Methyl iodide → HCID 67015634, compound

HRID 1617644Notes

Reaction equation

HRID 1617644 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH2:19][CH:20]([CH3:22])[CH3:21])[CH2:9][C:10]([C:12]2[CH:13]=[CH:14][C:15](=[O:18])[NH:16][CH:17]=2)=[O:11])=[CH:4][CH:3]=1.IC.[C:25](=O)([O-])[O-].[K+].[K+]>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]([CH2:19][CH:20]([CH3:22])[CH3:21])[CH2:9][C:10]([C:12]2[CH:13]=[CH:14][C:15](=[O:18])[N:16]([CH3:25])[CH:17]=2)=[O:11])=[CH:6][CH:7]=1

Participants

4

Reactant 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 67015631HCID 67015631, compound

Product 1

HCID 67015634HCID 67015634, compound

Procedure

In analogy to example 161, step 1, 5-[3-(4-bromo-phenyl)-5-methyl-hexanoyl]-1H-pyridin-2-one was reacted with iodomethane in the presence of potassium carbonate to give the title compound as a colorless oil, MS (ESI+): m/z=376.2 [M+H]+.

Sources & evidence

ORD record
ord-29d104ba2d5347be9a23021852a9dd40
Source dataset
uspto-grants-2014_07
Patent number
US08765730B2

Reaction notes

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