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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 323179생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/323179

반응식

참여 물질

역할이름HCID투입량
반응물2-ChlorobenzimidazoleHCID 78572—
반응물1-Benzyl-4-piperidylamineHCID 415852—
생성물N-(1-Benzylpiperidin-4-yl)-1H-benzimidazol-2-amineHCID 16640950—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211199B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-560697a9c71444b5a7705a1b92fc2c32
출처 메모uspto-grants-2001_04