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HRID 344382作成日:2026年10月27日
Potassium Carbonate → 4-amino-5-chloro-N-(1-(6-(2,3-dihydro-1,3-dioxo-1H-isoindol-2-yl)hexyl)-piperidin-4-ylmethyl)-2-methoxybenzamide
https://huagongshe.com/reaction/344382
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 6-Bromohexylphthalimide | HCID 21930853 | — |
| 反応物 | 4-Amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide hydrochloride | HCID 66780941 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-amino-5-chloro-N-(1-(6-(2,3-dihydro-1,3-dioxo-1H-isoindol-2-yl)hexyl)-piperidin-4-ylmethyl)-2-methoxybenzamide | HCID 54520676 | 62.7% |
反応手順
4-Amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide hydrochloride (8.5 g) was dissolved in dimethylformamide (100 ml). Potassium carbonate (10.5 g) and 6-bromohexylphthalimide (7.2 g) were added, and the mixture was stirred at 70° C. for 16 hr. The reaction mixture was concentrated under reduced pressure and the residue was extracted with ethyl acetate. The extract was dried over magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography to give 4.2 g of 4-amino-5-chloro-N-(1-(6-(2,3-dihydro-1,3-dioxo-1H-isoindol-2-yl)hexyl)-piperidin-4-ylmethyl)-2-methoxybenzamide.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05864039 |
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| 出典データセット | uspto-grants-1999_01 |
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| ORD ID | ord-b0302d1f48d04f79a5fc161d508661df |
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| 出典メモ | uspto-grants-1999_01 |
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