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HRID 54561作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物Methyl quinuclidine-3-carboxylateHCID 2736953—
反応物4-(1-Benzylpiperidin-4-yl)butanamide oximeHCID 86750726—
溶媒TetrahydrofuranHCID 8028—
生成物3-[3-(1-Benzylpiperidin-4-yl)propyl]-5-(quinuclidin-3-yl)-1,2,4-oxadiazoleHCID 1995916043.8%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05622976
出典データセットuspto-grants-1997_04
ORD IDord-50dec5ff3d014dcb9434de57ce76d919
出典メモuspto-grants-1997_04