反应 #1615851

ord-cc3c62749fa541638445e9673f30dee5

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

The title compound was prepared from (S)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-3-{(S)-1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-ethyl}-1,3-oxazinan-2-one and 3-(5-bromo-pyridin-2-yl)-3-hydroxy-1-methyl-pyrrolidin-2-one following a procedure analogous to that described in Example 1. Yield: 14% of theory; LC (method 3): tR=2.76 min; Mass spectrum (ESI+): m/z=544 [M+H]+.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09090605B2uspto-grants-2015_07