(S)-5-dibenzylamino-1-methylpiperidin-2-one → HCID 28064098, compound

HRID 449853Notes

Reaction equation

HRID 449853 reaction equation
C([N:8](CC1C=CC=CC=1)[C@@H:9]1[CH2:14][N:13]([CH3:15])[C:12](=[O:16])[CH2:11][CH2:10]1)C1C=CC=CC=1>CO.[Pd]>[NH2:8][C@@H:9]1[CH2:14][N:13]([CH3:15])[C:12](=[O:16])[CH2:11][CH2:10]1

Participants

4

Reactant 1

HCID 59708472(S)-5-dibenzylamino-1-methylpiperidin-2-one

Product 1

HCID 28064098HCID 28064098, compoundYield 101.6%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 887MethanolSolvent

Procedure

0.450 g (S)-5-dibenzylamino-1-methylpiperidin-2-one are suspended in 25 ml of methanol and hydrogenated with 0.150 g Pd/C 10% at a pressure of 3 bar and a temperature of 60° C. After 16 hours the catalyst is removed by suction filtering and the filtrate is evaporated to dryness. 0.190 g of the product are obtained as an oil. 1H NMR (400 MHz, DMSO): 2.76 (3H, s).

Workup

  1. customa temperature of 60° C
  2. customAfter 16 hours the catalyst is removed by suction
  3. filtrationfiltering
  4. customthe filtrate is evaporated to dryness

Sources & evidence

ORD record
ord-55a333474bcc4bcc991172b2b88a6fc4
Source dataset
uspto-grants-2013_07
Patent number
US08486948B2

Reaction notes

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