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HRID 330070作成日:2026年10月26日
Ethanamine, 2-fluoro-, hydrochloride → N-(2-chloroethyl)-(3-benzyl-5,6-diethylpyrazine-2-yl oxy) acetamide
https://huagongshe.com/reaction/330070
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethanamine, 2-fluoro-, hydrochloride | HCID 9995 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Pivaloyl chloride | HCID 62493 | — |
| 反応物 | (3-Benzyl-5,6-diethylpyrazine-2-yl oxy) acetate | HCID 86743689 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | N-(2-chloroethyl)-(3-benzyl-5,6-diethylpyrazine-2-yl oxy) acetamide | HCID 15170451 | 88.8% |
反応手順
Pivaloyl chloride (3.66 g, 30 mM) was added dropwise at -5° C. to compound 655 (8.62 g, 28.7 mM) and triethylamine (4.2 ml, 30 mM) dissolved in tetrahydrofuran (50 ml), then the mixture was stirred for 30 minutes. Chloroform (30 ml) in solution with 2-fluoroethylamine hydrochloride (3.48 g) and triethylamine (4.2 ml) was added dropwise thereto with cooling at 0° to -5° C. then the mixture was stirred for 1 hour with ice cooling and 4 hours at room temperature. Dilute aqueous potassium carbonate was added to the reaction mixture and the mixture was extracted three times with chloroform. The extract was dried with anhydrous magnesium sulfate, and concentrated in vacuo. The residue was charged on a column of silica gel (C-200, 175 g) and eluted successively with benzene and benzene-ethyl acetate (5:1) to obtain the product. (9.21 g, yield: 88.8%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04894453 |
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| 出典データセット | uspto-grants-1990_01 |
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| ORD ID | ord-fd7256a37c514635bd620f41b69d38a7 |
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| 出典メモ | uspto-grants-1990_01 |
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