HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

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

HRID 408099
Notes
Print preview

Reaction equation

HRID 408099 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
ParticipantsProcedureWorkupSources & evidenceReaction notes

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 eliminated 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. filtrationfiltering
  3. customthe filtrate is evaporated to dryness

Sources & evidence

ORD record
ord-73683245091147afbc8d3a467cc93464
Source dataset
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08759326B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes