反应详情

In a screw cap vial equipped with stir bar added 3-(5-Fluoro-2-pyridyl)-5-(3-fluoro-5-(3-pyridyl)phenyl)-1,2,4-oxadiazole (100 mg, 0.30 mmol), acetonitrile (2 ml) and benzyl bromide (0.05 ml, 0.39 mmol). Stirred the resulting mixture at 90° C. for 4 h. Cooled the mixture to room temperature, concentrated in-vacuo and triturated the residue with 30% ethyl acetate in hexanes to isolate the quarternary salt. The isolated solid was dissolved in methanol (2 ml) and treated with sodium borohydride (22.6 mg, 0.60 mmol) at 0° C. The bright yellow reaction mixture was stirred at room temperature for 2 h. The reaction mixture was concentrated in-vacuo and the residue was dissolved in dichloromethane (20 ml). The organic phase was sequentially washed with water (20 ml) and brine (20 ml), dried (sodium sulfate), filtered and concentrated in-vacuo. The crude residue was purified on silica gel using 30% ethyl acetate in hexanes to isolate the title compound (10.1 mg, 8%) as yellow oil. 1H-NMR (CDCl3), δ (ppm): 8.69 (d, 1H), 8.26 (dd, 1H), 8.02 (s, 1H), 7.80 (dd, 1H), 7.60 (dt, 1H), 7.32 (m, 6H), 6.34 (m, 1H), 3.73 (s, 2H), 3.40 (bs, 2H), 2.63 (t, 2H), 2.39 (m, 2H).

1. customIn a screw cap vial
2. customequipped
3. stirringStirred the resulting mixture at 90° C. for 4 h
4. concentrationconcentrated in-vacuo
5. customtriturated the residue with 30% ethyl acetate in hexanes
6. customto isolate the quarternary salt
7. stirringThe bright yellow reaction mixture was stirred at room temperature for 2 h
8. concentrationThe reaction mixture was concentrated in-vacuo
9. dissolutionthe residue was dissolved in dichloromethane (20 ml)
10. washThe organic phase was sequentially washed with water (20 ml) and brine (20 ml)
11. dry with materialdried (sodium sulfate)
12. filtrationfiltered
13. concentrationconcentrated in-vacuo
14. customThe crude residue was purified on silica gel using 30% ethyl acetate in hexanes