反应 #60714

ord-d924d161d22940deac503ffab5e90c9d

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他afforded

实验过程

Using alkylation method A, 3-chloro-N-[1-(4-fluoro-phenyl)-2-(piperidin-4-ylmethoxy)ethyl]-1H-indole-6-carboxamide (600 mg, 1.4 mmol) and acetone (10 mL, 135 mmol) afforded, after trituration (acetonitrile), 500 mg (76%) of the title compound.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07427632B2uspto-grants-2008_09