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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 572829생성일: 2026년 10월 24일

1H-Benzimidazole-2-carboxaldehyde → (1H-benzimidazol-2-ylmethylene)(1-methylpiperidin-4-yl)amine

https://huagongshe.com/ko/reaction/572829

반응식

참여 물질

역할이름HCID투입량
반응물1H-Benzimidazole-2-carboxaldehydeHCID 76826—
반응물4-Amino-1-methylpiperidineHCID 2737531—
용매EthanolHCID 702—
생성물(1H-benzimidazol-2-ylmethylene)(1-methylpiperidin-4-yl)amineHCID 136335844—

반응 단계

1H-Benzimidazole-2-carboxaldehyde (781 mg, can be prepared according to Fegy, K. Angewandte Chemie Int Ed, 1998, vol. 37, 1270-1273), 4-amino-1-methylpiperidine (781 mg) and 4 Å molecular sieves (15 g) in ethanol (100 mL) are heated under reflux for 4 h. The mixture is then filtered and the filtrate concentrated under reduced pressure to yield (1H-benzimidazol-2-ylmethylene)(1-methylpiperidin-4-yl)amine as a beige solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029357B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-09ad8afe261641bbbf1993569c1c8080
출처 메모uspto-grants-2015_05