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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 963444생성일: 2026년 10월 23일

Sodium hydride → 1-(3,4-Dichiorobenzyl)-2-pyridin-2-yl-1H-benzoimidazole

https://huagongshe.com/ko/reaction/963444

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-(2'-Pyridyl)benzimidazoleHCID 70821—
반응물4-(Bromomethyl)-1,2-dichlorobenzeneHCID 639726—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물1-(3,4-Dichiorobenzyl)-2-pyridin-2-yl-1H-benzoimidazoleHCID 1537622536.7%

반응 단계

2-Pyridin-2-yl-lH-benzoimidazole (1.95 g, 0.01 mol) was dissolved in DMF (50 mL) under an atmosphere of nitrogen. Sodium hydride (60% dispersion in oil, 0.48 g, 0.012 mol) was then added. The reaction mixture was stirred at ambient temperature for 0.5 hour. 3,4-Dichlorobenzyl bromide (2.4 g, 0.01 mol) was then added. The mixture was stirred at 80° C. for a period of 4 hours. The mixture was cooled and diluted with water. The mixture was then extracted with ethyl acetate. The organic extract was washed with water twice then evaporated. The residue was triturated with a small amount of ethyl acetate/hexane. The solid was collected and crystallized from ethanolic hydrogen chloride. The solid was collected to give the title compound (1.3 g, 36.7% yield) as a mono-hydrochloride, light brown solid, m.p. 227°-229° C. Anal. Calcd. for Cl9Hl3Cl2N3-HCl: C, 58.41; H, 3.61; N, 10.76.. Found: C, 58.21; H, 3.54; N, 10.80. Mass spectrum (+FAB; [M+H]+) 354/356/358. 1H-NMR (DMSO-d6 ; 400 MHz) 8 8.78 (d, 1H), 8.52 (d, 1H), 8.15 (t, 1H), 7.9 (d, 1H), 7.77 (d, 1H), 7.65 (d, 2H), 7.54 (d, 1H), 7.48-7.52 (m, 2H), 7.23 (d, 1H), and 6.22 ppm (s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05763473
출처 데이터셋uspto-grants-1998_06
ORD IDord-66f230093170450a8e296d34fd904649
출처 메모uspto-grants-1998_06