Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoate | HCID 242 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 22671955 | HCID 22671955 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12017704 | HCID 12017704 | — |
Reaction Steps
Methyl 4-[2-(N-isopropyl-phenylsulfonylamino)-5-trifluoromethyl-phenyl]aminomethyl]benzoate (200 mg) prepared by the same procedure as Example 17 by using methyl 4-(2-phenylsulfonylamino-5-trifluoromethyl-phenylaminomethyl)benzoate (prepared in Example 27) was dissolved in DMF (5 ml). Sodium hydride (64 mg) and methyl iodide (200 μl) were added thereto. The mixture was stirred for 24 hours at 60° C. The reaction mixture was extracted with H2O-AcOEt, washed, dried over, filtered and concentrated under the reduced pressure. The residue was purified on silica gel column chromatography (hexane:AcOEt=5:1) to give the title compound (105 mg) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06790866B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-b291a97798344867b87aafa567bda363 |
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| Source note | uspto-grants-2004_09 |
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