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HCID 21834430, compound → HCID 21834422, compound

HRID 1740940
Notes
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Reaction equation

HRID 1740940 reaction equation
[CH3:1][C:2]1[C:7]([C:8]#[C:9][CH2:10][CH2:11][CH3:12])=[CH:6][N:5]=[C:4]([NH:13][C:14](=[O:19])[C:15]([CH3:18])([CH3:17])[CH3:16])[CH:3]=1>C(OCC)(=O)C.[Pt]=O>[CH3:1][C:2]1[C:7]([CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])=[CH:6][N:5]=[C:4]([NH:13][C:14](=[O:19])[C:15]([CH3:18])([CH3:17])[CH3:16])[CH:3]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 21834430HCID 21834430, compound

Product 1

HCID 21834422HCID 21834422, compound

Reagents, catalysts & solvents 2

HCID 82844Platinum oxide (PtO)CatalystHCID 8857Ethyl AcetateSolvent

Procedure

A solution of 4-methyl-2-(trimethylacetyl)amino-5-(1-pentynyl)-pyridine (225 mg, 0.87 mmol) in ethyl acetate (4.5 mL) containing platinum oxide (45 mg) was hydrogenated at atmospheric pressure for 1.5 h. The catalyst was removed by filtration through a Millex-HV 0.45 um Filter Unit. Evaporation of the filtrate gave the title compound.

Workup

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
  • customThe catalyst was removed by filtration through a Millex-HV 0.45 um
  • filtrationFilter Unit
  • customEvaporation of the filtrate
  • Sources & evidence

    ORD record
    ord-fd33297981394917b02fba0ec53daf36
    Source dataset
    uspto-grants-1999_10
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05972975

    Reaction notes

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