反应 #1797557

ord-25d32477dbd8494ab0e363c119504647

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The title compound is synthesized
  2. 2
    其他Purification by chromatography on flash silica gel (eluent gradient: dichloromethane/0-10 vol. % ethanol)

实验过程

The title compound is synthesized as described for 7-[2-(6-{4-cyano-phen-1-yl}-3H-imidazo[4,5-b]pyridin-2-yl)-ethyl]-azepan-2-thione (compound A2) from 120 mg of 7-{2-[6-(4-methoxy-phenyl)-3H-imidazo[4,5-b]pyridin-2-yl]-ethyl}-azepan-2-one (compound B3) and 222 mg of Lawesson's reagent. Purification by chromatography on flash silica gel (eluent gradient: dichloromethane/0-10 vol. % ethanol) affords 104 mg of the title compound as a light yellow, waxy solid. ESI-MS: 381.2 (MH+). TLC: Rf=0.64 (dichloromethane/ethanol 10:1 parts by volume).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07790710B2uspto-grants-2010_09