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HRID 374215作成日:2026年10月27日
Sodium Iodide → 7-[3-[[(2,3-Dihydro-7-methoxy-1,4-benzodioxin-2-yl)methyl]amino]propoxy]-2H-1-benzopyran-2-one
https://huagongshe.com/reaction/374215
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Iodide | HCID 5238 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 2H-1-Benzopyran-2-one, 7-(3-chloropropoxy)- | HCID 1900666 | — |
| 反応物 | (7-Methoxy-2,3-dihydro-1,4-benzodioxin-2-YL)methanamine | HCID 18923874 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 7-[3-[[(2,3-Dihydro-7-methoxy-1,4-benzodioxin-2-yl)methyl]amino]propoxy]-2H-1-benzopyran-2-one | HCID 19778668 | 40.3% |
反応手順
2,3-Dihydro-7-methoxy-1,4-benzodioxin-2-methanamine (3.8 g, 20 mmole), 7-(3-chloropropoxy)coumarin (4.8 g, 20 mmole), diisopropylethylamine (2.6 g, 20 mmole) and sodium iodide (5.0 g, 33 mmole) were combined in 200 ml of DMF and heated at 100° C. for 24 hours under a nitrogen atmosphere. The solvent was then removed and replaced with 500 ml of dichloromethane. The mixture was washed with 300 ml portions of saturated aqueous sodium bicarbonate, with saturated aqueous sodium chloride, dried over sodium sulfate, filtered, and concentrated in vacuum. The residue was column chromatographed on 100 g of silica gel using first dichloromethane, then chloroform, and finally 2% methanol in chloroform as eluant. The product-containing fractions were combined and concentrated in vacuum and the residue crystallized from 100 ml of isopropanol with the addition of 5.0 ml of 4N isopropanolic HCl to give 3.2 g of title compound as a white solid, monohydrochloride, m.p. 223°- 225° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05166367 |
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| 出典データセット | uspto-grants-1992_11 |
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| ORD ID | ord-0fedae0cffc44585965de7dad80c3cb4 |
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| 出典メモ | uspto-grants-1992_11 |
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