HCID 178420347, compound → HCID 178511561, compound

HRID 2356294Notes

Reaction equation

HRID 2356294 reaction equation
C([N:8](CC1C=CC=CC=1)[C@H:9]1[CH2:14][CH2:13][C@@H:12]([CH2:15][O:16][CH2:17][CH2:18][CH:19]2[CH2:24][CH2:23][CH2:22][CH2:21][NH:20]2)[CH2:11][CH2:10]1)C1C=CC=CC=1>C(O)C.[OH-].[Pd+2].[OH-]>[NH:20]1[CH2:21][CH2:22][CH2:23][CH2:24][CH:19]1[CH2:18][CH2:17][O:16][CH2:15][C@@H:12]1[CH2:11][CH2:10][C@H:9]([NH2:8])[CH2:14][CH2:13]1

Participants

4

Reactant 1

HCID 178420347HCID 178420347, compound

Product 1

HCID 178511561HCID 178511561, compound

Reagents, catalysts & solvents 2

HCID 9942167Palladium hydroxideCatalystHCID 702EthanolSolvent

Procedure

cis-N,N-Dibenzyl-N-{4-[(2-piperidylethoxy)methyl]cyclohexyl}amine (2.84 g, 6.65 mmol) was dissolved in 20 mL of ethanol. Palladium hydroxide (20% weight) was added (50 mg) and the reaction was stirred overnight under an atmosphere of hydrogen. The catalyst was removed by filtration and washed with small portions of ethanol. The filtrate was concentrated and used without further purification. (quantitative yield): ES-MS (m/z) 241.

Workup

  1. customThe catalyst was removed by filtration
  2. washwashed with small portions of ethanol
  3. concentrationThe filtrate was concentrated
  4. customused without further purification

Sources & evidence

ORD record
ord-566c6f2b29c04708952bd31b574cafd5
Source dataset
uspto-grants-2010_07
Patent number
US07759342B2

Reaction notes

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