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HRID 453692作成日:2026年10月26日

4-Fluoro-2-hydroxyphenacyl bromide → (R)-1-(2-(4-fluoro-2-hydroxyphenyl)-2-oxoethyl)-3-((R)-2-phenyl-2-(phenylamino)acetoxy)-1-azoniabicyclo[2.2.2]octane bromide

https://huagongshe.com/reaction/453692

反応式

関与物質

役割名称HCID仕込み量
反応物4-Fluoro-2-hydroxyphenacyl bromideHCID 26986071—
反応物(R)-((R)-quinuclidin-3-yl) 2-phenyl-2-(phenylamino)acetateHCID 46840261—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物(R)-1-(2-(4-fluoro-2-hydroxyphenyl)-2-oxoethyl)-3-((R)-2-phenyl-2-(phenylamino)acetoxy)-1-azoniabicyclo[2.2.2]octane bromideHCID 8666030291%

反応手順

To a solution of (R)—((R)-quinuclidin-3-yl) 2-phenyl-2-(phenylamino)acetate (diastereomer 1 of I2) (100 mg, 0.30 mmol) in EtOAc (3 ml) and acetonitrile (2 ml), was added 2-bromo-1-(4-fluoro-2-hydroxyphenyl)ethanone (69.3 mg, 0.30 mmol), and the reaction was stirred at room temperature for 15 hours (UPLC-MS: complete conversion). The solvent was evaporated and the crude was triturated in i-Pr2O-EtOAc (1/1) to obtain (R)-1-(2-(4-fluoro-2-hydroxyphenyl)-2-oxoethyl)-3-((R)-2-phenyl-2-(phenylamino)acetoxy)-1-azoniabicyclo[2.2.2]octane bromide (154.0 mg, 91% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08492548B2
出典データセットuspto-grants-2013_07
ORD IDord-34f9f34d961a4db9a2ab4b5197a10bec
出典メモuspto-grants-2013_07