4-benzyloxy-1-(3-fluorobenzyl)-1H-pyridin-2-one → HCID 54724162, compound

HRID 1831903Notes

Reaction equation

HRID 1831903 reaction equation
C([O:8][C:9]1[CH:14]=[CH:13][N:12]([CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([F:22])[CH:17]=2)[C:11](=[O:23])[CH:10]=1)C1C=CC=CC=1>C(O)C>[F:22][C:18]1[CH:17]=[C:16]([CH:21]=[CH:20][CH:19]=1)[CH2:15][N:12]1[CH:13]=[CH:14][C:9]([OH:8])=[CH:10][C:11]1=[O:23]

Participants

3

Reactant 1

HCID 220502224-benzyloxy-1-(3-fluorobenzyl)-1H-pyridin-2-one

Product 1

HCID 54724162HCID 54724162, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

In a Fischer-Porter bottle, added a solution of 4-(benzyloxy)-1-(3-fluorobenzyl)pyridin-2(1H)-one (4.5 g, 14.56 mmol) in absolute ethanol-(20 mL). Flushed the solution with nitrogen then added palladium catalyst (1.05 g). Sealed bottle and evacuated system. The system was purged with hydrogen gas (2×15 psi) to check for leaks. The reaction was charged with hydrogen (35 psi) and stirred at room temperature for 45 min. The system was evacuated and flushed with nitrogen. The reaction was filtered and the catalyst was carefully washed with fresh ethanol. The filtrate was concentrated under reduced pressure.

Workup

  1. customFlushed the solution with nitrogen
  2. customSealed bottle
  3. customevacuated system
  4. customThe system was purged with hydrogen gas (2×15 psi)
  5. additionThe reaction was charged with hydrogen (35 psi)
  6. customThe system was evacuated
  7. customflushed with nitrogen
  8. filtrationThe reaction was filtered
  9. washthe catalyst was carefully washed with fresh ethanol
  10. concentrationThe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-c4bb582f305842b0b53556a4f1ff4944
Source dataset
uspto-grants-2006_06
Patent number
US07067540B2

Reaction notes

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