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HRID 404622作成日:2026年10月26日

4-(Chloromethyl)-2-phenyl-1,3-oxazole → (3R)-3-(2-phenyl-2-(piperidin-1-yl)acetoxy)-1-((2-phenyloxazol-4-yl)methyl)-1-azoniabicyclo[2.2.2]octane chloride

https://huagongshe.com/reaction/404622

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Chloromethyl)-2-phenyl-1,3-oxazoleHCID 3551196—
反応物(R)-quinuclidin-3-yl 2-phenyl-2-(piperidin-1-yl)acetateHCID 71603247—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物(3R)-3-(2-phenyl-2-(piperidin-1-yl)acetoxy)-1-((2-phenyloxazol-4-yl)methyl)-1-azoniabicyclo[2.2.2]octane chlorideHCID 8668888335.1%

反応手順

To a solution of (R)-quinuclidin-3-yl 2-phenyl-2-(piperidin-1-yl)acetate (100 mg, 0.30 mmol) in EtOAc (2 ml) and acetonitrile (1 ml), was added 4-(chloromethyl)-2-phenyloxazole (70.7 mg, 0.36 mmol). The reaction was stirred at room temperature for 30 hours and then the solvents were evaporated. Purification by flash chromatography (DCM/MeOH=9/1) followed by trituration with Et2O afforded (3R)-3-(2-phenyl-2-(piperidin-1-yl)acetoxy)-1-((2-phenyloxazol-4-yl)methyl)-1-azoniabicyclo[2.2.2]octane chloride (55 mg, 34.6% yield) as an off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08748613B2
出典データセットuspto-grants-2014_06
ORD IDord-df65fa96c2e449f494d5b424559754fc
出典メモuspto-grants-2014_06