Iodine → 2-Chloro-5-fluoro-4-iodopyridine

Temperature

-75 °C

A tetrahydrofuran (5 ml) solution containing 2-chloro-5-fluoropyridine (500 mg) was added to a tetrahydrofuran (20 ml) solution containing lithium-N,N-diisopropylamide (2M tetrahydrofuran/ethylbenzene/heptane solution) (2.9 ml) at −75° C. in a nitrogen atmosphere, followed by stirring at −75° C. for 3 hours. Subsequently, a tetrahydrofuran (5 ml) solution containing iodine (1.16 g) was added, followed by stirring at −75° C. for 1 hour. Then, water/tetrahydrofuran (2 ml/8 ml), water (10 ml), and 3M aqueous sodium thiosulfate were slowly added at −75° C., −50° C., and −35° C., respectively, to the reaction solution. The reaction solution was adjusted to room temperature, followed by extraction with ethyl acetate. The resultant was washed with saturated saline and dried over anhydrous sodium sulfate. Thereafter, the solvent was distilled away under reduced pressure, the obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate=20:1 to 10:1), and a white solid of 2-chloro-5-fluoro-4-iodopyridine (457 mg) was thus obtained.

1. additionwas added
2. stirringby stirring at −75° C. for 1 hour
3. custom−35° C.
4. customwas adjusted to room temperature
5. extractionfollowed by extraction with ethyl acetate
6. washThe resultant was washed with saturated saline
7. dry with materialdried over anhydrous sodium sulfate
8. distillationThereafter, the solvent was distilled away under reduced pressure
9. customthe obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate=20:1 to 10:1)

ORD record

ord-5182960f4d534d159d4c9f8191ae7e02

Source dataset

uspto-grants-2014_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08809371B2