Hydrazine → 4-(1-Isopropylpiperidin-4-yl)aniline

HRID 1366199Notes

Reaction equation

HRID 1366199 reaction equation
NN.[CH:3]([N:6]1[CH2:11][CH2:10][CH:9]([C:12]2[CH:17]=[CH:16][C:15]([N+:18]([O-])=O)=[CH:14][CH:13]=2)[CH2:8][CH2:7]1)([CH3:5])[CH3:4]>CCO.[Pd]>[CH:3]([N:6]1[CH2:7][CH2:8][CH:9]([C:12]2[CH:13]=[CH:14][C:15]([NH2:18])=[CH:16][CH:17]=2)[CH2:10][CH2:11]1)([CH3:5])[CH3:4]

Participants

5

Reactant 2

HCID 9321HydrazineHCID 574241751-Isopropyl-4-(4-nitrophenyl)piperidine

Product 1

HCID 575900714-(1-Isopropylpiperidin-4-yl)anilineYield 72.2%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 702EthanolSolvent

Procedure

Hydrazine (35% by weight in water, 0.67 mL, 7.2 nnol) and 10% Pd/C (38 mg, 0.03 mmol) are added to a solution of 1-isopropyl-4-(4-nitrophenyl)piperidine (180 mg, 0.72 mmol) in EtOH (10 mL) and the mixture is heated at reflux for 3 h. After cooling, the mixture is filtered through celite and the solvent evaporated. The residue is redissolved in DCM (25 mL), dried over MgSO4 and the solvent evaporated to afford the desired compound as a pale yellow solid (113 mg, 0.52 mmol) which was used without further purification.

Workup

  1. temperaturethe mixture is heated
  2. temperatureat reflux for 3 h
  3. temperatureAfter cooling
  4. filtrationthe mixture is filtered through celite
  5. customthe solvent evaporated
  6. dissolutionThe residue is redissolved in DCM (25 mL)
  7. dry with materialdried over MgSO4
  8. customthe solvent evaporated

Sources & evidence

ORD record
ord-f0b03dcf5fdd431f984901f3577f8760
Source dataset
uspto-grants-2011_02
Patent number
US07893058B2

Reaction notes

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