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HRID 1044034作成日:2026年10月27日

Dicyclohexylcarbodiimide → (R)-quinuclidin-3-yl 2-(4-fluorophenyl)-2-(3-fluorophenylamino)acetate

https://huagongshe.com/reaction/1044034

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物3-Quinuclidinol, (-)-HCID 91404—
反応物(4-Fluoro-phenyl)-(3-fluoro-phenylamino)-acetic acidHCID 54890833—
溶媒TetrahydrofuranHCID 8028—
生成物(R)-quinuclidin-3-yl 2-(4-fluorophenyl)-2-(3-fluorophenylamino)acetateHCID 5855696150%

反応手順

A mixture of 2-(4-fluorophenyl)-2-(3-fluorophenylamino)acetic acid (I3) (510 mg, 1.94 mmol), (R)-quinuclidin-3-ol (246 mg, 1.94 mmol), HOBT (356 mg, 2.32 mmol), and DCC (480 mg, 2.32 mmol) in THF (10 ml) was stirred at room temperature overnight (UPLC-MS monitoring: complete conversion). The solvent was evaporated, the crude was dissolved in EtOAc, and the insoluble was removed by filtration. The clear solution was washed with 1N K2CO3 and then with brine. The organic layer was dried over Na2SO4, filtered and evaporated. The crude product was purified by silica gel chromatography (EtOAc/MeOH=8/2) to give (R)-quinuclidin-3-yl 2-(4-fluorophenyl)-2-(3-fluorophenylamino)acetate (360 mg, 50% yield, mixture of diastereomers).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08563577B2
出典データセットuspto-grants-2013_10
ORD IDord-8bfe7afcb6cd4d8db3101347a360df3f
出典メモuspto-grants-2013_10