반응 #43317

ord-e0491db91f0f4cdfb76c6bf620a3cd51

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The reaction liquid
  2. 2
    여과was filtered
  3. 3
    세척washed thoroughly with methanol
  4. 4
    농축the filtrate was concentrated under reduced pressure
  5. 5
    workup.ADDITIONTHF was added to the resulting residue
  6. 6
    여과the formed precipitate was recovered by filtration
  7. 7
    기타dried

실험 절차

Into a THF (10 mL) solution of 4-benzyloxy-1-{4-[2-(1-piperidinyl)ethoxy]phenyl}-1H-pyridin-2-one (Example 2, 130 mg, 0.32 mmol), 10% palladium-on-carbon (165 mg) was added and stirred at room temperature for 10 hours in hydrogen atmosphere. The reaction liquid was filtered, washed thoroughly with methanol, and the filtrate was concentrated under reduced pressure. THF was added to the resulting residue and the formed precipitate was recovered by filtration and dried to provide the title compound (75 mg, 74%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07732456B2uspto-grants-2010_06