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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 402511생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/402511

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4,6-Dichloro-5-methylpyrimidineHCID 818860—
반응물4-(3-Isopropyl-1,2,4-oxadiazol-5-YL)piperidine hydrochlorideHCID 53400827—
용매DichloromethaneHCID 6344—
생성물5-(1-(6-Chloro-5-methylpyrimidin-4-yl)piperidin-4-yl)-3-isopropyl-1,2,4-oxadiazoleHCID 8666161143%

반응 조건

온도27 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08742117B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-1835680b8e5e4078a7d45ff6eb06ff2d
출처 메모uspto-grants-2014_06