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HRID 1044069作成日:2026年10月26日

3-(Chloromethyl)-5-phenyl-1,2,4-oxadiazole → (3R)-1-((5-phenyl-1,2,4-oxadiazol-3-yl)methyl)-3-(2-phenyl-2-(o-tolylamino)acetoxy)-1-azoniabicyclo[2.2.2]octane chloride

https://huagongshe.com/reaction/1044069

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Chloromethyl)-5-phenyl-1,2,4-oxadiazoleHCID 302154—
反応物(R)-quinuclidin-3-yl 2-phenyl-2-(o-tolylamino)acetateHCID 46840573—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物(3R)-1-((5-phenyl-1,2,4-oxadiazol-3-yl)methyl)-3-(2-phenyl-2-(o-tolylamino)acetoxy)-1-azoniabicyclo[2.2.2]octane chlorideHCID 5476623619.3%

反応手順

3-(Chloromethyl)-5-phenyl-1,2,4-oxadiazole (I45) (79 mg, 0.40 mmol) was added to a solution of (R)-quinuclidin-3-yl 2-phenyl-2-(o-tolylamino)acetate (I23) (129 mg, 0.37 mmol) in acetonitrile (1.2 ml) and ethyl acetate (2.4 ml). The yellow solution was stirred at room temperature for 48 hours. The solution was evaporated, and the residue was purified by flash chromatography (DCM/MeOH=9/1) to obtain (3R)-1-((5-phenyl-1,2,4-oxadiazol-3-yl)methyl)-3-(2-phenyl-2-(o-tolylamino)acetoxy)-1-azoniabicyclo[2.2.2]octane chloride (39 mg, 19% 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-e0eddd1fcbfc4ded98c93537f94d1c73
出典メモuspto-grants-2013_10