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HRID 2243314생성일: 2026년 10월 27일

9-Oxofluorene-4-carboxylic acid → 4-(1H-benzimidazol-2-yl)-fluoren-9-one

https://huagongshe.com/reaction/2243314

반응식

참여 물질

역할이름HCID투입량
반응물9-Oxofluorene-4-carboxylic acidHCID 80361—
반응물(2-Aminophenyl)amideHCID 86621027—
용매Acetic AcidHCID 176—
생성물4-(1H-benzimidazol-2-yl)-fluoren-9-oneHCID 59208194—

반응 조건

온도80 °C

반응 단계

In a 50-ml three-necked flask under an argon atmosphere, heat, at 80° C. for 2 hours, a solution of 3 g of the (2-amino-phenyl)amide of 9-oxo-9H-fluorene-4-carboxylic acid obtained in the preceding stage, in 150 ml of acetic acid. After cooling, the precipitate that formed is drained. After purification by silica gel flash chromatography, eluting with mixtures of dichloromethane and ethyl acetate (90-10 then 80-20 and finally 70-30 by volume), we obtain 1.73 g of 4-(1H-benzimidazol-2-yl)-fluoren-9-one in the form of a yellow powder, which is used as it is in the next stage, with the following characteristics:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07674795B2
출처 데이터셋uspto-grants-2010_03
ORD IDord-91000b449a9f4adba18f981a768e6866
출처 메모uspto-grants-2010_03