反应详情

温度

150 °C

To a 10 mL microwave vial is added 6-bromo-5-(2-fluoro-4-nitrophenoxy)-1-methyl-1H-indazole (500 mg, 1.37 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (73 mg, 123 μmol) and Pd2(dba)3 (38 mg, 41 μmol). The mixture is suspended in toluene (5 mL, 47 mmol) and benzophenone imine (272 mg, 1.5 mmol) and sodium tert-butoxide (203 mg, 2.05 mmol) are added. The mixture is heated at 150° C. for 20 min in a microwave reactor. After cooling, the reaction solution is concentrated to give a brown oil which is dissolved in DCM (150 mL) and washed with saturated aqueous sodium chloride (2×50 mL). The aqueous layers are combined and extracted with DCM (1×50 mL), dried with Na2SO4, filtered and concentrated to give a brown residue. The residue is purified on a silica gel column eluting with hexanes (A) and EtOAc (B), gradient from 85%(A): 15%(B) to 50%(A):50%(B) over 50 min to give a yellow solid material as the title compound (574 mg, 90.1% yield). MS (m/z): 467.2 (M+H).

1. temperatureAfter cooling
2. concentrationthe reaction solution is concentrated
3. customto give a brown oil which
4. washwashed with saturated aqueous sodium chloride (2×50 mL)
5. extractionextracted with DCM (1×50 mL)
6. dry with materialdried with Na2SO4
7. filtrationfiltered
8. concentrationconcentrated
9. customto give a brown residue
10. customThe residue is purified on a silica gel column
11. washeluting with hexanes (A) and EtOAc (B), gradient from 85%(A)