反应详情

The product of Example 9A (240 mg, 1 mmol) was coupled with the product of Example 28B (0.72, 2 mmol) under the catalysis of Pd2(dba)3 (24 mg, 0.025 mmol) and (tBu3P)2Pd (26 mg, 0.05 mmol) with CsF (Strem Chemicals, 228 mg, 1.5 mmol) in dioxane (8 mL) and DMF (Aldrich, 1 mL) at 80° C. under N2 for 16 hours according to the procedure of Example 20B. The title compound was purified by chromatography (SiO2, EtOAc:MeOH (v. 2% NH3.H2O), 50:50, Rf. 0.3) as yellow solid (350 mg, 79%). 1H NMR (300 MHz, MeOH-D4) δ 1.40 (s, 9H), 1.51-1.70 (m, 1H), 1.70-1.98 (m, 2H), 2.00-2.23 (m, 1H), 2.37-2.51 (m, 1H), 2.71-3.18 (m, 5H), 3.47-3.69 (m, 1H), 5.33-5.49 (m, 1H), 7.30 (d, J=9.2 Hz, 1H), 7.54 (d, J=8.5 Hz, 1H), 7.62 (s, 1H), 8.14 (d, J=9.5 Hz, 1H), 8.37 (dd, J=8.1, 2.0 Hz, 1H), 8.80 (d, J=2.0 Hz, 1H) ppm. MS (DCI/NH3): 442 (M+H)+.

1. customThe title compound was purified by chromatography (SiO2, EtOAc:MeOH (v. 2% NH3.H2O), 50:50, Rf. 0.3) as yellow solid (350 mg, 79%)