反应 #79965

ord-e54746e285824f6da11149c58367d4ea

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Following general procedure L and using 4-[(8-cyclopropyl-3,4-dihydro-4,4-dimethylspiro[2H-1-benzopyran-2,1′-cyclopropane]-6-yl)ethynyl]-2-fluoro-benzoic acid methyl ester (Compound 53, 0.019 g, 0.047 mmol), 5 mL of methanol and 1M sodium hydroxide solution (2 mL) followed by preparative reverse phase HPLC using 10% water in acetonitrile as the mobile phase, the title compound was obtained as a solid (0.01 g, 56%).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06713647B2uspto-grants-2004_03