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HRID 16196作成日:2026年10月24日

Water → N-(4-(6-chloropyrazin-2-ylthio)phenyl)cyclopropanecarboxamide

https://huagongshe.com/ja/reaction/16196

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物2,6-DichloropyrazineHCID 78504—
反応物N-(4-mercaptophenyl)cyclopropanecarboxamideHCID 16722082—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物N-(4-(6-chloropyrazin-2-ylthio)phenyl)cyclopropanecarboxamideHCID 5934340172%

反応手順

To a solution of N-(4-mercaptophenyl)cyclopropane carboxamide (16.1 mmol) in THF (25 mL) at 0° C. was added sodium hydride (16.1 mmol) portionwise. Once the addition was complete the resulting solution was stirred at room temperature for 30 min. After this time, the reaction mixture was cooled to 0° C. and a solution of 2,6-dichloropyrazine (13.4 mmol) was added and the resulting mixture stirred at room temperature for 16 h. Water (30 mL) and ethyl acetate (30 mL) were added and the layers separated. The aqueous layer was extracted further with ethyl acetate (2×30 mL), the combined organic layers dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography (EtOAc/Petroleum ether, 0-100% gradient EtOAc) to give the title compound (2.95 g, 72%) as a cream coloured solid; 1H NMR (400 MHz, DMSO-d6) δ 0.91 (2H, m), 1.13 (2H, m), 1.54 (1H, m), 7.53 (1H, br s), 7.57 (2H, m), 7.65 (2H, m), 7.96 (1H, s), 8.22 (1H, s); MS (ES+): m/e=306.14 (100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737151B2
出典データセットuspto-grants-2010_06
ORD IDord-828b4a785b5f43c68f2fdae5541d9a91
出典メモuspto-grants-2010_06