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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50874생성일: 2026년 10월 24일

Hydrochloric Acid → (E)-1-(6-Fluoropyridin-2-yl)-2-styryl-1H-benzimidazole hydrochloride

https://huagongshe.com/ko/reaction/50874

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2,6-DifluoropyridineHCID 73934—
반응물2-(2-Phenylethenyl)-1h-benzimidazoleHCID 242965—
반응물(E)-1-(2-pyridyl)-2-styryl-1H-benzimidazoleHCID 9796241—
용매Diethyl EtherHCID 3283—
생성물(E)-1-(6-Fluoropyridin-2-yl)-2-styryl-1H-benzimidazole hydrochlorideHCID 22736651—

반응 단계

Free base of the titled compound was prepared from 2-styryl-1H-benzimidazole and 2,6-difluoropyridine according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method B). The free base was dissolved into diethyl ether and hydrogen chloride gas was passed through the ether solution. Filtration and drying under vacuum yielded the titled compound as pale yellow solids. MW: 351.81; mp: 198.0-205.0° C.; 1H-NMR (DMSO-d6) δ: 8.43 (1H, ddd, J=8.1, 8.1, 8.1 Hz), 8.26 (1H, d, J=16.1 Hz), 7.90-7.80 (2H, m), 7.76-7.69 (2H, m), 7.66-755 (3H, m), 7.54-7.43 (4H, m), 7.28 (1H, d, J=16.1 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713482B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-0bc055b36fde4321966e8386c9ed2cc7
출처 메모uspto-grants-2004_03