Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 68470234 | HCID 68470234 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68469900 | HCID 68469900 | — |
Reaction Steps
Sodium hydride (60%, 16 mg) was added to a DMF (10 ml) solution of N-{1-[5-(2-chlorophenyl)-4-methyl-4H-1,2,4-triazol-3-yl]-1-methylethyl}benzamide (130 mg), followed by stirring at room temperature for 30 minutes. Then, methyl iodide (0.027 ml) was added thereto and the whole was stirred at room temperature for 1 hour. A saturated aqueous sodium hydrogen carbonate solution and chloroform were added to the reaction solution and then the organic layer was separated. Furthermore, the organic layer was washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate and filtered and then the solvent was removed by evaporation under reduced pressure. The resulting crude product was purified by flash column chromatography (chloroform:methanol=100:3) to obtain 104 mg of N-{1-[5-(2-chlorophenyl)-4-methyl-4H-1,2,4-triazol-3-yl]-1-methylethyl}-N-methylbenzamide (colorless solid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776897B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-e4dd630910324f9d8019a594c8619f61 |
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| Source note | uspto-grants-2010_08 |
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