돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50871생성일: 2026년 10월 24일

Hydrochloric Acid → (E)-1-(4-Methylpyrid-2-yl)-2-styryl-1H-benzimidazole hydrochloride

https://huagongshe.com/ko/reaction/50871

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-(2-Phenylethenyl)-1h-benzimidazoleHCID 242965—
반응물2-Fluoro-4-methylpyridineHCID 2737403—
반응물(E)-1-(2-pyridyl)-2-styryl-1H-benzimidazoleHCID 9796241—
용매MethanolHCID 887—
생성물(E)-1-(4-Methylpyrid-2-yl)-2-styryl-1H-benzimidazole hydrochlorideHCID 22736699—

반응 단계

Free base of the titled compound was prepared from 2-styryl-1H-benzimidazole and 2-fluoro-4-methylpyridine according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method B). The free base was treated with a 10% methanol solution of hydrogen chloride and concentrated to dryness. The residue was recrystallized from ethyl acetate/n-hexane to give the titled compound. MW: 358.68; mp: 221.0-222.5° C.; 1H-NMR (DMSO) δ: 8.66 (1H, d, J=5.1 Hz), 8.22-8.15 (1H, m), 7.86 (1H, d, J=7.7 Hz), 7.71-7.66 (3H, m), 7.59-7.44 (7H, m), 7.20 (1H, d, J=16.1 Hz), 2.53 (3H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713482B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-e7563a17df69493da72aa3c4147489d9
출처 메모uspto-grants-2004_03