Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 58244057 | HCID 58244057 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58244054 | HCID 58244054 | — |
Reaction Steps
Sodium hydride (55% mineral oil, 30 mg) was added to a mixture of 5-{5-[1-(4-chloro-2,6-difluorophenoxy)-1-methylethyl]-4-isopropyl-4H-1,2,4-triazol-3-yl}isoindolin-1-one (200 mg) and DMF (5 ml) under ice cooling, followed by stirring for one hour, iodomethane (0.084 ml) was added thereto, followed by stirring for one hour, while slowly elevating to room temperature. The reaction solution was concentrated, water was added to the residue, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate and the solvent was then evaporated. The resulting residue was purified by silica gel column chromatography (chloroform:methanol=100:0 to 90:10) and then was solidified from ethyl acetate-diisopropylether, and the solid was collected by filtration, washed with diisopropylether and then dried under reduced pressure to obtain 5-{5-[1-(4-chloro-2,6-difluorophenoxy)-1-methylethyl]-4-isopropyl-4H-1,2,4-triazol-3-yl}-2-methylisoindolin-1-one (111 mg) as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08377923B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-970e9c0e4eaf49c0b96f24b017faf761 |
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| Source note | uspto-grants-2013_02 |
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