참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 9-Oxofluorene-4-carboxylic acid | HCID 80361 | — |
| 반응물 | (2-Aminophenyl)amide | HCID 86621027 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 4-(1H-benzimidazol-2-yl)-fluoren-9-one | HCID 59208194 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07674795B2 |
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| 출처 데이터셋 | uspto-grants-2010_03 |
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| ORD ID | ord-91000b449a9f4adba18f981a768e6866 |
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| 출처 메모 | uspto-grants-2010_03 |
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