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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 582054생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/582054

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 번호US05922737
출처 데이터셋uspto-grants-1999_07
ORD IDord-d4d8e37fcd0a4bc8977bd503b9a5113f
출처 메모uspto-grants-1999_07