反应详情

The titled compound was prepared following the procedure C using N-{4-[(4-chlorophenyl)ethynyl]benzyl}-N-(2,2-dimethyl-4-oxo-4H-1,3-benzodioxin-6-yl)isoxazole-5-carboxamide and NaOH as a yellow solid (55%). M− (ESI): 470.7; M+ (ESI): 472.6. HPLC, Rt: 4.56 min (Purity: 71.3%).