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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1582337생성일: 2026년 10월 27일

Pyridine → 5-Benzyloxycarbonylamino-2-(2-methyl-imidazol-1-yl)fluorobenzene

https://huagongshe.com/reaction/1582337

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Benzyl chloroformateHCID 10387—
반응물Sodium BicarbonateHCID 516892—
반응물3-fluoro-4-(2-methyl-1H-imidazol-1-yl)anilineHCID 21876620—
용매DichloromethaneHCID 6344—
생성물5-Benzyloxycarbonylamino-2-(2-methyl-imidazol-1-yl)fluorobenzeneHCID 2187665193.5%

반응 단계

5-Amino-2-(2-methylimidazol-1-yl)fluorobenzene (34.25 g, 0.179 M) was dissolved in dry dichloromethane (600 ml) under nitrogen, and cooled to −5°. Pyridine (17.7 g, 0.224 M) was added, followed by benzyl chloroformate (33.7 g, 0.197 M) over 20 minutes. The mixture was stirred and the temperature allowed to rise to ambient over 16 hours. Aqueous sodium bicarbonate (5%, 250 ml) was added, the organic layer separated, the aqueous layer re-extracted with dichloromethane (2×300 ml), and combined extracts dried (magnesium sulfate). After filtration and evaporation, the residue was recrystallised from toluene (400 ml) to give title product (54.5 g). NMR (DMSO-d6) δ: 2.13 (s, 3H); 5.18 (s, 2H); 6.89 (s, 1H); 7.17 (s, 1H); 7.41 (overlapping m, 7H); 7.73 (dd, 1H); 10.21 (br, 1H). MS (ESP): 326 (MH+) for C18H16FN3O2

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06734200B1
출처 데이터셋uspto-grants-2004_05
ORD IDord-71348f1e773d4121a09a5c5e9061104a
출처 메모uspto-grants-2004_05