참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Aniline | HCID 6115 | — |
| 반응물 | Phenyl2-hydroxy-11H-benzo[a]carbazole-3-carboxylate | HCID 19933809 | — |
| 용매 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 생성물 | 2-Hydroxy-N-phenyl-11H-benzo[A]carbazole-3-carboxamide | HCID 15596992 | 166.2% |
반응 단계
The phenyl 2-hydroxy-11H-benzo(a)carbazole-3-carboxylate obtained from Example I (5 grams, 14 millimoles), aniline (2.75 grams, 28 millimoles) and 15 milliliters of N-methyl pyrrolidinone were charged in a 100 milliliter 3-neck flask equipped with a magnetic stirrer and a nitrogen inlet. The resulting mixture was stirred and was heated to reflux at an oil bath temperature of ~250° C. under a nitrogen atmosphere. After 3 hours, TLC analysis revealed that all the starting phenyl ester was consumed. The mixture was cooled to room temperature and was poured into a 1 liter beaker containing 400 milliliters of ice cold 5 percent of HCl. The yellow precipitate obtained was isolated by filtration. After washing with water (~200 milliliters) and ~20 milliliters of methanol and vacuum drying, 4.7 grams of crude product resulted. This product was then recrystallized from a mixture of (dimethylformamide) DMF/MeOH/H2O (~30 milliliter each) yielding 4.1 grams (83 percent) of 2-hydroxy-11H-benzo(a)carbazole-3-carboxanilide.
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-e182c9a22cc24161b9e73f13b2aeca9b |
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| 출처 메모 | uspto-grants-1992_07 |
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