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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 278022생성일: 2026년 10월 25일

4-Fluorobenzene-1,2-diamine → 5-(5-Fluorobenzimidazol-2-yl)-3-(1-Methylpiperidin-4-yl)-1H-Indole

https://huagongshe.com/reaction/278022

반응식

참여 물질

역할이름HCID투입량
반응물4-Fluorobenzene-1,2-diamineHCID 164584—
반응물5-Formyl-3-(1-Methylpiperidin-4-yl)-1H-IndoleHCID 22626786—
용매NitrobenzeneHCID 7416—
생성물5-(5-Fluorobenzimidazol-2-yl)-3-(1-Methylpiperidin-4-yl)-1H-IndoleHCID 1204181125%

반응 조건

온도155 °C

반응 단계

A solution of 5-formyl-3-(1-methylpiperidin-4-yl)-1H-indole (0.210 g, 0.90 mmol), and 4-fluoro-o-phenylenediamine (0.112 g, 0.90 mmol), in 15 mL of nitrobenzene was heated, with stirring, at 150-160° C. for 24 hours. An additional 0.5 equivalents of the diamine was added, and heating continued for an additional 24 hours. The solution was allowed to cool to room temperature, the solvent was removed in vacuo, and the residue was purified by silica gel chromatography (dichloromethane:methanol 10:1.5) to give the title compound (0.075 g, 25%) as an amorphous tan solid. FDMS m/e=348 (M+). EA calculated for C21H21N4F.¾ H2O: C, 69.69; H, 6.27; N, 15.48. Found: C, 69.61; H, 6.19; N, 15.17.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06358972B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-d4fb135a88004116a74448d718e06f2c
출처 메모uspto-grants-2002_03