反応 #46844

ord-b7a3483c68dd4a4d851dbaf158682c74

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他1-[2-(4-Chloro-phenyl)-ethyl]-4-(3-hydroxy-azetidine-1-carbonyl)-1H-benzoimidazole-2-carboxylic acid (1-isopropyl-piperidin-4-yl)-amide was prepared by a procedure

実験手順

1-[2-(4-Chloro-phenyl)-ethyl]-4-(3-hydroxy-azetidine-1-carbonyl)-1H-benzoimidazole-2-carboxylic acid (1-isopropyl-piperidin-4-yl)-amide was prepared by a procedure according to example 22 starting from 150 mg (0.29 mmol) 1-[2-(4-Chloro-phenyl)-ethyl]-2-(1-isopropyl-piperidin-4-ylcarbamoyl)-1H-benzoimidazole-4-carboxylic acid and 23.4 mg (0.32 mmol) 3-hydroxy-azetidine. The title compound was obtained as its formiate in form a white amorphous solid.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07741341B2uspto-grants-2010_06