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HRID 2421158作成日:2026年10月26日

Triethylamine → 2-(5-Cyclopropyl-3-phenyl-isoxazol-4-yl)-5-(2-methoxy-phenyl)-[1,3,4]oxadiazole

https://huagongshe.com/reaction/2421158

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物o-AnisohydrazideHCID 24051—
反応物2-chloro-1,3-dimethyl-1H-imidazol-3-ium chlorideHCID 11126651—
反応物5-Cyclopropyl-3-phenyl-1,2-oxazole-4-carboxylic acidHCID 22309080—
溶媒DichloromethaneHCID 6344—
生成物2-(5-Cyclopropyl-3-phenyl-isoxazol-4-yl)-5-(2-methoxy-phenyl)-[1,3,4]oxadiazoleHCID 1672290733%

反応手順

To a suspension of 5-cyclopropyl-3-phenyl-isoxazole-4-carboxylic acid (236 mg, 1.03 mmol) in dichloromethane (2 mL) were added 2-methoxybenzhydrazide (205 mg, 1.24 mmol), 2-chloro-1,3-dimethylimidazolium chloride (383 mg, 2.26 mmol) and triethylamine (0.52 ml, 5.15 mmol) at ambient temperature. The resulting suspension was stirred for 18 h at this temperature before diluting with dichloromethane (20 ml) and washing with water (20 mL) and brine (20 mL). The aqueous layers were extracted with dichlormethane and the combined organic layers dried over sodium sulfate. Purification by chromatography (SiO2, heptane:ethyl acetate:dichloromethane=70:10:20 to 40:40:20) afforded the title compound (121 mg, 33%) as a white solid. MS: m/e=360.2 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07956074B2
出典データセットuspto-grants-2011_06
ORD IDord-8db7792f09f3414b8d81fc4ead911587
出典メモuspto-grants-2011_06