HCID 68861190, compound → HCID 68861456, compound

HRID 1510394Notes

Reaction equation

HRID 1510394 reaction equation
[C:1]([O:5][C:6]([NH:8][C@@:9]1([CH2:23][F:24])[CH:13]([CH3:14])[CH2:12][N:11]([C@@H](C2C=CC=CC=2)C)[CH2:10]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]>C(O)C.[C].[Pd].[H][H]>[C:1]([O:5][C:6]([NH:8][C@@:9]1([CH2:23][F:24])[CH:13]([CH3:14])[CH2:12][NH:11][CH2:10]1)=[O:7])([CH3:3])([CH3:4])[CH3:2]

Participants

5

Reactant 1

HCID 68861190HCID 68861190, compound

Product 1

HCID 68861456HCID 68861456, compound

Reagents, catalysts & solvents 3

HCID 178418390HCID 178418390, compoundCatalystHCID 702EthanolSolventHCID 178418361HCID 178418361, compoundSolvent

Procedure

To a solution of (3S)-3-(tert-butoxycarbonylamino)-3-fluoromethyl-4-methyl-1-[(1R)-1-phenylethyl]pyrrolidine (200 mg, 0.594 mmol) in ethanol (12 mL) was added 10% palladium-carbon catalyst (containing 52.8% water, 200 mg), and the suspension was stirred in an oil bath at 40° C. for 2 hours in hydrogen gas atmosphere. After removing the catalyst by filtration, the solvent was removed by distillation under reduced pressure to obtain 150 mg (quantitative) of the crude title compound as a white solid.

Workup

  1. customAfter removing the catalyst
  2. filtrationby filtration
  3. customthe solvent was removed by distillation under reduced pressure

Sources & evidence

ORD record
ord-2bed2db5a9e54c618f4c7d62f9ae5ac5
Source dataset
uspto-grants-2012_07
Patent number
US08211910B2

Reaction notes

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