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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50882생성일: 2026년 10월 25일

Hydrochloric Acid → (E)-2-(2-Methylstyryl)-1-(2-pyridyl)-1H-benzimidazole hydrochloride

https://huagongshe.com/reaction/50882

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물N1-(pyridin-2-yl)benzene-1,2-diamineHCID 752150—
반응물(e)-3-o-Tolylacryloyl chlorideHCID 5706558—
반응물(E)-1-(2-pyridyl)-2-styryl-1H-benzimidazoleHCID 9796241—
용매MethanolHCID 887—
생성물(E)-2-(2-Methylstyryl)-1-(2-pyridyl)-1H-benzimidazole hydrochlorideHCID 22736767—

반응 단계

Free base of the titled compound was prepared from N-(2-pyridyl)-o-phenylenediamine and (E)-2-methylcinnamoyl chloride (Sekiya, T.; Hiranuma, H.; Hata, S.; Mizogami, S.; Hanazuka, M.; Yamada, S. J. Med. Chem., 1983, 26, 411) according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method A). The free base was dissolved with a 10% methanol solution of hydrogen chloride (5 ml). Concentration and recrystallization from ethyl acetate/ethanol yielded the titled compound. MW: 347.85; mp: 212.0-215.0° C.; 1H-NMR (CDCl3) δ: 9.26 (1H, d, J=16.1 Hz), 8.89-8.83 (1H, m), 8.24-8.12 (2H, m), 7.72-7.64 (2H, m), 7.59-7.43 (4H, m), 7.43-7.11 (3H, m), 6.92 (1H, d, J=16.1 Hz), 2.70 (3H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713482B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-788d893663f043699acd01d7179b5f29
출처 메모uspto-grants-2004_03