関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methylamine | HCID 6329 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | S-Ethylisothiuronium bromide | HCID 200213 | — |
| 反応物 | 1-Bromo-4-(4-bromophenyl)-3-(4-methoxyphenyl)butan-2-one | HCID 86650847 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 4-[2-(4-bromophenyl)-1-(4-methoxyphenyl)ethyl]-1-methyl-1H-imidazol-2-amine | HCID 44219587 | 100.7% |
反応手順
1-bromo-4-(4-bromophenyl)-3-(4-methoxyphenyl)butan-2-one (0.15 g, 0.36 mmol) was dissolved in methanol (1.8 mL) and methylamine (0.36 mL, 0.72 mmol, 2M solution in methanol) was added in one portion and the reaction was allowed to stir at 25° C. for 0.5 hour. S-ethylisothiourea hydrobromide (0.27 mg, 1.46 mmol) and NaOH (0.61 mL, 1.82 mmol, 3M solution in water) were added to the solution and the resulting solution was allowed to stir at 25° C. for 16 hours. The reaction was purified using reverse phase C-18 chromatography (acetontitrile and water system) to afford 140 mg of 4-[2-(4-bromophenyl)-1-(4-methoxyphenyl)ethyl]-1-methyl-1H-imidazol-2-amine as a yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08492387B2 |
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| 出典データセット | uspto-grants-2013_07 |
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| ORD ID | ord-af88c8423c9e4317bb520879787aed68 |
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| 出典メモ | uspto-grants-2013_07 |
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