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HRID 743852作成日:2026年10月26日

4-Benzyloxy [4-(4-pyridyl)piperazin-2-one-1-yl]benzene → 4-[4-(4-Pyridyl)piperazin-2-one-1-yl]phenol

https://huagongshe.com/reaction/743852

反応式

関与物質

役割名称HCID仕込み量
反応物4-Benzyloxy [4-(4-pyridyl)piperazin-2-one-1-yl]benzeneHCID 54227295—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物4-[4-(4-Pyridyl)piperazin-2-one-1-yl]phenolHCID 18918415—

反応手順

To a solution of the product of step (i) (1.1 g) in a mixture of methanol (500 ml) and tetrahydrofuran (100 ml) was added 30% palladium-on-charcoal catalyst (300 mg) and the mixture stirred in an atmosphere of hydrogen at ambient temperature and pressure until all the starting material had been consumed. After removal of the catalyst by filtration, the solvent was evaporated in vacuo to give 4-[4-(4-pyridyl)piperazin-2-one-1-yl]phenol as a colourless solid, essentially one spot by tlc, which was used without further purification or characterisation.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05556977
出典データセットuspto-grants-1996_09
ORD IDord-1e2ddc42f7424b8fbe1cba4ab884d3a6
出典メモuspto-grants-1996_09