反应详情

温度

120 °C

To a mixture of N-(6-chloro-4,5-dimethylpyridin-2-yl)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamide (25 mg, 0.067 mmol) and 2-methoxy-4-methylpyridin-5-ylboronic acid (21 mg, 0.1 mmol) in DME (0.7 mL) and Na2CO3 (2M, 0.065 mL, 0.13 mmol) was added Pd(PPh3)4 (4 mg, 0.003 mmol). The mixture was heated in microwave oven at 120° C. for 30 min. The reaction was re-partitioned between EtOAc and H2O and the aqueous layer was extracted with EtOAc twice. The combined organic layers were washed with brine and dried over MgSO4. After the removal of solvent, the residue was purified by column chromatography (0-20% EtOAc-Hexane) to yield 1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-N-(6′-methoxy-3,4,4′-trimethyl-2,3′-bipyridin-6-yl)cyclopropanecarboxamide (20 mg, 65%). 1H NMR (400 MHz, CDCl3) 8.05 (s, 1H), 7.86 (s, 1H), 7.59 (d, J=1.5 Hz, 1H), 7.21-7.16 (m, 2H), 7.04 (d, J=8.2 Hz, 1H), 6.62 (s, 1H), 3.92 (s, 3H), 2.34 (s, 3H), 2.00 (s, 3H), 1.96 (s, 3H), 1.74 (dd, J=3.9, 6.9 Hz, 2H), 1.15 (dd, J=3.9, 7.0 Hz, 2H). Retention time: 2.00 min; ESI-MS m/z calc. 467.5. found 468.2 (M+H)+.

1. customThe reaction was re-partitioned between EtOAc and H2O
2. extractionthe aqueous layer was extracted with EtOAc twice
3. washThe combined organic layers were washed with brine
4. dry with materialdried over MgSO4
5. customAfter the removal of solvent
6. customthe residue was purified by column chromatography (0-20% EtOAc-Hexane)