反応 #91268

ord-e38c0efc65fc4dc1b3568e4fbae16e5b

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他obtained in Step C of Preparation Example 64
  2. 2
    その他to react sequentially in the same manner as in Steps A and B of Example 1

実験手順

3-Chloromethyl-2-propylsulfanyl-pyridine (0.016 g, 0.08 mmol) obtained in Step C of Preparation Example 14 and 2-(3-fluoro-4-hydroxy-phenyl)-cyclopropane carboxylic acid methyl ester (less polar) (0.017 g, 0.08 mmol) obtained in Step C of Preparation Example 64 were used to react sequentially in the same manner as in Steps A and B of Example 1 to obtain the title compound (0.014 g, 48%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09447044B2uspto-grants-2016_09