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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 244463생성일: 2026년 10월 26일

1-Methyl-3-(trifluoroacetyl)-1H-indole → 1-(4-Fluorophenyl)-5-[2,2,2-trifluoro-1-hydroxy-1-(1-methyl-1H-indol-3-yl)ethyl]-1,3-dihydrobenzimidazol-2-one

https://huagongshe.com/reaction/244463

반응식

참여 물질

역할이름HCID투입량
반응물1-Methyl-3-(trifluoroacetyl)-1H-indoleHCID 3524388—
반응물5-Bromo-1-(4-fluorophenyl)-1,3-dihydrobenzimidazol-2-oneHCID 59437201—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매DiglymeHCID 8150—
생성물1-(4-Fluorophenyl)-5-[2,2,2-trifluoro-1-hydroxy-1-(1-methyl-1H-indol-3-yl)ethyl]-1,3-dihydrobenzimidazol-2-oneHCID 59437267—

반응 단계

To a chilled (−78° C.) solution of 5-bromo-1-(4-fluorophenyl)-1,3-dihydrobenzimidazol-2-one (152 mg, 0.5 mmol) in anhydrous bis(2-methoxyethyl)ether (10 mL) was added 0.5 mL (1.25 mmol) of a solution of 2.5 M n-butyllithium in hexanes. After 30 minutes, a solution of 2,2,2-trifluoro-1-(1-methyl-1H-indol-3-yl)ethanone (114 mg) in bis(2-methoxyethyl) in 1 mL of ether was added. The mixture stirred for 1 hour and was quenched with ammonium chloride solution. The resulting precipitate was filtered, washed with water, and dried to afford the title compound as an off-white solid. MS m/z 456 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658637B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-6fd87ebebfdd4b239aa9588f5450b660
출처 메모uspto-grants-2014_02