反応 #44841

ord-659f4c92bf4c415ea05c5b935dd9dae7

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The product was purified by column chromatography

実験手順

The title compound was prepared from 2-chlorobenzimidazole and 7-fluoro-1,2,3,4-tetrahydro-1-naphthylamine (prepared by Procedure B from 7-fluoro-1 -tetralone) by Procedure A. The product was purified by column chromatography to give the title compound as the free base and as a mixture of enantiomers (white solid, mp 181° C.). MS(ES+) m/z 282 ([M+1]+, 100).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07737167B2uspto-grants-2010_06