over sodium sulfate. The organic solvent was removed under reduced pressure and the residue was crystallised from a methanolic solution (20 mL). The resultant solid was filtered off and dried to afford 5-bromo-2-chloro-3-methylsulfonylpyridine (2.15 g, 73% yield); 1H NMR Spectrum: (CDCl3) 8.70 (1H, d); 8.59 (1H, d); 3.34 (3H, s); Mass Spectrum: M+H+ 270 and 272.

1. customThe organic phase was separated
2. washwashed twice with saturated aqueous sodium hydrogen carbonate solution
3. dry with materialdried over sodium sulfate
4. customThe organic solvent was removed under reduced pressure
5. customthe residue was crystallised from a methanolic solution (20 mL)
6. filtrationThe resultant solid was filtered off
7. customdried

ORDレコード

ord-576b8adf3bf249d5adefffd9ff4a04e1

出典データセット

uspto-grants-2011_01

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07868188B2