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HRID 454908作成日:2026年10月25日

2-(Azetidin-3-yloxy)-3-(3,6-dihydro-2H-pyran-4-YL)pyridine hydrochloride → 2-(azetidin-3-yloxy)-3-(tetrahydro-2H-pyran-4-yl)pyridine

https://huagongshe.com/reaction/454908

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Azetidin-3-yloxy)-3-(3,6-dihydro-2H-pyran-4-YL)pyridine hydrochlorideHCID 67477450—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物2-(azetidin-3-yloxy)-3-(tetrahydro-2H-pyran-4-yl)pyridineHCID 5854776597.3%

反応条件

温度30 °C

反応手順

A mixture of 2-(azetidin-3-yloxy)-3-(3,6-dihydro-2H-pyran-4-yl)pyridine hydrochloride (see PREPARATION P26.1; 3.5 g, 15 mmol) and wet Pd—C (50%, 1.0 g) in MeOH (100 ml) was stirred under H2 (40 psi) at 30° C. for 3 hours then the reaction mixture was filtered through CELITE® and the filtrate was concentrated in vacuo to give the title compound (3.2 g, 14.6 mmol, yield 91%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08497265B2
出典データセットuspto-grants-2013_07
ORD IDord-bf1e0e2146dd457d8b9c5e9e987f429a
出典メモuspto-grants-2013_07