戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 402511作成日:2026年10月27日

Diisopropylethylamine → 5-(1-(6-Chloro-5-methylpyrimidin-4-yl)piperidin-4-yl)-3-isopropyl-1,2,4-oxadiazole

https://huagongshe.com/reaction/402511

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物4,6-Dichloro-5-methylpyrimidineHCID 818860—
反応物4-(3-Isopropyl-1,2,4-oxadiazol-5-YL)piperidine hydrochlorideHCID 53400827—
溶媒DichloromethaneHCID 6344—
生成物5-(1-(6-Chloro-5-methylpyrimidin-4-yl)piperidin-4-yl)-3-isopropyl-1,2,4-oxadiazoleHCID 8666161143%

反応条件

温度27 °C

反応手順

A solution of 4-(3-isopropyl-1,2,4-oxadiazol-5-yl)piperidine hydrochloride (2.0 gm, 0.008369 moles) and diisopropylethylamine (2.78 gm, 0.0215 moles) in dichloromethane (30 ml) was added to an ice-cooled solution of 4,6-dichloro-5-methylpyrimidine (2.1 gm, 0.001295 moles) in dichloromethane (10 ml) and the reaction was stirred at 27° C. for 2 h. The reaction mixture was diluted with dichloromethane and washed with water and brine, dried over sodium sulfate and evaporated under reduced pressure. The crude was purified by flash column chromatography (silica gel, 15% ethyl acetate in hexane) to afford the title compound as a white solid (43% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08742117B2
出典データセットuspto-grants-2014_06
ORD IDord-1835680b8e5e4078a7d45ff6eb06ff2d
出典メモuspto-grants-2014_06