反应详情

To a mixture of (1R*,2S*)-2-(3-iodo-1H-indazol-6-yl)spiro[cyclopropane-1,3′-indolin]-2′-one (80.2 mg, 0.2 mmol) and 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide (68.2 mg, 0.24 mmol) in DME (4 mL) was added 1 M Na2CO3 (0.24 mL, 0.24 mmol), followed by Pd(PPh3)2Cl2 (14 mg, 0.02 mmol). The resulting mixture was purged with argon and microwaved 2 h at 120° C. It was diluted with H2O, extracted with EtOAc and dried (Na2SO4). Removal of solvents provided an oil which was triturated with EtOAc/hex then MeOH/CH2Cl2/hex to give the title compound as a white solid (7 mg, 8%). 1H NMR (400 MHz, DMSO-d6) δ 13.41 (s, 1H), 10.63 (s, 1H), 8.41 (s, 1H), 8.19 (d, J=6.8 Hz, 1H), 8.00 (d, J=8.4 Hz, 1H), 7.20 (d, J=8.0 Hz, 1H), 7.69 (t, J=7.6 Hz, 1H), 7.54 (s, 1H), 7.47 (s, 2H, NH2), 7.08 (d, J=8.4 Hz, 1H), 7.00 (t, J=7.2 Hz, 1H), 6.85 (d, J=6.8 Hz, 1H), 6.54 (t, J=7.4 Hz, 1H), 6.05 (d, J=6.4 Hz, 1H), 3.22 (t, J=7.6 Hz, 1H), 2.38-2.30 (m, 1H), 2.05-1.98 (m, 1H); MS ESI 431.1 [M+H]+, calcd for [C23H18N4O3S+H]+ 431.1.

1. customThe resulting mixture was purged with argon
2. custommicrowaved 2 h at 120° C
3. additionIt was diluted with H2O
4. extractionextracted with EtOAc
5. dry with materialdried (Na2SO4)
6. customRemoval of solvents
7. customprovided an oil which
8. customwas triturated with EtOAc/hex