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HRID 58526作成日:2026年10月26日

Triethylamine → N-(2-(5-chloro-1H-indol-3-yl)ethyl)-5-(chloromethyl)isoxazole-3-carboxamide

https://huagongshe.com/reaction/58526

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Thionyl ChlorideHCID 24386—
反応物5-Chloro-1H-indole-3-ethylamine monohydrochlorideHCID 2827494—
反応物5-(Hydroxymethyl)-1,2-oxazole-3-carboxylic acidHCID 8027249—
溶媒DichloromethaneHCID 6344—
生成物N-(2-(5-chloro-1H-indol-3-yl)ethyl)-5-(chloromethyl)isoxazole-3-carboxamideHCID 6683169922%

反応条件

温度80 °C

反応手順

Thionyl chloride (0.5 mL; 7.26 mmol) was added to a mixture of 5-(hydroxymethyl)isoxazole-3-carboxylic acid (0.207 g; 7.26 mmol) and stirred at 80° C. for 72 h. The solution was concentrated under reduced pressure and the crude material was dissolved in dichloromethane (5 mL) and added to a mixture of 2-(5-chloro-1H-indol-3-yl)ethanamine hydrochloride (0.370 g; 1.60 mmol) and triethylamine (0.524 mL; 3.62 mmol) in dichloromethane (5 mL). The resulting solution was stirred at room temperature for 20 min, concentrated under reduced pressure and the crude material was purified by flash chromatography on silica gel (eluent 2 to 20% ethyl acetate in dichloromethane) to afford N-(2-(5-chloro-1H-indol-3-yl)ethyl)-5-(chloromethyl)isoxazole-3-carboxamide 0.088 g (22%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434722B2
出典データセットuspto-grants-2016_09
ORD IDord-e8aeaa6de6af4bfbb528e1622eee4e5b
出典メモuspto-grants-2016_09