反应 #52288

ord-6ed0a590d3c8457395966c04bdee1df8

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONdescribed in Example 18, step (d), in an 8% yield as a mixture of E/Z isomers

实验过程

The title compound was synthesized from 7-[2-(1H-indol-5-yloxy)-ethyl]-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester and 3-biphenyl-4-yl-3-chloro-acrylic acid ethyl ester using the procedure described in Example 18, step (d), in an 8% yield as a mixture of E/Z isomers.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06855722B2uspto-grants-2005_02