Hydrazine → 3-(4-(4-Fluorophenyl)piperidin-1-yl)propan-1-amine

HRID 2187554Notes

Reaction equation

HRID 2187554 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[CH2:13][CH2:12][N:11]([CH2:14][CH2:15][CH2:16]C3C=CC=C4C(NC(=O)C=34)=O)[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[NH2:28]N>CO>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]2[CH2:9][CH2:10][N:11]([CH2:14][CH2:15][CH2:16][NH2:28])[CH2:12][CH2:13]2)=[CH:6][CH:7]=1

Participants

4

Reactant 2

HCID 9321HydrazineHCID 227294733-[4-(4-Fluorophenyl)piperidin-1-yl]propylphthalimide

Product 1

HCID 101985993-(4-(4-Fluorophenyl)piperidin-1-yl)propan-1-amine

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To a solution of 3-[4-(4-fluorophenyl)piperidin-1-yl] propylphthalimide (4.5 g, 12.3 mmol) in methanol (200 mL), hydrazine (4 mL) was added and the mixture was stirred and refluxed for 8 h. It was cooled, and the white solid was filtered and washed with methanol (20 mL). Solvent was evaporated, and the residue was dried under vacuum for 4 h. Chloroform (50 mL) was added to this material, it was stirred for 1 h and filtered. The white solid was washed with more chloroform (20 mL), and the solvent was evaporated from the combined filtrates to leave the crude product as an oil. It was purified by column chromatography on silica gel using dichloromethane/methanol/2M ammonia in methanol (10/3/1) as the eluent.

Workup

  1. temperaturerefluxed for 8 h
  2. temperatureIt was cooled
  3. filtrationthe white solid was filtered
  4. washwashed with methanol (20 mL)
  5. customSolvent was evaporated
  6. customthe residue was dried under vacuum for 4 h
  7. additionChloroform (50 mL) was added to this material, it
  8. stirringwas stirred for 1 h
  9. filtrationfiltered
  10. washThe white solid was washed with more chloroform (20 mL)
  11. customthe solvent was evaporated from the combined filtrates

Sources & evidence

ORD record
ord-9861c8bf20e4467f8224f7c45e24d6c1
Source dataset
uspto-grants-2002_06
Patent number
US06410554B1

Reaction notes

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