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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 4,6-Dichloro-5-methylpyrimidine | HCID 818860 | — |
| 반응물 | 4-(3-Isopropyl-1,2,4-oxadiazol-5-YL)piperidine hydrochloride | HCID 53400827 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 5-(1-(6-Chloro-5-methylpyrimidin-4-yl)piperidin-4-yl)-3-isopropyl-1,2,4-oxadiazole | HCID 86661611 | 43% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08742117B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-1835680b8e5e4078a7d45ff6eb06ff2d |
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| 출처 메모 | uspto-grants-2014_06 |
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