Methyl iodide → 5-(Methanesulfonyl-methylamino)-N-methyl-N-propyl-isophthalamic acid methyl ester

HRID 1436658Notes

Reaction equation

HRID 1436658 reaction equation
[CH3:1][O:2][C:3](=[O:22])[C:4]1[CH:16]=[C:15]([NH:17][S:18]([CH3:21])(=[O:20])=[O:19])[CH:14]=[C:6]([C:7]([N:9]([CH3:13])[CH2:10][CH2:11][CH3:12])=[O:8])[CH:5]=1.IC.[C:25](=O)([O-])[O-].[K+].[K+]>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.CN(C=O)C.C(OCC)(=O)C>[CH3:1][O:2][C:3](=[O:22])[C:4]1[CH:16]=[C:15]([N:17]([S:18]([CH3:21])(=[O:19])=[O:20])[CH3:25])[CH:14]=[C:6]([C:7]([N:9]([CH3:13])[CH2:10][CH2:11][CH3:12])=[O:8])[CH:5]=1

Participants

7

Procedure

Mix 5-methanesulfonylamino-N-methyl-N-propyl-isophthalamic acid methyl ester (2.09 g, 6.36 mmol), iodomethane (1.35 g, 9.55 mmol), potassium carbonate (1.38 g, 10 mmol), and tetrabutylammonium bromide (206 mg, 0.64 mmol) in DMF (10 mL) at room temperature for 30 min. Dilute with ethyl acetate and wash with 10% aqueous potassium carbonate, 1 N lithium chloride and saturated aqueous sodium chloride. Dry (magnesium sulfate), concentrate and purify (silica gel chromatography, eluting with 0:100 to 40:60 ethyl acetate:dichloromethane) to give the title compound as an oil.

Workup

  1. washwash with 10% aqueous potassium carbonate, 1 N lithium chloride and saturated aqueous sodium chloride
  2. dry with materialDry (magnesium sulfate)
  3. concentrationconcentrate
  4. custompurify
  5. wash(silica gel chromatography, eluting with 0:100 to 40:60 ethyl acetate:dichloromethane)

Sources & evidence

ORD record
ord-72fd23ae9dac49e3b308529baf3d7f3a
Source dataset
uspto-grants-2009_11
Patent number
US07618978B2

Reaction notes

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