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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

反応式

関与物質

役割名称HCID仕込み量
反応物Ethanamine, 2-fluoro-, hydrochlorideHCID 9995—
反応物Potassium CarbonateHCID 11430—
反応物Pivaloyl chlorideHCID 62493—
反応物(3-Benzyl-5,6-diethylpyrazine-2-yl oxy) acetateHCID 86743689—
溶媒ChloroformHCID 6212—
溶媒TetrahydrofuranHCID 8028—
溶媒TriethylamineHCID 8471—
生成物N-(2-chloroethyl)-(3-benzyl-5,6-diethylpyrazine-2-yl oxy) acetamideHCID 1517045188.8%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04894453
出典データセットuspto-grants-1990_01
ORD IDord-fd7256a37c514635bd620f41b69d38a7
出典メモuspto-grants-1990_01