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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1991209생성일: 2026년 10월 25일

Triethylamine → 2-(6,7-Difluoro-1H-benzimidazol-1-yl)-N-[3-(trifluoromethyl)phenyl]acetamide

https://huagongshe.com/reaction/1991209

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-bromo-N-[3-(trifluoromethyl)phenyl]acetamideHCID 2317152—
반응물4,5-DifluorobenzimidazoleHCID 2736916—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물2-(6,7-Difluoro-1H-benzimidazol-1-yl)-N-[3-(trifluoromethyl)phenyl]acetamideHCID 1123355725%

반응 단계

To a suspension of 4,5-difluoro-1H-benzimidazole (20 mg, 0.13 mmol) in toluene (260 μL), triethylamine (18 μL, 0.13 mmol) and 2-bromo-N-[3-(trifluoromethyl)phenyl]acetamide (37 mg, 0.13 mmol) were added. The reaction mixture was microwave-irradiated in a sealed vial at 120° C. for 30 min. The vial was cooled, opened and the contents dissolved in 20 mL ethyl acetate. The solution was washed with water (5 mL), saturated aqueous NaHCO3 (5 mL) and brine (5 mL), dried over anhydrous Na2SO4 and concentrated under reduced pressure. Separation of the isomers in the crude product was performed on flash silica column using neat ethyl acetate to yield the title compound (11.3 mg, 25%). MS (ESI) m/z: 355.8 [M+H] 1H NMR (400 MHz, MeOD) δ ppm 5.31 (s, 2H), 7.20 (ddd, J=11.4, 9.0, 7.5 Hz, 1H), 7.40 (d, J=7.8 Hz, 1H), 7.47 (ddd, J=8.9, 3.7, 1.3 Hz, 1H), 7.52 (t, J=8.1 Hz, 1H), 7.79 (d, J=8.8 Hz, 1H), 7.96 (s, 1H), 8.20 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07645784B2
출처 데이터셋uspto-grants-2010_01
ORD IDord-09f8c0b82a214a57862cb7729af5df37
출처 메모uspto-grants-2010_01