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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54561생성일: 2026년 10월 24일

Water → 3-[3-(1-Benzylpiperidin-4-yl)propyl]-5-(quinuclidin-3-yl)-1,2,4-oxadiazole

https://huagongshe.com/ko/reaction/54561

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물Methyl quinuclidine-3-carboxylateHCID 2736953—
반응물4-(1-Benzylpiperidin-4-yl)butanamide oximeHCID 86750726—
용매TetrahydrofuranHCID 8028—
생성물3-[3-(1-Benzylpiperidin-4-yl)propyl]-5-(quinuclidin-3-yl)-1,2,4-oxadiazoleHCID 1995916043.8%

반응 단계

A mixture of 4-(1-benzylpiperidin-4-yl)butanamide oxime (1.0 g), sodium hydride (0.15 g) and molecular sieves 4A (2.0 g) in tetrahydrofuran (50 ml) was stirred at ambient temperature for 30 minutes. To the mixture was added dropwise a solution of methyl 3-quinuclidine carboxylate (0.49 g) in tetrahydrofuran (10 ml) and refluxed for 6 hours. After cooling to room temperature, the mixture was poured into water and extracted with ethyl acetate. The extracts were successively washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was chromatographed on alumina eluting with chloroform to give 3-[3-(1-benzylpiperidin-4-yl)propyl]-5-(quinuclidin-3-yl)-1,2,4-oxadiazole (0.5 g) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05622976
출처 데이터셋uspto-grants-1997_04
ORD IDord-50dec5ff3d014dcb9434de57ce76d919
출처 메모uspto-grants-1997_04