반응 #796995

ord-aa5502d794854eb2986865365ccb6d07

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The solvent in the reaction mixture was evaporated under reduced pressure
  2. 2
    기타the residue was purified by silica gel column chromatography (ethyl acetate/hexane)

실험 절차

To a solution of ethyl 3-cyclopropyl-3-(2-((6-(2-fluoro-5-methoxyphenyl)-5-neopentylpyridin-3-yl)methoxy)pyridin-4-yl)propanoate (28 mg) in THF (1.0 mL) and methanol (0.50 ml) was added 1N aqueous sodium hydroxide solution (1.0 mL), and the mixture was stirred at room temperature for 1 hr. The solvent in the reaction mixture was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (21 mg) as a yellow amorphous solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09181186B2uspto-grants-2015_11