Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54559생성일: 2026년 10월 25일
2-(1-Benzylpiperidin-4-yl)ethan-1-amine → 5-(Quinuclidin-3-yl)-3-[{2-(1-benzylpiperidin-4-yl)ethyl}carbamoyl]-1,2,4-oxadiazole
https://huagongshe.com/reaction/54559
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2-(1-Benzylpiperidin-4-yl)ethan-1-amine | HCID 1867002 | — |
| 반응물 | 3-Ethoxycarbonyl-5-(quinuclidin-3-yl)-1,2,4-oxadiazole | HCID 14685546 | — |
| 생성물 | 5-(Quinuclidin-3-yl)-3-[{2-(1-benzylpiperidin-4-yl)ethyl}carbamoyl]-1,2,4-oxadiazole | HCID 19959165 | — |
반응 단계
A mixture of 3-ethoxycarbonyl-5-(quinuclidin-3-yl)-1,2,4-oxadiazole (0.2 g) and 1-benzyl-4-(2-aminoethyl)piperidine (0.26 g) was stirred and heated at 100° C. for 2 hours. The cooled mixture was chromatographed on alumina eluting with chloroform to give 5-(quinuclidin-3-yl)-3-[{2-(1-benzylpiperidin-4-yl)ethyl}carbamoyl]-1,2,4-oxadiazole as an oil. The compound was treated with an ethanol solution of hydrogen chloride, the solution was evaporated in vacuo and the residue was powdered with ether to give 5-(quinuclidin-3-yl)-3-[{2-(1-benzylpiperidin-4-yl)ethyl}carbamoyl]-1,2,4-oxadiazole dihydrochloride (0.2 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05622976 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-f63717e5f49849a488f00827e3ebbd54 |
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| 출처 메모 | uspto-grants-1997_04 |
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