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HRID 13282作成日:2026年10月25日
Iodoacetamide → 2-(2-(6-(4-Fluoro-phenoxy)-2-pyridin-2-yl-3H-benzimidazol-5-yl)-pyrrolidin-1-yl)-acetamide
https://huagongshe.com/reaction/13282
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Iodoacetamide | HCID 3727 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 5-(4-fluoro-phenoxy)-2-pyridin-2-yl-6-pyrrolidin-2-yl-1H-benzimidazole | HCID 23145575 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 2-(2-(6-(4-Fluoro-phenoxy)-2-pyridin-2-yl-3H-benzimidazol-5-yl)-pyrrolidin-1-yl)-acetamide | HCID 23145124 | — |
反応手順
11.4 mg of potassium carbonate and 11.1 mg of iodoacetamide were added in order to an acetonitrile (1 ml) solution of 20 mg of 5-(4-fluoro-phenoxy)-2-pyridin-2-yl-6-pyrrolidin-2-yl-1H-benzimidazole obtained in Example 168, and the reaction liquid was stirred overnight at room temperature. The reaction liquid was concentrated, and the resulting residue was purified through reversed-phase middle-pressure liquid chromatography [ODS-AS-360-CC (by YMC), mobile phase: water-acetonitrile-0.1% trifluoroacetic acid], and the resulting fraction was diluted with ethyl acetate, washed with aqueous saturated sodium bicarbonate and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure to obtain the entitled compound as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07728025B2 |
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| 出典データセット | uspto-grants-2010_06 |
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| ORD ID | ord-82f3e1f2420e4be1992565f49031ff26 |
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| 出典メモ | uspto-grants-2010_06 |
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