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HRID 749147作成日:2026年10月25日

3-Bromo-5-phenylpyridine → Ethyl 6-hydroxy-6-(5-phenyl-3-pyridinyl)-3-azabicyclo[3.2.1]octane-3-carboxylate

https://huagongshe.com/reaction/749147

反応式

関与物質

役割名称HCID仕込み量
反応物3-Bromo-5-phenylpyridineHCID 2762904—
反応物Ethyl 6-oxo-3-azabicyclo(3.2.1)octane-3-carboxylateHCID 53302214—
反応物HCID 178418918HCID 178418918—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 6-hydroxy-6-(5-phenyl-3-pyridinyl)-3-azabicyclo[3.2.1]octane-3-carboxylateHCID 5748635614.2%

反応手順

To a solution of 3-bromo-5-phenylpyridine (0.23 g, 1.0 mmol) in THF (5 mL) at ambient temperature was added 2.0 M isopropylmagnesium chloride in THF (0.5 mL). The reaction was stirred for an hour under nitrogen. Then a solution of ethyl 6-oxo-3-azabicyclo[3.2.1]octane-3-carboxylate (0.21 g, 1.0 mmol) in THF (2 mL) was added. The mixture was stirred at ambient temperature overnight, concentrated and quenched with water (1 mL). The mixture was extracted with chloroform (2×10 mL), and the combined extracts were dried over magnesium sulfate, filtered, and concentrated by rotary evaporation. The compound was purified by silica gel column chromatography (1:1 ethyl acetate/hexane) to yield 50 mg of product (13%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07402592B2
出典データセットuspto-grants-2008_07
ORD IDord-89737a3b41aa4b4ca0bdba7e3185248c
出典メモuspto-grants-2008_07