참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Aniline | HCID 6115 | — |
| 반응물 | Phenyl2-hydroxy-11H-benzo[a]carbazole-3-carboxylate | HCID 19933809 | — |
| 생성물 | 2-Hydroxy-N-phenyl-11H-benzo[A]carbazole-3-carboxamide | HCID 15596992 | — |
반응 단계
The aromatic ester is reacted with an aniline in a solvent and heating to form the anilide product. The reaction temperature can be varied to from about 140° C. to about 280° C. or above. Specifically, phenyl 2-hydroxy-11H-benzo(a)carbazole-3-carboxylate can be reacted with aniline in methyl N-pyrrolidinone at about 250° C. The ratio of the phenyl ester to aniline can vary, for example, from about 1:1 equivalent and up to about 20 equivalents. After the reaction is completed, the product mixture is cooled to room temperature, about 25° C., and discharged into an acidic aqueous solution, such as a 5 percent HCl ice cold solution. The precipitated anilide product, such as 2-hydroxy-11H-benzo(a)carbazole-3-carboxanilide, is isolated by filtration and washed with water and methanol. Purification can be accomplished by first dissolving the crude product in a hot solvent, such as DMF, and then precipitating the product by adding water or methanol, or a mixture of methanol and water. The purified product is then characterized by melting point, IR, mass spectrometry, NMR spectroscopy, especially 13C NMR as well as elemental analysis.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05130443 |
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| 출처 데이터셋 | uspto-grants-1992_07 |
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| ORD ID | ord-5dad97ebca7d4ec59c9dc23aec51fe7d |
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| 출처 메모 | uspto-grants-1992_07 |
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