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HRID 54569作成日:2026年10月25日

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 3-[(E)-2-[{2-(1-benzylpiperidin-4-yl)ethyl}carbamoyl]vinyl]-5-(4-cyanophenyl)-1,2,4-oxadiazole fumarate

https://huagongshe.com/reaction/54569

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物2-(1-Benzylpiperidin-4-yl)ethan-1-amineHCID 1867002—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物3-{(E)-2-carboxyvinyl}-5-(4-cyanophenyl)-1,2,4-oxadiazoleHCID 19959232—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物3-[(E)-2-[{2-(1-benzylpiperidin-4-yl)ethyl}carbamoyl]vinyl]-5-(4-cyanophenyl)-1,2,4-oxadiazole fumarateHCID 19959329110.7%

反応手順

To a mixture of 3-{(E)-2-carboxyvinyl}-5-(4-cyanophenyl)-1,2,4-oxadiazole (0.25 g), 2-(1-benzylpiperidin-4-yl)ethylamine (0.23 g) and 1-hydroxybenzotriazole hydrate (0.16 g) in N,N-dimethylformamide (5 ml) was added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (0.20 ml) at 5° C. After stirring for 1 hour at ambient temperature, the mixture was poured into water and extracted with ethyl acetate. The extract was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was chromatographed on silica eluting with 2% methanol in chloroform and the fractions containing the object compound were evaporated in vacuo. The residue was dissolved in a solution of fumaric acid (71 mg) in ethanol to give 3-[(E)-2-[{2-(1-benzylpiperidin-4-yl)ethyl}carbamoyl]vinyl]-5-(4-cyanophenyl)-1,2,4-oxadiazole fumarate (0.32 g ).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05622976
出典データセットuspto-grants-1997_04
ORD IDord-7a2c6b62bcb34a1096833904cd486b42
出典メモuspto-grants-1997_04