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HRID 323183作成日:2026年10月25日

Ethyl 4-amino-1-piperidinecarboxylate → (1-(2-ethoxyethyl)-1H-benzimidazol-2-yl)(1-ethoxycarbonyl-piperidin-4-yl)amine

https://huagongshe.com/reaction/323183

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 4-amino-1-piperidinecarboxylateHCID 100867—
反応物2-chloro-1-(2-ethoxyethyl)-1H-benzimidazoleHCID 10489356—
溶媒Ethyl acetate hexaneHCID 21226206—
生成物(1-(2-ethoxyethyl)-1H-benzimidazol-2-yl)(1-ethoxycarbonyl-piperidin-4-yl)amineHCID 22009481—

反応条件

温度170 °C

反応手順

Combine 1-(2-ethoxyethyl)-2-chloro-1H-benzimidazole (3.06 g, 13.62 mmol) and ethyl 4-aminopiperidine-1-carboxylate (5.16 g, 30 mmol) and heat to 150° C. After 12 hours, heat to 170° C. After 8 hours, cool the reaction mixture and partition between dichloromethane (150 mL) and water. Separate the layers and extract the organic layer with water. Dry the organic layer over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with ethyl acetate/hexane 1/1 to give (1-(2-ethoxyethyl)-1H-benzimidazol-2-yl)(1-ethoxycarbonyl-piperidin-4-yl)amine: Rf=0.15 (silica gel, ethyl acetate/hexane).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211199B1
出典データセットuspto-grants-2001_04
ORD IDord-f5b1e0492c1340f09d2a6f9c5b78700a
出典メモuspto-grants-2001_04