Methyl iodide → HCID 67227504, compound

HRID 1043188Notes

Reaction equation

HRID 1043188 reaction equation
[C:1]([O:5][C:6]([NH:8][C:9]1[N:14]=[CH:13][C:12]([O:15][C:16]2[CH:25]=[C:24]([F:26])[CH:23]=[CH:22][C:17]=2[C:18]([O:20][CH3:21])=[O:19])=[CH:11][CH:10]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[H-].[Na+].I[CH3:30]>CN(C)C=O>[C:1]([O:5][C:6]([N:8]([CH3:30])[C:9]1[N:14]=[CH:13][C:12]([O:15][C:16]2[CH:25]=[C:24]([F:26])[CH:23]=[CH:22][C:17]=2[C:18]([O:20][CH3:21])=[O:19])=[CH:11][CH:10]=1)=[O:7])([CH3:4])([CH3:2])[CH3:3]

Participants

5

Procedure

To a solution of EXAMPLE 377B (0.750 g) in N,N-dimethylformamide (5 mL) was added sodium hydride (0.091 g). The reaction was stirred for 30 minutes at room temperature and then iodomethane (0.142 mL) was added to the reaction and stirring was continued at room temperature for 2 hours. The reaction was quenched with water (25 mL) and extracted with ethyl acetate (75 mL). The organic layer was separated, washed with brine (50 mL), dried over magnesium sulfate, filtered, and concentrated. The residue was loaded onto silica gel (Reveleris 40 g) and eluted with a gradient of 5-15% ethyl acetate/hexanes over 30 minutes (flow=40 ml/min) to provide the title compound.

Workup

  1. stirringstirring
  2. waitwas continued at room temperature for 2 hours
  3. customThe reaction was quenched with water (25 mL)
  4. extractionextracted with ethyl acetate (75 mL)
  5. customThe organic layer was separated
  6. washwashed with brine (50 mL)
  7. dry with materialdried over magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated
  10. washeluted with a gradient of 5-15% ethyl acetate/hexanes over 30 minutes (flow=40 ml/min)

Sources & evidence

ORD record
ord-8431a06cf3ac436283b9079e11b0f7a9
Source dataset
uspto-grants-2013_10
Patent number
US08557983B2

Reaction notes

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