反应 #2125845

ord-f332e414e2e44d9f919b9b73a9093fb5

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The crude material was purified by HPLC Method A

实验过程

The title compound was prepared from 5-ethyl-2-fluoro-4-[3-(4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridin-2-yl)-1H-indazol-6-yl]-phenol trihydrobromide salt (Preparation 25, 50 mg, 80 μmol) and 6-phenoxy-pyridine-3-sulfonyl chloride (22 mg, 80 μmol) using the method of Example 6. The crude material was purified by HPLC Method A to afford 8.4 mg of the title compound.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08575336B2uspto-grants-2013_11