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HRID 32287作成日:2026年10月24日
4-Amino-N-[2-(diethylamino)ethyl]-2-methoxybenzamide → Benzo[1,3]-dioxole-5-carboxylic acid [4-(2-diethylamino-ethylcarbarnoyl)-5-methoxy-phenyl]-amide
https://huagongshe.com/ja/reaction/32287
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 4-Amino-N-[2-(diethylamino)ethyl]-2-methoxybenzamide | HCID 77374 | — |
| 反応物 | 1,3-Benzodioxole-5-carbonyl chloride | HCID 2734749 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | Benzo[1,3]-dioxole-5-carboxylic acid [4-(2-diethylamino-ethylcarbarnoyl)-5-methoxy-phenyl]-amide | HCID 59793341 | 67% |
反応手順
200 mg (0.75 mmol) of 4-amino-N-(2-diethylamino-ethyl)-2-methoxy-benzamide in 10 ml of chloroform is mixed with 5 ml of 3,4-methylenedioxybenzoic acid chloride (in chloroform) and this mixture is stirred for 3 hours at room temperature. After concentration by evaporation in a vacuum, the residue is taken up in 40 ml of dilute sodium bicarbonate solution and then extracted with 40 ml of methylene chloride. The methylene chloride phase is washed with water, dried, filtered and concentrated by evaporation. The crude product, 315 mg, is taken up in methylene chloride and purified on silica gel. As a mobile solvent, a mixture that consists of methylene chloride/methanol (97:3→90:10) is used. 210 mg (67% of theory) of benzo[1,3]dioxole-5-carboxylic acid [4-(2-diethylamino-ethylcarbamoyl)-5-methoxy-phenyl]-amide (melting point 131.1° C.) is obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07427390B2 |
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| 出典データセット | uspto-grants-2008_09 |
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| ORD ID | ord-edf55ea1959844a7beb69242da746a76 |
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| 出典メモ | uspto-grants-2008_09 |
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