反应 #592675

ord-fd99cb701e914fb1a1263246ae18f465

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

Following the procedures described in Example 1, Intermediate 3B was used in place of Intermediate 3A, and 2-fluoro-3-phenyl-acrylic acid was used in place of cinnamic acid to give (2S)-3-{3-bromo-4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)-ethoxy]-phenyl}-2-(2-fluoro-3-phenyl-acryloylamino)-propanoic acid as a white solid with the yield of 25% and mp of 243˜245° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07781468B2uspto-grants-2010_08