Dimethylformamide → 3,5-Dibromo-1,6-dimethylpyridin-2(1H)-one

HRID 593157Notes

Reaction equation

HRID 593157 reaction equation
[CH3:1]N(C=O)C.[Br:6][C:7]1[C:8](=[O:15])[NH:9][C:10]([CH3:14])=[C:11]([Br:13])[CH:12]=1.CI.C([O-])([O-])=O.[K+].[K+]>O>[Br:6][C:7]1[C:8](=[O:15])[N:9]([CH3:1])[C:10]([CH3:14])=[C:11]([Br:13])[CH:12]=1

Participants

6

Reactant 4

HCID 6228DimethylformamideHCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 2854813,5-Dibromo-6-methylpyridin-2-ol

Product 1

HCID 299237793,5-Dibromo-1,6-dimethylpyridin-2(1H)-oneYield 78%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

A 100-mL single-neck round-bottomed flask equipped with a magnetic stirrer was charged with DMF (50 mL), 327c (10.0 g, 37.5 mmol), CH3I (5.3 g, 37.5 mmol), and K2CO3 (7.8 g, 56.2 mmol). The mixture was stirred at room temperature for 5 h. Water (100 mL) was added and the resulting white solid was collected to afford 327d (8.2 g, 78%) as a white solid. MS-ESI: [M+H]+ 280.

Workup

  1. customA 100-mL single-neck round-bottomed flask equipped with a magnetic stirrer
  2. customthe resulting white solid was collected

Sources & evidence

ORD record
ord-e143c97c57644e5f8336875727855533
Source dataset
uspto-grants-2016_01
Patent number
US09238655B2

Reaction notes

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