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HRID 323179作成日:2026年10月27日

2-Chlorobenzimidazole → N-(1-Benzylpiperidin-4-yl)-1H-benzimidazol-2-amine

https://huagongshe.com/reaction/323179

反応式

関与物質

役割名称HCID仕込み量
反応物2-ChlorobenzimidazoleHCID 78572—
反応物1-Benzyl-4-piperidylamineHCID 415852—
生成物N-(1-Benzylpiperidin-4-yl)-1H-benzimidazol-2-amineHCID 16640950—

反応手順

Combine 2-chloro-1H-benzimidazole (5.0 g, 33 mmol) and 1-benzyl-4-aminopiperidine (14.2 g, 75 mmol) and heat to about 150° C. After 12 hours, cool and partition between water and chloroform, warming if necessary. Separate the layers and add methanol and toluene to the organic layer. Evaporate the organic layer in vacuo to give a solid. Triturate the solid with ethyl acetate, collect by filtration, and dry to give (1H-benzimidazol-2-yl)(1-benzylpiperidin-4-yl)amine: Rf=0.30 (2% triethylamine/10% methanol/ethyl acetate).

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-560697a9c71444b5a7705a1b92fc2c32
出典メモuspto-grants-2001_04